Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
about
VEGF stimulation of mitochondrial biogenesis: requirement of AKT3 kinaseMitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins.The complete sequence of the zebrafish (Danio rerio) mitochondrial genome and evolutionary patterns in vertebrate mitochondrial DNAMitochondrial disorders: challenges in diagnosis & treatmentDin7 and Mhr1 expression levels regulate double-strand-break-induced replication and recombination of mtDNA at ori5 in yeastEffect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseasesMitochondrial DNA disease and developmental implications for reproductive strategiesPersistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contractionStem cell-based models and therapies for neurodegenerative diseasesIdentification of small non-coding RNAs from mitochondria and chloroplasts.Targeting of mutant hogg1 in mammalian mitochondria and nucleus: effect on cellular survival upon oxidative stress.A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck.Mitochondrial medicine--recent advances.High rate of large deletions in Caenorhabditis briggsae mitochondrial genome mutation processes.Evolutionary toxicology: contaminant-induced genetic mutations in mosquitofish from Sumgayit, Azerbaijan.Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathyThe strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates.Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?Clinical mitochondrial genetics.Characterization of a human import component of the mitochondrial outer membrane, TOMM70A.Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Identification of sequence polymorphism in the D-Loop region of mitochondrial DNA as a risk factor for hepatocellular carcinoma with distinct etiology.Finding and interpreting genetic variations that are important to ophthalmologists.Gene therapy for the treatment of mitochondrial DNA disorders.In vivo quantification reveals extensive natural variation in mitochondrial form and function in Caenorhabditis briggsae.Stochastic modelling, Bayesian inference, and new in vivo measurements elucidate the debated mtDNA bottleneck mechanism.Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside.Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep.Conveniently pre-tagged and pre-packaged: extended molecular identification and metagenomics using complete metazoan mitochondrial genomes.Germline bottlenecks, biparental inheritance and selection on mitochondrial variants: a two-level selection modelGermline bottlenecks and the evolutionary maintenance of mitochondrial genomes.Replicative advantage and tissue-specific segregation of RR mitochondrial DNA between C57BL/6 and RR heteroplasmic miceElectrophile and oxidant damage of mitochondrial DNA leading to rapid evolution of homoplasmic mutations.Mhr1p-dependent concatemeric mitochondrial DNA formation for generating yeast mitochondrial homoplasmic cells.Peptide-based carbon nanotubes for mitochondrial targeting.Quantitative analysis of mitochondrial morphology and membrane potential in living cells using high-content imaging, machine learning, and morphological binning.Associations of mitochondrial haplogroups b4 and e with biliary atresia and differential susceptibility to hydrophobic bile Acid.Heteroplasmy in the mitochondrial genomes of human lice and ticks revealed by high throughput sequencing.Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy.From genotype to phenotype: genetics and medical practice in the new millennium.
P2860
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P2860
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
@en
type
label
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
@en
prefLabel
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
@en
P2093
P1433
P1476
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
@en
P2093
Lightowlers RN
Turnbull DM
P304
P356
10.1016/S0168-9525(97)01266-3
P577
1997-11-01T00:00:00Z