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Short body length phenotype is compensated by the upregulation of nidogen family members in a deleterious nid1a mutation of zebrafish

  • Published:2017-11 Issue:11 Volume:44 Page:553-556
  • ISSN:1673-8527
  • Container-title:Journal of Genetics and Genomics
  • language:en
  • Short-container-title:Journal of Genetics and Genomics

Author:

Zhu Peipei,Ma Zhipeng,Guo Liwei,Zhang Wei,Zhang Qinghe,Zhao Ting,Jiang Kunpeng,Peng Jinrong,Chen Jun

Funder

National Natural Science Foundation of China

Fundamental Research Funds

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology

Reference20 articles.

1. Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice;Bader;Mol. Cell. Biol.,2005

2. tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors;Berghmans;Proc. Natl. Acad. Sci. U. S. A.,2005

3. Loss of nidogen-1 and -2 results in syndactyly and changes in limb development;Bose;J. Biol. Chem.,2006

4. Entactin, a novel basal lamina-associated sulfated glycoprotein;Carlin;J. Biol. Chem.,1981

5. Transcriptional and phenotypic comparisons of Ppara knockout and siRNA knockdown mice;De Souza;Nucleic Acids Res.,2006

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