Literature DB >> 9425595

Role of HOX genes in human development.

J W Innis1.   

Abstract

Hox genes specify developmental boundaries and determine cell fate during morphogenesis. Recently, two human syndromes, synpolydactyly and hand-foot-genital were shown to result from mutations in HOX genes. Both disorders affect digital arch structures and can involve genitourinary malformations. These studies confirm the critical role of these highly conserved transcription factors in the specification of growth and patterning of skeletal elements and axial soft tissues in humans.

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Year:  1997        PMID: 9425595     DOI: 10.1097/00008480-199712000-00011

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  3 in total

1.  Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.

Authors:  Gopalrao V N Velagaleti; Judy C Hawkins; Neli I Panova; Lillian H Lockhart
Journal:  Indian J Pediatr       Date:  2008-09       Impact factor: 1.967

2.  Study of the dynamic expression of Meis1 in mice.

Authors:  Li Hai-Xia; Guo Xin-Yu; Xie Yan; Yuan Qi-Long; Ge Ming-Xiao; Zhang Jin-Yu
Journal:  Iran J Reprod Med       Date:  2013-02

3.  Transcriptomic analysis of the black tiger shrimp (Penaeus monodon) reveals insights into immune development in their early life stages.

Authors:  Pacharaporn Angthong; Tanaporn Uengwetwanit; Sopacha Arayamethakorn; Wanilada Rungrassamee
Journal:  Sci Rep       Date:  2021-07-06       Impact factor: 4.379

  3 in total

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