Sally Camper, Ph. D. - Publications

Human Genetics University of Michigan, Ann Arbor, Ann Arbor, MI 
Pituitary developement

195 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Brinkmeier ML, Bando H, Camarano AC, Fujio S, Yoshimoto K, de Souza FSJ, Camper SA. Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors. The Journal of Clinical Investigation. PMID 32453714 DOI: 10.1172/JCI136745  0.4
2019 Garnai SJ, Brinkmeier ML, Emery B, Aleman TS, Pyle LC, Veleva-Rotse B, Sisk RA, Rozsa FW, Ozel AB, Li JZ, Moroi SE, Archer SM, Lin CM, Sheskey S, Wiinikka-Buesser L, ... ... Camper SA, et al. Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. Plos Genetics. 15: e1008130. PMID 31048900 DOI: 10.1371/journal.pgen.1008130  0.4
2019 Mortensen AH, Fang Q, Fleming MT, Jones TJ, Daly AZ, Johnson KR, Camper SA. Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 30778664 DOI: 10.1007/s00335-019-09792-6  0.6
2018 Cheung LYM, George AS, McGee SR, Daly AZ, Brinkmeier ML, Ellsworth BS, Camper SA. Single-cell RNA sequencing reveals novel markers of male pituitary stem cells and hormone-producing cell-types. Endocrinology. PMID 30335147 DOI: 10.1210/en.2018-00750  0.4
2018 Pérez Millán MI, Vishnopolska SA, Daly AZ, Bustamante JP, Seilicovich A, Bergadá I, Braslavsky D, Keselman AC, Lemons RM, Mortensen AH, Marti MA, Camper SA, Kitzman JO. Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism. Molecular Genetics & Genomic Medicine. PMID 29739035 DOI: 10.1002/mgg3.395  0.6
2016 Fang Q, George AS, Brinkmeier ML, Mortensen AH, Gergics P, Cheung LY, Daly AZ, Ajmal A, Millán MI, Ozel AB, Kitzman JO, Mills RE, Li JZ, Camper SA. Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era. Endocrine Reviews. er20161101. PMID 27828722 DOI: 10.1210/er.2016-1101  0.6
2016 Mortensen AH, Camper SA. Cocaine-and Amphetamine Regulated Transcript (CART) Peptide Is Expressed in Precursor Cells and Somatotropes of the Mouse Pituitary Gland. Plos One. 11: e0160068. PMID 27685990 DOI: 10.1371/journal.pone.0160068  0.6
2016 Cheung LY, Davis SW, Brinkmeier ML, Camper SA, Pérez-Millán MI. Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways. Molecular and Cellular Endocrinology. PMID 27650955 DOI: 10.1016/j.mce.2016.09.016  0.4
2016 Pérez Millán MI, Brinkmeier ML, Mortensen AH, Camper SA. PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells. Elife. 5. PMID 27351100 DOI: 10.7554/eLife.14470  0.6
2016 Davis SW, Mortensen AH, Keisler JL, Zacharias AL, Gage PJ, Yamamura K, Camper SA. β-catenin is required in the neural crest and mesencephalon for pituitary gland organogenesis. Bmc Developmental Biology. 16: 16. PMID 27184910 DOI: 10.1186/s12861-016-0118-9  0.6
2016 Fang Q, Benedetti AF, Ma Q, Gregory L, Li JZ, Dattani M, Sadeghi-Nejad A, Arnhold IJ, de Mendonça BB, Camper SA, Carvalho LR. HESX1 Mutations in Patients with Congenital Hypopituitarism: Variable Phenotypes with the Same Genotype. Clinical Endocrinology. PMID 27000987 DOI: 10.1111/cen.13067  0.96
2016 Davis SW, Keisler JL, Pérez-Millán MI, Schade V, Camper SA. All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from Prop1 expressing progenitors. Endocrinology. en20151862. PMID 26812162 DOI: 10.1210/en.2015-1862  0.96
2015 Geister KA, Brinkmeier ML, Cheung LY, Wendt J, Oatley MJ, Burgess DL, Kozloff KM, Cavalcoli JD, Oatley JM, Camper SA. LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice. Plos Genetics. 11: e1005569. PMID 26496357 DOI: 10.1371/journal.pgen.1005569  0.96
2015 Brinkmeier ML, Geister KA, Jones M, Waqas M, Maillard I, Camper SA. The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice. Biology of Reproduction. PMID 26333994 DOI: 10.1095/biolreprod.115.131516  0.96
2015 Castinetti F, Brinkmeier ML, Mortensen AH, Vella KR, Gergics P, Brue T, Hollenberg AN, Gan L, Camper SA. ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism. Molecular Endocrinology (Baltimore, Md.). 29: 1510-21. PMID 26296153 DOI: 10.1210/me.2015-1192  0.96
2015 Polk RC, Gergics P, Steimle JD, Li H, Moskowitz IP, Camper SA, Reeves RH. The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model. Bmc Developmental Biology. 15: 30. PMID 26208718 DOI: 10.1186/s12861-015-0080-y  0.96
2015 Geister KA, Camper SA. Advances in Skeletal Dysplasia Genetics. Annual Review of Genomics and Human Genetics. 16: 199-227. PMID 25939055 DOI: 10.1146/annurev-genom-090314-045904  0.96
2015 Jones M, Chase J, Brinkmeier M, Xu J, Weinberg DN, Schira J, Friedman A, Malek S, Grembecka J, Cierpicki T, Dou Y, Camper SA, Maillard I. Ash1l controls quiescence and self-renewal potential in hematopoietic stem cells. The Journal of Clinical Investigation. 125: 2007-20. PMID 25866973 DOI: 10.1172/JCI78124  0.96
2015 Gergics P, Brinkmeier ML, Camper SA. Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia. Molecular Endocrinology (Baltimore, Md.). 29: 597-612. PMID 25668206 DOI: 10.1210/me.2014-1380  0.96
2015 Wang H, Graham I, Hastings R, Gunewardena S, Brinkmeier ML, Conn PM, Camper SA, Kumar TR. Gonadotrope-specific deletion of Dicer results in severely suppressed gonadotropins and fertility defects. The Journal of Biological Chemistry. 290: 2699-714. PMID 25525274 DOI: 10.1074/jbc.M114.621565  0.96
2015 Mortensen AH, Schade V, Lamonerie T, Camper SA. Deletion of OTX2 in neural ectoderm delays anterior pituitary development. Human Molecular Genetics. 24: 939-53. PMID 25315894 DOI: 10.1093/hmg/ddu506  0.96
2014 Millán MIP, Camper SA. The Biology of Pituitary Stem Cells Cellular Endocrinology in Health and Disease. 55-63. DOI: 10.1016/B978-0-12-408134-5.00004-4  0.96
2013 de Pater E, Kaimakis P, Vink CS, Yokomizo T, Yamada-Inagawa T, van der Linden R, Kartalaei PS, Camper SA, Speck N, Dzierzak E. Gata2 is required for HSC generation and survival. The Journal of Experimental Medicine. 210: 2843-50. PMID 24297996 DOI: 10.1084/jem.20130751  0.96
2013 Davis SW, Ellsworth BS, Peréz Millan MI, Gergics P, Schade V, Foyouzi N, Brinkmeier ML, Mortensen AH, Camper SA. Pituitary gland development and disease: from stem cell to hormone production. Current Topics in Developmental Biology. 106: 1-47. PMID 24290346 DOI: 10.1016/B978-0-12-416021-7.00001-8  0.96
2013 Pérez-Millán MI, Zeidler MG, Saunders TL, Camper SA, Davis SW. Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes. Genesis (New York, N.Y. : 2000). 51: 785-92. PMID 23996951 DOI: 10.1002/dvg.22425  0.96
2013 Geister KA, Brinkmeier ML, Hsieh M, Faust SM, Karolyi IJ, Perosky JE, Kozloff KM, Conti M, Camper SA. A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type. Human Molecular Genetics. 22: 345-57. PMID 23065701 DOI: 10.1093/hmg/dds432  0.96
2012 Lim KC, Hosoya T, Brandt W, Ku CJ, Hosoya-Ohmura S, Camper SA, Yamamoto M, Engel JD. Conditional Gata2 inactivation results in HSC loss and lymphatic mispatterning. The Journal of Clinical Investigation. 122: 3705-17. PMID 22996665 DOI: 10.1172/JCI61619  0.96
2012 Fang Q, Giordimaina AM, Dolan DF, Camper SA, Mustapha M. Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment. Journal of the Association For Research in Otolaryngology : Jaro. 13: 173-84. PMID 22143287 DOI: 10.1007/s10162-011-0302-3  0.96
2011 Nasonkin IO, Ward RD, Bavers DL, Beuschlein F, Mortensen AH, Keegan CE, Hammer GD, Camper SA. Aged PROP1 deficient dwarf mice maintain ACTH production. Plos One. 6: e28355. PMID 22145038 DOI: 10.1371/journal.pone.0028355  0.96
2011 Castinetti F, Brinkmeier ML, Gordon DF, Vella KR, Kerr JM, Mortensen AH, Hollenberg A, Brue T, Ridgway EC, Camper SA. PITX2 AND PITX1 regulate thyrotroph function and response to hypothyroidism. Molecular Endocrinology (Baltimore, Md.). 25: 1950-60. PMID 21964592 DOI: 10.1210/me.2010-0388  0.96
2011 Fang Q, Longo-Guess C, Gagnon LH, Mortensen AH, Dolan DF, Camper SA, Johnson KR. A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice. Genetics. 189: 665-73. PMID 21840860 DOI: 10.1534/genetics.111.130633  0.96
2011 Mortensen AH, MacDonald JW, Ghosh D, Camper SA. Candidate genes for panhypopituitarism identified by gene expression profiling. Physiological Genomics. 43: 1105-16. PMID 21828248 DOI: 10.1152/physiolgenomics.00080.2011  0.96
2011 Camper SA. Beta-catenin stimulates pituitary stem cells to form aggressive tumors. Proceedings of the National Academy of Sciences of the United States of America. 108: 11303-4. PMID 21719710 DOI: 10.1073/pnas.1108275108  0.96
2011 Castinetti F, Davis SW, Brue T, Camper SA. Pituitary stem cell update and potential implications for treating hypopituitarism. Endocrine Reviews. 32: 453-71. PMID 21493869 DOI: 10.1210/er.2010-0011  0.96
2011 Davis SW, Mortensen AH, Camper SA. Birthdating studies reshape models for pituitary gland cell specification. Developmental Biology. 352: 215-27. PMID 21262217 DOI: 10.1016/j.ydbio.2011.01.010  0.96
2011 Gay D, Saunders T, Camper S, Weigert M. Receptor editing: an approach by autoreactive B cells to escape tolerance. The Journal of Experimental Medicine. 1993. 177: 999-1008. Journal of Immunology (Baltimore, Md. : 1950). 186: 1303-12. PMID 21248268  0.96
2010 Bjork BC, Fujiwara Y, Davis SW, Qiu H, Saunders TL, Sandy P, Orkin S, Camper SA, Beier DR. A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development. Plos One. 5: e14375. PMID 21179568 DOI: 10.1371/journal.pone.0014375  0.96
2010 Carvalho LR, Brinkmeier ML, Castinetti F, Ellsworth BS, Camper SA. Corepressors TLE1 and TLE3 interact with HESX1 and PROP1. Molecular Endocrinology (Baltimore, Md.). 24: 754-65. PMID 20181723 DOI: 10.1210/me.2008-0359  0.96
2010 Davis SW, Castinetti F, Carvalho LR, Ellsworth BS, Potok MA, Lyons RH, Brinkmeier ML, Raetzman LT, Carninci P, Mortensen AH, Hayashizaki Y, Arnhold IJ, Mendonça BB, Brue T, Camper SA. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Molecular and Cellular Endocrinology. 323: 4-19. PMID 20025935 DOI: 10.1016/j.mce.2009.12.012  0.96
2009 Davis SW, Potok MA, Brinkmeier ML, Carninci P, Lyons RH, MacDonald JW, Fleming MT, Mortensen AH, Egashira N, Ghosh D, Steel KP, Osamura RY, Hayashizaki Y, Camper SA. Genetics, gene expression and bioinformatics of the pituitary gland. Hormone Research. 71: 101-15. PMID 19407506 DOI: 10.1159/000192447  0.96
2009 Mustapha M, Fang Q, Gong TW, Dolan DF, Raphael Y, Camper SA, Duncan RK. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 1212-23. PMID 19176829 DOI: 10.1523/JNEUROSCI.4957-08.2009  0.96
2009 Brinkmeier ML, Davis SW, Carninci P, MacDonald JW, Kawai J, Ghosh D, Hayashizaki Y, Lyons RH, Camper SA. Discovery of transcriptional regulators and signaling pathways in the developing pituitary gland by bioinformatic and genomic approaches. Genomics. 93: 449-60. PMID 19121383 DOI: 10.1016/j.ygeno.2008.11.010  0.96
2009 Nasonkin IO, Potok MA, Camper SA. Cre-mediated recombination in pituitary somatotropes. Genesis (New York, N.Y. : 2000). 47: 55-60. PMID 19039787 DOI: 10.1002/dvg.20462  0.96
2008 Charles MA, Mortensen AH, Potok MA, Camper SA. Pitx2 deletion in pituitary gonadotropes is compatible with gonadal development, puberty, and fertility. Genesis (New York, N.Y. : 2000). 46: 507-14. PMID 18802953 DOI: 10.1002/dvg.20398  0.96
2008 Egashira N, Minematsu T, Miyai S, Takekoshi S, Camper SA, Osamura RY. Pituitary changes in Prop1 transgenic mice: hormone producing tumors and signet-ring type gonadotropes. Acta Histochemica Et Cytochemica. 41: 47-57. PMID 18636109 DOI: 10.1267/ahc.08007  0.96
2008 Potok MA, Cha KB, Hunt A, Brinkmeier ML, Leitges M, Kispert A, Camper SA. WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 1006-20. PMID 18351662 DOI: 10.1002/dvdy.21511  0.96
2008 Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U. SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. Plos One. 3: e1709. PMID 18320030 DOI: 10.1371/journal.pone.0001709  0.96
2008 Ellsworth BS, Butts DL, Camper SA. Mechanisms underlying pituitary hypoplasia and failed cell specification in Lhx3-deficient mice. Developmental Biology. 313: 118-29. PMID 18037398 DOI: 10.1016/j.ydbio.2007.10.006  0.96
2007 Brinkmeier ML, Potok MA, Davis SW, Camper SA. TCF4 deficiency expands ventral diencephalon signaling and increases induction of pituitary progenitors. Developmental Biology. 311: 396-407. PMID 17919533 DOI: 10.1016/j.ydbio.2007.08.046  0.96
2007 Karolyi IJ, Dootz GA, Halsey K, Beyer L, Probst FJ, Johnson KR, Parlow AF, Raphael Y, Dolan DF, Camper SA. Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 596-608. PMID 17899304 DOI: 10.1007/s00335-007-9038-0  0.96
2007 Hughes ED, Qu YY, Genik SJ, Lyons RH, Pacheco CD, Lieberman AP, Samuelson LC, Nasonkin IO, Camper SA, Van Keuren ML, Saunders TL. Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 549-58. PMID 17828574 DOI: 10.1007/s00335-007-9054-0  0.96
2007 Mustapha M, Beyer LA, Izumikawa M, Swiderski DL, Dolan DF, Raphael Y, Camper SA. Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants. Journal of the Association For Research in Otolaryngology : Jaro. 8: 329-37. PMID 17619105 DOI: 10.1007/s10162-007-0083-x  0.96
2007 Ward RD, Davis SW, Cho M, Esposito C, Lyons RH, Cheng JF, Rubin EM, Rhodes SJ, Raetzman LT, Smith TP, Camper SA. Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 521-37. PMID 17557180 DOI: 10.1007/s00335-007-9008-6  0.96
2007 L'Honoré A, Coulon V, Marcil A, Lebel M, Lafrance-Vanasse J, Gage P, Camper S, Drouin J. Sequential expression and redundancy of Pitx2 and Pitx3 genes during muscle development. Developmental Biology. 307: 421-33. PMID 17540357 DOI: 10.1016/j.ydbio.2007.04.034  0.96
2007 Raetzman LT, Cai JX, Camper SA. Hes1 is required for pituitary growth and melanotrope specification. Developmental Biology. 304: 455-66. PMID 17367776 DOI: 10.1016/j.ydbio.2006.11.010  0.96
2007 Davis SW, Camper SA. Noggin regulates Bmp4 activity during pituitary induction. Developmental Biology. 305: 145-60. PMID 17359964 DOI: 10.1016/j.ydbio.2007.02.001  0.96
2007 Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system. The European Journal of Neuroscience. 25: 999-1005. PMID 17331196 DOI: 10.1111/j.1460-9568.2007.05332.x  0.96
2007 Savage JJ, Mullen RD, Sloop KW, Colvin SC, Camper SA, Franklin CL, Rhodes SJ. Transgenic mice expressing LHX3 transcription factor isoforms in the pituitary: effects on the gonadotrope axis and sex-specific reproductive disease. Journal of Cellular Physiology. 212: 105-17. PMID 17311285 DOI: 10.1002/jcp.21010  0.96
2006 Ellsworth BS, Egashira N, Haller JL, Butts DL, Cocquet J, Clay CM, Osamura RY, Camper SA. FOXL2 in the pituitary: molecular, genetic, and developmental analysis. Molecular Endocrinology (Baltimore, Md.). 20: 2796-805. PMID 16840539 DOI: 10.1210/me.2005-0303  0.96
2006 Raetzman LT, Wheeler BS, Ross SA, Thomas PQ, Camper SA. Persistent expression of Notch2 delays gonadotrope differentiation. Molecular Endocrinology (Baltimore, Md.). 20: 2898-908. PMID 16840533 DOI: 10.1210/me.2005-0394  0.96
2006 Gong TW, Karolyi IJ, Macdonald J, Beyer L, Raphael Y, Kohrman DC, Camper SA, Lomax MI. Age-related changes in cochlear gene expression in normal and shaker 2 mice. Journal of the Association For Research in Otolaryngology : Jaro. 7: 317-28. PMID 16794912 DOI: 10.1007/s10162-006-0046-7  0.96
2006 Solomon NM, Dackor J, Camper SA. 19th International Mouse Genome Conference. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 355-62. PMID 16688525 DOI: 10.1007/s00335-005-1900-3  0.96
2006 Kanzaki S, Beyer L, Karolyi IJ, Dolan DF, Fang Q, Probst FJ, Camper SA, Raphael Y. Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice. Hearing Research. 214: 37-44. PMID 16580798 DOI: 10.1016/j.heares.2006.01.017  0.96
2006 Ward RD, Stone BM, Raetzman LT, Camper SA. Cell proliferation and vascularization in mouse models of pituitary hormone deficiency. Molecular Endocrinology (Baltimore, Md.). 20: 1378-90. PMID 16556738 DOI: 10.1210/me.2005-0409  0.96
2006 Charles MA, Saunders TL, Wood WM, Owens K, Parlow AF, Camper SA, Ridgway EC, Gordon DF. Pituitary-specific Gata2 knockout: effects on gonadotrope and thyrotrope function. Molecular Endocrinology (Baltimore, Md.). 20: 1366-77. PMID 16543408 DOI: 10.1210/me.2005-0378  0.96
2006 Vesper AH, Raetzman LT, Camper SA. Role of prophet of Pit1 (PROP1) in gonadotrope differentiation and puberty. Endocrinology. 147: 1654-63. PMID 16384867 DOI: 10.1210/en.2005-1080  0.96
2005 Stewart L, Potok MA, Camper SA, Stifani S. Runx1 expression defines a subpopulation of displaced amacrine cells in the developing mouse retina. Journal of Neurochemistry. 94: 1739-45. PMID 16026391 DOI: 10.1111/j.1471-4159.2005.03336.x  0.96
2005 Meehan TP, Harmon BG, Overcast ME, Yu KK, Camper SA, Puett D, Narayan P. Gonadal defects and hormonal alterations in transgenic mice expressing a single chain human chorionic gonadotropin-lutropin receptor complex. Journal of Molecular Endocrinology. 34: 489-503. PMID 15821112 DOI: 10.1677/jme.1.01669  0.96
2005 Charles MA, Suh H, Hjalt TA, Drouin J, Camper SA, Gage PJ. PITX genes are required for cell survival and Lhx3 activation. Molecular Endocrinology (Baltimore, Md.). 19: 1893-903. PMID 15761027 DOI: 10.1210/me.2005-0052  0.96
2005 Ward RD, Raetzman LT, Suh H, Stone BM, Nasonkin IO, Camper SA. Role of PROP1 in pituitary gland growth. Molecular Endocrinology (Baltimore, Md.). 19: 698-710. PMID 15591534 DOI: 10.1210/me.2004-0341  0.96
2004 Nasonkin IO, Ward RD, Raetzman LT, Seasholtz AF, Saunders TL, Gillespie PJ, Camper SA. Pituitary hypoplasia and respiratory distress syndrome in Prop1 knockout mice. Human Molecular Genetics. 13: 2727-35. PMID 15459176 DOI: 10.1093/hmg/ddh311  0.96
2004 Cha KB, Karolyi IJ, Hunt A, Wenglikowski AM, Wilkinson JE, Dolan DF, Dootz G, Finnegan AA, Seasholtz AF, Hankenson KD, Siracusa LD, Camper SA. Skeletal dysplasia and male infertility locus on mouse chromosome 9. Genomics. 83: 951-60. PMID 15177549 DOI: 10.1016/j.ygeno.2003.12.020  0.96
2004 Cha KB, Douglas KR, Potok MA, Liang H, Jones SN, Camper SA. WNT5A signaling affects pituitary gland shape. Mechanisms of Development. 121: 183-94. PMID 15037319 DOI: 10.1016/j.mod.2003.12.002  0.96
2004 Camper SA. Sox3 and sexual dysfunction: it's in the head. Nature Genetics. 36: 217-9. PMID 14988719 DOI: 10.1038/ng0304-217  0.96
2004 Martin DM, Skidmore JM, Philips ST, Vieira C, Gage PJ, Condie BG, Raphael Y, Martinez S, Camper SA. PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain. Developmental Biology. 267: 93-108. PMID 14975719 DOI: 10.1016/j.ydbio.2003.10.035  0.96
2004 Raetzman LT, Ross SA, Cook S, Dunwoodie SL, Camper SA, Thomas PQ. Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression Developmental Biology. 265: 329-340. PMID 14732396 DOI: 10.1016/j.ydbio.2003.09.033  0.96
2003 Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. Human Molecular Genetics. 12: 2797-805. PMID 12966030 DOI: 10.1093/hmg/ddg308  0.96
2003 Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, ... Camper SA, et al. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Human Molecular Genetics. 12: 2049-61. PMID 12913076 DOI: 10.1093/hmg/ddg210  0.96
2003 Brinkmeier ML, Potok MA, Cha KB, Gridley T, Stifani S, Meeldijk J, Clevers H, Camper SA. TCF and Groucho-related genes influence pituitary growth and development. Molecular Endocrinology (Baltimore, Md.). 17: 2152-61. PMID 12907761 DOI: 10.1210/me.2003-0225  0.96
2003 Carninci P, Waki K, Shiraki T, Konno H, Shibata K, Itoh M, Aizawa K, Arakawa T, Ishii Y, Sasaki D, Bono H, Kondo S, Sugahara Y, Saito R, Osato N, ... ... Camper S, et al. Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Genome Research. 13: 1273-89. PMID 12819125 DOI: 10.1101/gr.1119703  0.96
2003 Keegan CE, Camper SA. Mouse knockout solves endocrine puzzle and promotes new pituitary lineage model. Genes & Development. 17: 677-82. PMID 12651886 DOI: 10.1101/gad.1085903  0.96
2003 Suszko MI, Lo DJ, Suh H, Camper SA, Woodruff TK. Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin. Molecular Endocrinology (Baltimore, Md.). 17: 318-32. PMID 12554780 DOI: 10.1210/me.2002-0081  0.96
2003 Marcil A, Dumontier E, Chamberland M, Camper SA, Drouin J. Pitx1 and Pitx2 are required for development of hindlimb buds. Development (Cambridge, England). 130: 45-55. PMID 12441290 DOI: 10.1242/dev.00192  0.96
2002 Martin DM, Skidmore JM, Fox SE, Gage PJ, Camper SA. Pitx2 distinguishes subtypes of terminally differentiated neurons in the developing mouse neuroepithelium. Developmental Biology. 252: 84-99. PMID 12453462 DOI: 10.1006/dbio.2002.0835  0.96
2002 Raetzman LT, Ward R, Camper SA. Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia. Development (Cambridge, England). 129: 4229-39. PMID 12183375  0.96
2002 Martin DM, Probst FJ, Fox SE, Schimmenti LA, Semina EV, Hefner MA, Belmont JW, Camper SA. Exclusion of PITX2 mutations as a major cause of CHARGE association. American Journal of Medical Genetics. 111: 27-30. PMID 12124729 DOI: 10.1002/ajmg.10473  0.96
2002 Kanzaki S, Ogawa K, Camper SA, Raphael Y. Transgene expression in neonatal mouse inner ear explants mediated by first and advanced generation adenovirus vectors. Hearing Research. 169: 112-20. PMID 12121744 DOI: 10.1016/S0378-5955(02)00347-7  0.96
2002 Suh H, Gage PJ, Drouin J, Camper SA. Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification. Development (Cambridge, England). 129: 329-37. PMID 11807026  0.96
2001 Douglas KR, Brinkmeier ML, Kennell JA, Eswara P, Harrison TA, Patrianakos AI, Sprecher BS, Potok MA, Lyons RH, MacDougald OA, Camper SA. Identification of members of the Wnt signaling pathway in the embryonic pituitary gland. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 843-51. PMID 11845287 DOI: 10.1007/s00335-001-2076-0  0.96
2001 Brinkmeier ML, Stahl JH, Gordon DF, Ross BD, Sarapura VD, Dowding JM, Kendall SK, Lloyd RV, Ridgway EC, Camper SA. Thyroid hormone-responsive pituitary hyperplasia independent of somatostatin receptor 2. Molecular Endocrinology (Baltimore, Md.). 15: 2129-36. PMID 11731614 DOI: 10.1210/mend.15.12.0744  0.96
2001 Cushman LJ, Camper SA. Molecular basis of pituitary dysfunction in mouse and human. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 485-94. PMID 11420609 DOI: 10.1007/s003350040002  0.96
2001 Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Hypomorphic phenotype in mice with pituitary-specific knockout of steroidogenic factor 1. Genesis (New York, N.Y. : 2000). 30: 65-9. PMID 11416865 DOI: 10.1002/gene.1034  0.96
2001 Cushman LJ, Watkins-Chow DE, Brinkmeier ML, Raetzman LT, Radak AL, Lloyd RV, Camper SA. Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility. Human Molecular Genetics. 10: 1141-53. PMID 11371507  0.96
2001 Seasholtz AF, Burrows HL, Karolyi IJ, Camper SA. Mouse models of altered CRH-binding protein expression. Peptides. 22: 743-51. PMID 11337087 DOI: 10.1016/S0196-9781(01)00387-4  0.96
2001 Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, et al. Sequence interpretation. Functional annotation of mouse genome sequences. Science (New York, N.Y.). 291: 1251-5. PMID 11233449 DOI: 10.1126/science.1058244  0.96
2001 Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function. Development (Cambridge, England). 128: 147-54. PMID 11124111  0.96
2000 Beyer LA, Odeh H, Probst FJ, Lambert EH, Dolan DF, Camper SA, Kohrman DC, Raphael Y. Hair cells in the inner ear of the pirouette and shaker 2 mutant mice. Journal of Neurocytology. 29: 227-40. PMID 11276175  0.96
2000 Douglas KR, Camper SA. Partial transcriptome of the developing pituitary gland. Genomics. 70: 335-46. PMID 11161784 DOI: 10.1006/geno.2000.6400  0.96
2000 Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Mouse embryonic stem (ES) cell lines established from neuronal cell-derived cloned blastocysts Genesis. 28: 156-163. PMID 11105058 DOI: 10.1002/1526-968X(200011/12)28:3/4<156::AID-GENE100>3.0.CO;2-T  0.96
2000 Martin DM, Probst FJ, Camper SA, Petty EM. Characterisation and genetic mapping of a new X linked deafness syndrome. Journal of Medical Genetics. 37: 836-41. PMID 11073537  0.96
2000 Anderson DW, Probst FJ, Belyantseva IA, Fridell RA, Beyer L, Martin DM, Wu D, Kachar B, Friedman TB, Raphael Y, Camper SA. The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells. Human Molecular Genetics. 9: 1729-38. PMID 10915760  0.96
2000 Brown NS, Smart A, Sharma V, Brinkmeier ML, Greenlee L, Camper SA, Jensen DR, Eckel RH, Krezel W, Chambon P, Haugen BR. Thyroid hormone resistance and increased metabolic rate in the RXR-γ- deficient mouse Journal of Clinical Investigation. 106: 73-79. PMID 10880050 DOI: 10.1172/JCI9422  0.96
2000 Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15. Advances in Oto-Rhino-Laryngology. 56: 131-44. PMID 10868225  0.96
1999 Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, et al. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics. 61: 243-58. PMID 10552926 DOI: 10.1006/geno.1999.5976  0.96
1999 Burrows HL, Douglas KR, Seasholtz AF, Camper SA. Genealogy of the Anterior Pituitary Gland: Tracing a Family Tree. Trends in Endocrinology and Metabolism: Tem. 10: 343-352. PMID 10511693 DOI: 10.1016/S1043-2760(99)00189-7  0.96
1999 Karolyi IJ, Burrows HL, Ramesh TM, Nakajima M, Lesh JS, Seong E, Camper SA, Seasholtz AF. Altered anxiety and weight gain in corticotropin-releasing hormone-binding protein-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 96: 11595-600. PMID 10500222 DOI: 10.1073/pnas.96.20.11595  0.96
1999 Gage PJ, Suh H, Camper SA. Dosage requirement of Pitx2 for development of multiple organs Development. 126: 4643-4651. PMID 10498698  0.96
1999 Probst FJ, Camper SA. The role of mouse mutants in the identification of human hereditary hearing loss genes. Hearing Research. 130: 1-6. PMID 10320095 DOI: 10.1016/S0378-5955(98)00231-7  0.96
1999 Stahl JH, Kendall SK, Brinkmeier ML, Greco TL, Watkins-Chow DE, Campos-Barros A, Lloyd RV, Camper SA. Thyroid hormone is essential for pituitary somatotropes and lactotropes. Endocrinology. 140: 1884-92. PMID 10098528 DOI: 10.1210/endo.140.4.6627  0.96
1999 Probst FJ, Chen KS, Zhao Q, Wang A, Friedman TB, Lupski JR, Camper SA. A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2). Genomics. 55: 348-52. PMID 10049592 DOI: 10.1006/geno.1998.5669  0.96
1999 Gage PJ, Suh H, Camper SA. The bicoid-related Pitx gene family in development Mammalian Genome. 10: 197-200. PMID 9922405 DOI: 10.1007/s003359900970  0.96
1998 Kulig E, Camper SA, Kuecker S, Jin L, Lloyd RV. Remodeling of Hyperplastic Pituitaries in Hypothyroid us-Subunit Knockout Mice After Thyroxine and 1713-Estradiol Treatment: Role of Apoptosis. Endocrine Pathology. 9: 261-274. PMID 12114718  0.36
1998 Yu RN, Ito M, Saunders TL, Camper SA, Jameson JL. Role of Ahch in gonadal development and gametogenesis Nature Genetics. 20: 353-357. PMID 9843206 DOI: 10.1038/3822  0.96
1998 Watkins-Chow DE, Camper SA. How many homeobox genes does it take to make a pituitary gland? Trends in Genetics. 14: 284-289. PMID 9676531 DOI: 10.1016/S0168-9525(98)01476-0  0.96
1998 Brinkmeier ML, Gordon DF, Dowding JM, Saunders TL, Kendall SK, Sarapura VD, Wood WM, Ridgway EC, Camper SA. Cell-specific expression of the mouse glycoprotein hormone α-subunit gene requires multiple interacting DNA elements in transgenic mice and cultured cells Molecular Endocrinology. 12: 622-633. PMID 9605925  0.96
1998 Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science (New York, N.Y.). 280: 1447-51. PMID 9603736 DOI: 10.1126/science.280.5368.1447  0.96
1998 Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science (New York, N.Y.). 280: 1444-7. PMID 9603735 DOI: 10.1126/science.280.5368.1444  0.96
1998 Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, ... ... Camper SA, et al. Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. American Journal of Human Genetics. 62: 904-15. PMID 9529344 DOI: 10.1086/301786  0.96
1998 Kulig E, Camper SA, Kuecker S, Jin L, Lloyd RV. Remodeling of hyperplastic pituitaries in hypothyroid α-subunit knockout mice after thyroxine and 17β-estradiol treatment: Role of apoptosis Endocrine Pathology. 9: 261-274.  0.96
1997 Lesh JS, Burrows HL, Seasholtz AF, Camper SA. Mapping of the mouse corticotropin-releasing hormone receptor 2 gene (Crhr2) to chromosome 6. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 944-5. PMID 9383293  0.96
1997 Watkins-Chow DE, Douglas KR, Buckwalter MS, Probst FJ, Camper SA. Construction of a 3-Mb contig and partial transcript map of the central region of mouse chromosome 11. Genomics. 45: 147-57. PMID 9339371 DOI: 10.1006/geno.1997.4931  0.96
1997 Brinkmeier ML, Camper SA. Localization of somatostatin receptor genes on mouse chromosomes 2, 11, 12, 15, and 17: Correlation with growth QTLs Genomics. 43: 9-14. PMID 9226367 DOI: 10.1006/geno.1997.4781  0.96
1997 Camper SA, Meisler MH. Meeting report: 10th International Mouse Genome Conference Mammalian Genome. 8: 461-463. PMID 9195987 DOI: 10.1007/s003359900476  0.96
1997 Gage PJ, Camper SA. Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation Human Molecular Genetics. 6: 457-464. PMID 9147650 DOI: 10.1093/hmg/6.3.457  0.96
1997 Watkins-Chow DE, Buckwalter MS, Newhouse MM, Lossie AC, Brinkmeier ML, Camper SA. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 40: 114-22. PMID 9070927 DOI: 10.1006/geno.1996.4532  0.96
1996 Gage PJ, Brinkmeier ML, Scarlett LM, Knapp LT, Camper SA, Mahon KA. The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation. Molecular Endocrinology (Baltimore, Md.). 10: 1570-81. PMID 8961267 DOI: 10.1210/mend.10.12.8961267  0.96
1996 Burrows HL, Birkmeier TS, Seasholtz AF, Camper SA. Targeted ablation of cells in the pituitary primordia of transgenic mice. Molecular Endocrinology (Baltimore, Md.). 10: 1467-77. PMID 8923471 DOI: 10.1210/mend.10.11.8923471  0.96
1996 Watkins-Chow D, Roller M, Newhouse MM, Buchberg AM, Camper SA. Encyclopedia of the mouse genome V. Mouse chromosome 11 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: S201-220. PMID 8800766  0.96
1996 Malý P, Thall A, Petryniak B, Rogers CE, Smith PL, Marks RM, Kelly RJ, Gersten KM, Cheng G, Saunders TL, Camper SA, Camphausen RT, Sullivan FX, Isogai Y, Hindsgaul O, et al. The alpha(1,3)fucosyltransferase Fuc-TVII controls leukocyte trafficking through an essential role in L-, E-, and P-selectin ligand biosynthesis. Cell. 86: 643-53. PMID 8752218 DOI: 10.1016/S0092-8674(00)80137-3  0.96
1996 Greco TL, Sussman DJ, Camper SA. Dishevelled-2 maps to human chromosome 17 and distal to Wnt3a and vestigial tail (vt) on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 475-6. PMID 8662242  0.96
1996 Chiang PW, Baldacci PA, Babinet C, Camper SA, Watkins-Chow D, Baker DD, Tsai CH, Ramamoorthy S, King E, Slack AC, Fogel E, Morahan G, Ashworth A, Blackburn CC, Kurnit DM. Linkage mapping of murine homolog of the yeast SPT6 gene to MMU11B1 Mammalian Genome. 7: 459-460. PMID 8662231  0.96
1996 Greco TL, Takada S, Newhouse MM, McMahon JA, McMahon AP, Camper SA. Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes & Development. 10: 313-24. PMID 8595882  0.96
1996 Gage PJ, Roller ML, Saunders TL, Scarlett LM, Camper SA. Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion Development. 122: 151-160. PMID 8565826  0.96
1995 Sorenson RC, Primo-Parmo SL, Camper SA, La Du BN. The genetic mapping and gene structure of mouse paraoxonase/arylesterase. Genomics. 30: 431-8. PMID 8825627 DOI: 10.1006/geno.1995.1261  0.96
1995 Zheng X, Saunders TL, Camper SA, Samuelson LC, Ginsburg D. Vitronectin is not essential for normal mammalian development and fertility Proceedings of the National Academy of Sciences of the United States of America. 92: 12426-12430. PMID 8618914 DOI: 10.1073/pnas.92.26.12426  0.96
1995 SPICER AP, ROLLER ML, CAMPER SA, MCPHERSON JD, WASMUTH JJ, HAKIM S, WANG C, TURLEY EA, MCDONALD JA. The Human and Mouse Receptors for Hyaluronan-Mediated Motility, RHAMM, Genes (HMMR) Map to Human Chromosome 5q33.2-qter and Mouse Chromosome 11 Genomics. 30: 115-117. PMID 8595891 DOI: 10.1006/geno.1995.0022  0.96
1995 Kalcheva I, Plass C, Sait S, Eddy R, Shows T, Watkins-Chow D, Camper S, Shibata H, Ueda T, Takagi N, Hayashizaki Y, Chapman V. Comparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and uman chromosome 5 Cytogenetic and Genome Research. 68: 19-24. PMID 7956352 DOI: 10.1159/000133881  0.96
1995 Gage PJ, Lossie AC, Scarlett LM, Lloyd RV, Camper SA. Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response Endocrinology. 136: 1161-1167. PMID 7867569 DOI: 10.1210/endo.136.3.7867569  0.96
1995 Chen C, Nagy Z, Radic MZ, Hardy RR, Huszar D, Camper SA, Weigert M. The site and stage of anti-DNA B-cell deletion Nature. 373: 252-255. PMID 7816141 DOI: 10.1038/373252a0  0.96
1995 Lossie AC, Haugen BR, Wood WM, Camper SA, Gordon DF. Chromosomal localization of the large subunit of mouse replication factor C in the mouse and human Mammalian Genome. 6: 58-59. PMID 7719032 DOI: 10.1007/BF00350900  0.96
1995 Burrows HL, Seasholtz AF, Camper SA. Localization of the corticotropin-releasing hormone receptor gene on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 55-6. PMID 7719029 DOI: 10.1007/BF00350896  0.96
1995 Camper SA, Saunders TL, Kendall SK, Keri RA, Seasholtz AF, Gordon DF, Birkmeier TS, Keegan CE, Karolyi IJ, Roller ML, Burrows HL, Samuelson LC. Implementing transgenic and embryonic stem cell technology to study gene expression, cell-cell interactions and gene function Biology of Reproduction. 52: 246-257. PMID 7711194 DOI: 10.1095/biolreprod52.2.246  0.96
1995 Radic MZ, Ibrahim SM, Rauch J, Camper SA, Weigert M. Constitutive secretion of transgene-encoded IgG2b autoantibodies leads to symptoms of autoimmune disease Journal of Immunology. 155: 3213-3222. PMID 7673734  0.96
1995 Roller ML, Camper SA. Localization of the thyrotropin-releasing hormone gene, Trh, on mouse Chromosome 6 Mammalian Genome. 6: 443-444. PMID 7647472 DOI: 10.1007/BF00355651  0.96
1995 Roller ML, Lossie AC, Koken MHM, Smit EME, Hagemeijer A, Camper SA. Localization of sequences related to the human RAD6 DNA repair gene on mouse Chromosomes 11 and 13 Mammalian Genome. 6: 305-306. PMID 7613042 DOI: 10.1007/BF00352425  0.96
1995 Roller ML, Camper SA. Chromosomal localization of the zinc finger protein 15, Zfp15, on Mouse Chromosome 4 Mammalian Genome. 6: 305. PMID 7613041 DOI: 10.1007/BF00352424  0.96
1995 Kendall SK, Samuelson LC, Saunders TL, Wood RI, Camper SA. Targeted disruption of the pituitary glycoprotein hormone alpha-subunit produces hypogonadal and hypothyroid mice. Genes & Development. 9: 2007-19. PMID 7544315  0.96
1994 Keegan CE, Herman JP, Karolyi IJ, O'Shea KS, Camper SA, Seasholtz AF. Differential expression of corticotropin-releasing hormone in developing mouse embryos and adult brain. Endocrinology. 134: 2547-55. PMID 8194481 DOI: 10.1210/endo.134.6.8194481  0.96
1994 Lossie AC, Vandenbergh DJ, Uhl GR, Camper SA. Localization of the dopamine transporter gene, Dat1, on mouse chromosome 13. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 117-8. PMID 8180472 DOI: 10.1007/BF00292340  0.96
1994 Chen C, Radic MZ, Erikson J, Camper SA, Litwin S, Hardy RR, Weigert M. Deletion and editing of B cells that express antibodies to DNA Journal of Immunology. 152: 1970-1982. PMID 8120401  0.96
1994 Ryan SG, Buckwalter MS, Lynch JW, Handford CA, Segura L, Shiang R, Wasmuth JJ, Camper SA, Schofield P, O'Connell P. A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse. Nature Genetics. 7: 131-5. PMID 7920629 DOI: 10.1038/ng0694-131  0.96
1994 Zhu W, Lossie AC, Camper SA, Gumucio DL. Chromosomal localization of the transcription factor YY1 in the mouse and human Mammalian Genome. 5: 234-236. PMID 7912122 DOI: 10.1007/BF00360552  0.96
1994 Buckwalter MS, Cook SA, Davisson MT, White WF, Camper SA. A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Human Molecular Genetics. 3: 2025-30. PMID 7874121  0.96
1994 Lossie AC, Eipper BA, Hand TA, Camper SA. Localization of the peptidylglycine alpha-amidating monooxygenase gene (Pam) introduces a region of homology between human chromosome 5q and mouse chromosome 1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 738-9. PMID 7873888 DOI: 10.1007/BF00426085  0.96
1994 Lossie AC, MacPhee M, Buchberg AM, Camper SA. Mouse chromosome 11 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: S164-180. PMID 7719004 DOI: 10.1007/BF00360837  0.96
1994 Keri RA, Wolfe MW, Saunders TL, Anderson I, Kendall SK, Wagner T, Yeung J, Gorski J, Nett TM, Camper SA. The proximal promoter of the bovine luteinizing hormone beta-subunit gene confers gonadotrope-specific expression and regulation by gonadotropin-releasing hormone, testosterone, and 17 beta-estradiol in transgenic mice. Molecular Endocrinology (Baltimore, Md.). 8: 1807-16. PMID 7708066 DOI: 10.1210/mend.8.12.7708066  0.96
1994 Keegan CE, Karolyi IJ, Knapp LT, Bourbonais FJ, Camper SA, Seasholtz AF. Expression of corticotropin-releasing hormone transgenes in neurons of adult and developing mice. Molecular and Cellular Neurosciences. 5: 505-14. PMID 7704423 DOI: 10.1006/mcne.1994.1062  0.96
1994 Kendall SK, Gordon DF, Birkmeier TS, Petrey D, Sarapura VD, O'Shea KS, Wood WM, Lloyd RV, Ridgway EC, Camper SA. Enhancer-mediated high level expression of mouse pituitary glycoprotein hormone α-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland Molecular Endocrinology. 8: 1420-1433. PMID 7531821 DOI: 10.1210/me.8.10.1420  0.96
1993 Lloyd RV, Jin L, Kulig E, Thiny MT, Fields K, Landefeld TD, Camper SA. Pit-1/ghf-1 transcription factor expression in rodent pituitaries. Endocrine Pathology. 4: 146-154. PMID 32370429 DOI: 10.1007/BF02915303  0.36
1993 Buckwalter MS, Testa CM, Noebels JL, Camper SA. Genetic mapping and evaluation of candidate genes for spasmodic, a neurological mouse mutation with abnormal startle response. Genomics. 17: 279-86. PMID 8406478 DOI: 10.1006/geno.1993.1322  0.96
1993 Buchberg AM, Camper SA. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 11 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: S164-175. PMID 8268671  0.96
1993 Knapp LT, Keegan CE, Seasholtz AF, Camper SA. Corticotropin-releasing hormone (Crh) maps to mouse chromosome 3. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 615-7. PMID 8268662 DOI: 10.1007/BF00361396  0.96
1993 Shlomchik MJ, Zharhary D, Saunders T, Camper SA, Weigert MG. A rheumatoid factor transgenic mouse model of autoantibody regulation. International Immunology. 5: 1329-41. PMID 8268138 DOI: 10.1093/intimm/5.10.1329  0.96
1993 Lossie AC, Buckwalter MS, Camper SA. Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 177-8. PMID 8094989 DOI: 10.1007/BF00352234  0.96
1993 Lossie AC, Gordon DF, Camper SA. Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15 Mammalian Genome. 4: 621-623. PMID 7903570 DOI: 10.1007/BF00361398  0.96
1993 Lloyd Rv, Jin L, Kulig E, Thiny MT, Fields K, Landefeld TD, Camper SA. Pit-1/ghf-1 transcription factor expression in rodent pituitaries Endocrine Pathology. 4: 146-154. DOI: 10.1007/BF02915303  0.96
1992 Golub EE, Harrison G, Taylor AG, Camper S, Shapiro IM. The role of alkaline phosphatase in cartilage mineralization Bone and Mineral. 17: 273-278. PMID 1611320 DOI: 10.1016/0169-6009(92)90750-8  0.96
1992 Buchberg AM, Buckwalter MS, Camper SA. Mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: S162-81. PMID 1498430 DOI: 10.1007/BF00648429  0.96
1992 Hu JM, Camper SA, Tilghman SM, Miller T, Georgoff I, Serra R, Isom HC. Functional analyses of albumin expression in a series of hepatocyte cell lines and in primary hepatocytes Cell Growth & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research. 3: 577-588. PMID 1419909  0.96
1992 Lloyd RV, Jin L, Chang A, Kulig E, Camper SA, Ross BD, Downs TR, Frohman LA. Morphologic effects of hGRH gene expression on the pituitary, liver, and pancreas of MT-hGRH transgenic mice: An in situ hybridization analysis American Journal of Pathology. 141: 895-906. PMID 1415483  0.96
1992 Vacher J, Camper SA, Krumlauf R, Compton RS, Tilghman SM. raf regulates the postnatal repression of the mouse α-fetoprotein gene at the posttranscriptional level Molecular and Cellular Biology. 12: 856-864. PMID 1370712  0.96
1992 Westbrook CA, Neuman WL, McPherson J, Camper S, Wasmuth J, Plaetke R, Williamson R. Report of the second international workshop on human chromosome 5 mapping. Cytogenetics and Cell Genetics. 61: 225-31. PMID 1362532 DOI: 10.1159/000133415  0.96
1992 Buckwalter MS, Lossie AC, Scarlett LM, Camper SA. Localization of the human chromosome 5q genes Gabra-1, Gabrg-2, Il-4, Il-5, and Irf-1 on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 604-7. PMID 1358285 DOI: 10.1007/BF00350629  0.96
1992 Karolyi IJ, Guénet JL, Rey-Campos J, Camper SA. The gene coding for variant hepatic nuclear factor 1 (Tcf-2), maps between the Edp-1 and Erba genes on mouse Chromosome 11 Mammalian Genome. 3: 184-185. PMID 1352161 DOI: 10.1007/BF00352466  0.96
1992 Westbrook CA, Neuman WL, McPherson J, Camper S, Wasmuth J, Plaetke R, Williamson R. Report of the second internal workshop on human chromosome 5 mapping Cytogenetics and Cell Genetics. 61: 226-231.  0.96
1991 Carmack CE, Camper SA, Mackle JJ, Gerhard WU, Weigert MG. Influence of a V kappa 8 L chain transgene on endogenous rearrangements and the immune response to the HA(Sb) determinant on influenza virus. Journal of Immunology (Baltimore, Md. : 1950). 147: 2024-33. PMID 1909739  0.96
1991 Erikson J, Radic MZ, Camper SA, Hardy RR, Carmack C, Weigert M. Expression of anti-DNA immunoglobulin transgenes in non-autoimmune mice Nature. 349: 331-334. PMID 1898987 DOI: 10.1038/349331a0  0.96
1991 Buckwalter MS, Katz RW, Camper SA. Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross. Genomics. 10: 515-26. PMID 1889803 DOI: 10.1016/0888-7543(91)90430-M  0.96
1991 Buchberg AM, Moskow JJ, Buckwalter MS, Camper SA. Mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 1: S158-91. PMID 1799798 DOI: 10.1007/BF00656492  0.96
1991 Camper SA, Tilghman SM. The activation and silencing of gene transcription in the liver Biotechnology (Reading, Mass.). 16: 81-87. PMID 1706634  0.96
1991 Kendall SK, Saunders TL, Jin L, Lloyd RV, Glode LM, Nett TM, Keri RA, Nilson JH, Camper SA. Targeted ablation of pituitary gonadotropes in transgenic mice. Molecular Endocrinology (Baltimore, Md.). 5: 2025-36. PMID 1665205 DOI: 10.1210/mend-5-12-2025  0.96
1991 Seasholtz AF, Bourbonais FJ, Harnden CE, Camper SA. Nucleotide sequence and expression of the mouse corticotropin-releasing hormone gene Molecular and Cellular Neuroscience. 2: 266-273. DOI: 10.1016/1044-7431(91)90054-R  0.96
1990 Camper SA, Saunders TL, Katz RW, Reeves RH. The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation Genomics. 8: 586-590. PMID 1981057 DOI: 10.1016/0888-7543(90)90050-5  0.96
1989 Camper SA, Godbout R, Tilghman SM. The developmental regulation of albumin and alpha-fetoprotein gene expression. Progress in Nucleic Acid Research and Molecular Biology. 36: 131-43. PMID 2471987 DOI: 10.1016/S0079-6603(08)60167-1  0.96
1989 Camper SA, Tilghman SM. Postnatal repression of the alpha-fetoprotein gene is enhancer independent Genes & Development. 3: 537-546. PMID 2470646  0.96
1987 Hammer RE, Krumlauf R, Camper SA, Brinster RL, Tilghman SM. Diversity of Alpha-Fetoprotein gene expression in mice is generated by a combination of separate enhancer elements Science. 235: 53-58. PMID 2432657  0.96
1987 Camper SA. Research applications of transgenic mice Biotechniques. 5: 638-650.  0.96
1986 Rottman F, Camper S, Goodwin E, Hampson R, Lyons R, Sakai D, Woychik R, Yao Y. Structure and regulated expression of bovine prolactin and bovine growth hormone genes Advances in Experimental Medicine and Biology. 205: 281-299. PMID 3466513  0.96
1986 Hammer RE, Krumlauf R, Camper S, Brinster RL, Tilghman SM. The regulation of α-foetoprotein minigene expression in the germline of mice Journal of Embryology and Experimental Morphology. 97: 257-262. PMID 2442281  0.96
1985 Camper SA, Yao YAS, Rottman FM. Hormonal regulation of the bovine prolactin promoter in rat pituitary tumor cell Journal of Biological Chemistry. 260: 12246-12251. PMID 2995368  0.96
1984 Camper SA, Albers RJ, Coward JK, Rottman FM. Effect of undermethylation on mRNA cytoplasmic appearance and half-life. Molecular and Cellular Biology. 4: 538-43. PMID 6201720  0.96
1984 Camper SA, Luck DN, Yao Y, Woychik RP, Goodwin RG, Lyons RH, Rottman FM. Characterization of the bovine prolactin gene Dna. 3: 237-249. PMID 6086257  0.96
1983 Nilson JH, Fink PA, Virgin JB, Cserbak MT, Camper SA, Rottman FM. Developmental expression of growth hormone and prolactin genes in the bovine pituitary. The Journal of Biological Chemistry. 258: 4565-70. PMID 6687594  0.96
1982 Woychik RP, Camper SA, Lyons RH, Horowitz S, Goodwin EC, Rottman FM. Cloning and nucleotide sequencing of the bovine growth hormone gene Nucleic Acids Research. 10: 7197-7210. PMID 6296767 DOI: 10.1093/nar/10.22.7197  0.96
1978 Meslar HW, Camper SA, White HB. Biotin-binding protein from egg yolk. A protein distinct from egg white avidin Journal of Biological Chemistry. 253: 6979-6982. PMID 567647  0.96
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