Delphine Leclerc
Overview
Explore the profile of Delphine Leclerc including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
114
Followers
0
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Recent Articles
1.
Paternoster M, Badoro B, Bourovali-Zade C, Castera C, Cordel H, Monteynard S, et al.
Sante Publique
. 2024 Jun;
36(3):39-48.
PMID: 38906813
Introduction: Pakistan has the second highest prevalence of hepatitis C globally. The Musafir study, set up in 2018 in a Parisian suburb to understand the representations of hepatitis and HIV...
2.
Doudnikoff C, Leclerc D, Angenard G, Gilot D, Coulouarn C, Mouriaux F
Mol Vis
. 2024 Apr;
30:160-166.
PMID: 38601020
Purpose: Uveal melanoma (UM) is a deadly cancer with limited therapeutic options. At advanced stages, UM cells metastasize almost exclusively into the liver, where targeting metastatic UM cells remain a...
3.
Leclerc D, Siroky M, Miller S
Curr Opin Biotechnol
. 2023 Dec;
85:103040.
PMID: 38103518
CRISPR-based genome editing holds promise for addressing genetic disease, infectious disease, and cancer and has rapidly advanced from primary research to clinical trials in recent years. However, the lack of...
4.
Louis C, Ferlier T, Leroux R, Pineau R, Desoteux M, Papoutsoglou P, et al.
JHEP Rep
. 2023 Nov;
5(12):100900.
PMID: 38023605
Background & Aims: Intrahepatic cholangiocarcinoma (iCCA) is a deadly cancer worldwide with an increasing incidence and limited therapeutic options. Therefore, there is an urgent need to open the field to...
5.
Mary L, Leclerc D, Labalme A, Bellaud P, Mazaud-Guittot S, Dreano S, et al.
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833200
Sexual development is a complex process relying on numerous genes. Disruptions in some of these genes are known to cause differences of sexual development (DSDs). Advances in genome sequencing allowed...
6.
Leclerc D, Goujon L, Jaillard S, Nouyou B, Cluzeau L, Damaj L, et al.
CRISPR J
. 2023 Jan;
6(1):17-31.
PMID: 36629845
Ganglioside-monosialic acid (GM1) gangliosidosis, a rare autosomal recessive disorder, is frequently caused by deleterious single nucleotide variants (SNVs) in gene. These variants result in reduced β-galactosidase (β-gal) activity, leading to...
7.
Hassold N, Brichler S, Gater Y, Leclerc D, Gordien E, Bouchaud O, et al.
J Clin Virol
. 2022 Dec;
158:105347.
PMID: 36476807
No abstract available.
8.
Quemener A, Bachelot L, Aubry M, Avner S, Leclerc D, Salbert G, et al.
Life Sci Alliance
. 2022 Oct;
5(12).
PMID: 36202613
Uveal melanoma (UM), the most common primary intraocular tumor in adults, has been extensively characterized by omics technologies during the last 5 yr. Despite the discovery of gene signatures, the...
9.
Mary L, Leclerc D, Gilot D, Belaud-Rotureau M, Jaillard S
Hum Mutat
. 2022 Apr;
43(9):1125-1148.
PMID: 35451537
PBX1 is a highly conserved atypical homeodomain transcription factor (TF) belonging to the TALE (three amino acid loop extension) family. Dimerized with other TALE proteins, it can interact with numerous...
10.
Goupil de Bouille J, Cordel H, Leclerc D, Faulcon C, Mubuanga A, Ouedraogo E, et al.
J Travel Med
. 2022 Mar;
29(4).
PMID: 35238905
No abstract available.