(Q22253448)

GOA release 2020-03-11

Syntrophin gamma 2

1 reference

GOA release 2020-03-11

V Nigro

10

V

Nigro

1 reference

7 February 2023

G Piluso

1

G

Piluso

1 reference

7 February 2023

M Mirabella

2

M

Mirabella

1 reference

7 February 2023

E Ricci

3

E

Ricci

1 reference

7 February 2023

A Belsito

4

A

Belsito

1 reference

7 February 2023

C Abbondanza

5

C

Abbondanza

1 reference

7 February 2023

S Servidei

6

S

Servidei

1 reference

7 February 2023

A A Puca

7

A A

Puca

1 reference

7 February 2023

P Tonali

8

P

Tonali

1 reference

7 February 2023

G A Puca

9

G A

Journal of Biological Chemistry

Puca

1 reference

7 February 2023

language of work or name

English

0 references

publication date

26 May 2000

0 references

published in

0 references

volume

275

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page(s)

15851-60

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issue

21

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cites work

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Agrin binding to alpha-dystroglycan. Domains of agrin necessary to induce acetylcholine receptor clustering are overlapping but not identical to the alpha-dystroglycan-binding region

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Caveolin-3 in muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Identification of the Syrian hamster cardiomyopathy gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

A postsynaptic Mr 58,000 (58K) protein concentrated at acetylcholine receptor-rich sites in Torpedo electroplaques and skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Syntrophin binds to an alternatively spliced exon of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Differential association of syntrophin pairs with the dystrophin complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Characterization of the dystrophin-syntrophin interaction using the two-hybrid system in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

beta-dystrobrevin, a member of the dystrophin-related protein family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Identification and characterization of a novel member of the dystrobrevin gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The pleckstrin homology domain: an intriguing multifunctional protein module

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

PDZ domains: targeting signalling molecules to sub-membranous sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Relation of neuronal APP-751/APP-695 mRNA ratio and neuritic plaque density in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The P-loop--a common motif in ATP- and GTP-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Direct binding of Torpedo syntrophin to dystrophin and the 87 kDa dystrophin homologue

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

A novel genetic system to detect protein-protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

The WW domain: a signalling site in dystrophin?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

ZZ and TAZ: new putative zinc fingers in dystrophin and other proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Dystrobrevin and dystrophin: an interaction through coiled-coil motifs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Up71 and up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Different dystrophin-like complexes are expressed in neurons and glia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

Duchenne muscular dystrophy--Meryon's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

A role for dystroglycan in basement membrane assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Mouse alpha 1- and beta 2-syntrophin gene structure, chromosome localization, and homology with a discs large domain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Heterogeneity of dystrophin-associated proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021

Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M000439200

7 January 2021