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MitochondriaMitochondrial disorders: challenges in diagnosis & treatmentEffect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseasesTransmission of mitochondrial DNA diseases and ways to prevent them.Mitochondrial respiratory chain disorders and the liver.The 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.Random genetic drift determines the level of mutant mtDNA in human primary oocytesA sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.Human mitochondrial genetics.Mitochondrial DNA sequence analysis of two mouse hepatocarcinoma cell lines.The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics.Epidemiology and treatment of mitochondrial disorders.Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.The biology of mitochondrial disease.Contrasting effects of in vitro fertilization and nuclear transfer on the expression of mtDNA replication factorsThe distribution of mitochondrial DNA heteroplasmy due to random genetic drift.Ovarian ageing: the role of mitochondria in oocytes and follicles.Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome.Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: a model using families from the Azores Islands (Portugal).Mitochondrial DNA content affects the fertilizability of human oocytes.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Mitochondrial genetics '98 is the bottleneck cracked?
@ast
Mitochondrial genetics '98 is the bottleneck cracked?
@en
Mitochondrial genetics '98 is the bottleneck cracked?
@nl
type
label
Mitochondrial genetics '98 is the bottleneck cracked?
@ast
Mitochondrial genetics '98 is the bottleneck cracked?
@en
Mitochondrial genetics '98 is the bottleneck cracked?
@nl
prefLabel
Mitochondrial genetics '98 is the bottleneck cracked?
@ast
Mitochondrial genetics '98 is the bottleneck cracked?
@en
Mitochondrial genetics '98 is the bottleneck cracked?
@nl
P2093
P2860
P356
P1476
Mitochondrial genetics '98 is the bottleneck cracked?
@en
P2093
D R Marchington
V Macaulay
P2860
P304
P356
10.1086/301811
P407
P577
1998-04-01T00:00:00Z