Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonuclease. (Q36137186)

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English	Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonuclease.	scientific article

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17 January 2020

Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonuclease (English)

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17 January 2020

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17 January 2020

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S R Bacman

1

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17 January 2020

S L Williams

2

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17 January 2020

C T Moraes

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17 January 2020

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1 December 2011

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17 January 2020

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17 January 2020

19

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17 January 2020

11

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17 January 2020

1101-1106

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17 January 2020

https://scigraph.springernature.com/pub.10.1038/gt.2011.196

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Zinc-finger nuclease based genome surgery: it's all about specificity

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2 October 2017

Therapeutic treatments of mtDNA diseases at the earliest stages of human development

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2 October 2017

Emerging therapeutic approaches to mitochondrial diseases

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2 October 2017

Engineered Zinc Finger Proteins for Manipulation of the Human Mitochondrial Genome

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2 October 2017

Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations

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2 October 2017

Organ-specific shifts in mtDNA heteroplasmy following systemic delivery of a mitochondria-targeted restriction endonuclease

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2 October 2017

Intra- and inter-molecular recombination of mitochondrial DNA after in vivo induction of multiple double-strand breaks

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2 October 2017

Progress and prospects: gene therapy for mitochondrial DNA disease

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2 October 2017

Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection

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2 October 2017

Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes

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2 October 2017

Modulating mtDNA heteroplasmy by mitochondria-targeted restriction endonucleases in a 'differential multiple cleavage-site' model

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Efficient whole-body transduction with trans-splicing adeno-associated viral vectors

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Efficient in vivo gene expression by trans-splicing adeno-associated viral vectors

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease

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2 October 2017

Mitochondrial respiratory-chain diseases

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2 October 2017

Mitochondrial threshold effects.

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2 October 2017

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

2 October 2017

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle

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2 October 2017

Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants

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2 July 2018

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

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2 July 2018

Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes

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23 September 2018

Systemic AAV-9 transduction in mice is influenced by animal age but not by the route of administration

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

23 September 2018

Recombinant adeno-associated virus serotype 9 leads to preferential cardiac transduction in vivo

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

23 September 2018

Utility of intraperitoneal administration as a route of AAV serotype 5 vector-mediated neonatal gene transfer

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23 September 2018

Efficient transduction of skeletal muscle using vectors based on adeno-associated virus serotype 6.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3410960

23 September 2018

High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.

1 reference

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23 September 2018

The use of adeno-associated virus to circumvent the maturation-dependent viral transduction of muscle fibers

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23 September 2018

Nuclear genetic control of mitochondrial DNA segregation

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21 October 2018

Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication

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21 October 2018

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

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Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders

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Prenatal diagnosis by amniocentesis and chorionic villus biopsy of mtDNA mutation 8993T > G

1 reference

https://pubmed.ncbi.nlm.nih.gov/22130448

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/22130448

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1038/GT.2011.196

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17 January 2020

PMC publication ID

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Europe PubMed Central

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17 January 2020

PubMed publication ID

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Europe PubMed Central

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17 January 2020

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