(Q24647603)

1

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Paolo Bernardi

object named as

Paolo Bernardi

10

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author name string

Alessia Angelin

2

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Tania Tiepolo

3

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Patrizia Sabatelli

5

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Alessandra Zamparelli

6

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Alessandra Ferlini

7

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Nadir M Maraldi

8

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Paolo Bonaldo

Proceedings of the National Academy of Sciences of the United States of America

9

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language of work or name

English

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publication date

1 April 2008

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published in

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volume

105

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page(s)

5225-9

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issue

13

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cites work

Collagen VI related muscle disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

The Ca2+-induced membrane transition in mitochondria. I. The protective mechanisms

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

The nonimmunosuppressive cyclosporin analogs NIM811 and UNIL025 display nanomolar potencies on permeability transition in brain-derived mitochondria.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Muscular dystrophy--reason for optimism?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Opening of the mitochondrial permeability transition pore causes depletion of mitochondrial and cytosolic NAD+ and is a causative event in the death of myocytes in postischemic reperfusion of the heart.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mitochondrial membrane potential and neuronal glutamate excitotoxicity: mortality and millivolts

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Fluctuations in mitochondrial membrane potential caused by repetitive gating of the permeability transition pore

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mitochondria and cell death. Mechanistic aspects and methodological issues

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Transient and long-lasting openings of the mitochondrial permeability transition pore can be monitored directly in intact cells by changes in mitochondrial calcein fluorescence

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Imaging the permeability pore transition in single mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Mitochondria are excitable organelles capable of generating and conveying electrical and calcium signals.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Calcium and pyridine nucleotide interaction in mitochondrial membranes

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy.

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Arachidonic acid causes cell death through the mitochondrial permeability transition. Implications for tumor necrosis factor-alpha aopototic signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Desensitization of the permeability transition pore by cyclosporin a prevents activation of the mitochondrial apoptotic pathway and liver damage by tumor necrosis factor-alpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Kongenitale, atonisch-sklerotische Muskeldystrophie, ein weiterer Typus der heredodegenerativen Erkrankungen des neuromuskulären Systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Interactions of cyclophilin with the mitochondrial inner membrane and regulation of the permeability transition pore, and cyclosporin A-sensitive channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

X-ray structure of a decameric cyclophilin-cyclosporin crystal complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23-24 November 2001, Naarden, The Netherlands

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800962105

Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278179

Quantitative assay by flow cytometry of the mitochondrial membrane potential in intact cells

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18362356

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0800962105

1 reference

1892048

ADS bibcode

2008PNAS..105.5225M

0 references

1892048

1 reference

1 reference

1 reference