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Year Number of Results
2001 1
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2004 2
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2010 2
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2024 0

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Page 1
Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy.
Angelini C, Tasca E, Nascimbeni AC, Fanin M. Angelini C, et al. Acta Myol. 2014 Dec;33(3):119-26. Acta Myol. 2014. PMID: 25873780 Free PMC article. Review.
In sarcoglycanopathies, the sarcolemmal nNOS reactivity varied from absent to reduced, depending on the residual level of sarcoglycan complex: in cases with complete sarcoglycan complex deficiency (mostly in beta-sarcoglycanopathy), the sarcolemmal nNOS reaction was absent and it …
In sarcoglycanopathies, the sarcolemmal nNOS reactivity varied from absent to reduced, depending on the residual level of sarcoglycan comple …
Caveolae and cancer: A new mechanical perspective.
Lamaze C, Torrino S. Lamaze C, et al. Biomed J. 2015 Sep-Oct;38(5):367-79. doi: 10.4103/2319-4170.164229. Biomed J. 2015. PMID: 26345539 Free article. Review.
Caveolae dysfunction, due to mutations in caveolins, has been linked to several human diseases called "caveolinopathies," including muscular dystrophies, cardiac disease, infection, osteoporosis, and cancer. ...
Caveolae dysfunction, due to mutations in caveolins, has been linked to several human diseases called "caveolinopathies," including m …
A Role for Caveolin-3 in the Pathogenesis of Muscular Dystrophies.
Pradhan BS, Prószyński TJ. Pradhan BS, et al. Int J Mol Sci. 2020 Nov 19;21(22):8736. doi: 10.3390/ijms21228736. Int J Mol Sci. 2020. PMID: 33228026 Free PMC article. Review.
Mutations in Caveolin-3 are known to cause muscular dystrophies that are collectively called caveolinopathies. Altered expression of Caveolin-3 is also observed in Duchenne's muscular dystrophy, which is likely a part of the pathological process leading to muscle weakness. …
Mutations in Caveolin-3 are known to cause muscular dystrophies that are collectively called caveolinopathies. Altered expression of …
[Updates in muscular dystrophies].
Erazo-Torricelli R. Erazo-Torricelli R. Rev Neurol. 2004 Nov 1-15;39(9):860-71. Rev Neurol. 2004. PMID: 15543503 Free article. Review. Spanish.
The others limb girdle muscular dystrophies, an heterogeneous phenotypical group, are detected by Western blot (mainly calpainopathies), or inmunohistochemistry in muscle (caveolinopathies) and blood (dysferlinopathies). Congenital muscular dystrophies with brain malformat …
The others limb girdle muscular dystrophies, an heterogeneous phenotypical group, are detected by Western blot (mainly calpainopathies), or …
Aquaporin expression in normal and pathological skeletal muscles: a brief review with focus on AQP4.
Wakayama Y. Wakayama Y. J Biomed Biotechnol. 2010;2010:731569. doi: 10.1155/2010/731569. Epub 2010 Mar 21. J Biomed Biotechnol. 2010. PMID: 20339523 Free PMC article. Review.
OAs were present in normal myofiber plasma membranes and were especially numerous in fast twitch type 2 myofibers; while OAs were lost from sarcolemmal plasma membranes of severely affected muscles with dystrophinopathy and dysferlinopathy but not with caveolinopathy. In t …
OAs were present in normal myofiber plasma membranes and were especially numerous in fast twitch type 2 myofibers; while OAs were lost from …
Sarcolemmopathy: muscular dystrophies with cell membrane defects.
Ozawa E, Nishino I, Nonaka I. Ozawa E, et al. Brain Pathol. 2001 Apr;11(2):218-30. doi: 10.1111/j.1750-3639.2001.tb00394.x. Brain Pathol. 2001. PMID: 11303797 Free PMC article. Review.
These disorders include Bethlem myopathy, merosinopathy, dystrophinopathy, sarcoglycanopathies, integrinopathy, dysferlinopathy and caveolinopathy. We refer to these diseases collectively as sarcolemmopathy. ...
These disorders include Bethlem myopathy, merosinopathy, dystrophinopathy, sarcoglycanopathies, integrinopathy, dysferlinopathy and caveo
Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies.
Bönnemann CG, Finkel RS. Bönnemann CG, et al. Semin Pediatr Neurol. 2002 Jun;9(2):81-99. doi: 10.1053/spen.2002.33795. Semin Pediatr Neurol. 2002. PMID: 12139001 Review.
The molecular findings are correlated with some of the clinical phenotypes that are part of the limb-girdle muscular dystrophy spectrum, including fukutin-related proteinopathy (LGMD 21), the sarcoglycanopathies (LGMD 2C-F), caveolinopathy (LGMD 1C), dysferlinopathy (LGMD …
The molecular findings are correlated with some of the clinical phenotypes that are part of the limb-girdle muscular dystrophy spectrum, inc …
The role of membrane-shaping BAR domain proteins in caveolar invagination: from mechanistic insights to pathophysiological consequences.
Kessels MM, Qualmann B. Kessels MM, et al. Biochem Soc Trans. 2020 Feb 28;48(1):137-146. doi: 10.1042/BST20190377. Biochem Soc Trans. 2020. PMID: 32104881 Review.
Muscle cells of syndapin III KO mice showed severe reductions of caveolae reminiscent of human caveolinopathies and were more vulnerable to membrane damage upon changes in membrane tensions. ...
Muscle cells of syndapin III KO mice showed severe reductions of caveolae reminiscent of human caveolinopathies and were more vulnera …
11 results