153 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
2022 Jamet S, Ha S, Ho TH, Houghtaling S, Timms A, Yu K, Paquette A, Maga AM, Greene NDE, Beier DR. The Arginine Methyltransferase Carm1 is Necessary for Heart Development. G3 (Bethesda, Md.). PMID 35736367 DOI: 10.1093/g3journal/jkac155  0.512
2020 Ha S, Tripathi PP, Daza RA, Hevner RF, Beier DR. Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis. Journal of Developmental Biology. 8. PMID 32962021 DOI: 10.3390/jdb8030020  0.628
2019 Bittermann E, Abdelhamed Z, Liegel RP, Menke C, Timms A, Beier DR, Stottmann RW. Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243. PMID 31386652 DOI: 10.1371/Journal.Pgen.1008243  0.687
2019 Geister KA, Lopez-Jimenez AJ, Houghtaling S, Ho TH, Vanacore R, Beier DR. Loss of function of disrupts collagen post-translational modification and causes musculoskeletal defects. Disease Models & Mechanisms. PMID 31101663 DOI: 10.1242/Dmm.037176  0.395
2019 Weghorn D, Balick DJ, Cassa C, Kosmicki JA, Daly MJ, Beier DR, Sunyaev SR. Applicability of the mutation-selection balance model to population genetics of heterozygous protein-truncating variants in humans. Molecular Biology and Evolution. PMID 31004148 DOI: 10.1093/Molbev/Msz092  0.398
2018 Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145. PMID 29317443 DOI: 10.1242/Dev.154500  0.692
2017 Geister KA, Timms AE, Beier DR. Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice. G3 (Bethesda, Md.). PMID 29208648 DOI: 10.1534/G3.117.300292  0.45
2017 Strassman A, Schnütgen F, Dai Q, Jones JC, Gomez AC, Pitstick L, Holton NE, Moskal R, Leslie ER, von Melchner H, Beier DR, Bjork BC. Generation of a multipurpose Prdm16 allele by targeted trapping. Disease Models & Mechanisms. PMID 28424158 DOI: 10.1242/Dmm.029561  0.518
2017 Cassa CA, Weghorn D, Balick DJ, Jordan DM, Nusinow D, Samocha KE, O'Donnell-Luria A, MacArthur DG, Daly MJ, Beier DR, Sunyaev SR. Estimating the selective effects of heterozygous protein-truncating variants from human exome data. Nature Genetics. PMID 28369035 DOI: 10.1038/Ng.3831  0.447
2017 Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 37: 960-971. PMID 28123028 DOI: 10.1523/Jneurosci.1826-16.2016  0.699
2016 Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 27986930 DOI: 10.1523/JNEUROSCI.1826-16.2016  0.677
2016 Jacobs DT, Silva LM, Allard BA, Schonfeld MP, Chatterjee A, Talbott GC, Beier DR, Tran PV. Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome. Disease Models & Mechanisms. 9: 789-98. PMID 27482817 DOI: 10.1242/Dmm.025791  0.326
2016 Gallego-Llamas J, Timms AE, Pitstick R, Peters J, Carlson GA, Beier DR. Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice. Plos One. 11: e0159377. PMID 27441645 DOI: 10.1371/Journal.Pone.0159377  0.424
2016 Ha S, Lindsay AM, Timms AE, Beier DR. Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice. G3 (Bethesda, Md.). PMID 27261005 DOI: 10.1534/G3.116.030791  0.631
2016 Beier DR. High-resolution genetic localization of a modifying locus affecting disease severity in the juvenile cystic kidneys (jck) mouse model of polycystic kidney disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 27114383 DOI: 10.1007/S00335-016-9633-Z  0.466
2016 Husson H, Moreno S, Smith LA, Smith MM, Russo RJ, Pitstick R, Sergeev M, Ledbetter SR, Bukanov NO, Lane M, Zhang K, Billot K, Carlson G, Shah J, Meijer L, ... Beier DR, et al. Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisis. Human Molecular Genetics. PMID 27053712 DOI: 10.1093/Hmg/Ddw093  0.32
2015 Gallego-Llamas J, Timms AE, Geister KA, Lindsay A, Beier DR. Variant mapping and mutation discovery in inbred mice using next-generation sequencing. Bmc Genomics. 16: 913. PMID 26552429 DOI: 10.1186/S12864-015-2173-1  0.485
2015 Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development. Genesis (New York, N.Y. : 2000). PMID 26177923 DOI: 10.1002/Dvg.22875  0.723
2015 Czarnecki PG, Gabriel GC, Manning DK, Sergeev M, Lemke K, Klena NT, Liu X, Chen Y, Li Y, San Agustin JT, Garnaas MK, Francis RJ, Tobita K, Goessling W, Pazour GJ, ... ... Beier DR, et al. ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning. Nature Communications. 6: 6023. PMID 25599650 DOI: 10.1038/Ncomms7023  0.34
2015 Ha S, Stottmann RW, Furley AJ, Beier DR. A forward genetic screen in mice identifies mutants with abnormal cortical patterning. Cerebral Cortex (New York, N.Y. : 1991). 25: 167-79. PMID 23968836 DOI: 10.1093/Cercor/Bht209  0.753
2015 Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development Genesis. DOI: 10.1002/dvg.22875  0.59
2014 Stottmann R, Beier D. ENU mutagenesis in the mouse Current Protocols in Mouse Biology. 4: 25-35. PMID 25723916 DOI: 10.1002/9780470942390.Mo140029  0.692
2014 Stottmann R, Beier D. ENU Mutagenesis in the Mouse. Current Protocols in Human Genetics. 82: 15.4.1-10. PMID 25042716 DOI: 10.1002/0471142905.hg1504s82  0.669
2014 Tran PV, Talbott GC, Turbe-Doan A, Jacobs DT, Schonfeld MP, Silva LM, Chatterjee A, Prysak M, Allard BA, Beier DR. Downregulating hedgehog signaling reduces renal cystogenic potential of mouse models. Journal of the American Society of Nephrology : Jasn. 25: 2201-12. PMID 24700869 DOI: 10.1681/Asn.2013070735  0.361
2014 Beier DR. Using Mutagenesis in Mice for Developmental Gene Discovery Principles of Developmental Genetics: Second Edition. 49-58. DOI: 10.1016/B978-0-12-405945-0.00003-X  0.328
2013 Stottmann RW, Donlin M, Hafner A, Bernard A, Sinclair DA, Beier DR. A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse. Human Molecular Genetics. 22: 4053-63. PMID 23727838 DOI: 10.1093/Hmg/Ddt255  0.725
2013 Manning DK, Sergeev M, van Heesbeen RG, Wong MD, Oh JH, Liu Y, Henkelman RM, Drummond I, Shah JV, Beier DR. Loss of the ciliary kinase Nek8 causes left-right asymmetry defects. Journal of the American Society of Nephrology : Jasn. 24: 100-12. PMID 23274954 DOI: 10.1681/Asn.2012050490  0.439
2013 Favero CB, Henshaw RN, Grimsley-Myers CM, Shrestha A, Beier DR, Dwyer ND. Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrain. The Journal of Comparative Neurology. 521: 677-96. PMID 22821687 DOI: 10.1002/Cne.23199  0.601
2012 Tao J, Koster MI, Harrison W, Moran JL, Beier DR, Roop DR, Overbeek PA. A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis. Plos One. 7: e50634. PMID 23226340 DOI: 10.1371/Journal.Pone.0050634  0.506
2012 Velupillai P, Sung CK, Andrews E, Moran J, Beier D, Kagan J, Benjamin T. Polymorphisms in toll-like receptor 4 underlie susceptibility to tumor induction by the mouse polyomavirus. Journal of Virology. 86: 11541-7. PMID 22896604 DOI: 10.1128/Jvi.01614-12  0.31
2012 Liem KF, Ashe A, He M, Satir P, Moran J, Beier D, Wicking C, Anderson KV. The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking. The Journal of Cell Biology. 197: 789-800. PMID 22689656 DOI: 10.1083/Jcb.201110049  0.378
2012 Leshchiner I, Alexa K, Kelsey P, Adzhubei I, Austin-Tse CA, Cooney JD, Anderson H, King MJ, Stottmann RW, Garnaas MK, Ha S, Drummond IA, Paw BH, North TE, Beier DR, et al. Mutation mapping and identification by whole-genome sequencing. Genome Research. 22: 1541-8. PMID 22555591 DOI: 10.1101/Gr.135541.111  0.754
2012 Weiss J, Hurley LA, Harris RM, Finlayson C, Tong M, Fisher LA, Moran JL, Beier DR, Mason C, Jameson JL. ENU mutagenesis in mice identifies candidate genes for hypogonadism. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 346-55. PMID 22258617 DOI: 10.1007/S00335-011-9388-5  0.521
2011 Stottmann RW, Turbe-Doan A, Tran P, Kratz LE, Moran JL, Kelley RI, Beier DR. Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo. Plos Genetics. 7: e1002224. PMID 21912524 DOI: 10.1371/Journal.Pgen.1002224  0.668
2011 Cozzi E, Ackerman KG, Lundequist A, Drazen JM, Boyce JA, Beier DR. The naive airway hyperresponsiveness of the A/J mouse is Kit-mediated. Proceedings of the National Academy of Sciences of the United States of America. 108: 12787-92. PMID 21768379 DOI: 10.1073/Pnas.1106582108  0.385
2011 Stottmann RW, Moran JL, Turbe-Doan A, Driver E, Kelley M, Beier DR. Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse. Genetics. 188: 615-24. PMID 21515572 DOI: 10.1534/Genetics.111.126862  0.745
2011 Dwyer ND, Manning DK, Moran JL, Mudbhary R, Fleming MS, Favero CB, Vock VM, O'Leary DD, Walsh CA, Beier DR. A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype. Neural Development. 6: 3. PMID 21214893 DOI: 10.1186/1749-8104-6-3  0.711
2011 Stottmann RW, Beier D. ENU mutagenesis identifies novel genes required for forebrain development Developmental Biology. 356: 159. DOI: 10.1016/J.Ydbio.2011.05.589  0.721
2011 Chong H, Cozzi E, Lundquist A, Boyce J, Beier D. Strain-dependent Influences On C-kit Function Alter The Mast Cell Phenotype Of Hyperresponsive A/J Mice Journal of Allergy and Clinical Immunology. 127: AB131-AB131. DOI: 10.1016/J.Jaci.2010.12.523  0.314
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  0.584
2010 Beier DR. New genetic resources for mammalian developmental biologists. F1000 Biology Reports. 2: 72. PMID 21173845 DOI: 10.3410/B2-72  0.418
2010 Hellman NE, Liu Y, Merkel E, Austin C, Le Corre S, Beier DR, Sun Z, Sharma N, Yoder BK, Drummond IA. The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch. Proceedings of the National Academy of Sciences of the United States of America. 107: 18499-504. PMID 20937855 DOI: 10.1073/Pnas.1005998107  0.315
2010 Stottmann RW, Beier DR. Using ENU mutagenesis for phenotype-driven analysis of the mouse. Methods in Enzymology. 477: 329-48. PMID 20699149 DOI: 10.1016/S0076-6879(10)77017-8  0.729
2010 Kamp A, Peterson MA, Svenson KL, Bjork BC, Hentges KE, Rajapaksha TW, Moran J, Justice MJ, Seidman JG, Seidman CE, Moskowitz IP, Beier DR. Genome-wide identification of mouse congenital heart disease loci. Human Molecular Genetics. 19: 3105-13. PMID 20511334 DOI: 10.1093/Hmg/Ddq211  0.445
2010 Stottmann RW, Bjork BC, Doyle JB, Beier DR. Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. Genesis (New York, N.Y. : 2000). 48: 303-8. PMID 20196077 DOI: 10.1002/Dvg.20618  0.735
2010 Shiba D, Manning DK, Koga H, Beier DR, Yokoyama T. Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia. Cytoskeleton (Hoboken, N.J.). 67: 112-9. PMID 20169535 DOI: 10.1002/Cm.20428  0.415
2010 Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, ... ... Beier DR, et al. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. The New England Journal of Medicine. 362: 206-16. PMID 20089971 DOI: 10.1056/Nejmoa0900158  0.679
2010 Bjork BC, Turbe-Doan A, Prysak M, Herron BJ, Beier DR. Prdm16 is required for normal palatogenesis in mice. Human Molecular Genetics. 19: 774-89. PMID 20007998 DOI: 10.1093/Hmg/Ddp543  0.428
2010 Vock VM, Fleming M, Rasoul B, Beier D, Walsh C, Dwyer ND. Abnormal cortical development and cell division defects in magoo mutant mice International Journal of Developmental Neuroscience. 28: 656-657. DOI: 10.1016/J.Ijdevneu.2010.07.046  0.543
2009 Heydemann A, Ceco E, Lim JE, Hadhazy M, Ryder P, Moran JL, Beier DR, Palmer AA, McNally EM. Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. The Journal of Clinical Investigation. 119: 3703-12. PMID 19884661 DOI: 10.1172/Jci39845  0.347
2009 Douglas DS, Moran JL, Bermingham JR, Chen XJ, Brindley DN, Soliven B, Beier DR, Popko B. Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 12089-100. PMID 19793967 DOI: 10.1523/Jneurosci.2029-09.2009  0.482
2009 Stottmann RW, Tran PV, Turbe-Doan A, Beier DR. Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain. Developmental Biology. 335: 166-78. PMID 19732765 DOI: 10.1016/J.Ydbio.2009.08.023  0.68
2009 Pettitt SJ, Liang Q, Rairdan XY, Moran JL, Prosser HM, Beier DR, Lloyd KC, Bradley A, Skarnes WC. Agouti C57BL/6N embryonic stem cells for mouse genetic resources. Nature Methods. 6: 493-5. PMID 19525957 DOI: 10.1038/Nmeth.1342  0.413
2009 Fernandez L, Marchuk DA, Moran JL, Beier DR, Rockman HA. An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 296-304. PMID 19387734 DOI: 10.1007/S00335-009-9184-7  0.49
2009 Stottmann RW, Turbe-Doan A, Qui H, Beier D. An ENU screen reveals novel genes in mammalian forebrain development Developmental Biology. 331: 495. DOI: 10.1016/J.Ydbio.2009.05.408  0.697
2008 Beckstead WA, Bjork BC, Stottmann RW, Sunyaev S, Beier DR. SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 687-90. PMID 18958524 DOI: 10.1007/S00335-008-9149-2  0.681
2008 Seale P, Bjork B, Yang W, Kajimura S, Chin S, Kuang S, Scimè A, Devarakonda S, Conroe HM, Erdjument-Bromage H, Tempst P, Rudnicki MA, Beier DR, Spiegelman BM. PRDM16 controls a brown fat/skeletal muscle switch. Nature. 454: 961-7. PMID 18719582 DOI: 10.1038/Nature07182  0.318
2008 Tran PV, Haycraft CJ, Besschetnova TY, Turbe-Doan A, Stottmann RW, Herron BJ, Chesebro AL, Qiu H, Scherz PJ, Shah JV, Yoder BK, Beier DR. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nature Genetics. 40: 403-10. PMID 18327258 DOI: 10.1038/Ng.105  0.695
2008 Sohara E, Luo Y, Zhang J, Manning DK, Beier DR, Zhou J. Nek8 regulates the expression and localization of polycystin-1 and polycystin-2. Journal of the American Society of Nephrology : Jasn. 19: 469-76. PMID 18235101 DOI: 10.1681/Asn.2006090985  0.419
2008 Trapp ML, Galtseva A, Manning DK, Beier DR, Rosenblum ND, Quarmby LM. Defects in ciliary localization of Nek8 is associated with cystogenesis. Pediatric Nephrology (Berlin, Germany). 23: 377-87. PMID 18189147 DOI: 10.1007/S00467-007-0692-Y  0.41
2008 Leder A, McMenamin J, Zhou F, Moran JL, Beier DR, Leder P. Genome-wide SNP analysis of Tg.AC transgenic mice reveals an oncogenic collaboration between v-Ha-ras and Ink4a, which is absent in p53 deficiency. Oncogene. 27: 2456-65. PMID 17952114 DOI: 10.1038/Sj.Onc.1210866  0.555
2008 Stottmann RW, Yun Y, Beier D. An Enu screen reveals novel genes required for mammalian forebrain development Developmental Biology. 319: 599. DOI: 10.1016/J.Ydbio.2008.05.424  0.7
2007 Poirier C, Moran JL, Kovanci E, Petit DC, Beier DR, Bishop CE. Three loci on mouse chromosome 5 and 10 modulate sex determination in XX Ods/+ mice. Genesis (New York, N.Y. : 2000). 45: 452-5. PMID 17607692 DOI: 10.1002/Dvg.20312  0.436
2007 Matera I, Cockroft JL, Moran JL, Beier DR, Goldowitz D, Pavan WJ. A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 20: 210-5. PMID 17516928 DOI: 10.1111/J.1600-0749.2007.00371.X  0.494
2007 Moran JL, Qiu H, Turbe-Doan A, Yun Y, Boeglin WE, Brash AR, Beier DR. A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrier. The Journal of Investigative Dermatology. 127: 1893-7. PMID 17429434 DOI: 10.1038/Sj.Jid.5700825  0.443
2007 Ackerman KG, Wang J, Luo L, Fujiwara Y, Orkin SH, Beier DR. Gata4 is necessary for normal pulmonary lobar development. American Journal of Respiratory Cell and Molecular Biology. 36: 391-7. PMID 17142311 DOI: 10.1165/Rcmb.2006-0211Rc  0.533
2007 Ideraabdullah FY, Kim K, Pomp D, Moran JL, Beier D, De Villena FPM. Rescue of the mouse DDK syndrome by parent-of-origin-dependent modifiers Biology of Reproduction. 76: 286-293. PMID 17050856 DOI: 10.1095/Biolreprod.106.056739  0.39
2007 Stottmann RW, Yun Y, Beier D. An ENU screen for novel genes required in mammalian forebrain development Developmental Biology. 306: 302. DOI: 10.1016/J.Ydbio.2007.03.086  0.651
2006 Holland KD, Fleming MT, Cheek S, Moran JL, Beier DR, Meisler MH. De novo exon duplication in a new allele of mouse Glra1 (spasmodic). Genetics. 174: 2245-7. PMID 17028313 DOI: 10.1534/Genetics.106.065532  0.453
2006 Lehoczky JA, Cai WW, Douglas JA, Moran JL, Beier DR, Innis JW. Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 903-13. PMID 16964440 DOI: 10.1007/S00335-006-0041-7  0.392
2006 Smith LA, Bukanov NO, Husson H, Russo RJ, Barry TC, Taylor AL, Beier DR, Ibraghimov-Beskrovnaya O. Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease. Journal of the American Society of Nephrology : Jasn. 17: 2821-31. PMID 16928806 DOI: 10.1681/Asn.2006020136  0.373
2006 Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, Manning DK, Bjork BC, Li C, Montgomery K, Siepka SM, Vitaterna MH, Takahashi JS, Wiltshire T, Kwiatkowski DJ, Kucherlapati R, ... Beier DR, et al. Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Research. 16: 436-40. PMID 16461637 DOI: 10.1101/Gr.4563306  0.65
2005 Ackerman KG, Herron BJ, Vargas SO, Huang H, Tevosian SG, Kochilas L, Rao C, Pober BR, Babiuk RP, Epstein JA, Greer JJ, Beier DR. Fog2 is required for normal diaphragm and lung development in mice and humans. Plos Genetics. 1: 58-65. PMID 16103912 DOI: 10.1371/Journal.Pgen.0010010  0.444
2005 Fatma N, Kubo E, Sharma P, Beier DR, Singh DP. Impaired homeostasis and phenotypic abnormalities in Prdx6-/-mice lens epithelial cells by reactive oxygen species: increased expression and activation of TGFbeta. Cell Death and Differentiation. 12: 734-50. PMID 15818411 DOI: 10.1038/Sj.Cdd.4401597  0.365
2005 Herron BJ, Rao C, Liu S, Laprade L, Richardson JA, Olivieri E, Semsarian C, Millar SE, Stubbs L, Beier DR. A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice. Human Molecular Genetics. 14: 667-77. PMID 15661756 DOI: 10.1093/Hmg/Ddi063  0.452
2005 Ackerman KG, Huang H, Grasemann H, Puma C, Singer JB, Hill AE, Lander E, Nadeau JH, Churchill GA, Drazen JM, Beier DR. Interacting genetic loci cause airway hyperresponsiveness. Physiological Genomics. 21: 105-11. PMID 15657107 DOI: 10.1152/Physiolgenomics.00267.2004  0.387
2004 McDonald JD, Beier D. ENU mutagenesis in the mouse. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 15.4. PMID 18428357 DOI: 10.1002/0471142905.Hg1504S39  0.406
2004 Beier DR, Herron BJ. Genetic mapping and ENU mutagenesis. Genetica. 122: 65-9. PMID 15619962 DOI: 10.1007/978-1-4020-5057-2_7  0.422
2003 Carroll EA, Gerrelli D, Gasca S, Berg E, Beier DR, Copp AJ, Klingensmith J. Cordon-bleu is a conserved gene involved in neural tube formation. Developmental Biology. 262: 16-31. PMID 14512015 DOI: 10.1016/S0012-1606(03)00323-3  0.404
2003 Layer K, Lin G, Nencioni A, Hu W, Schmucker A, Antov AN, Li X, Takamatsu S, Chevassut T, Dower NA, Stang SL, Beier D, Buhlmann J, Bronson RT, Elkon KB, et al. Autoimmunity as the consequence of a spontaneous mutation in Rasgrp1. Immunity. 19: 243-55. PMID 12932358 DOI: 10.1016/S1074-7613(03)00209-7  0.356
2003 Rao C, Foernzler D, Loftus SK, Liu S, McPherson JD, Jungers KA, Apte SS, Pavan WJ, Beier DR. A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation. Development (Cambridge, England). 130: 4665-72. PMID 12925592 DOI: 10.1242/Dev.00668  0.453
2003 Li Z, Stuart RO, Eraly SA, Gittes G, Beier DR, Nigam SK. Debt91, a putative zinc finger protein differentially expressed during epithelial morphogenesis. Biochemical and Biophysical Research Communications. 306: 623-8. PMID 12810064 DOI: 10.1016/S0006-291X(03)00875-1  0.408
2002 Beier DR. ENU mutagenesis: a work in progress. Physiological Genomics. 11: 111-3. PMID 12464687 DOI: 10.1152/Physiolgenomics.00140.2002  0.305
2002 Fröhlich L, Liu Z, Beier DR, Lanske B. Genomic structure and refined chromosomal localization of the mouse Ptch2 gene. Cytogenetic and Genome Research. 97: 106-10. PMID 12438747 DOI: 10.1159/000064064  0.334
2002 Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA, Beier DR. A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development (Cambridge, England). 129: 5839-46. PMID 12421721 DOI: 10.1242/Dev.00173  0.495
2002 Phelan SA, Beier DR, Higgins DC, Paigen B. Confirmation and high resolution mapping of an atherosclerosis susceptibility gene in mice on Chromosome 1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 548-53. PMID 12420131 DOI: 10.1007/S00335-002-2196-1  0.385
2002 Schymeinsky J, Nedbal S, Miosge N, Pöschl E, Rao C, Beier DR, Skarnes WC, Timpl R, Bader BL. Gene structure and functional analysis of the mouse nidogen-2 gene: nidogen-2 is not essential for basement membrane formation in mice. Molecular and Cellular Biology. 22: 6820-30. PMID 12215539 DOI: 10.1128/Mcb.22.19.6820-6830.2002  0.414
2002 Lee MLT, Lu W, Whitmore GA, Beier D. Models for microarray gene expression data Journal of Biopharmaceutical Statistics. 12: 1-19. PMID 12146717 DOI: 10.1081/Bip-120005737  0.354
2002 Hou X, Mrug M, Yoder BK, Lefkowitz EJ, Kremmidiotis G, D'Eustachio P, Beier DR, Guay-Woodford LM. Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. The Journal of Clinical Investigation. 109: 533-40. PMID 11854326 DOI: 10.1172/Jci14099  0.442
2002 Mátés L, Korpos E, Déak F, Liu Z, Beier DR, Aszódi A, Kiss I. Comparative analysis of the mouse and human genes (Matn2 and MATN2) for matrilin-2, a filament-forming protein widely distributed in extracellular matrices. Matrix Biology : Journal of the International Society For Matrix Biology. 21: 163-74. PMID 11852232 DOI: 10.1016/S0945-053X(01)00194-9  0.402
2002 Herron BJ, Lu W, Rao C, Liu S, Peters H, Bronson RT, Justice MJ, McDonald JD, Beier DR. Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis. Nature Genetics. 30: 185-9. PMID 11818962 DOI: 10.1038/Ng812  0.471
2001 Stuart RO, Pavlova A, Beier D, Li Z, Krijanovski Y, Nigam SK. EEG1, a putative transporter expressed during epithelial organogenesis: comparison with embryonic transporter expression during nephrogenesis. American Journal of Physiology. Renal Physiology. 281: F1148-56. PMID 11704567 DOI: 10.1152/Ajprenal.2001.281.6.F1148  0.388
2001 Mrug M, Green WJ, DasGupta S, Beier DR, Lu W, D'Eustachio P, Guay-Woodford LM. An integrated genetic and physical map of the 650-kb region containing the congenital polycystic kidney (cpk) locus on mouse chromosome 12. Cytogenetics and Cell Genetics. 94: 55-61. PMID 11701955 DOI: 10.1159/000048783  0.473
2001 Chen F, Collin GB, Liu KC, Beier DR, Eccles M, Nishina PM, Moshang T, Epstein JA. Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndrome. Genomics. 74: 219-27. PMID 11386758 DOI: 10.1006/Geno.2001.6539  0.483
2000 Jilek A, Engel E, Beier D, Lepperdinger G. Murine Bv8 gene maps near a synteny breakpoint of mouse chromosome 6 and human 3p21 Gene. 256: 189-195. PMID 11054548 DOI: 10.1016/S0378-1119(00)00355-3  0.325
2000 Beier DR. Sequence-based analysis of mutagenized mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 594-7. PMID 10886029 DOI: 10.1007/S003350010113  0.433
2000 Pavlova A, Sakurai H, Leclercq B, Beier DR, Yu AS, Nigam SK. Developmentally regulated expression of organic ion transporters NKT (OAT1), OCT1, NLT (OAT2), and Roct. American Journal of Physiology. Renal Physiology. 278: F635-43. PMID 10751225 DOI: 10.1152/Ajprenal.2000.278.4.F635  0.317
2000 Guay-Woodford LM, Green WJ, Lindsey JR, Beier DR. Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated. Human Molecular Genetics. 9: 769-78. PMID 10749984 DOI: 10.1093/Hmg/9.5.769  0.398
2000 Wagener R, Kobbe B, Aszódi A, Liu Z, Beier DR, Paulsson M. Structure and mapping of the mouse matrilin-3 gene (Matn3), a member of a gene family containing a U12-type AT-AC intron. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 85-90. PMID 10656920 DOI: 10.1007/S003350010018  0.425
2000 Kuida S, Beier DR. Genetic localization of interacting modifiers affecting severity in a murine model of polycystic kidney disease. Genome Research. 10: 49-54. PMID 10645949 DOI: 10.1101/Gr.10.1.49  0.385
1999 Iakoubova O, Dushkin H, Pacella L, Beier DR. Genetic analysis of modifying loci on mouse chromosome 1 that affect disease severity in a model of recessive PKD. Physiological Genomics. 1: 101-5. PMID 11015567 DOI: 10.1152/Physiolgenomics.1999.1.2.101  0.395
1999 Deák F, Mátés L, Krysan K, Liu Z, Szabó PE, Mann JR, Beier DR, Kiss I. Characterization and chromosome location of the mouse link protein gene (Crtl1). Cytogenetics and Cell Genetics. 87: 75-9. PMID 10640815 DOI: 10.1159/000015395  0.385
1999 Cohen DE, Green RM, Wu MK, Beier DR. Cloning, tissue-specific expression, gene structure and chromosomal localization of human phosphatidylcholine transfer protein. Biochimica Et Biophysica Acta. 1447: 265-70. PMID 10542325 DOI: 10.1016/S0167-4781(99)00163-3  0.37
1999 Dangond F, Foerznler D, Weremowicz S, Morton CC, Beier DR, Gullans SR. Cloning and expression of a murine histone deacetylase 3 (mHdac3) cDNA and mapping to a region of conserved synteny between murine chromosome 18 and human chromosome 5. Molecular Cell Biology Research Communications : McBrc. 2: 91-6. PMID 10542131 DOI: 10.1006/Mcbr.1999.0156  0.377
1999 In KH, Silverman ES, Asano K, Beier D, Fischer AR, Keith TP, Serino K, Yandava C, De Sanctis GT, Drazen JM. Mutations in the human 5-lipoxygenase gene. Clinical Reviews in Allergy & Immunology. 17: 59-69. PMID 10436859 DOI: 10.1007/Bf02737597  0.453
1999 Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, Pihlajaniemi T. Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue. Matrix Biology : Journal of the International Society For Matrix Biology. 18: 261-74. PMID 10429945 DOI: 10.1016/S0945-053X(99)00018-9  0.439
1999 Marks PW, Bandura JL, Shieh DB, Foernzler D, Beier DR, Kwiatkowski DJ. The spontaneous coat color mutant white nose (wn) maps to murine chromosome 15. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 750-2. PMID 10384053 DOI: 10.1007/S003359901084  0.465
1999 Brady KP, Dushkin H, Förnzler D, Koike T, Magner F, Her H, Gullans S, Segre GV, Green RM, Beier DR. A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics. 56: 254-61. PMID 10087192 DOI: 10.1006/Geno.1998.5722  0.479
1999 Mount DB, Baekgaard A, Hall AE, Plata C, Xu J, Beier DR, Gamba G, Hebert SC. Isoforms of the Na-K-2Cl cotransporter in murine TAL I. Molecular characterization and intrarenal localization. The American Journal of Physiology. 276: F347-58. PMID 10070158 DOI: 10.1152/Ajprenal.1999.276.3.F347  0.307
1999 Davidson AJ, Postlethwait JH, Yan YL, Beier DR, van Doren C, Foernzler D, Celeste AJ, Crosier KE, Crosier PS. Isolation of zebrafish gdf7 and comparative genetic mapping of genes belonging to the growth/differentiation factor 5, 6, 7 subgroup of the TGF-beta superfamily. Genome Research. 9: 121-9. PMID 10022976  0.34
1999 Foernzler D, Beier DR. Gene mapping in zebrafish using single-strand conformation polymorphism analysis. Methods in Cell Biology. 60: 185-93. PMID 9891338 DOI: 10.1016/S0091-679X(08)61901-9  0.347
1998 Phelan SA, Johnson KA, Beier DR, Paigen B. Characterization of the murine gene encoding Aop2 (antioxidant protein 2) and identification of two highly related genes. Genomics. 54: 132-9. PMID 9806838 DOI: 10.1006/Geno.1998.5568  0.417
1998 Twist CJ, Beier DR, Disteche CM, Edelhoff S, Tedder TF. The mouse Cd83 gene: structure, domain organization, and chromosome localization. Immunogenetics. 48: 383-93. PMID 9799334 DOI: 10.1007/S002510050449  0.342
1998 Strobl B, Wechselberger C, Beier DR, Lepperdinger G. Structural organization and chromosomal localization of Hyal2, a gene encoding a lysosomal hyaluronidase. Genomics. 53: 214-9. PMID 9790770 DOI: 10.1006/Geno.1998.5472  0.434
1998 Förnzler D, Her H, Knapik EW, Clark M, Lehrach H, Postlethwait JH, Zon LI, Beier DR. Gene mapping in zebrafish using single-strand conformation polymorphism analysis. Genomics. 51: 216-22. PMID 9722944 DOI: 10.1006/Geno.1998.5386  0.389
1998 Heaney C, Shalev H, Elbedour K, Carmi R, Staack JB, Sheffield VC, Beier DR. Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation. Human Molecular Genetics. 7: 1407-10. PMID 9700194 DOI: 10.1093/Hmg/7.9.1407  0.372
1998 Thompson MA, Ransom DG, Pratt SJ, MacLennan H, Kieran MW, Detrich HW, Vail B, Huber TL, Paw B, Brownlie AJ, Oates AC, Fritz A, Gates MA, Amores A, Bahary N, ... ... Beier DR, et al. The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis. Developmental Biology. 197: 248-69. PMID 9630750 DOI: 10.1006/Dbio.1998.8887  0.319
1998 Aszódi A, Beier DR, Hiripi L, Bösze Z, Fässler R. Sequence, structure and chromosomal localization of Crtm gene encoding mouse cartilage matrix protein and its exclusion as a candidate for murine achondroplasia. Matrix Biology : Journal of the International Society For Matrix Biology. 16: 563-73. PMID 9569124 DOI: 10.1016/S0945-053X(98)90067-1  0.457
1998 Landgren C, Beier DR, Fässler R, HeinegÃ¥rd D, Sommarin Y. The mouse chondroadherin gene: characterization and chromosomal localization. Genomics. 47: 84-91. PMID 9465299 DOI: 10.1006/Geno.1997.5085  0.444
1998 Neuhaus IM, Beier DR. Efficient localization of mutations by interval haplotype analysis. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 150-4. PMID 9457677 DOI: 10.1007/S003359900706  0.419
1998 Beier DR. Zebrafish: genomics on the fast track. Genome Research. 8: 9-17. PMID 9445483 DOI: 10.1101/Gr.8.1.9  0.411
1998 Lammert F, Cohen DE, Paigen B, Carey MC, Beier DR. The gene encoding the multispecific organic anion transporter (Cmoat) of the hepatocyte canalicular membrane maps to mouse chromosome 19. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 87-8. PMID 9434956 DOI: 10.1007/S003359900689  0.348
1997 Skvorak AB, Robertson NG, Yin Y, Weremowicz S, Her H, Bieber FR, Beisel KW, Lynch ED, Beier DR, Morton CC. An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics. 46: 191-9. PMID 9417906 DOI: 10.1006/Geno.1997.5026  0.402
1997 Brady KP, Rowe LB, Her H, Stevens TJ, Eppig J, Sussman DJ, Sikela J, Beier DR. Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Research. 7: 1085-93. PMID 9371744 DOI: 10.1101/Gr.7.11.1085  0.383
1997 Iakoubova OA, Dushkin H, Beier DR. Genetic analysis of a quantitative trait in a mouse model of polycystic kidney disease. American Journal of Respiratory and Critical Care Medicine. 156: S72-7. PMID 9351583 DOI: 10.1164/Ajrccm.156.4.12-Tac-0  0.422
1997 Bui TD, Beier DR, Jonssen M, Smith K, Dorrington SM, Kaklamanis L, Kearney L, Regan R, Sussman DJ, Harris AL. cDNA cloning of a human dishevelled DVL-3 gene, mapping to 3q27, and expression in human breast and colon carcinomas. Biochemical and Biophysical Research Communications. 239: 510-6. PMID 9344861 DOI: 10.1006/Bbrc.1997.7500  0.382
1997 Apte SS, Fukai N, Beier DR, Olsen BR. The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesis. The Journal of Biological Chemistry. 272: 25511-7. PMID 9325265 DOI: 10.1074/Jbc.272.41.25511  0.305
1997 Rauch U, Meyer H, Brakebusch C, Seidenbecher C, Gundelfinger ED, Beier DR, Fässler R. Sequence and chromosomal localization of the mouse brevican gene. Genomics. 44: 15-21. PMID 9286696 DOI: 10.1006/Geno.1997.4853  0.413
1997 Fleming MD, Trenor CC, Su MA, Foernzler D, Beier DR, Dietrich WF, Andrews NC. Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nature Genetics. 16: 383-6. PMID 9241278 DOI: 10.1038/Ng0897-383  0.392
1997 Iakoubova OA, Pacella LA, Her H, Beier DR. LTW4 protein on mouse chromosome 1 is a member of a family of antioxidant proteins. Genomics. 42: 474-8. PMID 9205120 DOI: 10.1006/Geno.1997.4762  0.441
1997 Langer-Safer PR, Fitz LJ, Whitley MZ, Wood CR, Beier DR. Strategies for the application of functional genomics technology to biopharmaceutical drug discovery Drug Development Research. 41: 173-179. DOI: 10.1002/(Sici)1098-2299(199707/08)41:3/4<173::Aid-Ddr7>3.0.Co;2-I  0.383
1996 Tsang M, Lijam N, Yang Y, Beier DR, Wynshaw-Boris A, Sussman DJ. Isolation and characterization of mouse dishevelled-3. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 207: 253-62. PMID 8922524 DOI: 10.1002/(Sici)1097-0177(199611)207:3<253::Aid-Aja2>3.0.Co;2-G  0.448
1996 Klingensmith J, Yang Y, Axelrod JD, Beier DR, Perrimon N, Sussman DJ. Conservation of dishevelled structure and function between flies and mice: isolation and characterization of Dvl2. Mechanisms of Development. 58: 15-26. PMID 8887313 DOI: 10.1016/S0925-4773(96)00549-7  0.424
1996 Beier DR, Dushkin H, Stone LV, Sherman GF. A transgene insertion at perinatal lethality (ple) is associated with abnormalities of the cortex. Brain Research. 727: 196-204. PMID 8842398 DOI: 10.1016/0006-8993(96)00380-0  0.427
1995 Li Y, Lacerda DA, Warman ML, Beier DR, Yoshioka H, Ninomiya Y, Oxford JT, Morris NP, Andrikopoulos K, Ramirez F. A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis. Cell. 80: 423-30. PMID 7859283 DOI: 10.1016/0092-8674(95)90492-1  0.402
1995 Iakoubova OA, Dushkin H, Beier DR. Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity. Genomics. 26: 107-14. PMID 7782068 DOI: 10.1016/0888-7543(95)80088-4  0.422
1995 Beier DR, Dushkin H, Telle T. Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 269-72. PMID 7613032 DOI: 10.1007/Bf00352414  0.384
1995 Rauch U, Grimpe B, Kulbe G, Arnold-Ammer I, Beier DR, Fässler R. Structure and chromosomal localization of the mouse neurocan gene. Genomics. 28: 405-10. PMID 7490074 DOI: 10.1006/Geno.1995.1168  0.425
1994 Kaiser UB, Dushkin H, Altherr MR, Beier DR, Chin WW. Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5. Genomics. 20: 506-8. PMID 8034328 DOI: 10.1006/Geno.1994.1211  0.334
1994 Crosier PS, Lewis PM, Hall LR, Vitas MR, Morris CM, Beier DR, Wood CR, Crosier KE. Isolation of a receptor tyrosine kinase (DTK) from embryonic stem cells: structure, genetic mapping and analysis of expression. Growth Factors (Chur, Switzerland). 11: 125-36. PMID 7857657 DOI: 10.3109/08977199409001054  0.329
1994 Warman ML, McCarthy MT, Perälä M, Vuorio E, Knoll JH, McDaniels CN, Mayne R, Beier DR, Olsen BR. The genes encoding alpha 2(IX) collagen (COL9A2) map to human chromosome 1p32.3-p33 and mouse chromosome 4. Genomics. 23: 158-62. PMID 7829066 DOI: 10.1006/Geno.1994.1472  0.312
1994 Ord DC, Edelhoff S, Dushkin H, Zhou LJ, Beier DR, Disteche C, Tedder TF. CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7. Immunogenetics. 39: 322-8. PMID 7513297 DOI: 10.1007/Bf00189228  0.372
1993 Atala A, Freeman MR, Mandell J, Beier DR. Juvenile cystic kidneys (jck): a new mouse mutation which causes polycystic kidneys. Kidney International. 43: 1081-5. PMID 8510385 DOI: 10.1038/Ki.1993.151  0.427
1993 Shultz LD, Schweitzer PA, Rajan TV, Yi T, Ihle JN, Matthews RJ, Thomas ML, Beier DR. Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene. Cell. 73: 1445-54. PMID 8324828 DOI: 10.1016/0092-8674(93)90369-2  0.51
1993 Peichel CL, Scherer SW, Tsui LC, Beier DR, Vogt TF. Mapping the midkine family of developmentally regulated signaling molecules. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 632-8. PMID 8281012 DOI: 10.1007/Bf00360899  0.415
1993 Beier DR. Single-strand conformation polymorphism (SSCP) analysis as a tool for genetic mapping. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 627-31. PMID 8281011 DOI: 10.1007/Bf00360898  0.309
1992 Beier DR, Dushkin H, Sussman DJ. Mapping genes in the mouse using single-strand conformation polymorphism analysis of recombinant inbred strains and interspecific crosses. Proceedings of the National Academy of Sciences of the United States of America. 89: 9102-6. PMID 1409609 DOI: 10.1073/Pnas.89.19.9102  0.375
1991 Beier DR, Chaillet JR, Schmidt EV, Leder P. Close linkage of a transgene insertion site to the steel (Sl) locus on mouse chromosome 10. Genomics. 10: 1003-8. PMID 1655629 DOI: 10.1016/0888-7543(91)90191-G  0.583
1991 Chaillet JR, Vogt TF, Beier DR, Leder P. Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis. Cell. 66: 77-83. PMID 1649008 DOI: 10.1016/0092-8674(91)90140-T  0.42
1990 Huang E, Nocka K, Beier DR, Chu TY, Buck J, Lahm HW, Wellner D, Leder P, Besmer P. The hematopoietic growth factor KL is encoded by the Sl locus and is the ligand of the c-kit receptor, the gene product of the W locus. Cell. 63: 225-33. PMID 1698557 DOI: 10.1016/0092-8674(90)90303-V  0.537
1989 Beier DR, Morton CC, Leder A, Wallace R, Leder P. Perinatal lethality (ple): a mutation caused by integration of a transgene into distal mouse chromosome 15. Genomics. 4: 498-504. PMID 2744761 DOI: 10.1016/0888-7543(89)90272-3  0.577
1985 Beier DR, Sledziewski A, Young ET. Deletion analysis identifies a region, upstream of the ADH2 gene of Saccharomyces cerevisiae, which is required for ADR1-mediated derepression. Molecular and Cellular Biology. 5: 1743-9. PMID 3160930 DOI: 10.1128/Mcb.5.7.1743  0.332
1982 Beier DR, Young ET. Characterization of a regulatory region upstream of the ADR2 locus of S. cerevisiae. Nature. 300: 724-8. PMID 6757760 DOI: 10.1038/300724A0  0.38
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