Literature DB >> 11897833

Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q.

M P Hitchins, S Abu-Amero, S Apostolidou, D Monk, P Stanier, M A Preece, G E Moore.   

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Year:  2002        PMID： 11897833      PMCID： PMC1735072          DOI： 10.1136/jmg.39.3.e13

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

Review 1.  The genetics of the Silver-Russell syndrome.

Authors:  Michael A Preece
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

2.  Hypomethylation in the 11p15 telomeric imprinting domain in a patient with Silver-Russell syndrome with a CSH1 deletion (17q24) renders a functional role of this alteration unlikely.

Authors:  Thomas Eggermann; Nadine Schönherr; Katja Eggermann; Hartmut Wollmann
Journal:  J Med Genet       Date:  2007-04       Impact factor: 6.318

3.  Tyrosine phosphorylation of growth factor receptor-bound protein-7 by focal adhesion kinase in the regulation of cell migration, proliferation, and tumorigenesis.

Authors:  Pei-Yu Chu; Ling-Ya Huang; Chun-Hua Hsu; Chun-Chi Liang; Jun-Lin Guan; Ting-Hsuan Hung; Tang-Long Shen
Journal:  J Biol Chem       Date:  2009-05-27       Impact factor: 5.157

4.  Genomic organization and control of the grb7 gene family.

Authors:  E Lucas-Fernández; I García-Palmero; A Villalobo
Journal:  Curr Genomics       Date:  2008-03       Impact factor: 2.236
  4 in total

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