unnamed protein product [Homo sapiens]

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Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients. [Biomolecules. 2019]
Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients.
Zerr I, Villar-Piqué A, Schmitz VE, Poleggi A, Pocchiari M, Sánchez-Valle R, Calero M, Calero O, Baldeiras I, Santana I, et al. Biomolecules. 2019 Nov 28; 9(12). Epub 2019 Nov 28.
MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathy. [Hum Genet. 2019]
MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathy.
Broeks MH, Shamseldin HE, Alhashem A, Hashem M, Abdulwahab F, Alshedi T, Alobaid I, Zwartkruis F, Westland D, Fuchs S, et al. Hum Genet. 2019 Dec; 138(11-12):1247-1257. Epub 2019 Sep 19.
Cytosolic malate dehydrogenase activity helps support glycolysis in actively proliferating cells and cancer. [Oncogene. 2017]
Cytosolic malate dehydrogenase activity helps support glycolysis in actively proliferating cells and cancer.
Hanse EA, Ruan C, Kachman M, Wang D, Lowman XH, Kelekar A. Oncogene. 2017 Jul 6; 36(27):3915-3924. Epub 2017 Mar 6.

RefSeq genomic sequence
See the genomic reference sequence for the MDH1 gene (NG_028144.2).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the MDH1 gene.

Nucleotide
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cytosolic malate dehydrogenase [Homo sapiens]
cytosolic malate dehydrogenase [Homo sapiens]
gi|1255604|dbj|BAA09513.1|

Protein
RecName: Full=Malate dehydrogenase, cytoplasmic; AltName: Full=Aromatic alpha-ke...
RecName: Full=Malate dehydrogenase, cytoplasmic; AltName: Full=Aromatic alpha-keto acid reductase; Short=KAR; AltName: Full=Cytosolic malate dehydrogenase
gi|1708967|sp|P40925.4|MDHC_HUMAN

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Protein