(Q39720312)

14 September 2017

Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genes (English)

1 reference

14 September 2017

Y Michikawa

1

1 reference

14 September 2017

G Hofhaus

series ordinal

2

1 reference

14 September 2017

L S Lerman

series ordinal

3

1 reference

14 September 2017

G Attardi

series ordinal

4

1 reference

14 September 2017

language of work or name

English

0 references

publication date

1 June 1997

1 reference

14 September 2017

Nucleic Acids Research

1 reference

14 September 2017

25

1 reference

14 September 2017

12

1 reference

14 September 2017

2455-2463

1 reference

Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Mitochondrial DNA sequence variation in human evolution and disease.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

The development of mitochondrial medicine

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Sequence and organization of the human mitochondrial genome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Detection and localization of single base changes by denaturing gradient gel electrophoresis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

The excised leader of human cytochrome c oxidase subunit I mRNA which contains the origin of mitochondrial DNA light-strand synthesis accumulates in mitochondria and is polyadenylated

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Unexpected behavior of H2Kb mutant DNAs in denaturing gradient gel electrophoresis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Mapping point mutations in the Drosophila rosy locus using denaturing gradient gel blots

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Diseases of the mitochondrial DNA.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

'Broad-range' DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase gene

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Intramolecular DNA melting between stable helical segments: melting theory and metastable states

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Human aging is associated with stochastic somatic mutations of mitochondrial DNA.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Inverted repeat sequences can influence the melting transitions of linear DNAs

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) gene.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

In vitro replication of human mitochondrial DNA: accurate initiation at the origin of light-strand synthesis

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

A general method for introducing a series of mutations into cloned DNA using the polymerase chain reaction

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

Biochemical characterization of a pedigree with mitochondrially inherited deafness

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146751

[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

17 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Sequence-Determined DNA Separations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Use of denaturing gradient gel electrophoresis to study conformational transitions in nucleic acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Mitochondrial DNA mutations in cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Mitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F25.12.2455

Use of chemical clamps in denaturing gradient gel electrophoresis: application in the detection of the most frequent Mediterranean beta-thalassemic mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9171099

12 December 2020

inferred from PubMed ID database lookup

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9171099

12 December 2020

inferred from PubMed ID database lookup

Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9171099

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/NAR/25.12.2455

1 reference

release_na3rlltjyzbgjbbyql3eni3qt4

14 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/na3rlltjyzbgjbbyql3eni3qt4

24 November 2022

mapped directly with Wikidata item

1 reference

14 September 2017

PubMed publication ID

9171099

1 reference