Jabs EW - Search Results

1

Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chain.

Myers JC, Sun MJ, D'Ippolito JA, Jabs EW, Neilson EG, Dion AS. Myers JC, et al. Among authors: jabs ew. Gene. 1993 Jan 30;123(2):211-7. doi: 10.1016/0378-1119(93)90126-n. Gene. 1993. PMID: 7916703

2

Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 --> q22.

Huebner K, Cannizzaro LA, Jabs EW, Kivirikko S, Manzone H, Pihlajaniemi T, Myers JC. Huebner K, et al. Among authors: jabs ew. Genomics. 1992 Oct;14(2):220-4. doi: 10.1016/s0888-7543(05)80209-5. Genomics. 1992. PMID: 1427836

3

Cloning and chromosomal localization of the human BARX2 homeobox protein gene.

Krasner A, Wallace L, Thiagalingam A, Jones C, Lengauer C, Minahan L, Ma Y, Kalikin L, Feinberg AP, Jabs EW, Tunnacliffe A, Baylin SB, Ball DW, Nelkin BD. Krasner A, et al. Among authors: jabs ew. Gene. 2000 May 30;250(1-2):171-80. doi: 10.1016/s0378-1119(00)00169-4. Gene. 2000. PMID: 10854790 Free article.

4

Partial structure and mapping of the human myelin P2 protein gene.

Narayanan V, Ripepi B, Jabs EW, Hawkins A, Griffin C, Tennekoon G. Narayanan V, et al. Among authors: jabs ew. J Neurochem. 1994 Dec;63(6):2010-3. doi: 10.1046/j.1471-4159.1994.63062010.x. J Neurochem. 1994. PMID: 7525873 Free article.

5

Complete cDNA sequence of a human dioxin-inducible mRNA identifies a new gene subfamily of cytochrome P450 that maps to chromosome 2.

Sutter TR, Tang YM, Hayes CL, Wo YY, Jabs EW, Li X, Yin H, Cody CW, Greenlee WF. Sutter TR, et al. Among authors: jabs ew. J Biol Chem. 1994 May 6;269(18):13092-9. J Biol Chem. 1994. PMID: 8175734 Free article.

6

Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.

Ben J, Jabs EW, Chong SS. Ben J, et al. Among authors: jabs ew. Gene Expr Patterns. 2005 Jun;5(5):629-38. doi: 10.1016/j.modgep.2005.03.002. Epub 2005 Apr 19. Gene Expr Patterns. 2005. PMID: 15939375

7

A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form.

VanderMeer JE, Lozano R, Sun M, Xue Y, Daentl D, Jabs EW, Wilcox WR, Ahituv N. VanderMeer JE, et al. Among authors: jabs ew. Hum Mutat. 2014 Aug;35(8):945-8. doi: 10.1002/humu.22581. Epub 2014 Jun 3. Hum Mutat. 2014. PMID: 24777739 Free PMC article.

8

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.

Zhao X, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X. Zhao X, et al. Among authors: jabs ew. Am J Hum Genet. 2007 Feb;80(2):361-71. doi: 10.1086/511387. Epub 2007 Jan 3. Am J Hum Genet. 2007. PMID: 17236141 Free PMC article.

9

Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients.

Jehee FS, Alonso LG, Cavalcanti DP, Kim C, Wall SA, Mulliken JB, Sun M, Jabs EW, Boyadjiev SA, Wilkie AO, Passos-Bueno MR. Jehee FS, et al. Among authors: jabs ew. Cleft Palate Craniofac J. 2006 Mar;43(2):148-51. doi: 10.1597/04-206.1. Cleft Palate Craniofac J. 2006. PMID: 16526918

10

p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

Wang Y, Zhou X, Oberoi K, Phelps R, Couwenhoven R, Sun M, Rezza A, Holmes G, Percival CJ, Friedenthal J, Krejci P, Richtsmeier JT, Huso DL, Rendl M, Jabs EW. Wang Y, et al. Among authors: jabs ew. J Clin Invest. 2012 Jun;122(6):2153-64. doi: 10.1172/JCI62644. Epub 2012 May 15. J Clin Invest. 2012. PMID: 22585574 Free PMC article.

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