Found: 12
Select item for more details and to access through your institution.
Selenoprotein N deficiency in mice is associated with abnormal lung development.
- Published in:
- FASEB Journal, 2013, v. 27, n. 4, p. 1585, doi. 10.1096/fj.12-212688
- By:
- Publication type:
- Article
Integrated multi‐omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex.
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2024, v. 15, n. 3, p. 1003, doi. 10.1002/jcsm.13470
- By:
- Publication type:
- Article
Sarcomeric and nonmuscle α‐actinin isoforms exhibit differential dynamics at skeletal muscle Z‐lines.
- Published in:
- Cytoskeleton, 2018, v. 75, n. 5, p. 213, doi. 10.1002/cm.21442
- By:
- Publication type:
- Article
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 1, p. 17, doi. 10.1038/ng713
- By:
- Publication type:
- Article
X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene.
- Published in:
- Skeletal Muscle, 2015, v. 5, n. 1, p. 1, doi. 10.1186/s13395-014-0025-3
- By:
- Publication type:
- Article
X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene.
- Published in:
- Skeletal Muscle, 2015, v. 5, n. 1, p. 1, doi. 10.1186/s13395-014-0025-3
- By:
- Publication type:
- Article
Mutations of tropomyosin 3 ( TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.
- Published in:
- Human Mutation, 2010, v. 31, n. 2, p. 176, doi. 10.1002/humu.21157
- By:
- Publication type:
- Article
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
- Published in:
- Muscle & Nerve, 2009, v. 39, n. 6, p. 739, doi. 10.1002/mus.21230
- By:
- Publication type:
- Article
Abnormal lysosomal and ubiquitin‐proteasome pathways in 19p13.3 distal myopathy.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 1, p. 133
- By:
- Publication type:
- Article
Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2467, doi. 10.1093/hmg/ddg264
- By:
- Publication type:
- Article
Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression pattern.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 9, p. 1045, doi. 10.1093/hmg/ddg115
- By:
- Publication type:
- Article
Adenylosuccinic Acid: An Orphan Drug with Untapped Potential.
- Published in:
- Pharmaceuticals (14248247), 2023, v. 16, n. 6, p. 822, doi. 10.3390/ph16060822
- By:
- Publication type:
- Article