Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.
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The rise of mitochondria in medicineEvolutionary defined role of the mitochondrial DNA in fertility, disease and ageingMitochondrial DNA disease and developmental implications for reproductive strategiesRecurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy NumberPhenotypic rescue of a Drosophila model of mitochondrial ANT1 disease.Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions.An exploratory analysis of mitochondrial haplotypes and allogeneic hematopoietic cell transplantation outcomes.Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutationsMolecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yieldPrivate mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.Misfolding of mutant adenine nucleotide translocase in yeast supports a novel mechanism of Ant1-induced muscle diseases.Mitochondrial functions modulate neuroendocrine, metabolic, inflammatory, and transcriptional responses to acute psychological stressMitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons.Adenine nucleotide translocase, mitochondrial stress, and degenerative cell death.Mitochondrial DNA variation and virologic and immunological HIV outcomes in African Americans.Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.Adeno-associated virus-mediated gene therapy for metabolic myopathy.The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex disease.The genetic landscape of cardiomyopathy and its role in heart failure.Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA.Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.MtDNA-maintenance defects: syndromes and genes.Cardiac and skeletal muscles show molecularly distinct responses to cancer cachexia.Cdkal1, a type 2 diabetes susceptibility gene, regulates mitochondrial function in adipose tissue.Risks inherent to mitochondrial replacementLeber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.The aetiology of cardiovascular disease: a role for mitochondrial DNA?Psychological Stress and Mitochondria: A Conceptual Framework.Relations of mitochondrial genetic variants to measures of vascular function.Inborn errors of metabolism and the human interactome: a systems medicine approach.Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome.Mitonuclear linkage disequilibrium in human populations.
P2860
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P2860
Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.
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2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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name
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@ast
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@en
type
label
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@ast
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@en
prefLabel
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@ast
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@en
P2093
P2860
P356
P1476
Severity of cardiomyopathy ass ...... relates with mtDNA haplogroup.
@en
P2093
D Holmes Morton
Douglas C Wallace
Erik G Puffenberger
Julia Platt
Kevin A Strauss
Lauren DuBiner
Mariella Simon
Michael Zaragoza
Navneet Narula
Partho P Sengupta
P2860
P304
P356
10.1073/PNAS.1300690110
P407
P50
P577
2013-02-11T00:00:00Z