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Assembly of the membrane domain of ATP synthase in human mitochondria | PNAS
Assembly of the membrane domain of ATP synthase in human mitochondria | PNAS

PDF] Two mutations in mitochondrial ATP6 gene of ATP synthase, related to  human cancer, affect ROS, calcium homeostasis and mitochondrial  permeability transition in yeast. | Semantic Scholar
PDF] Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human cancer, affect ROS, calcium homeostasis and mitochondrial permeability transition in yeast. | Semantic Scholar

Overlapping mutations in mt-ATP6 and mt-ATP8. Comparison between a... |  Download Scientific Diagram
Overlapping mutations in mt-ATP6 and mt-ATP8. Comparison between a... | Download Scientific Diagram

MT-ATP6 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, |  Fisher Scientific
MT-ATP6 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific

IJMS | Free Full-Text | A Mutation in Mouse MT-ATP6 Gene Induces  Respiration Defects and Opposed Effects on the Cell Tumorigenic Phenotype
IJMS | Free Full-Text | A Mutation in Mouse MT-ATP6 Gene Induces Respiration Defects and Opposed Effects on the Cell Tumorigenic Phenotype

Frontiers | ATP Synthase Diseases of Mitochondrial Genetic Origin
Frontiers | ATP Synthase Diseases of Mitochondrial Genetic Origin

Isolation and in silico functional analysis of MtATP6, a 6-kDa subunit of  mitochondrial F₁F0-ATP synthase, in response to abiotic stress. | Semantic  Scholar
Isolation and in silico functional analysis of MtATP6, a 6-kDa subunit of mitochondrial F₁F0-ATP synthase, in response to abiotic stress. | Semantic Scholar

Variety in Mitochondrial Disease Tied to MT-ATP6 Mutations Warrants Better  Tests, Study Says
Variety in Mitochondrial Disease Tied to MT-ATP6 Mutations Warrants Better Tests, Study Says

Molecular model of ATP9 - ATP6 subcomplex from shrimp L. vannamei . a... |  Download Scientific Diagram
Molecular model of ATP9 - ATP6 subcomplex from shrimp L. vannamei . a... | Download Scientific Diagram

MT-ATP6 - Wikipedia
MT-ATP6 - Wikipedia

Translation of MT-ATP6 pathogenic variants reveals distinct regulatory  consequences from the co-translational quality control of mitochondrial  protein synthesis | bioRxiv
Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis | bioRxiv

A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP  (neuropathy, ataxia, and retinitis pigmentosa) syndrome - ScienceDirect
A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome - ScienceDirect

Supplement to Mitochondrial Encephalomyopathy in Drosophila | Journal of  Neuroscience
Supplement to Mitochondrial Encephalomyopathy in Drosophila | Journal of Neuroscience

Cells | Free Full-Text | Clinical Heterogeneity in MT-ATP6 Pathogenic  Variants: Same Genotype—Different Onset
Cells | Free Full-Text | Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype—Different Onset

MT-ATP6 - Wikiwand
MT-ATP6 - Wikiwand

MT-ATP6 Antibody | Cell Signaling Technology
MT-ATP6 Antibody | Cell Signaling Technology

MT-ATP6 Gene - GeneCards | ATP6 Protein | ATP6 Antibody
MT-ATP6 Gene - GeneCards | ATP6 Protein | ATP6 Antibody

The molecular model of the p.MT-ATP6 subunit. ( A ) View of subunit a... |  Download Scientific Diagram
The molecular model of the p.MT-ATP6 subunit. ( A ) View of subunit a... | Download Scientific Diagram

The biogenesis and assembly of the human ATP synthase | MRC Mitochondrial  Biology Unit
The biogenesis and assembly of the human ATP synthase | MRC Mitochondrial Biology Unit

Diagnosis and Discussion -- Case1064
Diagnosis and Discussion -- Case1064

MT‐ATP6 mitochondrial disease variants: Phenotypic and biochemical features  analysis in 218 published cases and cohort of 14 new cases - Ganetzky -  2019 - Human Mutation - Wiley Online Library
MT‐ATP6 mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases - Ganetzky - 2019 - Human Mutation - Wiley Online Library

Figures_Page_7.jpg
Figures_Page_7.jpg

MT-ATP6 antibody | Anti-MT-ATP6 | stjohnslabs
MT-ATP6 antibody | Anti-MT-ATP6 | stjohnslabs

Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human  cancer, affect ROS, calcium homeostasis and mitochondrial permeability  transition in yeast - ScienceDirect
Two mutations in mitochondrial ATP6 gene of ATP synthase, related to human cancer, affect ROS, calcium homeostasis and mitochondrial permeability transition in yeast - ScienceDirect

A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome  with ataxia, peripheral neuropathy, diabetes mellitus, and  hypergonadotropic hypogonadism | SpringerLink
A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism | SpringerLink

Allotopic Expression of ATP6 in Mouse as a Transgenic Model of  Mitochondrial Disease | SpringerLink
Allotopic Expression of ATP6 in Mouse as a Transgenic Model of Mitochondrial Disease | SpringerLink

MT-ATP6 antibody (ABIN950556)
MT-ATP6 antibody (ABIN950556)