(Q48070846)

English

Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

mitochondrial DNA

0 references

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

Valeria Tiranti

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

author name string

C Mariotti

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

G Uziel

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

F Carrara

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

A Prelle

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

S DiDonato

7

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

M Zeviani

8

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

publication date

1 September 1995

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

242

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

9

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

547-556

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

https://scigraph.springernature.com/pub.10.1007/bf00868806

0 references

Sequence and organization of the human mitochondrial genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Similarity of human mitochondrial transcription factor 1 to high mobility group proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid isolation of animal mitochondrial DNA by alkaline extraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infantile liver failure associated with mitochondrial DNA depletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human mitochondrial DNA variation and evolution: analysis of nucleotide sequences from seven individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein measurement with the Folin phenol reagent

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple abnormalities of ectoglycosyltransferases in cultured fibroblasts from patients with mucolipidosis II: Possible indication for abnormal plasma membrane glycoproteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/8551315

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00868806

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8551315

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48070846&oldid=2183731262"