Product References
Mitochondrial FAD shortage in SLC25A32 deficiency affects folate-mediated one-carbon metabolism.
Cellular and molecular life sciences : CMLS
Peng MZ,Shao YX,Li XZ,Zhang KD,Cai YN,Lin YT,Jiang MY,Liu ZC,Su XY,Zhang W,Jiang XL,Liu L
Tue Jun 21 00:00:00 UTC 2022
Propofol Inhibits Proliferation and Augments the Anti-Tumor Effect of Doxorubicin and Paclitaxel Partly Through Promoting Ferroptosis in Triple-Negative Breast Cancer Cells.
Frontiers in oncology
Sun C,Liu P,Pei L,Zhao M,Huang Y
Fri Apr 15 00:00:00 UTC 2022
Propofol Inhibits Proliferation and Augments the Anti-Tumor Effect of Doxorubicin and Paclitaxel Partly Through Promoting Ferroptosis in Triple-Negative Breast Cancer Cells.
Frontiers in oncology
Sun C,Liu P,Pei L,Zhao M,Huang Y
Fri Apr 15 00:00:00 UTC 2022
Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: a single-center retrospective study.
Human molecular genetics
Wen B,Tang S,Lv X,Li D,Xu J,Olsen RKJ,Zhao Y,Li W,Wang T,Shao K,Zhao D,Yan C
Thu Mar 31 00:00:00 UTC 2022
CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease
Liu XY,Chen XJ,Zhao M,Wang ZQ,Chen HZ,Li HF,Wang CJ,Wu SF,Peng C,Yin Y,Fu HX,Lin MT,Yu L,Xiong ZQ,Wu ZY,Wang N
Mon Mar 01 00:00:00 UTC 2021
CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease
Liu XY,Chen XJ,Zhao M,Wang ZQ,Chen HZ,Li HF,Wang CJ,Wu SF,Peng C,Yin Y,Fu HX,Lin MT,Yu L,Xiong ZQ,Wu ZY,Wang N
Mon Mar 01 00:00:00 UTC 2021
Expression and significance of ETFDH in hepatocellular carcinoma.
Pathology, research and practice
Wu Y,Zhang X,Shen R,Huang J,Lu X,Zheng G,Chen X
Sun Dec 01 00:00:00 UTC 2019
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.
Annals of neurology
Xu J,Li D,Lv J,Xu X,Wen B,Lin P,Liu F,Ji K,Shan J,Li H,Li W,Zhao Y,Zhao D,Pok JY,Yan C
Thu Nov 01 00:00:00 UTC 2018
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.
Annals of neurology
Xu J,Li D,Lv J,Xu X,Wen B,Lin P,Liu F,Ji K,Shan J,Li H,Li W,Zhao Y,Zhao D,Pok JY,Yan C
Thu Nov 01 00:00:00 UTC 2018
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.
Annals of neurology
Xu J,Li D,Lv J,Xu X,Wen B,Lin P,Liu F,Ji K,Shan J,Li H,Li W,Zhao Y,Zhao D,Pok JY,Yan C
Thu Nov 01 00:00:00 UTC 2018
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Fu HX,Liu XY,Wang ZQ,Jin M,Wang DN,He JJ,Lin MT,Wang N
Fri Jul 01 00:00:00 UTC 2016
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Fu HX,Liu XY,Wang ZQ,Jin M,Wang DN,He JJ,Lin MT,Wang N
Fri Jul 01 00:00:00 UTC 2016
Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
Journal of molecular medicine (Berlin, Germany)
Wang ZQ,Chen XJ,Murong SX,Wang N,Wu ZY
Wed Jun 01 00:00:00 UTC 2011
Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
Journal of molecular medicine (Berlin, Germany)
Wang ZQ,Chen XJ,Murong SX,Wang N,Wu ZY
Wed Jun 01 00:00:00 UTC 2011
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.
Journal of neurology, neurosurgery, and psychiatry
Wen B,Dai T,Li W,Zhao Y,Liu S,Zhang C,Li H,Wu J,Li D,Yan C
Mon Feb 01 00:00:00 UTC 2010
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.
Journal of neurology, neurosurgery, and psychiatry
Wen B,Dai T,Li W,Zhao Y,Liu S,Zhang C,Li H,Wu J,Li D,Yan C
Mon Feb 01 00:00:00 UTC 2010