(Q24291338)

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Identification of two nuclear genes (ATP11, ATP12) required for assembly of the yeast F1-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

ATP synthase of yeast mitochondria. Isolation of subunit j and disruption of the ATP18 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Bovine coupling factor 6, with just 14.5% shared identity, replaces subunit h in the yeast ATP synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

The assembly factor Atp11p binds to the beta-subunit of the mitochondrial F(1)-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

The alpha-subunit of the mitochondrial F(1) ATPase interacts directly with the assembly factor Atp12p

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

The Drosophila gene 2A5 complements the defect in mitochondrial F1-ATPase assembly in yeast lacking the molecular chaperone Atp11p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Nucleotide sequence of a cDNA for the alpha subunit of human mitochondrial ATP synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Human F1-ATPase: molecular cloning of cDNA for the beta subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Yeast/E. coli shuttle vectors with multiple unique restriction sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

A physical map of 30,000 human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

A comprehensive view of human chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

An STS-based map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

A novel genetic system to detect protein-protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

High efficiency transformation of intact yeast cells using single stranded nucleic acids as a carrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Report of the fifth international workshop on human chromosome 1 mapping 1999.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Human diseases with defects in oxidative phosphorylation. 2. F1F0 ATP-synthase defects in Alzheimer disease revealed by blue native polyacrylamide gel electrophoresis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Interstitial deletion of (17)(p11.2p11.2) in nine patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

A novel deficiency of mitochondrial ATPase of nuclear origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

Bacterial production and characterization of ATP11, a yeast protein required for mitochondrial F1-ATPase assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

7 January 2021

Identification of functional domains in Atp11p. Protein required for assembly of the mitochondrial F1-ATPase in yeast

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

7 January 2021

Mutational studies with Atp12p, a protein required for assembly of the mitochondrial F1-ATPase in yeast. Identification of domains important for Atp12p function and oligomerization

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104133200

7 January 2021

Identifiers

DOI

10.1074/JBC.M104133200

1 reference

Consolidated OpenCitations Corpus – April 2017

release_ieuvorbw6nfwrmbjvsrwdu4aqe

4764493

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ieuvorbw6nfwrmbjvsrwdu4aqe

24 November 2022

mapped directly with Wikidata item

4764493

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference