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Lab affiliation
1Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, VIC, 3010, Australia 2Murdoch Children’s Research Institute, Melbourne, VIC 3052, Australia 3Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Melbourne, VIC, 3052, Australia
(1)
Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, Biomedicum, 171 65 Solna, Sweden Max Planck Institute Biology of Ageing - Karolinska Institutet Laboratory, Karolinska Institutet, Stockholm, Sweden
(1)
Head of Proteomics, Dept of Immunology, University of Oslo and Oslo University Hospital
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Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan
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Max Delbrueck Center for Molecular Medicine (MDC), Berlin, Germany
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xref:PubMed:28132834
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xref:PubMed:42342683
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xref:PubMed:39024447
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xref:PubMed:41819105
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Proteomics of SEMA5A, MT-ATP6, ZNF662, and KDM4C in zebrafish embryos
Proteomics of SEMA5A, MT-ATP6, ZNF662, and KDM4C in zebrafish embryos
ORGANISM(S):
Danio Rerio
2024-02-05
|
PXD049175
|
Cite
Evaluating the MT-CYB and MT-ATP6 variations in COVID-19 patients: A case-control study.
Not available
S-EPMC12370035
|
biostudies-literature
Cite
Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease.
Not available
S-EPMC3525307
|
biostudies-literature
Cite
Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening.
Not available
S-EPMC8578202
|
biostudies-literature
Cite
A lack of a definite correlation between male sub-fertility and single nucleotide polymorphisms in sperm mitochondrial genes MT-CO3, MT-ATP6 and MT-ATP8.
Not available
S-EPMC9618475
|
biostudies-literature
Cite
Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6.
Not available
S-EPMC10201920
|
biostudies-literature
Cite
Threshold of heteroplasmic truncating MT-ATP6 mutation in reprogramming, Notch hyperactivation and motor neuron metabolism.
Not available
S-EPMC8947243
|
biostudies-literature
Cite
MT-ATP6 mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases.
Not available
S-EPMC6506718
|
biostudies-literature
Cite
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia.
Not available
S-EPMC8563540
|
biostudies-literature
Cite
Transcriptome of SEMA5A, MT-ATP6, ZNF662, and KDM4C in zebrafish embryos
PRJNA1073183
|
ENA
Cite
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