Literature DB >> 10809382

Id genes in nervous system development.

P J Andres-Barquin1, M C Hernandez, M A Israel.   

Abstract

Id genes encode helix-loop-helix proteins that function to mediate processes important for normal development including cellular differentiation, proliferation and apoptosis. Id proteins act as negative regulators of other transcription factors, which are essential for cell determination and differentiation in diverse cell types, and interact with proteins important for cell cycle regulation. Studies of Id gene expression in the nervous system and in neural cells in culture indicate that Id proteins contribute to the regulation of mammalian nervous system development. Also, recognition of a wide variety of proteins with which Id transcription factors are capable of interacting suggests that it will be possible to understand more precisely their specific functions and importantly how these are integrated.

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Year:  2000        PMID: 10809382     DOI: 10.14670/HH-15.603

Source DB:  PubMed          Journal:  Histol Histopathol        ISSN: 0213-3911            Impact factor:   2.303


  22 in total

Review 1.  Inhibitors of DNA binding in neural cell proliferation and differentiation.

Authors:  Shun-Fen Tzeng
Journal:  Neurochem Res       Date:  2003-01       Impact factor: 3.996

Review 2.  Helix-loop-helix proteins in mammary gland development and breast cancer.

Authors:  Pierre-Yves Desprez; Tomoki Sumida; Jean-Philippe Coppé
Journal:  J Mammary Gland Biol Neoplasia       Date:  2003-04       Impact factor: 2.673

3.  To proliferate or to die: role of Id3 in cell cycle progression and survival of neural crest progenitors.

Authors:  Yun Kee; Marianne Bronner-Fraser
Journal:  Genes Dev       Date:  2005-03-15       Impact factor: 11.361

4.  Impaired terminal differentiation of hippocampal granule neurons and defective contextual memory in PC3/Tis21 knockout mice.

Authors:  Stefano Farioli-Vecchioli; Daniele Saraulli; Marco Costanzi; Luca Leonardi; Irene Cinà; Laura Micheli; Michele Nutini; Patrizia Longone; S Paul Oh; Vincenzo Cestari; Felice Tirone
Journal:  PLoS One       Date:  2009-12-17       Impact factor: 3.240

5.  Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Authors:  Sailaja Peddada; Dag H Yasui; Janine M LaSalle
Journal:  Hum Mol Genet       Date:  2006-05-08       Impact factor: 6.150

6.  Id4 suppresses MMP2-mediated invasion of glioblastoma-derived cells by direct inactivation of Twist1 function.

Authors:  G J Rahme; M A Israel
Journal:  Oncogene       Date:  2014-01-13       Impact factor: 9.867

7.  The transcriptional repressor ID2 can interact with the canonical clock components CLOCK and BMAL1 and mediate inhibitory effects on mPer1 expression.

Authors:  Sarah M Ward; Shanik J Fernando; Tim Y Hou; Giles E Duffield
Journal:  J Biol Chem       Date:  2010-09-22       Impact factor: 5.157

8.  Molecular regulation of vasculogenic mimicry in tumors and potential tumor-target therapy.

Authors:  Yue-Zu Fan; Wei Sun
Journal:  World J Gastrointest Surg       Date:  2010-04-27

9.  Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations.

Authors:  Jennifer L Larimore; Christopher A Chapleau; Shinichi Kudo; Anne Theibert; Alan K Percy; Lucas Pozzo-Miller
Journal:  Neurobiol Dis       Date:  2009-01-03       Impact factor: 5.996

10.  Hypoxia-induced gene expression in human macrophages: implications for ischemic tissues and hypoxia-regulated gene therapy.

Authors:  Bernard Burke; Athina Giannoudis; Kevin P Corke; Dalvir Gill; Michael Wells; Loems Ziegler-Heitbrock; Claire E Lewis
Journal:  Am J Pathol       Date:  2003-10       Impact factor: 4.307

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