Search details
1.
Analysis of the Healthy Platelet Proteome Identifies a New Form of Domain-Specific O-Fucosylation.
Mol Cell Proteomics
; 23(2): 100717, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38237698
2.
Poglut2/3 double knockout in mice results in neonatal lethality with reduced levels of fibrillin in lung tissues.
J Biol Chem
; : 107445, 2024 Jun 04.
Article
in English
| MEDLINE | ID: mdl-38844137
3.
Structure of the IFNγ receptor complex guides design of biased agonists.
Nature
; 567(7746): 56-60, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30814731
4.
In vivo evidence for GDP-fucose transport in the absence of transporter SLC35C1 and putative transporter SLC35C2.
J Biol Chem
; 299(12): 105406, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-38270391
5.
Lfng and Dll3 cooperate to modulate protein interactions in cis and coordinate oscillatory Notch pathway activation in the segmentation clock.
Dev Biol
; 487: 42-56, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35429490
6.
Cancer-associated Notch receptor variants lead to O-fucosylation defects that deregulate Notch signaling.
J Biol Chem
; 298(12): 102616, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36265581
7.
Fringe GlcNAc-transferases differentially extend O-fucose on endogenous NOTCH1 in mouse activated T cells.
J Biol Chem
; 298(7): 102064, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35623385
8.
O-fucosylation stabilizes the TSR3 motif in thrombospondin-1 by interacting with nearby amino acids and protecting a disulfide bond.
J Biol Chem
; 298(6): 102047, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35597280
9.
Two NOTCH1 O-fucose sites have opposing functions in mouse retinal angiogenesis.
Glycobiology
; 33(8): 661-672, 2023 10 06.
Article
in English
| MEDLINE | ID: mdl-37329502
10.
O-fucosylation of thrombospondin type I repeats is dispensable for trafficking thrombospondin 1 to platelet secretory granules.
Glycobiology
; 33(4): 301-310, 2023 05 17.
Article
in English
| MEDLINE | ID: mdl-36721988
11.
Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling.
Cell
; 132(2): 247-58, 2008 Jan 25.
Article
in English
| MEDLINE | ID: mdl-18243100
12.
POGLUT2 and POGLUT3 O-glucosylate multiple EGF repeats in fibrillin-1, -2, and LTBP1 and promote secretion of fibrillin-1.
J Biol Chem
; 297(3): 101055, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34411563
13.
Peters plus syndrome mutations affect the function and stability of human ß1,3-glucosyltransferase.
J Biol Chem
; 297(1): 100843, 2021 07.
Article
in English
| MEDLINE | ID: mdl-34058199
14.
Identification, function, and biological relevance of POGLUT2 and POGLUT3.
Biochem Soc Trans
; 50(2): 1003-1012, 2022 04 29.
Article
in English
| MEDLINE | ID: mdl-35411374
15.
Canonical Notch ligands and Fringes have distinct effects on NOTCH1 and NOTCH2.
J Biol Chem
; 295(43): 14710-14722, 2020 10 23.
Article
in English
| MEDLINE | ID: mdl-32820046
16.
O-Fucosylation of ADAMTSL2 is required for secretion and is impacted by geleophysic dysplasia-causing mutations.
J Biol Chem
; 295(46): 15742-15753, 2020 11 13.
Article
in English
| MEDLINE | ID: mdl-32913123
17.
Hydrocephalus in mouse B3glct mutants is likely caused by defects in multiple B3GLCT substrates in ependymal cells and subcommissural organ.
Glycobiology
; 31(8): 988-1004, 2021 09 09.
Article
in English
| MEDLINE | ID: mdl-33909046
18.
O-Fucose and Fringe-modified NOTCH1 extracellular domain fragments as decoys to release niche-lodged hematopoietic progenitor cells.
Glycobiology
; 31(5): 582-592, 2021 06 03.
Article
in English
| MEDLINE | ID: mdl-33351914
19.
ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome.
Hum Mol Genet
; 28(24): 4053-4066, 2019 12 15.
Article
in English
| MEDLINE | ID: mdl-31600785
20.
Emerging structural insights into glycosyltransferase-mediated synthesis of glycans.
Nat Chem Biol
; 15(9): 853-864, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31427814