(Q24317420)

GOA release 2020-03-11

muscle organ development

1 reference

GOA release 2020-03-11

1 reference

16

E P Hoffman

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author name string

Y K Hayashi

1

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F L Chou

2

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E Engvall

3

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M Ogawa

4

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C Matsuda

5

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S Hirabayashi

6

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K Yokochi

7

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B L Ziober

8

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R H Kramer

9

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S J Kaufman

10

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E Ozawa

11

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Y Goto

12

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I Nonaka

13

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T Tsukahara

14

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J Z Wang

15

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K Arahata

https://scigraph.springernature.com/pub.10.1038/ng0598-94

17

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language of work or name

English

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publication date

May 1998

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published in

Nature Genetics

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volume

19

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page(s)

94-7

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issue

1

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exact match

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cites work

H36-alpha 7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis

1 reference

Distinct alpha 7A beta 1 and alpha 7B beta 1 integrin expression patterns during mouse development: alpha 7A is restricted to skeletal muscle but alpha 7B is expressed in striated muscle, vasculature, and nervous system

20 April 2017

1 reference

Absence of integrin alpha 7 causes a novel form of muscular dystrophy

20 April 2017

1 reference

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

20 April 2017

1 reference

Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa

20 April 2017

1 reference

Synaptic integrins in developing, adult, and mutant muscle: selective association of alpha1, alpha7A, and alpha7B integrins with the neuromuscular junction

20 April 2017

1 reference

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

20 April 2017

1 reference

Expression of the avian alpha 7-integrin in developing nervous system and myotome

20 April 2017

1 reference

Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia.

21 January 2018

1 reference

Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice.

21 January 2018

1 reference

Abnormal localization of laminin subunits in muscular dystrophies

21 January 2018

1 reference

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

21 January 2018

1 reference

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

21 January 2018

1 reference

Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy

21 January 2018

1 reference

7 January 2021

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle

1 reference

7 January 2021

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa

1 reference

7 January 2021

A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia

1 reference

7 January 2021

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses

1 reference

7 January 2021

Expression of utrophin (dystrophin-related protein) and dystrophin-associated glycoproteins in muscles from patients with Duchenne muscular dystrophy

1 reference

7 January 2021

A dystrophin-associated glycoprotein, A3a (one of 43DAG doublets), is retained in Duchenne muscular dystrophy muscle

1 reference

7 January 2021