Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ] (Q48686462)

14 February 2018

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title

Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ] (English)

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

6 November 2022

Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1713858

6 November 2022

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6 November 2022

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

6 November 2022

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

6 November 2022

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

6 November 2022

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6 November 2022

author name string

Obermaier-Kusser B

1

1 reference

14 February 2018

Paetzke-Brunner I

2

1 reference

14 February 2018

Müller-Höcker J

4

1 reference

14 February 2018

B. Obermaier-Kusser

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1713858

6 November 2022

I. Paetzke-Brunner

2

1 reference

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6 November 2022

C. Enter

3

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6 November 2022

J. Müller-Höcker

4

1 reference

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6 November 2022

S. Zierz

5

1 reference

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6 November 2022

W. Ruitenbeek

6

1 reference

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6 November 2022

K. D. Gerbitz

7

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6 November 2022

language of work or name

English

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publication date

1 July 1991

1 reference

14 February 2018

29 July 1991

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1713858

full work available at URL

6 November 2022

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2F0014-5793%2891%2980942-V

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2F0014-5793(91)80942-V

6 November 2022

1 reference

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http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(91)80942-V/fullpdf

6 November 2022

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6 November 2022

1 reference

14 February 2018

volume

286

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14 February 2018

issue

1-2

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14 February 2018

page(s)

67-70

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14 February 2018

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

cites work

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

21 January 2018

1 reference

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Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.

21 January 2018

1 reference

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

21 January 2018

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Cloning of human mitochondrial DNA in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2F0014-5793%2891%2980942-V

Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method

21 January 2018

1 reference

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A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changes

21 January 2018

1 reference

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Biochemical and Biophysical Research Communications

21 January 2018

4

author name string

Enter

publication date

1990

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

6 November 2022

10

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie

6 November 2022

11

28

241

Gerbitz

1990

1 reference

https://api.crossref.org/works/10.1016/0014-5793(91)80942-V

6 November 2022

Identifiers

1 reference

14 February 2018

1 reference

14 February 2018