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MYH9 (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "MYH9" in German language version.

refsWebsite
Global rank German rank
8nih.gov
4th place
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3doi.org
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2ucsc.edu
3,619th place
3,290th place

doi.org

  • W. H. Linda Kao u. a.: MYH9 is associated with nondiabetic end-stage renal disease in African Americans. In: Nature Genetics. Band 40, Nr. 10, Oktober 2008, S. 1185–1192, doi:10.1038/ng.232, PMID 18794854.
  • Jeffrey B Kopp u. a.: MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis. In: Nature Genetics. Band 40, Nr. 10, Oktober 2008, S. 1175–1184, doi:10.1038/ng.226, PMID 18794856.
  • Giulio Genovese u. a.: Association of trypanolytic ApoL1 variants with kidney disease in African Americans. In: Science. Band 329, Nr. 5993, 13. August 2010, S. 841–845, doi:10.1126/science.1193032, PMID 20647424.

nih.gov

ncbi.nlm.nih.gov

  • J. A. Martignetti u. a.: The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1. In: Am J Hum Genet. 66/2000, S. 1449–1454. PMID 10739770.
  • M. Picu u. a.: An 8-Year-Old Girl With Thrombocytopenia. In: Archives of Pathology & Laboratory Medicine. Band 129, 2005, S. 214–217. PMID 16329740.
  • K. E. Heath u. a.: Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. In: Am J Hum Genet. 69/2001, S. 1033–1045. PMID 11590545.
  • W. H. Linda Kao u. a.: MYH9 is associated with nondiabetic end-stage renal disease in African Americans. In: Nature Genetics. Band 40, Nr. 10, Oktober 2008, S. 1185–1192, doi:10.1038/ng.232, PMID 18794854.
  • Jeffrey B Kopp u. a.: MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis. In: Nature Genetics. Band 40, Nr. 10, Oktober 2008, S. 1175–1184, doi:10.1038/ng.226, PMID 18794856.
  • Giulio Genovese u. a.: Association of trypanolytic ApoL1 variants with kidney disease in African Americans. In: Science. Band 329, Nr. 5993, 13. August 2010, S. 841–845, doi:10.1126/science.1193032, PMID 20647424.
  • E. Pays, B. Vanhollebeke, L. Vanhamme, F. Paturiaux-Hanocq, D. P. Nolan, D. Pérez-Morga: The trypanolytic factor of human serum. In: Nat Rev Microbiol. 4(6), Jun 2006, S. 477–486. PMID 16710327.
  • M. D’Apolito u. a.: Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes. In: Gene. 286/2002, S. 215–222. PMID 11943476.

ucsc.edu

genome.ucsc.edu