Titin mutations as the molecular basis for dilated cardiomyopathy (Q24292301)

Titin-cap

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titin

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cardiac muscle contraction

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dilated cardiomyopathy

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5

Takuro Arimura

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author name string

Manatsu Itoh-Satoh

1

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Takeharu Hayashi

2

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Hirofumi Nishi

3

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Yoshinori Koga

4

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Takeshi Koyanagi

6

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Megumi Takahashi

7

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Shigeru Hohda

8

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Kazuo Ueda

9

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Tatsuhito Nouchi

10

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Michiaki Hiroe

11

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Fumiaki Marumo

12

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Tsutomu Imaizumi

13

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Michio Yasunami

14

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Akinori Kimura

Biochemical and Biophysical Research Communications

15

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language of work or name

English

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publication date

22 February 2002

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published in

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volume

291

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issue

2

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page(s)

385-93

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cites work

The N-terminal Z repeat 5 of connectin/titin binds to the C-terminal region of alpha-actinin

1 reference

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7 January 2021

Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese

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7 January 2021

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

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7 January 2021

Tissue-specific expression and alpha-actinin binding properties of the Z-disc titin: implications for the nature of vertebrate Z-discs

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7 January 2021

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy

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7 January 2021

Novel missense mutation in cardiac beta myosin heavy chain gene found in a Japanese patient with hypertrophic cardiomyopathy

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7 January 2021

Passive tension in cardiac muscle: contribution of collagen, titin, microtubules, and intermediate filaments

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7 January 2021

Telethonin, a novel sarcomeric protein of heart and skeletal muscle

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DNA typing of HLA class II genes in Japanese patients with dilated cardiomyopathy.

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

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The Genetic Basis for Cardiomyopathy

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

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Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

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7 January 2021

The role of cytoskeletal proteins in cardiomyopathies

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Structural basis for activation of the titin kinase domain during myofibrillogenesis

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7 January 2021

Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy

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7 January 2021

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

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7 January 2021

A novel X-linked gene, G4.5. is responsible for Barth syndrome

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7 January 2021

Genetics and dilated cardiomyopathy: limitations of candidate gene strategies

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The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

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Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

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7 January 2021

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

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Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

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7 January 2021

Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence

1 reference

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7 January 2021

Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

The NH2 terminus of titin spans the Z-disc: its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

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7 January 2021

Molecular structure of the sarcomeric Z-disk: two types of titin interactions lead to an asymmetrical sorting of alpha-actinin.

1 reference

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7 January 2021

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

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https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Titins: giant proteins in charge of muscle ultrastructure and elasticity

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7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

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7 January 2021

Cardiac titin isoforms are coexpressed in the half-sarcomere and extend independently

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7 January 2021

Carnitine palmitoyltransferase in patients with cardiac ischemia due to atherosclerotic coronary artery disease and in patients with idiopathic dilated cardiomyopathy

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https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system

1 reference

https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

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https://api.crossref.org/works/10.1006%2FBBRC.2002.6448

7 January 2021