(Q58052162)

6

0 references

Mayana Zatz

4

object named as

Mayana Zatz

0 references

author name string

Telma L. F. Gouveia

1

0 references

Patrícia M. Kossugue

2

0 references

Julia F. Paim

3

0 references

Louise V. B. Anderson

Journal of Molecular Medicine

5

0 references

publication date

30 January 2007

0 references

published in

0 references

volume

85

0 references

issue

4

0 references

page(s)

415-420

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s00109-007-0163-8

0 references

cites work

Dystrophin-associated proteins in muscular dystrophy

1 reference

12 December 2020

Caveolin-3 in muscular dystrophy

1 reference

12 December 2020

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions

1 reference

12 December 2020

Zeta-sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex

1 reference

12 December 2020

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

1 reference

12 December 2020

Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan.

1 reference

12 December 2020

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

1 reference

12 December 2020

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

1 reference

12 December 2020

Sequential expression of genes involved in muscular dystrophies during human development.

1 reference

12 December 2020

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies

1 reference

12 December 2020

Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family

1 reference

12 December 2020

Myotilin is mutated in limb girdle muscular dystrophy 1A

1 reference

12 December 2020

Sarcoglycans in muscular dystrophy

1 reference

12 December 2020

Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes

1 reference

12 December 2020

The beta-delta-core of sarcoglycan is essential for deposition at the plasma membrane.

1 reference

12 December 2020

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31

1 reference

12 December 2020

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

1 reference

12 December 2020

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.

1 reference

12 December 2020

Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

1 reference

12 December 2020

Novel sarcoglycan gene mutations in a large cohort of Italian patients.

1 reference

12 December 2020

Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies

1 reference

12 December 2020

Developmental expression of sarcoglycan gene products in cultured myocytes

1 reference

12 December 2020

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

1 reference

12 December 2020

Limb-girdle muscular dystrophies: an overview

1 reference

12 December 2020

The limb-girdle muscular dystrophies-multiple genes, multiple mechanisms

1 reference

12 December 2020

Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations

1 reference

12 December 2020

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population

1 reference

12 December 2020

Association of dystrophin and an integral membrane glycoprotein.

1 reference

12 December 2020

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

12 December 2020

Expanding the clinical spectrum of POMT1 phenotype.

1 reference

12 December 2020

Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex

1 reference

12 December 2020

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

1 reference

12 December 2020

Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations

1 reference

12 December 2020

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G

1 reference

12 December 2020

The 10 autosomal recessive limb-girdle muscular dystrophies

1 reference

12 December 2020

Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC Consortium on Limb-Girdle Dystrophies

1 reference

12 December 2020

A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F

1 reference

12 December 2020

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7

1 reference

12 December 2020

A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.

1 reference

12 December 2020

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

1 reference

12 December 2020