Literature DB >> 9286712

Lhx4, a LIM homeobox gene.

T Yamashita1, K Moriyama, H Z Sheng, H Westphal.   

Abstract

LIM homeobox genes are well conserved in evolution and play important roles as transcriptional regulators of embryonic development. Here we report on the structure of LIM domains of the mouse Lhx4 (Gsh4) gene. The cDNA was generated by modified reverse transcription-PCR from midgestation embryo templates, using a degenerate consensus primer. The deduced amino acid sequence of the first LIM domain reveals 77% identity and that of the second domain reveals 86% identity with the corresponding sequences of the closely related Lhx3 gene. In addition, there is 38-56% similarity to other members of the Lhx gene family. The LIM consensus sequence is well conserved in Lhx4.

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Year:  1997        PMID: 9286712     DOI: 10.1006/geno.1997.4852

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Expression of LIM-homeodomain transcription factors in the developing and mature mouse retina.

Authors:  Revathi Balasubramanian; Andrew Bui; Qian Ding; Lin Gan
Journal:  Gene Expr Patterns       Date:  2013-12-10       Impact factor: 1.224

2.  Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

Authors:  K Machinis; J Pantel; I Netchine; J Léger; O J Camand; M L Sobrier; F Dastot-Le Moal; P Duquesnoy; M Abitbol; P Czernichow; S Amselem
Journal:  Am J Hum Genet       Date:  2001-09-20       Impact factor: 11.025

Review 3.  LIM-homeodomain genes in mammalian development and human disease.

Authors:  Chad S Hunter; Simon J Rhodes
Journal:  Mol Biol Rep       Date:  2005-06       Impact factor: 2.316

4.  Generation and characterization of Lhx4tdT reporter knock-in and Lhx4loxP conditional knockout mice.

Authors:  Xuhui Dong; Xiaoling Xie; Luming Guo; Jiadong Xu; Mei Xu; Guoqing Liang; Lin Gan
Journal:  Genesis       Date:  2019-07-17       Impact factor: 2.487

5.  Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue.

Authors:  Claire Rochette; Nicolas Jullien; Alexandru Saveanu; Emmanuelle Caldagues; Ignacio Bergada; Debora Braslavsky; Marija Pfeifer; Rachel Reynaud; Jean-Paul Herman; Anne Barlier; Thierry Brue; Alain Enjalbert; Frederic Castinetti
Journal:  PLoS One       Date:  2015-05-08       Impact factor: 3.240

6.  Molecular and Clinical Findings in Patients with LHX4 and OTX2 Mutations.

Authors:  Toshihiro Tajima; Katsura Ishizu; Akie Nakamura
Journal:  Clin Pediatr Endocrinol       Date:  2013-04-26
  6 in total

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