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Molecular and developmental genetics of mouse coat color.
Jackson IJ. Jackson IJ. Annu Rev Genet. 1994;28:189-217. doi: 10.1146/annurev.ge.28.120194.001201. Annu Rev Genet. 1994. PMID: 7893123 Review. No abstract available.
Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletions.
Rinchik EM, Bell JA, Hunsicker PR, Friedman JM, Jackson IJ, Russell LB. Rinchik EM, et al. Among authors: jackson ij. Genetics. 1994 Jul;137(3):845-54. Genetics. 1994. PMID: 7916309 Free PMC article.
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans.
Valverde P, Healy E, Jackson I, Rees JL, Thody AJ. Valverde P, et al. Among authors: jackson i. Nat Genet. 1995 Nov;11(3):328-30. doi: 10.1038/ng1195-328. Nat Genet. 1995. PMID: 7581459
Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf.
Taylor KL, Lister JA, Zeng Z, Ishizaki H, Anderson C, Kelsh RN, Jackson IJ, Patton EE. Taylor KL, et al. Among authors: jackson ij. Development. 2011 Aug;138(16):3579-89. doi: 10.1242/dev.064014. Epub 2011 Jul 19. Development. 2011. PMID: 21771814 Free PMC article.
Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited.
Wilkie AL, Jordan SA, Jackson IJ. Wilkie AL, et al. Among authors: jackson ij. Development. 2002 Jul;129(14):3349-57. Development. 2002. PMID: 12091305
Genetic determinants of hair and eye colours in the Scottish and Danish populations.
Mengel-From J, Wong TH, Morling N, Rees JL, Jackson IJ. Mengel-From J, et al. Among authors: jackson ij. BMC Genet. 2009 Dec 30;10:88. doi: 10.1186/1471-2156-10-88. BMC Genet. 2009. PMID: 20042077 Free PMC article.
Humanized MC1R transgenic mice reveal human specific receptor function.
Jackson IJ, Budd PS, Keighren M, McKie L. Jackson IJ, et al. Hum Mol Genet. 2007 Oct 1;16(19):2341-8. doi: 10.1093/hmg/ddm191. Epub 2007 Jul 25. Hum Mol Genet. 2007. PMID: 17652101
Cardiac malformations and midline skeletal defects in mice lacking filamin A.
Hart AW, Morgan JE, Schneider J, West K, McKie L, Bhattacharya S, Jackson IJ, Cross SH. Hart AW, et al. Among authors: jackson ij. Hum Mol Genet. 2006 Aug 15;15(16):2457-67. doi: 10.1093/hmg/ddl168. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825286
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.
Cross SH, Morgan JE, Pattyn A, West K, McKie L, Hart A, Thaung C, Brunet JF, Jackson IJ. Cross SH, et al. Among authors: jackson ij. Hum Mol Genet. 2004 Jul 15;13(14):1433-9. doi: 10.1093/hmg/ddh156. Epub 2004 May 18. Hum Mol Genet. 2004. PMID: 15150159
PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins.
Hall EA, Nahorski MS, Murray LM, Shaheen R, Perkins E, Dissanayake KN, Kristaryanto Y, Jones RA, Vogt J, Rivagorda M, Handley MT, Mali GR, Quidwai T, Soares DC, Keighren MA, McKie L, Mort RL, Gammoh N, Garcia-Munoz A, Davey T, Vermeren M, Walsh D, Budd P, Aligianis IA, Faqeih E, Quigley AJ, Jackson IJ, Kulathu Y, Jackson M, Ribchester RR, von Kriegsheim A, Alkuraya FS, Woods CG, Maher ER, Mill P. Hall EA, et al. Among authors: jackson ij. Am J Hum Genet. 2017 May 4;100(5):706-724. doi: 10.1016/j.ajhg.2017.03.008. Epub 2017 Apr 13. Am J Hum Genet. 2017. PMID: 28413018 Free PMC article.
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