Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Muscular dystrophy in the mouse caused by an allele at the dy-locus.

Literature DB >> 5434356

Muscular dystrophy in the mouse caused by an allele at the dy-locus.

H Meier, J L Southard.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 1970 PMID： 5434356 DOI： 10.1016/0024-3205(70)90306-1

Source DB: PubMed Journal: Life Sci ISSN： 0024-3205 Impact factor: 5.037

Keyword Cloud
Cited

× No keyword cloud information.

19 in total

Review 1. Laminins in peripheral nerve development and muscular dystrophy.

Authors: Wei-Ming Yu; Huaxu Yu; Zu-Lin Chen
Journal: Mol Neurobiol Date: 2007-06 Impact factor: 5.590

2. Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies.

Authors: P C G Onofre-Oliveira; A L F Santos; P M Martins; D Ayub-Guerrieri; M Vainzof
Journal: Neuromolecular Med Date: 2012-02-24 Impact factor: 3.843

3. Elimination of polyneuronal innervation in a fast muscle of normal and dystrophic mice.

Authors: J Dangain; G Vrbová
Journal: J Physiol Date: 1983-09 Impact factor: 5.182

4. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.

Authors: W Kuang; H Xu; P H Vachon; L Liu; F Loechel; U M Wewer; E Engvall
Journal: J Clin Invest Date: 1998-08-15 Impact factor: 14.808

5. Successful treatment of murine muscular dystrophy with the proteinase inhibitor leupeptin.

Authors: J H Sher; A Stracher; S A Shafiq; J Hardy-Stashin
Journal: Proc Natl Acad Sci U S A Date: 1981-12 Impact factor: 11.205

Review 6. Myocardial diseases of animals.

Authors: J F Van Vleet; V J Ferrans
Journal: Am J Pathol Date: 1986-07 Impact factor: 4.307

Muscular dystrophy in the mouse caused by an allele at the dy-locus.

Review 1. Laminins in peripheral nerve development and muscular dystrophy.

2. Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies.

3. Elimination of polyneuronal innervation in a fast muscle of normal and dystrophic mice.

4. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.

5. Successful treatment of murine muscular dystrophy with the proteinase inhibitor leupeptin.

Review 6. Myocardial diseases of animals.

7. Calcium and strontium activation of single skinned muscle fibres of normal and dystrophic mice.

Review 8. The role of laminins in the organization and function of neuromuscular junctions.

9. Ultrastructure of muscle spindles in C57BL/6J dy2J/dy2J dystrophic mice.

10. A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments.