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Page 1
Variants in ZNF365 isoform D are associated with Crohn's disease.
Haritunians T, Jones MR, McGovern DP, Shih DQ, Barrett RJ, Derkowski C, Dubinsky MC, Dutridge D, Fleshner PR, Ippoliti A, King L, Leshinsky-Silver E, Levine A, Melmed GY, Mengesha E, Vasilauskas EA, Ziaee S, Rotter JI, Targan SR, Taylor KD. Haritunians T, et al. Among authors: king l. Gut. 2011 Aug;60(8):1060-7. doi: 10.1136/gut.2010.227256. Epub 2011 Jan 21. Gut. 2011. PMID: 21257989 Free PMC article.
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease.
McGovern DP, Rotter JI, Mei L, Haritunians T, Landers C, Derkowski C, Dutridge D, Dubinsky M, Ippoliti A, Vasiliauskas E, Mengesha E, King L, Pressman S, Targan SR, Taylor KD. McGovern DP, et al. Among authors: king l. Inflamm Bowel Dis. 2009 Jun;15(6):883-9. doi: 10.1002/ibd.20855. Inflamm Bowel Dis. 2009. PMID: 19235914 Free PMC article.
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.
McGovern DP, Jones MR, Taylor KD, Marciante K, Yan X, Dubinsky M, Ippoliti A, Vasiliauskas E, Berel D, Derkowski C, Dutridge D, Fleshner P, Shih DQ, Melmed G, Mengesha E, King L, Pressman S, Haritunians T, Guo X, Targan SR, Rotter JI; International IBD Genetics Consortium. McGovern DP, et al. Among authors: king l. Hum Mol Genet. 2010 Sep 1;19(17):3468-76. doi: 10.1093/hmg/ddq248. Epub 2010 Jun 22. Hum Mol Genet. 2010. PMID: 20570966 Free PMC article.
MAGI2 genetic variation and inflammatory bowel disease.
McGovern DP, Taylor KD, Landers C, Derkowski C, Dutridge D, Dubinsky M, Ippoliti A, Vasiliauskas E, Mei L, Mengesha E, King L, Pressman S, Targan SR, Rotter JI. McGovern DP, et al. Among authors: king l. Inflamm Bowel Dis. 2009 Jan;15(1):75-83. doi: 10.1002/ibd.20611. Inflamm Bowel Dis. 2009. PMID: 18720471 Free PMC article.
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.
Steiner C, Ehtesham N, Taylor KD, Sebald E, Cantor R, King LM, Guo X, Hang T, Hu MS, Cui JR, Friedman B, Norato D, Allanson J, Honeywell C, Mettler G, Field F, Lachman R, Cohn DH, Krakow D. Steiner C, et al. Among authors: king lm. J Med Genet. 2004 Apr;41(4):266-9. doi: 10.1136/jmg.2003.012252. J Med Genet. 2004. PMID: 15060099 Free PMC article.
A transcriptional profile of human fetal cartilage.
Pogue R, Sebald E, King L, Kronstadt E, Krakow D, Cohn DH. Pogue R, et al. Among authors: king l. Matrix Biol. 2004 Aug;23(5):299-307. doi: 10.1016/j.matbio.2004.07.003. Matrix Biol. 2004. PMID: 15464362
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrum.
Briggs MD, Mortier GR, Cole WG, King LM, Golik SS, Bonaventure J, Nuytinck L, De Paepe A, Leroy JG, Biesecker L, Lipson M, Wilcox WR, Lachman RS, Rimoin DL, Knowlton RG, Cohn DH. Briggs MD, et al. Among authors: king lm. Am J Hum Genet. 1998 Feb;62(2):311-9. doi: 10.1086/301713. Am J Hum Genet. 1998. PMID: 9463320 Free PMC article.
3,041 results