Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy (Q35754519)

10 August 2017

title

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy (English)

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10 August 2017

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E Arbustini

1

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author name string

M Diegoli

2

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10 August 2017

R Fasani

3

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10 August 2017

M Grasso

4

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10 August 2017

P Morbini

5

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10 August 2017

N Banchieri

6

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10 August 2017

O Bellini

7

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10 August 2017

B Dal Bello

8

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10 August 2017

A Pilotto

9

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10 August 2017

G Magrini

10

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10 August 2017

C Campana

11

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10 August 2017

P Fortina

12

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10 August 2017

A Gavazzi

13

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10 August 2017

J Narula

14

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10 August 2017

M Viganò

15

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10 August 2017

language of work or name

English

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publication date

1 November 1998

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The American Journal of Pathology

10 August 2017

published in

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10 August 2017

volume

153

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10 August 2017

issue

5

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10 August 2017

page(s)

1501-1510

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An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study

10 August 2017

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2 October 2017

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2 October 2017

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2 October 2017

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Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects

2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases

2 October 2017

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Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia

2 October 2017

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2 October 2017

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PCR-SSCP: a method for detection of mutations

2 October 2017

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Human heart mast cells. Isolation, purification, ultrastructure, and immunologic characterization

2 October 2017

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A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene

27 July 2018

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Idiopathic cardiomyopathy. Mitochondrial and cytoplasmic alterations in heart and liver.

27 July 2018

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Percutaneous transvenous endomyocardial biopsy in human heart recipients. Experience with a new technique

27 July 2018

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Expression of tumor necrosis factor in human acute cardiac rejection. An immunohistochemical and immunoblotting study

27 July 2018

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A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

25 September 2018

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Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy

25 September 2018

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A Novel mtDNA Point Mutation in Maternally Inherited Cardiomyopathy

7 January 2021

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An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

7 January 2021

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Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

7 January 2021

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Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy

7 January 2021

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Mitochondrial mutation in fatal infantile cardiomyopathy

7 January 2021

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Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy

7 January 2021

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A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy

7 January 2021

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Restrictive Cardiomyopathy, Atrioventricular Block and Mild to Subclinical Myopathy in Patients With Desmin-Immunoreactive Material Deposits

7 January 2021

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Leber′s Hereditary Optic Neuropathy (LHON)-Related Mitochondrial DNA Sequence Changes in Italian Patients Presenting with Sporadic Bilateral Optic Neuritis

7 January 2021

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[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

7 January 2021

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Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

7 January 2021

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Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy

7 January 2021

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A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

7 January 2021

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Ischaemic colitis due to mitochondrial cytopathy

7 January 2021

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)65738-0

1 reference

10 August 2017

1 reference

10 August 2017

1 reference