A novel human UDP-N-acetyl-D-galactosamine:polypeptideN-acetylgalactosaminyltransferase, GalNAc-T7, with specificity for partial GalNAc-glycosylated acceptor substrates-Reference-Cited by-同舟云学术

A novel human UDP-N-acetyl-D-galactosamine:polypeptideN-acetylgalactosaminyltransferase, GalNAc-T7, with specificity for partial GalNAc-glycosylated acceptor substrates

Published:1999-10-25 Issue:2 Volume:460 Page:226-230
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Bennett Eric Paul,Hassan Helle,Hollingsworth Michael A.,Clausen Henrik

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(99)01268-5/fullpdf

Reference29 articles.

1. A family of UDP-GalNAc: polypeptide N-acetylgalactosaminyl-transferases control the initiation of mucin-type O-linked glycosylation

2. Isolation and expression of a cDNA clone encoding a bovine UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase

3. Purification and cDNA Cloning of a Human UDP-N-acetyl-α- D-galactosamine:polypeptide N-Acetylgalactosaminyltransferase

4. cDNA Cloning and Expression of a Novel Human UDP- -acetyl-α-D-galactosamine

5. Cloning of a Human UDP-N-Acetyl-α-d-Galactosamine:PolypeptideN-Acetylgalactosaminyltransferase That Complements Other GalNAc-Transferases in Complete O-Glycosylation of the MUC1 Tandem Repeat

Cited by 122 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. Reading and Writing the Human Glycocode;Annual Review of Biochemistry;2024-08-02

2. ISOGlyP: O-Glycosylation Site Prediction Using Peptide Sequences and GALNTs;Methods in Molecular Biology;2024

3. Glycosylation as regulator of human B-cell leukaemias in bone marrow;Frontiers in Hematology;2023-11-16

4. Bump-and-hole engineering of human polypeptide N-acetylgalactosamine transferases to dissect their protein substrates and glycosylation sites in cells;STAR Protocols;2023-03

5. Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology;Developmental Biology;2022-10