Isabelle Callebaut
Overview
Explore the profile of Isabelle Callebaut including associated specialties, affiliations and a list of published articles.
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Articles
183
Citations
4782
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Recent Articles
1.
Garrigue A, Kermasson L, Susini S, Fert I, Mahony C, Sadek H, et al.
J Clin Invest
. 2025 Jan;
PMID: 39847438
Oncostatin M (OSM) is a cytokine with the unique ability to interact with both the OSM receptor (OSMR) and the leukemia inhibitory factor receptor (LIFR). On the other hand, OSMR...
2.
Elbahnsi A, Dudas B, Callebaut I, Hinzpeter A, Miteva M
Pharmaceuticals (Basel)
. 2025 Jan;
17(12.
PMID: 39770445
The ATP-binding cassette (ABC) and solute carrier (SLC) transporters play pivotal roles in cellular transport mechanisms, influencing a wide range of physiological processes and impacting various medical conditions. Recent advancements...
3.
Castanier S, Elbahnsi A, Chevalier B, Baatallah N, Pranke I, Berri L, et al.
Cell Mol Life Sci
. 2024 Oct;
81(1):426.
PMID: 39373784
CFTR is an anion channel that has evolved from the mold of an ABC transporter. It possesses specific structural features, including a lateral portal between the cytoplasmic extensions of its...
4.
Benavides-Nieto M, Adam F, Martin E, Boussard C, Lagresle-Peyrou C, Callebaut I, et al.
J Clin Invest
. 2024 Sep;
134(17).
PMID: 39225097
The ubiquitously expressed small GTPase Ras-related protein 1B (RAP1B) acts as a molecular switch that regulates cell signaling, cytoskeletal remodeling, and cell trafficking and activates integrins in platelets and lymphocytes....
5.
Uguen K, Le Tertre M, Tchernitchko D, Elbahnsi A, Maestri S, Gourlaouen I, et al.
HGG Adv
. 2024 Jul;
5(4):100335.
PMID: 39039793
Heterozygous mutations in SLC40A1, encoding a multi-pass membrane protein of the major facilitator superfamily known as ferroportin 1 (FPN1), are responsible for two distinct hereditary iron-overload diseases: ferroportin disease, which...
6.
Debbiche R, Elbahnsi A, Uguen K, Ka C, Callebaut I, Le Gac G
FASEB J
. 2024 Jul;
38(13):e23725.
PMID: 38959016
SLC40A1 is the sole iron export protein reported in mammals. In humans, its dysfunction is responsible for ferroportin disease, an inborn error of iron metabolism transmitted as an autosomal dominant...
7.
Gaschignard G, Millet M, Bruley A, Benzerara K, Dezi M, Skouri-Panet F, et al.
Proteins
. 2024 Jan;
92(6):776-794.
PMID: 38258321
Three-dimensional (3D) structure information, now available at the proteome scale, may facilitate the detection of remote evolutionary relationships in protein superfamilies. Here, we illustrate this with the identification of a...
8.
Bertrand A, Ba I, Kermasson L, Pirabakaran V, Chable N, Lainey E, et al.
Hum Mol Genet
. 2024 Jan;
33(7):612-623.
PMID: 38176734
Telomeres are nucleoprotein structures that protect the chromosome ends from degradation and fusion. Telomerase is a ribonucleoprotein complex essential to maintain the length of telomeres. Germline defects that lead to...
9.
Houngue R, Sangare L, Alayi T, Dieng A, Bitard-Feildel T, Boulogne C, et al.
Cell Rep
. 2023 Dec;
43(1):113601.
PMID: 38157297
Apicomplexan parasites possess specialized secretory organelles called rhoptries, micronemes, and dense granules that play a vital role in host infection. In this study, we demonstrate that TgREMIND, a protein found...
10.
Serres M, Shaughnessy R, Escot S, Hammich H, Cuvelier F, Salles A, et al.
Dev Cell
. 2023 Oct;
58(22):2477-2494.e8.
PMID: 37875118
Cilia protrude from the cell surface and play critical roles in intracellular signaling, environmental sensing, and development. Reduced actin-dependent contractility and intracellular trafficking are both required for ciliogenesis, but little...