(Q36268463)

English

The development of novel quantification assay for mitochondrial DNA heteroplasmy aimed at preimplantation genetic diagnosis of Leigh encephalopathy

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scholarly article

1 reference

Europe PubMed Central

13 August 2017

The development of novel quantification assay for mitochondrial DNA heteroplasmy aimed at preimplantation genetic diagnosis of Leigh encephalopathy (English)

1 reference

Europe PubMed Central

13 August 2017

mitochondrial DNA

0 references

1 reference

based on heuristic

inferred from title

author name string

Hiroto Tajima

1

1 reference

Europe PubMed Central

13 August 2017

Kou Sueoka

2

1 reference

Europe PubMed Central

13 August 2017

Sung Yung Moon

3

1 reference

Europe PubMed Central

13 August 2017

Akira Nakabayashi

4

1 reference

Europe PubMed Central

13 August 2017

Tomoyoshi Sakurai

5

1 reference

Europe PubMed Central

13 August 2017

Yukitaka Murakoshi

6

1 reference

Europe PubMed Central

13 August 2017

Hiroyoshi Watanabe

7

1 reference

Europe PubMed Central

13 August 2017

Soukichi Iwata

8

1 reference

Europe PubMed Central

13 August 2017

Tsuyoshi Hashiba

9

1 reference

Europe PubMed Central

13 August 2017

Shingo Kato

10

1 reference

Europe PubMed Central

13 August 2017

Yu-Ichi Goto

11

1 reference

Europe PubMed Central

13 August 2017

Yasunori Yoshimura

12

1 reference

Europe PubMed Central

13 August 2017

publication date

8 March 2007

1 reference

Europe PubMed Central

13 August 2017

Journal of Assisted Reproduction and Genetics

1 reference

Europe PubMed Central

13 August 2017

24

1 reference

Europe PubMed Central

13 August 2017

6

1 reference

Europe PubMed Central

13 August 2017

227-232

1 reference

Europe PubMed Central

13 August 2017

https://scigraph.springernature.com/pub.10.1007/s10815-007-9114-0

0 references

Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Rapid segregation of heteroplasmic bovine mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Unequal partitioning of bovine mitochondrial genotypes among siblings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Replacement of bovine mitochondrial DNA by a sequence variant within one generation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

30 September 2017

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

29 June 2018

Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

22 September 2018

Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

22 September 2018

MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

22 September 2018

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3454964

22 September 2018

Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17342424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA in mammalian reproduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17342424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/17342424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of cytochrome c oxidase deficiency in cultured amniocytes is hazardous

1 reference

https://pubmed.ncbi.nlm.nih.gov/17342424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17342424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10815-007-9114-0

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

ResearchGate publication ID

0 references

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