Marie-Ange Krzewinski-Recchi
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Explore the profile of Marie-Ange Krzewinski-Recchi including associated specialties, affiliations and a list of published articles.
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22
Citations
477
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Recent Articles
1.
Kasprowicz A, Cavdarli S, Delannoy P, Le Guezennec X, Defebvre C, Spriet C, et al.
Mol Cell Biochem
. 2024 Oct;
PMID: 39395135
O-acetylated GD2 (OAcGD2) is a cancer-related antigen that is currently being explored for therapeutic use. Exploring the intricate mechanisms behind OAcGD2 synthesis in cancer cells has long been a challenge....
2.
Wavelet-Vermuse C, Groux-Degroote S, Vicogne D, Cogez V, Venturi G, Trinchera M, et al.
Biochim Biophys Acta Gene Regul Mech
. 2021 Sep;
1864(11-12):194747.
PMID: 34500083
Background: The Sd antigen and corresponding biosynthetic enzyme B4GALNT2 are primarily expressed in normal colonic mucosa and are down-regulated to a variable degree in colon cancer tissues. Although their expression...
3.
Roy A, Miskinyte S, Garat A, Hovnanian A, Krzewinski-Recchi M, Foulquier F
Biochimie
. 2020 Apr;
174:159-170.
PMID: 32335229
TMEM165 is a Golgi protein whose deficiency causes a Congenital Disorder of Glycosylation (CDG). We have demonstrated that Mn supplementation could suppress the glycosylation defects observed in TMEM165-deficient cells and...
4.
Dulary E, Yu S, Houdou M, de Bettignies G, Decool V, Potelle S, et al.
Biochim Biophys Acta Gen Subj
. 2017 Nov;
1862(3):394-402.
PMID: 29108953
The Golgi ion homeostasis is tightly regulated to ensure essential cellular processes such as glycosylation, yet our understanding of this regulation remains incomplete. Gdt1p is a member of the conserved...
5.
Potelle S, Dulary E, Climer L, Duvet S, Morelle W, Vicogne D, et al.
Biochem J
. 2017 Mar;
474(9):1481-1493.
PMID: 28270545
TMEM165 deficiencies lead to one of the congenital disorders of glycosylation (CDG), a group of inherited diseases where the glycosylation process is altered. We recently demonstrated that the Golgi glycosylation...
6.
Krzewinski-Recchi M, Potelle S, Mir A, Vicogne D, Dulary E, Duvet S, et al.
Biochim Biophys Acta Gen Subj
. 2017 Jan;
1861(4):737-748.
PMID: 28088503
Background: Defects in TMEM165 gene cause a type-II Congenital Disorder of Glycosylation affecting Golgi glycosylation processes. TMEM165 patients exhibit psychomotor retardation, important osteoporosis, scoliosis, irregular epiphyses and thin bone cortex....
7.
Colomb F, Krzewinski-Recchi M, Steenackers A, Vincent A, Harduin-Lepers A, Delannoy P, et al.
Biochem J
. 2016 Nov;
474(1):65-78.
PMID: 27821620
We have previously shown that tumor necrosis factor (TNF) induced the up-regulation of the sialyltransferase gene ST3GAL4 (α2,3-sialyltransferase gene) BX transcript through mitogen- and stress-activated kinase 1/2 (MSK1/2), extracellular signal-regulated...
8.
Gilormini P, Lion C, Noel M, Krzewinski-Recchi M, Harduin-Lepers A, Guerardel Y, et al.
Glycobiology
. 2016 Aug;
26(11):1151-1156.
PMID: 27543325
Natural and synthetically modified cytidine monophosphate activated sialic acids (CMP-Sias) are essential research assets in the field of glycobiology: among other applications, they can be used to probe glycans, detect...
9.
Potelle S, Morelle W, Dulary E, Duvet S, Vicogne D, Spriet C, et al.
Hum Mol Genet
. 2016 Mar;
25(8):1489-500.
PMID: 27008884
Congenital disorders of glycosylation (CDG) are severe inherited diseases in which aberrant protein glycosylation is a hallmark. From this genetically and clinically heterogenous group, a significant subgroup due to Golgi...
10.
Van Slambrouck S, Groux-Degroote S, Krzewinski-Recchi M, Cazet A, Delannoy P, Steelant W
Biosci Rep
. 2014 Aug;
34(5).
PMID: 25137483
Complex interplays among proteins, lipids and carbohydrates can alter the phenotype and are suggested to have a crucial role in tumour metastasis. Our previous studies indicated that a complex of...