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Teresa M. Gunn - Publications

Affiliations: 
2001-2009 Biomedical Sciences Cornell University, Ithaca, NY, United States 
 2009- McLaughlin Research Institute, Great Falls, MT, United States 
Area:
Neuroscience Biology, Animal Physiology Biology, Biochemistry
Website:
http://mclaughlinresearch.org/research-scientists/faculty/teresa-gunn/
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49 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
2023 Ratz-Mitchem ML, Leary G, Grindeland A, Silvius D, Guter J, Kavanaugh MP, Gunn TM. Generation and characterization of a knock-in mouse model for spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM). Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 37642681 DOI: 10.1007/s00335-023-10013-4  0.307
2023 Ratz ML, Leary G, Grindeland A, Silvius D, Guter J, Kavanaugh MP, Gunn TM. Generation and characterization of a knock-in mouse model for Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM). Research Square. PMID 37162879 DOI: 10.21203/rs.3.rs-2839029/v1  0.303
2020 Kong JH, Young CB, Pusapati GV, Patel CB, Ho S, Krishnan A, Lin JI, Devine W, Moreau de Bellaing A, Athni TS, Aravind L, Gunn TM, Lo CW, Rohatgi R. A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. Developmental Cell. PMID 32966817 DOI: 10.1016/j.devcel.2020.08.012  0.37
2019 Gunn TM, Silvius D, Lester A, Gibbs B. Chronic and age-dependent effects of the spongiform neurodegeneration-associated MGRN1 E3 ubiquitin ligase on mitochondrial homeostasis. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 31089807 DOI: 10.1007/S00335-019-09802-7  0.419
2016 Walker WP, Oehler A, Edinger AL, Wagner KU, Gunn TM. Oligodendroglial deletion of ESCRT-I component TSG101 causes spongiform encephalopathy. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. PMID 27406702 DOI: 10.1111/Boc.201600014  0.743
2015 Besio R, Maruelli S, Gioia R, Villa I, Grabowski P, Gallagher O, Bishop NJ, Foster S, De Lorenzi E, Colombo R, Diaz JL, Moore-Barton H, Deshpande C, Aydin HI, Tokatli A, ... ... Gunn TM, et al. Lack of prolidase causes a bone phenotype both in human and in mouse. Bone. 72: 53-64. PMID 25460580 DOI: 10.1016/J.Bone.2014.11.009  0.385
2015 Anderson SR, Lee I, Ebeling C, Stephenson DA, Schweitzer KM, Baxter D, Moon TM, LaPierre S, Jaques B, Silvius D, Wegner M, Hood LE, Carlson G, Gunn TM. Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 26: 80-93. PMID 25399070 DOI: 10.1007/S00335-014-9548-5  0.498
2013 Gunn TM, Carlson GA. RML prions act through Mahogunin and Attractin-independent pathways. Prion. 7: 267-71. PMID 23787699 DOI: 10.4161/Pri.25054  0.428
2013 Jesty SA, Jung SW, Cordeiro JM, Gunn TM, Di Diego JM, Hemsley S, Kornreich BG, Hooker G, Antzelevitch C, Moïse NS. Cardiomyocyte calcium cycling in a naturally occurring German shepherd dog model of inherited ventricular arrhythmia and sudden cardiac death. Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology. 15: 5-14. PMID 23434243 DOI: 10.1016/J.Jvc.2012.07.005  0.517
2013 Silvius D, Pitstick R, Ahn M, Meishery D, Oehler A, Barsh GS, DeArmond SJ, Carlson GA, Gunn TM. Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease. Plos One. 8: e55575. PMID 23383230 DOI: 10.1371/Journal.Pone.0055575  0.612
2013 Gunn TM, Silvius D, Bagher P, Sun K, Walker KK. MGRN1-dependent pigment-type switching requires its ubiquitination activity but not its interaction with TSG101 or NEDD4. Pigment Cell & Melanoma Research. 26: 263-8. PMID 23253940 DOI: 10.1111/Pcmr.12059  0.781
2012 Gunn TM. Functional annotation and ENU. Bmc Research Notes. 5: 580. PMID 23095518 DOI: 10.1186/1756-0500-5-580  0.368
2011 Jung S, Silvius D, Nolan KA, Borchert GL, Millet YH, Phang JM, Gunn TM. Developmental cardiac hypertrophy in a mouse model of prolidase deficiency. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 204-17. PMID 21472842 DOI: 10.1002/Bdra.20789  0.362
2011 Friedenberg SG, Zhu L, Zhang Z, Foels Wv, Schweitzer PA, Wang W, Fisher PJ, Dykes NL, Corey E, Vernier-Singer M, Jung SW, Sheng X, Hunter LS, McDonough SP, Lust G, ... ... Gunn TM, et al. Evaluation of a fibrillin 2 gene haplotype associated with hip dysplasia and incipient osteoarthritis in dogs. American Journal of Veterinary Research. 72: 530-40. PMID 21453155 DOI: 10.2460/Ajvr.72.4.530  0.542
2010 Walker WP, Gunn TM. Shades of meaning: the pigment-type switching system as a tool for discovery. Pigment Cell & Melanoma Research. 23: 485-95. PMID 20465596 DOI: 10.1111/J.1755-148X.2010.00721.X  0.736
2010 Walker WP, Gunn TM. Piecing together the pigment-type switching puzzle. Pigment Cell & Melanoma Research. 23: 4-6. PMID 20042018 DOI: 10.1111/J.1755-148X.2009.00654.X  0.682
2009 Jiao J, Sun K, Walker WP, Bagher P, Cota CD, Gunn TM. Abnormal regulation of TSG101 in mice with spongiform neurodegeneration. Biochimica Et Biophysica Acta. 1792: 1027-35. PMID 19703557 DOI: 10.1016/J.Bbadis.2009.08.009  0.761
2009 Jiao J, Kim HY, Liu RR, Hogan CA, Sun K, Tam LM, Gunn TM. Transgenic analysis of the physiological functions of Mahogunin Ring Finger-1 isoforms. Genesis (New York, N.Y. : 2000). 47: 524-34. PMID 19422019 DOI: 10.1002/Dvg.20529  0.735
2009 Zhang Z, Alpert D, Francis R, Chatterjee B, Yu Q, Tansey T, Sabol SL, Cui C, Bai Y, Koriabine M, Yoshinaga Y, Cheng JF, Chen F, Martin J, Schackwitz W, ... Gunn TM, et al. Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy. Proceedings of the National Academy of Sciences of the United States of America. 106: 3219-24. PMID 19218456 DOI: 10.1073/Pnas.0813400106  0.419
2009 Cruickshank J, Quaas RL, Li J, Hemsley S, Gunn TM, Moïse NS. Genetic analysis of ventricular arrhythmia in young German shepherd dogs Journal of Veterinary Internal Medicine. 23: 264-270. PMID 19210315 DOI: 10.1111/J.1939-1676.2009.0265.X  0.316
2008 Cota CD, Liu RR, Sumberac TM, Jung S, Vencato D, Millet YH, Gunn TM. Genetic and phenotypic studies of the dark-like mutant mouse. Genesis (New York, N.Y. : 2000). 46: 562-73. PMID 18821597 DOI: 10.1002/Dvg.20432  0.677
2007 Walker WP, Aradhya S, Hu CL, Shen S, Zhang W, Azarani A, Lu X, Barsh GS, Gunn TM. Genetic analysis of attractin homologs. Genesis (New York, N.Y. : 2000). 45: 744-56. PMID 18064672 DOI: 10.1002/Dvg.20351  0.799
2007 Sun K, Johnson BS, Gunn TM. Mitochondrial dysfunction precedes neurodegeneration in mahogunin (Mgrn1) mutant mice. Neurobiology of Aging. 28: 1840-52. PMID 17720281 DOI: 10.1016/J.Neurobiolaging.2007.07.012  0.632
2007 Hackett SR, Jung SW, Kirkness E, Cruickshank J, Vikstrom KL, Moïse NS, Gunn TM. Identification and characterization of canine microsatellite markers in cardiac genes. Animal Genetics. 38: 89-91. PMID 17257202 DOI: 10.1111/J.1365-2052.2007.01556.X  0.533
2007 Azouz A, Gunn TM, Duke-Cohan JS. Juvenile-onset loss of lipid-raft domains in attractin-deficient mice. Experimental Cell Research. 313: 761-71. PMID 17196964 DOI: 10.1016/J.Yexcr.2006.11.018  0.372
2006 Bagher P, Jiao J, Owen Smith C, Cota CD, Gunn TM. Characterization of Mahogunin Ring Finger-1 expression in mice. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 19: 635-43. PMID 17083490 DOI: 10.1111/J.1600-0749.2006.00340.X  0.794
2006 Cota CD, Bagher P, Pelc P, Smith CO, Bodner CR, Gunn TM. Mice with mutations in Mahogunin ring finger-1 (Mgrn1) exhibit abnormal patterning of the left-right axis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 235: 3438-47. PMID 17075880 DOI: 10.1002/Dvdy.20992  0.77
2006 Liu W, Hackett SR, Cruickshank J, Vikstrom KL, Moïse NS, Gunn TM. Canine microsatellites associated with genes implicated in cardiac development and function. Animal Genetics. 37: 87-8. PMID 16441309 DOI: 10.1111/J.1365-2052.2005.01410.X  0.308
2003 He L, Eldridge AG, Jackson PK, Gunn TM, Barsh GS. Accessory proteins for melanocortin signaling: attractin and mahogunin. Annals of the New York Academy of Sciences. 994: 288-98. PMID 12851328 DOI: 10.1111/J.1749-6632.2003.Tb03192.X  0.596
2003 He L, Lu XY, Jolly AF, Eldridge AG, Watson SJ, Jackson PK, Barsh GS, Gunn TM. Spongiform degeneration in mahoganoid mutant mice. Science (New York, N.Y.). 299: 710-2. PMID 12560552 DOI: 10.1126/Science.1079694  0.642
2002 Barsh GS, He L, Gunn TM. Genetic and biochemical studies of the Agouti-attractin system. Journal of Receptor and Signal Transduction Research. 22: 63-77. PMID 12503608 DOI: 10.1081/Rrs-120014588  0.59
2002 Gunn TM, Azarani A, Kim PH, Hyman RW, Davis RW, Barsh GS. Identification and preliminary characterization of mouse Adam33. Bmc Genetics. 3: 2. PMID 11897009 DOI: 10.1186/1471-2156-3-2  0.511
2001 Juriloff DM, Gunn TM, Harris MJ, Mah DG, Wu MK, Dewell SL. Multifactorial genetics of exencephaly in SELH/Bc mice. Teratology. 64: 189-200. PMID 11598925 DOI: 10.1002/Tera.1064  0.659
2001 Gunn TM, Inui T, Kitada K, Ito S, Wakamatsu K, He L, Bouley DM, Serikawa T, Barsh GS. Molecular and phenotypic analysis of Attractin mutant mice. Genetics. 158: 1683-95. PMID 11514456  0.551
2001 He L, Gunn TM, Bouley DM, Lu XY, Watson SJ, Schlossman SF, Duke-Cohan JS, Barsh GS. A biochemical function for attractin in agouti-induced pigmentation and obesity. Nature Genetics. 27: 40-7. PMID 11137996 DOI: 10.1038/83741  0.585
2000 Barsh G, Gunn T, He L, Wilson B, Lu X, Gantz I, Watson S. Neuroendocrine regulation by the Agouti/Agrp-melanocortin system Endocrine Research. 26: 571. PMID 11196430 DOI: 10.3109/07435800009048572  0.59
2000 Gunn TM, Barsh GS. Mahogany/attractin: en route from phenotype to function. Trends in Cardiovascular Medicine. 10: 76-81. PMID 11150734 DOI: 10.1016/S1050-1738(00)00052-9  0.601
2000 Barsh G, Gunn T, He L, Schlossman S, Duke-Cohan J. Biochemical and genetic studies of pigment-type switching. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 13: 48-53. PMID 11041357 DOI: 10.1034/J.1600-0749.13.S8.10.X  0.567
2000 Tang W, Gunn TM, McLaughlin DF, Barsh GS, Schlossman SF, Duke-Cohan JS. Secreted and membrane attractin result from alternative splicing of the human ATRN gene. Proceedings of the National Academy of Sciences of the United States of America. 97: 6025-30. PMID 10811918 DOI: 10.1073/pnas.110139897  0.485
1999 Barsh GS, Ollmann MM, Wilson BD, Miller KA, Gunn TM. Molecular pharmacology of Agouti protein in vitro and in vivo. Annals of the New York Academy of Sciences. 885: 143-52. PMID 10816647 DOI: 10.1111/J.1749-6632.1999.Tb08671.X  0.634
1999 Lu Xy, Gunn TM, Shieh Kr, Barsh GS, Akil H, Watson SJ. Distribution of Mahogany/Attractin mRNA in the rat central nervous system. Febs Letters. 462: 101-7. PMID 10580100 DOI: 10.1016/S0014-5793(99)01494-5  0.461
1999 Gunn TM, Miller KA, He L, Hyman RW, Davis RW, Azarani A, Schlossman SF, Duke-Cohan JS, Barsh GS. The mouse mahogany locus encodes a transmembrane form of human attractin. Nature. 398: 152-6. PMID 10086356 DOI: 10.1038/18217  0.543
1997 Miller KA, Gunn TM, Carrasquillo MM, Lamoreux ML, Galbraith DB, Barsh GS. Genetic studies of the mouse mutations mahogany and mahoganoid. Genetics. 146: 1407-15. PMID 9258683  0.539
1996 Gunn TM, Juriloff DM, Harris MJ. Exencephaly and cleft cerebellum in SELH/Bc mouse embryos are alternative developmental consequences of the same underlying genetic defect Teratology. 54: 230-236. PMID 9035344 DOI: 10.1002/(Sici)1096-9926(199611)54:5<230::Aid-Tera3>3.0.Co;2-3  0.667
1995 Gunn TM, Juriloff DM, Harris MJ. Genetically determined absence of an initiation site of cranial neural tube closure is causally related to exencephaly in SELH/Bc mouse embryos Teratology. 52: 101-108. PMID 8588181 DOI: 10.1002/Tera.1420520206  0.639
1994 Harris MJ, Juriloff DM, Gunn TM, Miller JE. Development of the cerebellar defect in ataxic SELH/Bc mice. Teratology. 50: 63-73. PMID 7974256 DOI: 10.1002/Tera.1420500109  0.642
1993 Juriloff DM, Harris MJ, Harrod ML, Gunn TM, Miller JE. Ataxia and a cerebellar defect in the exencephaly-prone SELH/Bc mouse stock. Teratology. 47: 333-40. PMID 8322227 DOI: 10.1002/Tera.1420470410  0.703
1993 Gunn TM, Juriloff DM, Vogl W, Harris MJ, Miller JE. Histological study of the cranial neural folds of mice genetically liable to exencephaly. Teratology. 48: 459-71. PMID 8303615 DOI: 10.1002/Tera.1420480510  0.628
1992 Gunn TM, Juriloff DM, Harris MJ. Further genetic studies of the cause of exencephaly in SELH mice Teratology. 45: 679-686. PMID 1412061 DOI: 10.1002/Tera.1420450613  0.669
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