(Q34657783)

3 August 2017

1 reference

title

Muscle development genes: their relevance in neuromuscular disorders (English)

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3 August 2017

Sue Brown

2

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Francesco Muntoni

series ordinal

1

object named as

Francesco Muntoni

1 reference

3 August 2017

Caroline Sewry

3

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3 August 2017

Ketan Patel

series ordinal

4

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3 August 2017

publication date

1 June 2002

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3 August 2017

published in

Neuromuscular Disorders

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3 August 2017

volume

12

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3 August 2017

issue

5

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3 August 2017

page(s)

438-446

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Genes that control the development of migrating muscle precursor cells.

3 August 2017

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The importance of timing differentiation during limb muscle development

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Pax7 is required for the specification of myogenic satellite cells

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From insect eye to vertebrate muscle: redeployment of a regulatory network

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Mox2 is a component of the genetic hierarchy controlling limb muscle development

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Functional redundancy of the muscle-specific transcription factors Myf5 and myogenin

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Early specification of limb muscle precursor cells by the homeobox gene Lbx1h.

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Myogenic stem cell function is impaired in mice lacking the forkhead/winged helix protein MNF

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The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

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Dedifferentiation of mammalian myotubes induced by msx1

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

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7 January 2021

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

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Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

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Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders

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In situ hybridization analysis for expression of myogenic regulatory factors in regenerating muscle of mdx mouse

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Inactivation of Myf-6 and Myf-5 genes in mice leads to alterations in skeletal muscle development

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7 January 2021

MyoD(-/-) satellite cells in single-fiber culture are differentiation defective and MRF4 deficient

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7 January 2021

Myotube formation is delayed but not prevented in MyoD-deficient skeletal muscle: studies in regenerating whole muscle grafts of adult mice

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7 January 2021

MyoD is required for myogenic stem cell function in adult skeletal muscle

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7 January 2021

Expression of MyoD and myogenin in dystrophic mice, mdx and dy, during regeneration

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7 January 2021

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

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7 January 2021

Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva

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7 January 2021

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

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7 January 2021

A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient

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7 January 2021

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

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7 January 2021

A nonsense mutation in MSX1 causes Witkop syndrome

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7 January 2021

Myostatin and the control of skeletal muscle mass

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7 January 2021

Uncoupling of Grb2 from the Met receptor in vivo reveals complex roles in muscle development

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7 January 2021

Altered primary myogenesis in NFATC3(-/-) mice leads to decreased muscle size in the adult

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7 January 2021

Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene

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7 January 2021

Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathies

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7 January 2021

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

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Elevated basic fibroblast growth factor in the serum of patients with Duchenne muscular dystrophy

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7 January 2021

Fibroblast growth factor in the extracellular matrix of dystrophic (mdx) mouse muscle

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7 January 2021

An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy

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7 January 2021

Organization of the human myostatin gene and expression in healthy men and HIV-infected men with muscle wasting

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7 January 2021

Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowing.

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7 January 2021

Part I. Amyoplasia: A common, sporadic condition with congenital contractures

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7 January 2021

Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?

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7 January 2021

Skeletal myogenic progenitors originating from embryonic dorsal aorta coexpress endothelial and myogenic markers and contribute to postnatal muscle growth and regeneration

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7 January 2021

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Identifiers

DOI

1 reference

3 August 2017

1 reference