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SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications

Governing glutaminolysis by regulation of glutaminase succinylation | Protein & Cell
Governing glutaminolysis by regulation of glutaminase succinylation | Protein & Cell

SUCLA2 gene | Semantic Scholar
SUCLA2 gene | Semantic Scholar

SUCLA2 Antibody (NBP1-33015): Novus Biologicals
SUCLA2 Antibody (NBP1-33015): Novus Biologicals

Screening of small molecules that selectively kill SUCLA2-deleted... | Download Scientific Diagram
Screening of small molecules that selectively kill SUCLA2-deleted... | Download Scientific Diagram

Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect

Anti-SUCLA2 Antibody | Rabbit anti-Human Polyclonal ICC,IHC,WB | LSBio
Anti-SUCLA2 Antibody | Rabbit anti-Human Polyclonal ICC,IHC,WB | LSBio

SUCLA2抗体(A-9) | SCBT - Santa Cruz Biotechnology
SUCLA2抗体(A-9) | SCBT - Santa Cruz Biotechnology

SUCLA2 Antibody (NBP1-33015): Novus Biologicals
SUCLA2 Antibody (NBP1-33015): Novus Biologicals

SUCLA2 - an overview | ScienceDirect Topics
SUCLA2 - an overview | ScienceDirect Topics

SUCLA2 Gene - GeneCards | SUCB1 Protein | SUCB1 Antibody
SUCLA2 Gene - GeneCards | SUCB1 Protein | SUCB1 Antibody

SUCLA2 Antibody (ABIN2856701)
SUCLA2 Antibody (ABIN2856701)

Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram
Analysis of the effects of SUCLA2 missense mutations on the structure... | Download Scientific Diagram

SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications

Thymoquinone targets SUCLA2 loss that collaterally takes place with RB1... | Download Scientific Diagram
Thymoquinone targets SUCLA2 loss that collaterally takes place with RB1... | Download Scientific Diagram

SUCLA2 Polyclonal Antibody (PA5-118292)
SUCLA2 Polyclonal Antibody (PA5-118292)

Advanced prostate cancer has an unexpected we | EurekAlert!
Advanced prostate cancer has an unexpected we | EurekAlert!

SUCLA2 Gene - GeneCards | SUCB1 Protein | SUCB1 Antibody
SUCLA2 Gene - GeneCards | SUCB1 Protein | SUCB1 Antibody

SUCLA2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology
SUCLA2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology

SUCLA2 Fusion Protein Ag3319 | Proteintech
SUCLA2 Fusion Protein Ag3319 | Proteintech

Recombinant Anti-SUCLA2 antibody [EPR14925] (ab183513) | Abcam
Recombinant Anti-SUCLA2 antibody [EPR14925] (ab183513) | Abcam

Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS
Succinyl-CoA ligase ADP-forming subunit beta promotes stress granule assembly to regulate redox and drive cancer metastasis | PNAS

PDF) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
PDF) SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness

SUCLA2 gene | Semantic Scholar
SUCLA2 gene | Semantic Scholar

Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 | SpringerLink
Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 | SpringerLink

進行前立腺がんの新しい治療薬を開発 – 金沢大学
進行前立腺がんの新しい治療薬を開発 – 金沢大学

Targeting metabolic vulnerability in advanced prostate cancer | Cancer Community
Targeting metabolic vulnerability in advanced prostate cancer | Cancer Community

Succinyl-CoA Ligase Deficiency: A Mitochondrial Hepatoencephalomyopathy | Pediatric Research
Succinyl-CoA Ligase Deficiency: A Mitochondrial Hepatoencephalomyopathy | Pediatric Research