Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis (Q38574817)

4 September 2017

title

Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis (English)

1 reference

4 September 2017

0 references

Hubert J M Smeets

1

1 reference

4 September 2017

Suzanne C E H Sallevelt

2

1 reference

4 September 2017

Jos C F M Dreesen

3

1 reference

4 September 2017

Christine E M de Die-Smulders

4

1 reference

4 September 2017

Irenaeus F M de Coo

5

1 reference

4 September 2017

language of work or name

English

0 references

publication date

27 August 2015

1 reference

Annals of the New York Academy of Sciences

4 September 2017

published in

1 reference

4 September 2017

volume

1350

1 reference

4 September 2017

page(s)

29-36

1 reference

A neurological perspective on mitochondrial disease.

4 September 2017

cites work

1 reference

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

Mitochondrial DNA content affects the fertilizability of human oocytes

21 January 2018

1 reference

PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.

21 January 2018

1 reference

The transmission of OXPHOS disease and methods to prevent this

21 January 2018

1 reference

Transmission of mitochondrial DNA diseases and ways to prevent them.

21 January 2018

1 reference

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

21 January 2018

1 reference

Random genetic drift determines the level of mutant mtDNA in human primary oocytes

21 January 2018

1 reference

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system

21 January 2018

1 reference

Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition

21 January 2018

1 reference

Risk of developing a mitochondrial DNA deletion disorder

21 January 2018

1 reference

Pathogenic mitochondrial DNA mutations are common in the general population

21 January 2018

1 reference

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

21 January 2018

1 reference

Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome

21 January 2018

1 reference

Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation

21 January 2018

1 reference

Mosaicism for mitochondrial DNA polymorphic variants in placenta has implications for the feasibility of prenatal diagnosis in mtDNA diseases.

21 January 2018

1 reference

Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development

21 January 2018

1 reference

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

21 January 2018

1 reference

Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.

21 January 2018

1 reference

Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success

21 January 2018

1 reference

Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis.

21 January 2018

1 reference

Blastocyst preimplantation genetic diagnosis (PGD) of a mitochondrial DNA disorder

21 January 2018

1 reference

Limitations of preimplantation genetic diagnosis for mitochondrial DNA diseases

21 January 2018

1 reference

174th ENMC international workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: implications of scientific advances 19-21 March 2010, Naarden, The Netherlands.

21 January 2018

1 reference

PGD to reduce reproductive risk: the case of mitochondrial DNA disorders.

21 January 2018

1 reference

Avoiding transgenerational risks of mitochondrial DNA disorders: a morally acceptable reason for sex selection?

21 January 2018

1 reference

Preventing the transmission of pathogenic mitochondrial DNA mutations: Can we achieve long-term benefits from germ-line gene transfer?

21 January 2018

1 reference

Mitochondrial DNA disease: new options for prevention

21 January 2018

1 reference

Mitochondrial gene replacement in primate offspring and embryonic stem cells

21 January 2018

1 reference

Towards germline gene therapy of inherited mitochondrial diseases

21 January 2018

1 reference

Polar body genome transfer for preventing the transmission of inherited mitochondrial diseases

21 January 2018

1 reference

Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants

21 January 2018

1 reference

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

21 January 2018

1 reference

Ethics of mitochondrial gene replacement: from bench to bedside

21 January 2018

1 reference

Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks.

21 January 2018

1 reference

Selective elimination of mitochondrial mutations in the germline by genome editing

21 January 2018

1 reference

mtDNA point mutations are present at various levels of heteroplasmy in human oocytes

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/NYAS.12866

1 reference

4 September 2017

1 reference