תמונות העטיפה

Short-chain L-3-hydroxyacyl-CoA dehydrogenase: A novel vital oncogene or tumor suppressor gene in cancers

The reprogramming of cellular metabolism is frequently linked to tumorigenesis. Glucose, fatty acids, and amino acids are the specific substrates involved in how an organism maintains metabolic equilibrium. The HADH gene codes for the short-chain L-3-hydroxyacyl-CoA dehydrogenase (HADH), a crucial e...

תיאור מלא

שמור ב:

מידע ביבליוגרפי
Main Authors:	He Fang (Author), Hanyang Li (Author), Hang Zhang (Author), Shu Wang (Author), Shuang Xu (Author), Li Chang (Author), Yongsheng Yang (Author), Ranji Cui (Author)
פורמט:	ספר
יצא לאור:	Frontiers Media S.A., 2022-10-01T00:00:00Z.
נושאים:	article
גישה מקוונת:	Connect to this object online.
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

פריטים דומים

New Acylcarnitine Ratio as a Reliable Indicator of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
מאת: Galina V. Baydakova, et al.
יצא לאור: (2023)

Newborn Screening for Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase and Mitochondrial Trifunctional Protein Deficiencies Using Acylcarnitines Measurement in Dried Blood Spots-A Systematic Review of Test Accuracy
מאת: Chris Stinton, et al.
יצא לאור: (2021)

Medium chain acyl-CoA dehydrogenase deficiency in a premature infant
מאת: Steven F. Dobrowolski, et al.
יצא לאור: (2017)

Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives
מאת: Soler-Alfonso C, et al.
יצא לאור: (2016)

The value of fasting in the diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
מאת: Carmen R Vargas, et al.
יצא לאור: (2020)

Compound heterozygous mutations of gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review
מאת: Se Jin An, et al.
יצא לאור: (2016)

Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives
מאת: Sarah Crawford, et al.
יצא לאור: (2023)

Neonatal Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency-Alternative Approaches
מאת: Rodney J. Pollitt
יצא לאור: (2016)

Oncogene/Tumor Suppressor Molecular Pathways
מאת: Dan Cushman, et al.
יצא לאור: (2010)

Parental Experiences of Raising a Child With Medium Chain Acyl-CoA Dehydrogenase Deficiency
מאת: Hilary Piercy, et al.
יצא לאור: (2017)

Acyl-CoA Dehydrogenase Deficiency and RS
מאת: J Gordon Millichap
יצא לאור: (1994)

Histone H3K9 butyrylation is regulated by dietary fat and stress via an Acyl-CoA dehydrogenase short chain-dependent mechanism
מאת: Zhi Yang, et al.
יצא לאור: (2021)

Long-term monitoring for short/branched-chain acyl-CoA dehydrogenase deficiency: A single-center 4-year experience and open issues
מאת: Alessandro Rossi, et al.
יצא לאור: (2022)

Cost-effectiveness analysis of universal newborn screening for medium chain acyl-CoA dehydrogenase deficiency in France
מאת: Hamers Françoise F, et al.
יצא לאור: (2012)

The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontario
מאת: Fisher Lawrence, et al.
יצא לאור: (2010)

"It's Just Always Eating": The Experiences of Young People Growing up Medium Chain Acyl-coA Dehydrogenase Deficiency
מאת: Hilary Piercy, et al.
יצא לאור: (2021)

Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart Review
מאת: Maria Al Bandari, et al.
יצא לאור: (2024)

Neonatal Screening on Tandem Mass Spectrometry as a Powerful Tool for the Reassessment of the Prevalence of Underestimated Diseases in Newborns and Their Family Members: A Focus on Short Chain Acyl-CoA Dehydrogenase Deficiency
מאת: MariaAnna Messina, et al.
יצא לאור: (2020)

Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency
מאת: Ryan Iverson, et al.
יצא לאור: (2024)

Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing
מאת: Aashish N. Adhikari, et al.
יצא לאור: (2020)

Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype
מאת: Lovera Cristina, et al.
יצא לאור: (2012)

Case report: Diagnosis of a patient with Sifrim-Hitz-Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency
מאת: Naim Zeka, et al.
יצא לאור: (2023)

Fibroblast Fatty-Acid Oxidation Flux Assays Stratify Risk in Newborns with Presumptive-Positive Results on Screening for Very-Long Chain Acyl-CoA Dehydrogenase Deficiency
מאת: Simon E. Olpin, et al.
יצא לאור: (2017)

Biosynthesis of clinically used antibiotic fusidic acid and identification of two short-chain dehydrogenase/reductases with converse stereoselectivity
מאת: Zhiqin Cao, et al.
יצא לאור: (2019)

Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan
מאת: Go Tajima, et al.
יצא לאור: (2024)

Beneficial Effect of N-Carbamylglutamate in a Neonatal Form of Multiple Acyl-CoA Dehydrogenase Deficiency
מאת: Sinziana Stanescu, et al.
יצא לאור: (2020)

Characteristics of long‐chain acyl‐CoA synthetases in metabolism and cancer
מאת: Linlin Zhang, et al.
יצא לאור: (2023)

"Omics" data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy
מאת: Nzali V. Campbell, et al.
יצא לאור: (2018)

Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review
מאת: Maria Anna Siano, et al.
יצא לאור: (2021)

Neonatal Screening for Medium-Chain Acyl-CoA Deficiency-Insights and Unexpected Challenges
מאת: Esther M. Maier
יצא לאור: (2015)

Clinical, biochemical and metabolic characterization of patients with short-chain enoyl-CoA hydratase(ECHS1) deficiency: two case reports and the review of the literature
מאת: Hua Yang, et al.
יצא לאור: (2020)

Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report
מאת: Liuh Ling Goh, et al.
יצא לאור: (2018)

Small Molecule Cjoc42 Improves Chemo-Sensitivity and Increases Levels of Tumor Suppressor Proteins in Hepatoblastoma Cells and in Mice by Inhibiting Oncogene Gankyrin
מאת: Amber M. D'Souza, et al.
יצא לאור: (2021)

Loss of the Drosophila branched-chain α-ketoacid dehydrogenase complex results in neuronal dysfunction
מאת: Hui-Ying Tsai, et al.
יצא לאור: (2020)

A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report
מאת: Loredana De Pasquale, et al.
יצא לאור: (2022)

A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene
מאת: Robin Chautard, et al.
יצא לאור: (2020)

Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency
מאת: Gaopin Yuan, et al.
יצא לאור: (2023)

The tumor suppressor 5A2, a synthetic miR-7-5p mimic, targets oncogenic and metabolic pathways, as revealed by transcriptome-wide analysis
מאת: Marion T. J. van den Bosch, et al.
יצא לאור: (2023)

Expression of acyl-CoA synthetase medium-chain 3 is associated with obesity in melanoma patients and correlates with androgen receptor
מאת: Yuan Zheng, et al.
יצא לאור: (2023)

miR-134: A Human Cancer Suppressor?
מאת: Jing-Yu Pan, et al.
יצא לאור: (2017)