Julie A. Kerns, Ph.D. - Publications

Stanford University, Palo Alto, CA 
pigmentation, melanocortin system

18 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
2014 Daugherty MD, Young JM, Kerns JA, Malik HS. Rapid evolution of PARP genes suggests a broad role for ADP-ribosylation in host-virus conflicts. Plos Genetics. 10: e1004403. PMID 24875882 DOI: 10.1371/Journal.Pgen.1004403  0.405
2010 Koyanagi M, Kerns JA, Chung L, Zhang Y, Brown S, Moldoveanu T, Malik HS, Bix M. Diversifying selection and functional analysis of interleukin-4 suggests antagonism-driven evolution at receptor-binding interfaces. Bmc Evolutionary Biology. 10: 223. PMID 20649995 DOI: 10.1186/1471-2148-10-223  0.338
2008 OhAinle M, Kerns JA, Li MM, Malik HS, Emerman M. Antiretroelement activity of APOBEC3H was lost twice in recent human evolution. Cell Host & Microbe. 4: 249-59. PMID 18779051 DOI: 10.1016/J.Chom.2008.07.005  0.359
2008 Kerns JA, Emerman M, Malik HS. Positive selection and increased antiviral activity associated with the PARP-containing isoform of human zinc-finger antiviral protein. Plos Genetics. 4: e21. PMID 18225958 DOI: 10.1371/Journal.Pgen.0040021  0.343
2008 Barsh G, Candille S, He L, Aradhya S, Kerns J. The role of accessory proteins in melanocortin receptor signaling Experimental Dermatology. 13: 569-569. DOI: 10.1111/J.0906-6705.2004.00212H.X  0.652
2007 Candille SI, Kaelin CB, Cattanach BM, Yu B, Thompson DA, Nix MA, Kerns JA, Schmutz SM, Millhauser GL, Barsh GS. A -defensin mutation causes black coat color in domestic dogs. Science (New York, N.Y.). 318: 1418-23. PMID 17947548 DOI: 10.1126/Science.1147880  0.634
2007 Kerns JA, Cargill EJ, Clark LA, Candille SI, Berryere TG, Olivier M, Lust G, Todhunter RJ, Schmutz SM, Murphy KE, Barsh GS. Linkage and segregation analysis of black and brindle coat color in domestic dogs. Genetics. 176: 1679-89. PMID 17483404 DOI: 10.1534/Genetics.107.074237  0.648
2006 OhAinle M, Kerns JA, Malik HS, Emerman M. Adaptive evolution and antiviral activity of the conserved mammalian cytidine deaminase APOBEC3H. Journal of Virology. 80: 3853-62. PMID 16571802 DOI: 10.1128/Jvi.80.8.3853-3862.2006  0.399
2005 Berryere TG, Kerns JA, Barsh GS, Schmutz SM. Association of an Agouti allele with fawn or sable coat color in domestic dogs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 262-72. PMID 15965787 DOI: 10.1007/S00335-004-2445-6  0.625
2004 Kerns JA, Newton J, Berryere TG, Rubin EM, Cheng JF, Schmutz SM, Barsh GS. Characterization of the dog Agouti gene and a nonagoutimutation in German Shepherd Dogs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 798-808. PMID 15520882 DOI: 10.1007/S00335-004-2377-1  0.661
2003 Kerns JA, Olivier M, Lust G, Barsh GS. Exclusion of melanocortin-1 receptor (mc1r) and agouti as candidates for dominant black in dogs. The Journal of Heredity. 94: 75-9. PMID 12692166  0.631
2003 Schmutz SM, Berryere TG, Ellinwood NM, Kerns JA, Barsh GS. MC1R studies in dogs with melanistic mask or brindle patterns. The Journal of Heredity. 94: 69-73. PMID 12692165 DOI: 10.1093/Jhered/Esg014  0.602
1997 Ollmann MM, Wilson BD, Yang YK, Kerns JA, Chen Y, Gantz I, Barsh GS. Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein. Science (New York, N.Y.). 278: 135-8. PMID 9311920 DOI: 10.1126/Science.278.5335.135  0.537
1996 Wevrick R, Kerns JA, Francke U. The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome. Acta Geneticae Medicae Et Gemellologiae. 45: 191-7. PMID 8872030 DOI: 10.1017/S000156600000129X  0.312
1995 Derry JM, Wiedemann P, Blair P, Wang Y, Kerns JA, Lemahieu V, Godfrey VL, Wilkinson JE, Francke U. The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome. Genomics. 29: 471-7. PMID 8666397 DOI: 10.1006/Geno.1995.9979  0.403
1995 Derry JM, Kerns JA, Francke U. RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain. Human Molecular Genetics. 4: 2307-11. PMID 8634703 DOI: 10.1093/Hmg/4.12.2307  0.381
1995 Derry JM, Kerns JA, Weinberg KI, Ochs HD, Volpini V, Estivill X, Walker AP, Francke U. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Human Molecular Genetics. 4: 1127-35. PMID 8528199 DOI: 10.1093/Hmg/4.7.1127  0.341
1994 Wevrick R, Kerns JA, Francke U. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Human Molecular Genetics. 3: 1877-82. PMID 7849716 DOI: 10.1093/Hmg/3.10.1877  0.33
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