MYH9-Related Disease-Reference-Cited by-同舟云学术

MYH9-Related Disease

Published:2003-05 Issue:3 Volume:82 Page:203-215
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Seri Marco,Pecci Alessandro,Di Bari Filomena,Cusano Roberto,Savino Maria,Panza Emanuele,Nigro Alessandra,Noris Patrizia,Gangarossa Simone,Rocca Bianca,Gresele Paolo,Bizzaro Nicola,Malatesta Paola,Koivisto Pasi A.,Longo Ilaria,Musso Roberto,Pecoraro Carmine,Iolascon Achille,Magrini Umberto,Soriano Juan Rodriguez,Renieri Alessandra,Ghiggeri Gian Marco,Ravazzolo Roberto,Balduini Carlo L.,Savoia Anna

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference29 articles.

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2. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes.;Arrondel;J Am Soc Nephrol,2002

3. Expression of non-muscle myosin isoforms in rabbit myometrium is estrogen-dependent.;Chiavegato;Cell Tissue Res,1996

4. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.;Chomczynski;Anal Biochem,1987

5. Hereditary thrombocytopenia, deafness, and renal disease.;Eckstein;Ann Intern Med,1975

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3. MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approaches;Research and Practice in Thrombosis and Haemostasis;2024-08

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