Literature DB >> 14671068

Double nucleotidic mutation of the MYH9 gene in a young patient with end-stage renal disease.

Maria Capria1, Michele Andreucci, Laura Fuiano, Domenico Mancuso, Paola Cianfrone, Nicola Comi, Giuseppe Mazza, Alfredo Caglioti, Giorgio Fuiano.   

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Year:  2004        PMID： 14671068     DOI： 10.1093/ndt/gfg475

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  3 in total

Review 1.  Non-muscle myosin II takes centre stage in cell adhesion and migration.

Authors:  Miguel Vicente-Manzanares; Xuefei Ma; Robert S Adelstein; Alan Rick Horwitz
Journal:  Nat Rev Mol Cell Biol       Date:  2009-11       Impact factor: 94.444

2.  Renin-angiotensin System Blockade Therapy for Early Renal Involvement in MYH9-related Disease with an E1841K Mutation.

Authors:  Mari Tanaka; Sho Miki; Hirona Saita; Hiroki Shimada; Seira Nishikawa; Keisuke Taniguchi; Koichiro Hagihara; Sachio Iwanari; Masaki Ikeda; Shinji Kunishima; Hiroya Takeoka
Journal:  Intern Med       Date:  2019-06-27       Impact factor: 1.271

3.  Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders.

Authors:  Béatrice Saposnik; Sylvie Binard; Odile Fenneteau; Alan Nurden; Paquita Nurden; Marie-Françoise Hurtaud-Roux; Nicole Schlegel
Journal:  Mol Genet Genomic Med       Date:  2014-02-07       Impact factor: 2.183
  3 in total

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