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TRPV6 Calcium Channel Targeting by Antibodies Raised against Extracellular Epitopes Induces Prostate Cancer Cell Apoptosis.
- Published in:
- Cancers, 2023, v. 15, n. 6, p. 1825, doi. 10.3390/cancers15061825
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- Publication type:
- Article
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.
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- Human Molecular Genetics, 2022, v. 31, n. 15, p. 2571, doi. 10.1093/hmg/ddac055
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- Publication type:
- Article
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation.
- Published in:
- Human Genetics, 2022, v. 141, n. 7, p. 1279, doi. 10.1007/s00439-021-02400-1
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- Publication type:
- Article
SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation.
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- Human Genetics, 2022, v. 141, n. 7, p. 1287, doi. 10.1007/s00439-021-02420-x
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- Publication type:
- Article
Towards understanding the extensive diversity of protein N‐glycan structures in eukaryotes.
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- Biological Reviews, 2022, v. 97, n. 2, p. 732, doi. 10.1111/brv.12820
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- Publication type:
- Article
TMEM165 a new player in proteoglycan synthesis: loss of TMEM165 impairs elongation of chondroitin- and heparan-sulfate glycosaminoglycan chains of proteoglycans and triggers early chondrocyte differentiation and hypertrophy.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41419-021-04458-1
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- Publication type:
- Article
Variation of the serum N‐glycosylation during the pregnancy of a MPI‐CDG patient.
- Published in:
- 2021
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- Publication type:
- Case Study
Les mécanismes de régulation de la glycosylation: Exemples d'altérations des chaînes glycanniques dans les cancers.
- Published in:
- Médecine Sciences, 2021, v. 37, n. 6/7, p. 609, doi. 10.1051/medsci/2021082
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- Publication type:
- Article
SLC37A4‐CDG: Second patient.
- Published in:
- Journal of Inherited Metabolic Disease Reports, 2021, v. 58, n. 1, p. 122, doi. 10.1002/jmd2.12195
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- Publication type:
- Article
Serum bikunin isoforms in congenital disorders of glycosylation and linkeropathies.
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- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 6, p. 1349, doi. 10.1002/jimd.12291
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- Publication type:
- Article
Anomalies congénitales de la glycosylation (CDG): 1980-2020, 40 ans pour comprendre.
- Published in:
- Médecine Sciences, 2020, v. 36, n. 8/9, p. 735, doi. 10.1051/medsci/2020128
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- Publication type:
- Article
Sialic Acid Metabolic Engineering of Breast Cancer Cells Interferes with Adhesion and Migration.
- Published in:
- Molecules, 2020, v. 25, n. 11, p. 2632, doi. 10.3390/molecules25112632
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- Publication type:
- Article
Potential Plasticity of the Mannoprotein Repertoire Associated to Mycobacterium tuberculosis Virulence Unveiled by Mass Spectrometry-Based Glycoproteomics.
- Published in:
- Molecules, 2020, v. 25, n. 10, p. 2348, doi. 10.3390/molecules25102348
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- Publication type:
- Article
Fetal bovine serum impacts the observed N‐glycosylation defects in TMEM165 KO HEK cells.
- Published in:
- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 2, p. 357, doi. 10.1002/jimd.12161
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- Publication type:
- Article
Investigating the functional link between TMEM165 and SPCA1.
- Published in:
- Biochemical Journal, 2019, v. 476, n. 21, p. 3281, doi. 10.1042/BCJ20190488
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- Publication type:
- Article
Involvement of thapsigargin- and cyclopiazonic acid-sensitive pumps in the rescue of TMEM165-associated glycosylation defects by Mn<sup>2+</sup>.
- Published in:
- FASEB Journal, 2019, v. 33, n. 2, p. 2669, doi. 10.1096/fj.201800387R
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- Publication type:
- Article
Use of Endoglycosidase H as a diagnostic tool for MAN1B1‐CDG patients.
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- Electrophoresis, 2018, v. 39, n. 24, p. 3133, doi. 10.1002/elps.201800020
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- Publication type:
- Article
Protein N-glycosylation alteration and glycolysis inhibition both contribute to the antiproliferative action of 2-deoxyglucose in breast cancer cells.
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 171, n. 3, p. 581, doi. 10.1007/s10549-018-4874-z
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- Publication type:
- Article
The extended cytoplasmic tail of the human B4GALNT2 is critical for its Golgi targeting and post‐Golgi sorting.
- Published in:
- FEBS Journal, 2018, v. 285, n. 18, p. 3442, doi. 10.1111/febs.14621
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- Publication type:
- Article
Chemical glycomics enrichment: imaging the recycling of sialic acid in living cells.
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- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 3, p. 515, doi. 10.1007/s10545-017-0118-3
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- Publication type:
- Article
Manganese-induced turnover of TMEM165.
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- Biochemical Journal, 2017, v. 474, n. 9, p. 1481, doi. 10.1042/BCJ20160910
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- Publication type:
- Article
Participation of 3- O-sulfated heparan sulfates in the protection of macrophages by herpes simplex virus-1 glycoprotein D and cyclophilin B against apoptosis.
- Published in:
- FEBS Open Bio, 2017, v. 7, n. 2, p. 133, doi. 10.1002/2211-5463.12145
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- Publication type:
- Article
Mutations in TRAPPC11 are associated with a congenital disorder of glycosylation.
- Published in:
- Human Mutation, 2017, v. 38, n. 2, p. 148, doi. 10.1002/humu.23145
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- Publication type:
- Article
Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.
- Published in:
- 2017
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- Publication type:
- journal article
Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 8, p. 1489, doi. 10.1093/hmg/ddw026
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- Publication type:
- Article
Yeast Gdt1 is a Golgi-localized calcium transporter required for stress-induced calcium signaling and protein glycosylation.
- Published in:
- Scientific Reports, 2016, p. 24282, doi. 10.1038/srep24282
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- Publication type:
- Article
Golgi post-translational modifications and associated diseases.
- Published in:
- Journal of Inherited Metabolic Disease, 2015, v. 38, n. 4, p. 741, doi. 10.1007/s10545-015-9851-7
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- Publication type:
- Article
Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG.
- Published in:
- Glycobiology, 2015, v. 25, n. 6, p. 669, doi. 10.1093/glycob/cwv009
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- Publication type:
- Article
MAN1B1 Deficiency: An Unexpected CDG-II.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 12, p. 1, doi. 10.1371/journal.pgen.1003989
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- Publication type:
- Article
Insulin signaling controls the expression of O-GlcNAc transferase and its interaction with lipid microdomains.
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- FASEB Journal, 2013, v. 27, n. 9, p. 3478, doi. 10.1096/fj.12-217984
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- Publication type:
- Article
Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2914, doi. 10.1093/hmg/ddt146
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- Publication type:
- Article
Glycosylation disorders of membrane trafficking.
- Published in:
- Glycoconjugate Journal, 2013, v. 30, n. 1, p. 23, doi. 10.1007/s10719-012-9389-y
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- Publication type:
- Article
COG5-CDG: expanding the clinical spectrum.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 1, doi. 10.1186/1750-1172-7-94
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- Publication type:
- Article
PUGNAc treatment leads to an unusual accumulation of free oligosaccharides in CHO cells.
- Published in:
- Journal of Biochemistry, 2012, v. 151, n. 4, p. 439, doi. 10.1093/jb/mvs012
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- Publication type:
- Article
COG5-CDG: expanding the clinical spectrum.
- Published in:
- 2012
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- Publication type:
- journal article
How Golgi glycosylation meets and needs trafficking: the case of the COG complex.
- Published in:
- Glycobiology, 2011, v. 21, n. 7, p. 853, doi. 10.1093/glycob/cwq179
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- Publication type:
- Article
Differential effects of lobe A and lobe B of the Conserved Oligomeric Golgi complex on the stability of β1,4-galactosyltransferase 1 and α2,6-sialyltransferase 1.
- Published in:
- Glycobiology, 2011, v. 21, n. 7, p. 864, doi. 10.1093/glycob/cwq176
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- Publication type:
- Article
Overexpression of Man2C1 leads to protein underglycosylation and upregulation of endoplasmic reticulum-associated degradation pathway.
- Published in:
- Glycobiology, 2011, v. 21, n. 3, p. 363, doi. 10.1093/glycob/cwq169
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- Publication type:
- Article
Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4350, doi. 10.1093/hmg/ddp389
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- Publication type:
- Article
RFT1 deficiency in three novel CDG patients.
- Published in:
- Human Mutation, 2009, v. 30, n. 10, p. 1428, doi. 10.1002/humu.21085
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- Publication type:
- Article
Golgi function and dysfunction in the first COG4-deficient CDG type II patient.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3244, doi. 10.1093/hmg/ddp262
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- Publication type:
- Article
Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient.
- Published in:
- Glycobiology, 2009, v. 19, n. 8, p. 910, doi. 10.1093/glycob/cwp067
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- Publication type:
- Article
Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 3, p. 517
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- Publication type:
- Article
A rapid mass spectrometric strategy for the characterization of N- and O-glycan chains in the diagnosis of defects in glycan biosynthesis.
- Published in:
- Proteomics, 2007, v. 7, n. 11, p. 1800, doi. 10.1002/pmic.200600977
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- Publication type:
- Article
A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1–Cog8 interaction in COG complex formation.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 717, doi. 10.1093/hmg/ddl476
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- Publication type:
- Article