肌浆内六边形交联管状阵列对小窝蛋白-3进行免疫染色：一种过度的小窝蛋白病？ - Suppr

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Sarcoplasmic hexagonally cross-linked tubular arrays immunostain for caveolin-3: an excess caveolinopathy?

作者信息

Lach Boleslaw, Tarnopolsky Mark, Nguyen Clara

出版信息

Acta Neuropathol. 2009 Mar;117(3):339-41. doi: 10.1007/s00401-009-0487-2. Epub 2009 Jan 31.

DOI:10.1007/s00401-009-0487-2

PMID:19184067

Abstract

摘要

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Sarcoplasmic hexagonally cross-linked tubular arrays immunostain for caveolin-3: an excess caveolinopathy?

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引用本文的文献

169th ENMC International Workshop Rare Structural Congenital Myopathies 6-8 November 2009, Naarden, The Netherlands.

Neuromuscul Disord. 2011 May;21(5):363-74. doi: 10.1016/j.nmd.2011.02.009. Epub 2011 Mar 29.

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Sarcoplasmic hexagonally cross-linked tubular arrays immunostain for caveolin-3: an excess caveolinopathy?

作者信息

Lach Boleslaw, Tarnopolsky Mark, Nguyen Clara

出版信息

Acta Neuropathol. 2009 Mar;117(3):339-41. doi: 10.1007/s00401-009-0487-2. Epub 2009 Jan 31.

DOI:10.1007/s00401-009-0487-2

PMID:19184067

Abstract

摘要

相似文献

Sarcoplasmic hexagonally cross-linked tubular arrays immunostain for caveolin-3: an excess caveolinopathy?

Acta Neuropathol. 2009 Mar;117(3):339-41. doi: 10.1007/s00401-009-0487-2. Epub 2009 Jan 31.

Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entity.

Neuromuscul Disord. 2010 Nov;20(11):701-8. doi: 10.1016/j.nmd.2010.06.006. Epub 2010 Jul 15.

[Myocyte sarcolemmal and cytoskeleton proteins in inherited muscular diseases].

Duodecim. 2003;119(3):179-86.

Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy.

Neuromuscul Disord. 2010 May;20(5):326-9. doi: 10.1016/j.nmd.2010.02.003. Epub 2010 Mar 7.

Polysaccharide storage myopathy--case report and literature review.

Clin Neuropathol. 2005 May-Jun;24(3):126-32.

A novel missense mutation in the caveolin-3 gene in rippling muscle disease.

Muscle Nerve. 2007 Aug;36(2):258-60. doi: 10.1002/mus.20781.

Cylindrical spirals in skeletal muscle: a further observation with clinical, morphological, and biochemical analysis.

Muscle Nerve. 1983 Nov-Dec;6(9):646-55. doi: 10.1002/mus.880060905.

Tiny percutaneous needle biopsy: An efficient method for studying cellular and molecular aspects of skeletal muscle in humans.

Int J Mol Med. 2011 Mar;27(3):361-7. doi: 10.3892/ijmm.2010.582. Epub 2010 Dec 14.

Nucleolar characteristics of reducing bodies in reducing body myopathy.

Acta Neuropathol. 2004 Mar;107(3):265-71. doi: 10.1007/s00401-003-0806-y. Epub 2004 Jan 20.

Adult-onset muscular dystrophy in a cat associated with a presumptive alteration in trafficking of caveolin-3.

J Comp Pathol. 2012 Aug-Oct;147(2-3):253-8. doi: 10.1016/j.jcpa.2011.12.012. Epub 2012 Feb 3.

引用本文的文献

169th ENMC International Workshop Rare Structural Congenital Myopathies 6-8 November 2009, Naarden, The Netherlands.

Neuromuscul Disord. 2011 May;21(5):363-74. doi: 10.1016/j.nmd.2011.02.009. Epub 2011 Mar 29.