(Q35790141)

10 August 2017

title

Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutation (English)

1 reference

real-time polymerase chain reaction

10 August 2017

main subject

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inferred from title

author

Andrew Tym Hattersley

series ordinal

3

object named as

Andrew Hattersley

1 reference

10 August 2017

Sian Ellard

2

0 references

author name string

Rinki Singh

series ordinal

1

1 reference

10 August 2017

Lorna W Harries

series ordinal

4

1 reference

10 August 2017

language of work or name

1 reference

1 May 2006

1 reference

The Journal of Molecular Diagnostics

10 August 2017

published in

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10 August 2017

volume

8

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10 August 2017

issue

2

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10 August 2017

page(s)

225-230

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High-sensitivity detection of the A3243G mutation of mitochondrial DNA by a combination of allele-specific PCR and peptide nucleic acid-directed PCR clamping

10 August 2017

cites work

1 reference

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Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems.

27 July 2018

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

27 July 2018

1 reference

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Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study

27 July 2018

1 reference

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Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene

27 July 2018

1 reference

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New sensitive method for the detection of the A3243G mutation of human mitochondrial deoxyribonucleic acid in diabetes mellitus patients by ligation-mediated polymerase chain reaction

27 July 2018

1 reference

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Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

27 July 2018

1 reference

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Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

27 July 2018

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

27 July 2018

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Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

27 July 2018

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Accurate detection and quantitation of heteroplasmic mitochondrial point mutations by pyrosequencing.

27 July 2018

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Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.

25 September 2018

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Accumulation of somatic mutation in mitochondrial DNA and atherosclerosis in diabetic patients.

25 September 2018

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Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients

25 September 2018

1 reference

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The level of the mitochondrial mutation A3243G decreases upon ageing in epithelial cells from individuals with diabetes and deafness

25 September 2018

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Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression

25 September 2018

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The spectrum of hearing loss due to mitochondrial DNA defects

25 September 2018

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The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families.

25 September 2018

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Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region

25 September 2018

1 reference

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Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation

25 September 2018

1 reference

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The mitochondrial A3243G mutation presenting as severe cardiomyopathy

25 September 2018

1 reference

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Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene

25 September 2018

1 reference

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HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness

25 September 2018

1 reference

12 December 2020

Clinical features of diabetic patients with 0.01-0.1% heteroplasmy A3243G mutation in leukocyte mitochondrial DNA

1 reference

12 December 2020

Molecular analysis of diabetes mellitus-associated A3243G mitochondrial DNA mutation in Taiwanese cases

1 reference

12 December 2020

Content of mutant mitochondrial DNA and organ dysfunction in a patient with a MELAS subgroup of mitochondrial encephalomyopathies

1 reference

12 December 2020

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

1 reference

12 December 2020

In situ characterization of islets in diabetes with a mitochondrial DNA mutation at nucleotide position 3243

1 reference

12 December 2020

Detection of MELAS A3243G point mutation in muscle, blood and hair follicles

1 reference

12 December 2020

Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 detected in patients with type 1 diabetes

1 reference

12 December 2020

10.2353/JMOLDX.2006.050067

Identifiers

DOI

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10 August 2017

1 reference

10 August 2017

1 reference