Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere (Q24316399)

Tropomyosin 1

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Troponin T2, cardiac type

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troponin T binding

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hypertrophic cardiomyopathy

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familial hypertrophic cardiomyopathy

inferred from title

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inferred from title

author

Hugh Christian Watkins

object named as

H Watkins

2

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Jonathan G Seidman

7

object named as

J G Seidman

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author name string

L Thierfelder

1

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C MacRae

3

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R Lamas

4

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W McKenna

5

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H P Vosberg

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C E Seidman

The molecular basis for tropomyosin isoform diversity

8

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language of work or name

English

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publication date

3 June 1994

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published in

Cell

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volume

77

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issue

5

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page(s)

701-12

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cites work

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Human myosin-binding protein H (MyBP-H): complete primary sequence, genomic organization, and chromosomal localization

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Chromosomal localization and genomic cloning of the mouse alpha-tropomyosin gene Tpm-1.

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A cDNA encoding a muscle-type tropomyosin cloned from a human epithelial cell line: identity with human fibroblast tropomyosin TM1

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Molecular cloning and developmental expression of human cardiac troponin T.

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Complete nucleotide sequence of the fast skeletal troponin T gene. Alternatively spliced exons exhibit unusual interspecies divergence

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Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities

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Complete nucleotide sequence and structural organization of rat cardiac troponin T gene

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Using bacteriophage P1 system to clone high molecular weight genomic DNA

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Interaction of tropomyosin and troponin T: a proton nuclear magnetic resonance study

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Bovine cardiac troponin T: amino acid sequences of the two isoforms

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Structure of co-crystals of tropomyosin and troponin

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A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

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The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families

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Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (2).

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Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

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Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

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Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

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Characterization of muscle and non muscle Xenopus laevis tropomyosin mRNAs transcribed from the same gene. Developmental and tissue-specific expression

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Exon definition may facilitate splice site selection in RNAs with multiple exons

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Isolation and characterization of a cDNA that encodes mouse fibroblast tropomyosin isoform 2

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Human hTM alpha gene: expression in muscle and nonmuscle tissue

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Hypertrophic cardiomyopathy: one disease or several?

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Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction

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Growth factors, proto-oncogenes, and plasticity of the cardiac phenotype

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Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

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Troponin T isoform expression in humans. A comparison among normal and failing adult heart, fetal heart, and adult and fetal skeletal muscle

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Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

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Troponin T Expression in Normal and Pressure-Loaded Fetal Sheep Heart

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

1408579

1408579

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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