Capucine Trollet
Overview
Explore the profile of Capucine Trollet including associated specialties, affiliations and a list of published articles.
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52
Citations
1120
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Recent Articles
11.
Kim E, Wu F, Lim D, Zeuthen C, Zhang Y, Allen J, et al.
Front Cell Dev Biol
. 2022 Jun;
10:875209.
PMID: 35669512
Skeletal muscle stem cells, known as satellite cells (SCs), are quiescent in normal adult limb muscles. Injury stimulates SC proliferation, differentiation, and fusion to regenerate muscle structure. In pharyngeal muscles,...
12.
Bensalah M, Muraine L, Boulinguiez A, Giordani L, Albert V, Ythier V, et al.
J Cachexia Sarcopenia Muscle
. 2022 Mar;
13(3):1771-1784.
PMID: 35319169
Background: Fibrosis is defined as an excessive accumulation of extracellular matrix (ECM) components. Many organs are subjected to fibrosis including the lung, liver, heart, skin, kidney, and muscle. Muscle fibrosis...
13.
Trollet C, Cheng A, Sylow L, Batista Jr M, Pillon N
Front Physiol
. 2021 May;
12:683088.
PMID: 33995133
No abstract available.
14.
Strings-Ufombah V, Malerba A, Kao S, Harbaran S, Roth F, Cappellari O, et al.
Mol Ther Nucleic Acids
. 2021 Mar;
24:67-78.
PMID: 33738139
Oculopharyngeal muscular dystrophy (OPMD) is a rare autosomal dominant disease that results from an alanine expansion in the N-terminal domain of Poly-A Binding Protein Nuclear-1 (PABPN1). We have recently demonstrated...
15.
Bamia A, Sinane M, Nait-Saidi R, Dhiab J, Keruzore M, Nguyen P, et al.
Neurotherapeutics
. 2021 Feb;
18(2):1137-1150.
PMID: 33533011
Prion diseases are caused by the propagation of PrP, the pathological conformation of the PrP prion protein. The molecular mechanisms underlying PrP propagation are still unsolved and no therapeutic solution...
16.
Muraine L, Bensalah M, Dhiab J, Cordova G, Arandel L, Marhic A, et al.
Hum Gene Ther
. 2019 Dec;
31(3-4):233-240.
PMID: 31880951
The adeno-associated virus (AAV) vector is an efficient tool for gene delivery in skeletal muscle. AAV-based therapies show promising results for treatment of various genetic disorders, including muscular dystrophy. These...
17.
Vargas J, Loria F, Wu Y, Cordova G, Nonaka T, Bellow S, et al.
EMBO J
. 2019 Oct;
38(23):e101230.
PMID: 31625188
Tunneling nanotubes (TNTs) are actin-based transient tubular connections that allow direct communication between distant cells. TNTs play an important role in several physiological (development, immunity, and tissue regeneration) and pathological...
18.
Malerba A, Klein P, Lu-Nguyen N, Cappellari O, Strings-Ufombah V, Harbaran S, et al.
Hum Mol Genet
. 2019 Jul;
28(19):3301-3308.
PMID: 31294444
Oculopharyngeal muscular dystrophy (OPMD) is a rare autosomal dominant late-onset muscular dystrophy affecting approximately 1:100 000 individuals in Europe. OPMD is mainly characterized by progressive eyelid drooping (ptosis) and dysphagia...
19.
Harish P, Malerba A, Lu-Nguyen N, Forrest L, Cappellari O, Roth F, et al.
J Cachexia Sarcopenia Muscle
. 2019 May;
10(5):1016-1026.
PMID: 31066242
Background: Oculopharyngeal muscular dystrophy (OPMD) is a late-onset muscle disease affecting one per 80 000 of the general population characterized by profound dysphagia and ptosis, and limb weakness at later...
20.
Bensalah M, Klein P, Riederer I, Chaouch S, Muraine L, Savino W, et al.
PLoS One
. 2019 May;
14(5):e0211522.
PMID: 31048846
Xenotransplantation of human cells into immunodeficient mouse models is a very powerful tool and an essential step for the pre-clinical evaluation of therapeutic cell- and gene- based strategies. Here we...