A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency
about
Decoding Warburg's hypothesis: tumor-related mutations in the mitochondrial respiratory chainThe deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriersA mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastA novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.Impact of the mitochondrial genetic background in complex III deficiencyA novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome.De novo mtDNA point mutations are common and have a low recurrence risk.Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene.Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.Effects of mutations in mitochondrial cytochrome b in yeast and man. Deficiency, compensation and disease.Mitochondrial DNA mutations in human disease.Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.MT-CYB mutations in hypertrophic cardiomyopathy.Application of 16s rDNA and cytochrome b ribosomal markers in studies of lineage and fish populations structure of aquatic species.Mitochondrial injury and dysfunction in hypertension-induced cardiac damage.Mitochondria: a pathogenic paradigm in hypertensive renal disease.Multipronged approach to identify and validate a novel upstream regulator of Sncg in mouse retinal ganglion cells.Prevalence and progression of mitochondrial diseases: a study of 50 patients.Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated CardiomyopathySynonymous codon usage pattern in mitochondrial CYB gene in pisces, aves, and mammals.Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene
P2860
Q26783724-13685346-DC93-480E-ABE4-4B17D41A081FQ28239925-CEBDA837-1E0B-4648-B66A-D2B1E364FE4DQ28260897-674C2ED5-4291-4F3B-9B85-BEFFF9EC3F7BQ28345777-48576197-8404-4B06-A880-5E9B6EF693EEQ28475526-BB7F04E1-343F-4D79-89AE-AF7056A945B7Q30575264-DD29AC98-0D38-4634-B145-F4F25BCA0E4FQ33886230-E985F5D3-E8EA-4EF5-A8B1-401AE038C531Q34095207-360AF87A-83A2-4837-9DA1-D6BDE9CCFF1BQ34144271-09D00C99-B007-4173-8726-5C9C734A60C1Q34169851-78A70E58-5604-4245-B1A6-485337C81752Q34386730-3EF6C82A-DE01-46A8-877B-E64B34EB5483Q34386775-A1D2F315-2FEE-43EF-9305-07127A176082Q35552917-860F7296-3250-4BAD-B8AC-43CDC05EF94AQ37483898-5AA8B46F-2598-487D-8580-ADF70902423BQ37968181-A93078BB-C5EC-480A-BABF-6AEBB7203E1EQ38266758-3749EE80-7A48-4821-9248-366D6C85DBC8Q38268844-A0DF918B-CFC9-4F88-BAF7-913B387939C1Q38453700-0540370B-91A2-49A4-912C-C4E3F2D83C4EQ39670018-BA1C8CB1-11F6-4F9A-A12B-1387BDC2C18AQ41813058-010FB9AD-E4B5-4CF1-922B-09CAF2A9EDCFQ53393325-F9821B53-D6B2-4E1B-85CD-8A45F4126E7EQ56761880-B76EBF20-2A43-4BC9-A012-06165DF98DF1
P2860
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@ast
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@en
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@nl
type
label
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@ast
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@en
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@nl
prefLabel
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@ast
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@en
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@nl
P2093
P356
P1433
P1476
A mitochondrial cytochrome b m ...... ctase (complex III) deficiency
@en
P2093
D Chretien
J Kachaner
P de Lonlay
P2888
P356
10.1007/S004390050988
P407
P577
1999-06-01T00:00:00Z
P5875
P6179
1037234039