A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome (original) (raw)

Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome

Inge Cuppen

Journal of Clinical Investigation

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EP.123Selenoprotein-related congenital myopathy in two siblings

Faruk İncecik

Neuromuscular Disorders, 2019

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Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species Comparisons

Benedikt Schoser

Journal of neuropathology and experimental neurology, 2016

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Faculty Opinions recommendation of Requirement of myomaker-mediated stem cell fusion for skeletal muscle hypertrophy

TROY HORNBERGER

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature

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Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy (XMEA)

Paula Onofre-Oliveira

Disease Models & Mechanisms

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MUSK, a new target for mutations causing congenital myasthenic syndrome

Daniel Hantaï

Human molecular genetics, 2004

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Bi-allelic mutations in MYL1 cause a severe congenital myopathy

Caroline Sewry

Human molecular genetics, 2018

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MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis

Anupama Vydyanath

Human Molecular Genetics, 2013

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Hereditary Inclusion Body Myopathy: A decade of progress

Marjan Huizing

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2009

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Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy

Kazuhiro Ogata

The American Journal of Human Genetics, 2017

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Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy

Teresa Gidaro

Neurology, 2010

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Extensive morphological and immunohistochemical characterization in myotubular myopathy

Michel Fardeau

Brain and Behavior, 2013

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The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs crossbridge detachment and cycling in adult muscle

Michael Regnier

Human molecular genetics, 2015

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X-linked recessive myotubular myopathy with MTM1 mutations

Han-Wook Yoo

Korean journal of pediatrics, 2013

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Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate Myopathy

Mauro Coluccia

Frontiers in Cell and Developmental Biology, 2021

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Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction

Caroline Sewry

Nature reviews. Neurology, 2018

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Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro- Muscular Center

Jean-louis Mandel

Human Molecular Genetics, 1997

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Natural history of a mouse model of X-linked myotubular myopathy

Ege Sarikaya

2021

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Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

Ichizo Nishino

Neurogenetics, 2012

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Congenital myopathies

Enrico Bertini

Current Opinion in Neurology, 2008

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Molecular mechanisms of myoblast fusion across species

Grace Pavlath

Advances in experimental medicine and biology, 2011

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Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism

Weikang Ma

Nature Communications

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Phenotypic and functional reversion of muscular dysgenesis by heterotypic fibroblast-myotube fusion in vitro

Francois Rieger

Advances in experimental medicine and biology, 1990

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Mutations in the MTM1 gene implicated in X-linked myotubular myopathy

Niklas Dahl

1997

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Filopodia powered by class X myosin promote fusion of mammalian myoblasts

Lee Sweeney

eLife

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Pathological defects in congenital myopathies

Caroline Sewry

Journal of Muscle Research and Cell Motility, 2008

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Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report

Roberto Massa

BMC Medical Genetics, 2016

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