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

Figures_Page_7.jpg
Figures_Page_7.jpg

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

INA complex liaises the F1Fo-ATP synthase membrane motor modules | Nature  Communications
INA complex liaises the F1Fo-ATP synthase membrane motor modules | Nature Communications

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

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

Model for the transmembrane helices of the ATP6 subunit of the F 1 F... |  Download Scientific Diagram
Model for the transmembrane helices of the ATP6 subunit of the F 1 F... | Download Scientific Diagram

MT-ATP6 - Wikiwand
MT-ATP6 - Wikiwand

Anti-MT-ATP6 Antibody, clone 1G7-1G2 | MABS1995
Anti-MT-ATP6 Antibody, clone 1G7-1G2 | MABS1995

catastrophegw325 contains a copper sensitive mutation in the vacuolar (H+)  ATPase Atp6.
catastrophegw325 contains a copper sensitive mutation in the vacuolar (H+) ATPase Atp6.

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

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

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

Association of a point mutation (m.9176T>G) of the MT-ATP6 gene with Leigh  syndrome: A case report | Biomedical Research and Therapy
Association of a point mutation (m.9176T>G) of the MT-ATP6 gene with Leigh syndrome: A case report | Biomedical Research and Therapy

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

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

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

MT-ATP6 - Wikipedia
MT-ATP6 - Wikipedia

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

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

ATP6 antibody (55313-1-AP) | Proteintech
ATP6 antibody (55313-1-AP) | Proteintech

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

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

Anti-MT-ATP6 Antibody (A28298) | Antibodies.com
Anti-MT-ATP6 Antibody (A28298) | Antibodies.com

MT-ATP6 - Wikipedia
MT-ATP6 - Wikipedia

MT-ATP6 antibody (ABIN6137340)
MT-ATP6 antibody (ABIN6137340)

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

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