(Q39669065)

English

Impairment of F1F0-ATPase, adenine nucleotide translocator and adenylate kinase causes mitochondrial energy deficit in human skin fibroblasts with chromosome 21 trisomy

scientific article published on October 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Impairment of F1F0-ATPase, adenine nucleotide translocator and adenylate kinase causes mitochondrial energy deficit in human skin fibroblasts with chromosome 21 trisomy (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

6

object named as

Ersilia Marra

0 references

Mariano Francesco Caratozzolo

object named as

Mariano F Caratozzolo

3

0 references

Daniela Valenti

object named as

Daniela Valenti

1

0 references

Rosa Anna Vacca

object named as

Rosa A Vacca

7

0 references

author name string

Apollonia Tullo

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Riccardo S Merafina

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Paolo Scartezzini

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

language of work or name

0 references

publication date

1 October 2010

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Biochemical Journal

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

431

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

299-310

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Down syndrome--recent progress and future prospects

1 reference

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21 January 2018

Alzheimer disease and Down syndrome: factors in pathogenesis

1 reference

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21 January 2018

Mental retardation in Down syndrome: from gene dosage imbalance to molecular and cellular mechanisms

1 reference

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21 January 2018

Understanding the basis for Down syndrome phenotypes

1 reference

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21 January 2018

Mitochondrial dysfunction and tau hyperphosphorylation in Ts1Cje, a mouse model for Down syndrome.

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Mitochondrial dysfunction and Down's syndrome.

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Molecular pathogenesis of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Proteomic evaluation of intermediary metabolism enzyme proteins in fetal Down's syndrome cerebral cortex

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Altered metabolism of the amyloid beta precursor protein is associated with mitochondrial dysfunction in Down's syndrome

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Down syndrome fibroblast model of Alzheimer-related endosome pathology: accelerated endocytosis promotes late endocytic defects

1 reference

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21 January 2018

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

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Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

In the early phase of programmed cell death in Tobacco Bright Yellow 2 cells the mitochondrial adenine nucleotide translocator, adenylate kinase and nucleoside diphosphate kinase are impaired in a reactive oxygen species-dependent manner

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Caspase-dependent alteration of the ADP/ATP translocator triggers the mitochondrial permeability transition which is not required for the low-potassium-dependent apoptosis of cerebellar granule cells.

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Dynamics of nucleotide metabolism as a supporter of life phenomena

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

DNA supercoiling suppresses real-time PCR: a new approach to the quantification of mitochondrial DNA damage and repair

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Differential expression of beta 1c integrin messenger ribonucleic acid and protein levels in human endometrium and decidua during the menstrual cycle and pregnancy

1 reference

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21 January 2018

10-N nonyl-acridine orange: a fluorescent probe which stains mitochondria independently of their energetic state.

1 reference

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21 January 2018

Increase in the ADP/ATP exchange in rat liver mitochondria irradiated in vitro by helium-neon laser

1 reference

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21 January 2018

Tissue-specific transcription pattern of the adenine nucleotide translocase isoforms in humans.

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Altered signaling pathways underlying abnormal hippocampal synaptic plasticity in the Ts65Dn mouse model of Down syndrome

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Energy substrate modulates mitochondrial structure and oxidative capacity in cancer cells

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Cyclic AMP produced inside mitochondria regulates oxidative phosphorylation

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Mitochondrial oxidative phosphorylation disorders presenting in neonates: clinical manifestations and enzymatic and molecular diagnoses.

1 reference

https://api.crossref.org/works/10.1042%2FBJ20100581

21 January 2018

Identifiers

10.1042/BJ20100581

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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