Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency-Reference-Cited by-同舟云学术

Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency

Published:2001-04 Issue:4 Volume:68 Page:839-847
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Binzak Barbara A.,Wevers Ron A.,Moolenaar Sytske H.,Lee Yu-May,Hwu Wuh-Liang,Poggi-Bach Jo,Engelke Udo F.H.,Hoard Heidi M.,Vockley Joseph G.,Vockley Jerry

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. Serum betaine, N, N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism;Allen;Metabolism,1993

2. Molecular cloning and tissue distribution of rat sarcosine dehydrogenase;Bergeron;Eur J Biochem,1998

3. Identification of the catalytic residue of human short/branched chain acyl-CoA dehydrogenase by in vitro mutagenesis;Binzak;Biochim Biophys Acta,1998

4. Structure and analysis of the human dimethylglycine dehydrogenase;Binzak;Mol Genet Metab,2000

5. Identification of the covalently bound flavin of dimethylglycine dehydrogenase and sarcosine dehydrogenase from rat liver mitochondria;Cook;J Biol Chem,1984

Cited by 61 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. New Mechanism of Bone Cancer Pain: Tumor Tissue-Derived Endogenous Formaldehyde Induced Bone Cancer Pain via TRPV1 Activation;Translational Research in Pain and Itch;2024

2. Pharmacokinetics of some newly synthesized 1, 5- benzothiazepine scaffolds: A molecular docking and molecular dynamics simulation approach;Journal of King Saud University - Science;2023-04

3. Salvia miltiorrhiza polysaccharides alleviates florfenicol-induced liver metabolic disorder in chicks by regulating drug and amino acid metabolic signaling pathways;Poultry Science;2022-09

4. Biochemical Phenotypes of Questionable Clinical Significance;Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases;2022

5. Disorders of Peptide and Amine Metabolism;Inborn Metabolic Diseases;2022