肌球蛋白是问题的核心所在。 - Suppr

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Myosin at the heart of the problem.

作者信息

Tardiff Jil C

机构信息

Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

N Engl J Med. 2004 Jul 29;351(5):424-6. doi: 10.1056/NEJMp048142.

DOI:10.1056/NEJMp048142

PMID:15282349

Abstract

摘要

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Myosin at the heart of the problem.

N Engl J Med. 2004 Jul 29;351(5):424-6. doi: 10.1056/NEJMp048142.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8.

Mutation of perinatal myosin heavy chain associated with a Carney complex variant.

N Engl J Med. 2004 Jul 29;351(5):460-9. doi: 10.1056/NEJMoa040584.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8. doi: 10.1056/NEJM200412093512420.

Mutation linked to variant of Carney complex.

Lancet Oncol. 2004 Sep;5(9):521. doi: 10.1016/s1470-2045(04)01555-4.

Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.

Am J Med Genet A. 2006 Nov 15;140(22):2387-93. doi: 10.1002/ajmg.a.31495.

["Heart myxoma syndrome" a hereditary disease?].

Pathologe. 1988 Jul;9(4):204-10.

[Combination of heart myxoma with primary nodular adrenal cortex dysplasia, spot-shaped skin pigmentation and myxoma-like tumors in other locations--a rare familial symptom complex ("Swiss syndrome")].

Schweiz Med Wochenschr. 1987 Apr 18;117(16):591-4.

Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice.

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Myosin at the heart of the problem.

作者信息

Tardiff Jil C

机构信息

Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

N Engl J Med. 2004 Jul 29;351(5):424-6. doi: 10.1056/NEJMp048142.

DOI:10.1056/NEJMp048142

PMID:15282349

Abstract

摘要

相似文献

Myosin at the heart of the problem.

N Engl J Med. 2004 Jul 29;351(5):424-6. doi: 10.1056/NEJMp048142.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8.

Mutation of perinatal myosin heavy chain associated with a Carney complex variant.

N Engl J Med. 2004 Jul 29;351(5):460-9. doi: 10.1056/NEJMoa040584.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8.

Mutation of perinatal myosin heavy chain.

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8. doi: 10.1056/NEJM200412093512420.

Mutation linked to variant of Carney complex.

Lancet Oncol. 2004 Sep;5(9):521. doi: 10.1016/s1470-2045(04)01555-4.

Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.

Am J Med Genet A. 2006 Nov 15;140(22):2387-93. doi: 10.1002/ajmg.a.31495.

["Heart myxoma syndrome" a hereditary disease?].

Pathologe. 1988 Jul;9(4):204-10.

Schweiz Med Wochenschr. 1987 Apr 18;117(16):591-4.

Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice.

Nat Genet. 1998 Jun;19(2):117-8. doi: 10.1038/470.