(Q50170483)

26 February 2018

title

The polymerase chain reaction in the study of mitochondrial genetics. (English)

1 reference

26 February 2018

author name string

Kapsa R

1

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26 February 2018

Siregar N

2

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26 February 2018

Quigley A

3

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26 February 2018

Ojaimi J

4

1 reference

26 February 2018

Katsabanis S

5

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26 February 2018

Sue C

6

1 reference

26 February 2018

Byrne E

7

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26 February 2018

publication date

1 December 1997

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26 February 2018

published in

Journal of Proteomics

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26 February 2018

volume

36

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26 February 2018

issue

1

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26 February 2018

page(s)

31-50

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26 February 2018

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Rapid and noninvasive screening of patients with mitochondrial myopathy

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Sequence and organization of the human mitochondrial genome

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Mitochondrial DNA polymorphism in substantia nigra.

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

A rapid polymerase-chain-reaction-directed sequencing strategy using a thermostable DNA polymerase from Thermus flavus

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

In vitro amplification of DNA fragments greater than 10 kb

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Complete mitochondrial genome amplification

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation").

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

Occurrence of a particular base substitution (3243 A to G) in mitochondrial DNA of tissues of ageing humans

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

The trouble with 'PCR' machines

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https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

The trouble with PCR machines: fill up the empty spaces!

1 reference

https://api.crossref.org/works/10.1016%2FS0165-022X%2897%2900044-4

7 January 2021

10.1016/S0165-022X(97)00044-4

Identifiers

DOI

1 reference

26 February 2018

1 reference

26 February 2018