編集部に宛てた手紙

Same author

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.

Orphanet journal of rare diseases·2022

Same author

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2011

Same author

Desmin mutations in a St. Petersburg cohort of cardiomyopathies.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2007

Same author

[Quality assurance of secondary prevention of coronary artery disease. Ongoing project offers possibilities for improved treatment].

Lakartidningen·2001

Same author

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

Human molecular genetics·1999

Same author

Pediatric rhabdomyosarcomas express the intermediate filament nestin.

Pediatric research·1998

Same journal

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Science (New York, N.Y.)·2026

Same journal

Local signals, systemic decline.

Science (New York, N.Y.)·2026

Same journal

The mechanics of liver regeneration.

Science (New York, N.Y.)·2026

Same journal

Computing in a memory with physics.

Science (New York, N.Y.)·2026

Same journal

Retraction.

Science (New York, N.Y.)·2026

Same journal

Making time.

Science (New York, N.Y.)·2026

関連する実験動画

編集部に宛てた手紙

関連する概念動画

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

Desmin mutations in a St. Petersburg cohort of cardiomyopathies.

[Quality assurance of secondary prevention of coronary artery disease. Ongoing project offers possibilities for improved treatment].

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

Pediatric rhabdomyosarcomas express the intermediate filament nestin.

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Local signals, systemic decline.

The mechanics of liver regeneration.

Computing in a memory with physics.

Retraction.

Making time.

関連する実験動画

編集部に宛てた手紙

関連する概念動画

関連記事

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

Desmin mutations in a St. Petersburg cohort of cardiomyopathies.

[Quality assurance of secondary prevention of coronary artery disease. Ongoing project offers possibilities for improved treatment].

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

Pediatric rhabdomyosarcomas express the intermediate filament nestin.

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Local signals, systemic decline.

The mechanics of liver regeneration.

Computing in a memory with physics.

Retraction.

Making time.