Mutations in the SLC35C1 gene, contributing to significant differences in fucosylation patterns, may underlie the diverse phenotypic manifestations observed in leukocyte adhesion deficiency type II patients-Reference-Cited by-同舟云学术

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Mutations in the SLC35C1 gene, contributing to significant differences in fucosylation patterns, may underlie the diverse phenotypic manifestations observed in leukocyte adhesion deficiency type II patients

Published:2024-08 Issue: Volume:173 Page:106602
ISSN:1357-2725
Container-title:The International Journal of Biochemistry & Cell Biology
language:en
Short-container-title:The International Journal of Biochemistry & Cell Biology

Author:

Skurska E.,Szulc B.,Kreczko K.,Olczak M.

Publisher

Elsevier BV

Reference35 articles.

1. Substitutions in the N-glycan core as regulators of biorecognition: the case of core-fucose and bisecting moieties;André;Biochemistry,2007

2. From structural to functional glycomics: core substitutions as molecular switches for shape and lectin affinity of N-glycans;André;Biol. Chem.,2009

3. Turning universal O into rare Bombay type blood;Anso;Nat. Commun.,2023

4. Lysine at position 329 within a C-terminal dilysine motif is crucial for the ER localization of human SLC35B4;Bazan;PloS One,2018

5. The many routes of Golgi-dependent trafficking;Boncompain;Histochem Cell Biol.,2013

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