PubMed for Bookshelf ID: 1436686

Year	Number of Results
1989	1
1992	2
1993	1
1994	5
1995	3
1996	7
1997	9
1998	4
1999	3
2000	6
2001	6
2002	3
2003	7
2024	0

1

Molecular and cellular biology of caveolae paradoxes and plasticities.

Couet J, Shengwen L, Okamoto T, Scherer PE, Lisanti MP. Couet J, et al. Trends Cardiovasc Med. 1997 May;7(4):103-10. doi: 10.1016/S1050-1738(97)00001-7. Trends Cardiovasc Med. 1997. PMID: 21235872

2

Caveolae, caveolin and caveolin-rich membrane domains: a signalling hypothesis.

Lisanti MP, Scherer PE, Tang Z, Sargiacomo M. Lisanti MP, et al. Trends Cell Biol. 1994 Jul;4(7):231-5. doi: 10.1016/0962-8924(94)90114-7. Trends Cell Biol. 1994. PMID: 14731661

3

Modulation of myoblast fusion by caveolin-3 in dystrophic skeletal muscle cells: implications for Duchenne muscular dystrophy and limb-girdle muscular dystrophy-1C.

Volonte D, Peoples AJ, Galbiati F. Volonte D, et al. Mol Biol Cell. 2003 Oct;14(10):4075-88. doi: 10.1091/mbc.e03-03-0161. Epub 2003 Aug 7. Mol Biol Cell. 2003. PMID: 14517320 Free PMC article.

4

Transgenic overexpression of caveolin-3 in the heart induces a cardiomyopathic phenotype.

Aravamudan B, Volonte D, Ramani R, Gursoy E, Lisanti MP, London B, Galbiati F. Aravamudan B, et al. Hum Mol Genet. 2003 Nov 1;12(21):2777-88. doi: 10.1093/hmg/ddg313. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966035

5

Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene.

Figarella-Branger D, Pouget J, Bernard R, Krahn M, Fernandez C, Lévy N, Pellissier JF. Figarella-Branger D, et al. Neurology. 2003 Aug 26;61(4):562-4. doi: 10.1212/01.wnl.0000076486.57572.5c. Neurology. 2003. PMID: 12939441 Review.

6

Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease.

Sotgia F, Woodman SE, Bonuccelli G, Capozza F, Minetti C, Scherer PE, Lisanti MP. Sotgia F, et al. Am J Physiol Cell Physiol. 2003 Nov;285(5):C1150-60. doi: 10.1152/ajpcell.00166.2003. Epub 2003 Jul 2. Am J Physiol Cell Physiol. 2003. PMID: 12839838 Free article.

7

Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.

Kubisch C, Schoser BG, von Düring M, Betz RC, Goebel HH, Zahn S, Ehrbrecht A, Aasly J, Schroers A, Popovic N, Lochmüller H, Schröder JM, Brüning T, Malin JP, Fricke B, Meinck HM, Torbergsen T, Engels H, Voss B, Vorgerd M. Kubisch C, et al. Ann Neurol. 2003 Apr;53(4):512-20. doi: 10.1002/ana.10501. Ann Neurol. 2003. PMID: 12666119

8

Consequences of a novel caveolin-3 mutation in a large German family.

Fischer D, Schroers A, Blümcke I, Urbach H, Zerres K, Mortier W, Vorgerd M, Schröder R. Fischer D, et al. Ann Neurol. 2003 Feb;53(2):233-41. doi: 10.1002/ana.10442. Ann Neurol. 2003. PMID: 12557291

9

Limb-girdle muscular dystrophy.

Mathews KD, Moore SA. Mathews KD, et al. Curr Neurol Neurosci Rep. 2003 Jan;3(1):78-85. doi: 10.1007/s11910-003-0042-9. Curr Neurol Neurosci Rep. 2003. PMID: 12507416 Review.

10

Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene.

Merlini L, Carbone I, Capanni C, Sabatelli P, Tortorelli S, Sotgia F, Lisanti MP, Bruno C, Minetti C. Merlini L, et al. J Neurol Neurosurg Psychiatry. 2002 Jul;73(1):65-7. doi: 10.1136/jnnp.73.1.65. J Neurol Neurosurg Psychiatry. 2002. PMID: 12082049 Free PMC article.

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