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Publications by M Sata

Functional Analysis of the Mutations in the Human Cardiac Beta-Myosin That Are Responsible for Familial Hypertrophic Cardiomyopathy. Implication for the Clinical Outcome.

Journal of Clinical Investigation

Medicine

1996

English

Demonstration of Reversed Flow in Segmental Branches of the Portal Vein With Hand-Held Color Doppler Ultrasonography After Hematopoietic Stem Cell Transplantation

Bone Marrow Transplantation

Transplantation

Hematology

2005

English

Related publications

On the Functional Assessment of Hypertrophic Cardiomyopathy-Causing Mutations in Human Β-Cardiac Myosin and the Role of Myosin Binding Protein-C

Biophysical Journal

Biophysics

2019

English

Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.

Journal of Medical Genetics

Genetics

1998

English

Impact of Hypertrophic Cardiomyopathy Mutations on the Cardiac Myosin Super-Relaxed State

Biophysical Journal

Biophysics

2019

English

Myosin Phosphorylation-Mediated Rescue of Cardiac Function in Familial Hypertrophic Cardiomyopathy

Biophysical Journal

Biophysics

2018

English

Impact of Human Beta-Cardiac Myosin Mutation Implicated in Both Hypertrophic and Dilated Cardiomyopathy

Biophysical Journal

Biophysics

2019

English

The Effect of Regulatory Light Chain Phosphorylation on Myosin Bearing Familial Hypertrophic Cardiomyopathy-Linked Mutations

Biophysical Journal

Biophysics

2013

English

Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations That Cause Familial Hypertrophic Cardiomyopathy

Journal of Biological Chemistry

English

Single-Molecule Mechanics of R403Q Cardiac Myosin Isolated From the Mouse Model of Familial Hypertrophic Cardiomyopathy

Circulation Research

Cardiovascular Medicine

Physiology

Cardiology

2000

English

Familial Hypertrophic Cardiomyopathy: Unequal Expression of Mutant and Wildtype Myosin in Individual Myocytes as Trigger for Functional Impairment of the Heart?

Biophysical Journal

Biophysics

2014

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by M Sata

Functional Analysis of the Mutations in the Human Cardiac Beta-Myosin That Are Responsible for Familial Hypertrophic Cardiomyopathy. Implication for the Clinical Outcome.

Demonstration of Reversed Flow in Segmental Branches of the Portal Vein With Hand-Held Color Doppler Ultrasonography After Hematopoietic Stem Cell Transplantation

Related publications

On the Functional Assessment of Hypertrophic Cardiomyopathy-Causing Mutations in Human Β-Cardiac Myosin and the Role of Myosin Binding Protein-C

Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.

Impact of Hypertrophic Cardiomyopathy Mutations on the Cardiac Myosin Super-Relaxed State

Myosin Phosphorylation-Mediated Rescue of Cardiac Function in Familial Hypertrophic Cardiomyopathy

Impact of Human Beta-Cardiac Myosin Mutation Implicated in Both Hypertrophic and Dilated Cardiomyopathy

The Effect of Regulatory Light Chain Phosphorylation on Myosin Bearing Familial Hypertrophic Cardiomyopathy-Linked Mutations

Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations That Cause Familial Hypertrophic Cardiomyopathy

Single-Molecule Mechanics of R403Q Cardiac Myosin Isolated From the Mouse Model of Familial Hypertrophic Cardiomyopathy

Familial Hypertrophic Cardiomyopathy: Unequal Expression of Mutant and Wildtype Myosin in Individual Myocytes as Trigger for Functional Impairment of the Heart?