Literature DB >> 1284527

Characterization of the human HOX 7 cDNA and identification of polymorphic markers.

B J Padanilam1, H S Stadler, K A Mills, L B McLeod, M Solursh, B Lee, F Ramirez, K H Buetow, J C Murray.   

Abstract

cDNA clones for a human HOX 7 gene obtained with homologous clones of Drosophila were used in human gene mapping studies. The human cDNA clone was isolated from a library constructed from human embryonic craniofacial material. The sequence of the cDNA demonstrates significant homology with mouse HOX 7. A search for RFLPs identified MboII and BstEII variants. A CA dinucleotide repeat with 5 alleles was also identified and allowed placement of HOX 7 into a defined linkage map. Evidence for linkage disequilibrium was found with markers tested. These results place the human HOX 7 gene in a defined position on 4p.

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Year:  1992        PMID： 1284527     DOI： 10.1093/hmg/1.6.407

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


  12 in total

1.  Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Authors:  H S Stadler; B J Padanilam; K Buetow; J C Murray; M Solursh
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

2.  Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.

Authors:  Deborah A Driscoll; Torrey Boland; Beverly S Emanuel; Richard E Kirschner; Don LaRossa; Jeanne Manson; Donna McDonald-McGinn; Peter Randall; Cynthia Solot; Elaine Zackai; Laura E Mitchell
Journal:  Cleft Palate Craniofac J       Date:  2006-07

3.  Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.

Authors:  Munefumi Kamamoto; Junichiro Machida; Seishi Yamaguchi; Masashi Kimura; Takao Ono; Peter A Jezewski; Yujiro Higashi; Atsuo Nakayama; Kazuo Shimozato; Yoshihito Tokita
Journal:  Eur J Hum Genet       Date:  2011-03-30       Impact factor: 4.246

4.  Evaluation of candidate genes for familial brachydactyly.

Authors:  J M Mastrobattista; P Dollé; S H Blanton; H Northrup
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

5.  Endogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammals.

Authors:  C Blin-Wakkach; F Lezot; S Ghoul-Mazgar; D Hotton; S Monteiro; C Teillaud; L Pibouin; S Orestes-Cardoso; P Papagerakis; M Macdougall; B Robert; A Berdal
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-05       Impact factor: 11.205

6.  Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.

Authors:  P Nieminen; S Arte; S Pirinen; L Peltonen; I Thesleff
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

7.  Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region.

Authors:  Rebecca L Slayton; Laura Williams; Jeffrey C Murray; James J Wheeler; Andrew C Lidral; Carla J Nishimura
Journal:  Cleft Palate Craniofac J       Date:  2003-05

8.  Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Authors:  A C Lidral; P A Romitti; A M Basart; T Doetschman; N J Leysens; S Daack-Hirsch; E V Semina; L R Johnson; J Machida; A Burds; T J Parnell; J L Rubenstein; J C Murray
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

9.  Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.

Authors:  P A Jezewski; A R Vieira; C Nishimura; B Ludwig; M Johnson; S E O'Brien; S Daack-Hirsch; R E Schultz; A Weber; B Nepomucena; P A Romitti; K Christensen; I M Orioli; E E Castilla; J Machida; N Natsume; J C Murray
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

10.  Genetic significance of muscle segment homeo box1 gene in South Indian population for cleft lip and palate.

Authors:  Venkanna S Prasad; Venkatesh Shivani
Journal:  Indian J Hum Genet       Date:  2012-09
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