(Q34415490)

English

Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Francis Collins

3

object named as

Collins FS

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Russell MW

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

du Manoir S

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Brody LC

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

1 January 1997

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

number of pages

2

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

8

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Europe PubMed Central

PubMed publication ID

2 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

60-61

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

https://scigraph.springernature.com/pub.10.1007/s003359900596

0 references

Expression of the novel basic helix-loop-helix gene eHAND in neural crest derivatives and extraembryonic membranes during mouse development

1 reference

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Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

1 reference

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Gsh-2, a murine homeobox gene expressed in the developing brain

1 reference

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HLH proteins, fly neurogenesis, and vertebrate myogenesis

1 reference

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Cardiac hypertrophy. Mechanical, neural, and endocrine dependence

1 reference

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Molecular pathways controlling heart development

1 reference

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The MyoD family of transcription factors and skeletal myogenesis

1 reference

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21 January 2018

A subclass of bHLH proteins required for cardiac morphogenesis

1 reference

https://api.crossref.org/works/10.1007%2FS003359900596

21 January 2018

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

1 reference

https://api.crossref.org/works/10.1007%2FS003359900596

21 January 2018

The helix-loop-helix gene E2A is required for B cell formation

1 reference

https://api.crossref.org/works/10.1007%2FS003359900596

21 January 2018

Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

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Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

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The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

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Preparation and screening of an arrayed human genomic library generated with the P1 cloning system

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

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Basic local alignment search tool

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

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Sequences of 20 subunits of NADH:ubiquinone oxidoreductase from bovine heart mitochondria. Application of a novel strategy for sequencing proteins using the polymerase chain reaction

1 reference

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A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene

1 reference

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

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The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

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inferred from PubMed ID database lookup

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of the electron transport chain in idiopathic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

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inferred from PubMed ID database lookup

How do polypeptides cross the mitochondrial membranes?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9021153

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S003359900596

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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