Glutamyl ribose 5-phosphate storage disease. A hereditary defect in the degradation of poly(ADP-ribosylated) proteins.-Reference-Cited by-同舟云学术

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Glutamyl ribose 5-phosphate storage disease. A hereditary defect in the degradation of poly(ADP-ribosylated) proteins.

Published:1984-01 Issue:2 Volume:259 Page:1037-1042
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Williams J C,Chambers J P,Liehr J G

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference28 articles.

1. A new type of carbohydrate-protein linkage in a glycopeptide from normal human urine.

2. Identification of digalactosylcysteine in a glycopeptide isolated from urine by a new preparative technique

3. Poly (ADP-Ribose) and ADP-Ribosylation of Proteins

4. Poly(adenosine diphosphate ribose)

Cited by 25 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. Poly‐ADP‐ribosylation dynamics, signaling, and analysis;Environmental and Molecular Mutagenesis;2024-09-02

2. Functional roles of ADP-ribosylation writers, readers and erasers;Frontiers in Cell and Developmental Biology;2022-08-11

3. Targeting dePARylation for cancer therapy;Cell & Bioscience;2020-01-29

4. ADP-ribosylation signalling and human disease;Open Biology;2019-04

5. Poly-ADP ribosylation in DNA damage response and cancer therapy;Mutation Research/Reviews in Mutation Research;2019-04

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