(Q28299243)

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S D Wilton

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P A Akkari

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S Dorosz

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K Boundy

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C Kneebone

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P Blumbergs

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S White

Human hTM alpha gene: expression in muscle and nonmuscle tissue

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language of work or name

English

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publication date

January 1995

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75-9

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cites work

1 reference

Isolation and characterization of cDNA clones encoding the skeletal and smooth muscle Xenopus laevis beta tropomyosin isoforms

21 January 2018

1 reference

21 January 2018

Congenital myopathies

1 reference

7 January 2021

NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY

1 reference

7 January 2021

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation

1 reference

7 January 2021

Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation

1 reference

7 January 2021

Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisation

1 reference

7 January 2021

Differential control of tropomyosin mRNA levels during myogenesis suggests the existence of an isoform competition-autoregulatory compensation control mechanism

1 reference

7 January 2021

Organization of the hTMnm gene. Implications for the evolution of muscle and non-muscle tropomyosins

1 reference

7 January 2021

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

1 reference

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

7 January 2021

New evidence for excessive accumulation of Z-band material in nemaline myopathy

1 reference

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

7 January 2021

Exclusion of two candidate loci for autosomal recessive nemaline myopathy

1 reference

7 January 2021

An actin-interacting heptapeptide in the cofilin sequence

1 reference

7 January 2021

Tropomyosin has discrete actin-binding sites with sevenfold and fourteenfold periodicities

1 reference

7 January 2021

Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

1 reference

7 January 2021

Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization.

1 reference

7 January 2021

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1

1 reference

7 January 2021

Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation

1 reference

7 January 2021

Complete nucleotide sequence of the adult skeletal isoform of human skeletal muscleβ-tropomyosin

1 reference

7 January 2021

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

1 reference

7 January 2021

Organization of contractile protein genes within the 88F subdivision of the D. melanogaster third chromosome

1 reference

7 January 2021

Characterization of a tropomyosin cDNA from the hydrozoan Podocoryne carnea

1 reference

7 January 2021