Russell Norris to Mutation
This is a "connection" page, showing publications Russell Norris has written about Mutation.
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0.387
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Mutations in DCHS1 cause mitral valve prolapse. Nature. 2015 Sep 03; 525(7567):109-13.
Score: 0.087
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Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation. Biochim Biophys Acta. 2014 Feb; 1843(2):234-44.
Score: 0.077
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Periostin regulates collagen fibrillogenesis and the biomechanical properties of connective tissues. J Cell Biochem. 2007 Jun 01; 101(3):695-711.
Score: 0.049
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The identification of Prx1 transcription regulatory domains provides a mechanism for unequal compensation by the Prx1 and Prx2 loci. J Biol Chem. 2001 Jul 20; 276(29):26829-37.
Score: 0.032
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Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome. Mamm Genome. 2000 Nov; 11(11):1000-5.
Score: 0.031
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New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study. Eur Heart J. 2018 04 14; 39(15):1269-1277.
Score: 0.026
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The exocyst is required for photoreceptor ciliogenesis and retinal development. J Biol Chem. 2017 09 08; 292(36):14814-14826.
Score: 0.025
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Mutations in the TGF-? repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm. Nat Genet. 2012 Nov; 44(11):1249-54.
Score: 0.018
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Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-?. J Clin Invest. 2010 Oct; 120(10):3520-9.
Score: 0.015
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Developmental basis of adult cardiovascular diseases: valvular heart diseases. Ann N Y Acad Sci. 2010 Feb; 1188:177-83.
Score: 0.015
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Versican proteolysis mediates myocardial regression during outflow tract development. Dev Dyn. 2007 Mar; 236(3):671-83.
Score: 0.012