MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

A New Equation to Estimate Glomerular Filtration Rate

(2013) Andrew S. Levey et al.   ANNALS OF INTERNAL MEDICINE

The mechanism of the converter domain rotation in the recovery stroke of myosin motor protein

(2013) Andrij Baumketner   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations

(2012) Daniela De Rocco et al.   European Journal of Medical Genetics

A Trp33Arg Mutation at Exon 1 of theMYH9Gene in a Korean Patient with May-Hegglin Anomaly

(2012) Moon Ju Jang et al.   YONSEI MEDICAL JOURNAL

Phosphorylation of the myosin IIA tailpiece regulates single myosin IIA molecule association with lytic granules to promote NK-cell cytotoxicity

(2011) K. B. Sanborn et al.   BLOOD

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias

(2011) Carlo L. Balduini et al.   BRITISH JOURNAL OF HAEMATOLOGY

Renal manifestations of patients with MYH9-related disorders

(2011) Kyoung Hee Han et al.   PEDIATRIC NEPHROLOGY

Structural and Functional Insights into the Myosin Motor Mechanism

(2010) H. Lee Sweeney et al.   Annual Review of Biophysics

Advances in the understanding of MYH9 disorders

(2010) Shinji Kunishima et al.   CURRENT OPINION IN HEMATOLOGY

Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

(2010) Takashi Sekine et al.   KIDNEY INTERNATIONAL

Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

(2010) Daniela De Rocco et al.   THROMBOSIS AND HAEMOSTASIS

MYH-9 Related Platelet Disorders: Strategies for Management and Diagnosis

(2010) Karina Althaus et al.   TRANSFUSION MEDICINE AND HEMOTHERAPY

MYH9related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype

(2009) Alessandro Pecci et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

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

(2009) Miguel Vicente-Manzanares et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

MYH9related disease: A novel missense Ala95Asp mutation of theMYH9gene

(2009) Daniela de Rocco et al.   PLATELETS

MYH9-Related Platelet Disorders

(2009) Karina Althaus et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Head–Head and Head–Tail Interaction: A General Mechanism for Switching Off Myosin II Activity in Cells

(2008) Hyun Suk Jung et al.   MOLECULAR BIOLOGY OF THE CELL

Renin-angiotensin system blockade is effective in reducing proteinuria of patients with progressive nephropathy caused by MYH9 mutations (Fechtner-Epstein syndrome)

(2008) A. Pecci et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history ofMYH9-related disease

(2007) Alessandro Pecci et al.   HUMAN MUTATION