Causes and consequences of impaired methionine synthase activity in acquired and inherited disorders of vitamin B12 metabolism-Reference-Cited by-同舟云学术

Causes and consequences of impaired methionine synthase activity in acquired and inherited disorders of vitamin B12 metabolism

Published:2021-10-05 Issue: Volume: Page:1-23
ISSN:1040-9238
Container-title:Critical Reviews in Biochemistry and Molecular Biology
language:en
Short-container-title:Critical Reviews in Biochemistry and Molecular Biology

Author:

Guéant Jean-Louis¹²,Guéant-Rodriguez Rosa-Maria¹²,Kosgei Viola J.¹,Coelho David¹

Affiliation:

1. UMR Inserm 1256 N-GERE (Nutrition, Génetique et Exposition aux Risques Environmentaux), Université de Lorraine, Vandoeuvre-lès-Nancy, France

2. Departments of Digestive Diseases and Molecular Medicine and National Center of Inborn Errors of Metabolism, University Hospital Center, Université de Lorraine, Vandoeuvre-lès-Nancy, France

Funder

FHU ARRIMAGE

French PIA GEENAGE project

Lorraine Université d’Excellence

OMAGE project

Region Grand-Est of France

FEDER

Publisher

Informa UK Limited

Subject

Molecular Biology,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10409238.2021.1979459

Reference146 articles.

1. Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

2. Effect of Proteolytic Enzymes on the Binding of Cobalamin to R Protein and Intrinsic Factor

3. Biochemical and clinical response to hydroxocobalamin versus cyanocobalamin treatment in patients with methylmalonic acidemia and homocystinuria (cblC)

4. Neuropathology of vitamin B 12 deficiency in the Cd320 −/− mouse

5. Maternofetal transport of vitamin B 12 : role of TCblR/ CD320 and megalin

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