Hepatic D-Glycerate Dehydrogenase and Glyoxylate Reductase Deficiency in Primary Hyperoxaluria Type 2

Biochemical Society Transactions - United Kingdom
doi 10.1042/bst0160626
Full Text
Abstract

Available in full text

Categories
Biochemistry
Date
Authors
Publisher

Portland Press Ltd.

Related search

Primary Hyperoxaluria Type III—a Model for Studying Perturbations in Glyoxylate Metabolism

Journal of Molecular Medicine
Molecular MedicineDrug DiscoveryGenetics
2012English

Glyoxylate Reductase Activity of Lactate Dehydrogenase

THE JOURNAL OF VITAMINOLOGY
1965English

Calcified Nodules on Fingers in Primary Hyperoxaluria Type 2

The Lancet Diabetes and Endocrinology
Internal MedicineEndocrinologyMetabolismDiabetes
2016English

Pd03-07 Rna Interference of Hepatic Lactate Dehydrogenase Reduces Urinary Oxalate in a Mouse Model of Primary Hyperoxaluria Type 1

Journal of Urology
Urology
2018English

Primary Hyperoxaluria Type 3

2020English

Identification of Mutations Associated With Peroxisome-To-Mitochondrion Mistargeting of Alanine/Glyoxylate Aminotransferase in Primary Hyperoxaluria Type 1

Journal of Cell Biology
MedicineCell Biology
1990English

Subunits and Sulfhydryl Groups of Beef Liver D-Glycerate Dehydrogenase.

Agricultural and Biological Chemistry
1975English

Combined Hepatic and Renal Transplantation in Primary Hyperoxaluria Type I: Clinical Report of Nine Cases

American Journal of Medicine
Medicine
1991English

Cortisone-Reductase Deficiency Associated With Heterozygous Mutations in 11 -Hydroxysteroid Dehydrogenase Type 1

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2011English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy