Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease (Q24607578)

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31 January 2020

title

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease (English)

1 reference

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31 January 2020

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1 reference

6

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Mary Herbert

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Douglass Matthew Turnbull

31 January 2020

12

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Robert William Taylor

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object named as

Robert W Taylor

1 reference

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8

Patrick F Chinnery

1 reference

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31 January 2020

2

Helen A Tuppen

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Robert N Lightowlers

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31 January 2020

1

Lyndsey Craven

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31 January 2020

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Julie L Murphy

1 reference

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author name string

Gareth D Greggains

3

1 reference

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31 January 2020

Stephen J Harbottle

4

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Alison P Murdoch

7

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31 January 2020

language of work or name

English

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publication date

14 April 2010

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31 January 2020

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volume

465

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issue

7294

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31 January 2020

page(s)

82-85

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describes a project that uses

31 January 2020

ImageQuant

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11 June 2022

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inferred from PubMed Central ID database lookup

cites work

Mitochondrial gene replacement in primate offspring and embryonic stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Mitochondrial DNA mutations in human disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

The epidemiology of Leber hereditary optic neuropathy in the North East of England

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Treatment for mitochondrial disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Mitochondrial disorders in the nervous system

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Pathogenic mitochondrial DNA mutations are common in the general population

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Prevalence of mitochondrial DNA disease in adults

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Can 'abnormally' fertilized zygotes give rise to viable embryos?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Transmission of mitochondrial DNA disorders: possibilities for the future.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Mitochondrial genotype segregation in a mouse heteroplasmic lineage produced by embryonic karyoplast transplantation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Influence of maternal age on meiotic spindle assembly in oocytes from naturally cycling women.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Adult phenotype in the mouse can be affected by epigenetic events in the early embryo.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Prevalence of mitochondrial 1555A-->G mutation in adults of European descent.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Comparison of mitochondrial DNA contents in human embryos with good or poor morphology at the 8-cell stage.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Quantification of human ooplasmic mitochondria

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

The effect of temperature fluctuations on the cytoskeletal organisation and chromosomal constitution of the human oocyte.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2875160

Prevalence of Mitochondrial 1555A→G Mutation in European Children

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20393463

12 December 2020

inferred from PubMed ID database lookup

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20393463

12 December 2020

inferred from PubMed ID database lookup

A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20393463

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NATURE08958

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20393463%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

31 January 2020

1028142309

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20393463%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

2 references