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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
1999 1
2001 3
2002 1
2003 1
2009 2
2010 1
2012 1
2013 4
2014 2
2015 3
2016 3
2017 1
2018 3
2019 1
2020 9
2021 4
2022 5
2023 2
2024 0

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45 results

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Page 1
Therapeutic Strategies Targeting DUX4 in FSHD.
Le Gall L, Sidlauskaite E, Mariot V, Dumonceaux J. Le Gall L, et al. Among authors: dumonceaux j. J Clin Med. 2020 Sep 7;9(9):2886. doi: 10.3390/jcm9092886. J Clin Med. 2020. PMID: 32906621 Free PMC article. Review.
Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy.
Mariot V, Dumonceaux J. Mariot V, et al. Among authors: dumonceaux j. Front Genome Ed. 2022 Jul 15;4:937879. doi: 10.3389/fgeed.2022.937879. eCollection 2022. Front Genome Ed. 2022. PMID: 35910413 Free PMC article. Review.
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles.
Le Gall L, Duddy WJ, Martinat C, Mariot V, Connolly O, Milla V, Anakor E, Ouandaogo ZG, Millecamps S, Lainé J, Vijayakumar UG, Knoblach S, Raoul C, Lucas O, Loeffler JP, Bede P, Behin A, Blasco H, Bruneteau G, Del Mar Amador M, Devos D, Henriques A, Hesters A, Lacomblez L, Laforet P, Langlet T, Leblanc P, Le Forestier N, Maisonobe T, Meininger V, Robelin L, Salachas F, Stojkovic T, Querin G, Dumonceaux J, Butler Browne G, González De Aguilar JL, Duguez S, Pradat PF. Le Gall L, et al. Among authors: dumonceaux j. J Cachexia Sarcopenia Muscle. 2022 Apr;13(2):1385-1402. doi: 10.1002/jcsm.12945. Epub 2022 Feb 22. J Cachexia Sarcopenia Muscle. 2022. PMID: 35194965 Free PMC article.
DUX4 Expression in FSHD Muscles: Focus on Its mRNA Regulation.
Sidlauskaite E, Le Gall L, Mariot V, Dumonceaux J. Sidlauskaite E, et al. Among authors: dumonceaux j. J Pers Med. 2020 Jul 28;10(3):73. doi: 10.3390/jpm10030073. J Pers Med. 2020. PMID: 32731450 Free PMC article. Review.
One-hour universal protocol for mouse genotyping.
Joubert R, Mariot V, Dumonceaux J. Joubert R, et al. Among authors: dumonceaux j. Muscle Nerve. 2020 Jun;61(6):801-807. doi: 10.1002/mus.26841. Epub 2020 Mar 6. Muscle Nerve. 2020. PMID: 32086834
268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trials.
Montagnese F, de Valle K, Lemmers RJLF, Mul K, Dumonceaux J, Voermans N; 268th ENMC workshop participants. Montagnese F, et al. Among authors: dumonceaux j. Neuromuscul Disord. 2023 May;33(5):447-462. doi: 10.1016/j.nmd.2023.04.005. Epub 2023 Apr 8. Neuromuscul Disord. 2023. PMID: 37099914 No abstract available.
Meeting report: The 2022 FSHD International Research Congress.
Leung DG, Kinoshita J, Arjomand J, Dumonceaux J; 2022 FSHD IRC Program committee and co-chairs. Leung DG, et al. Among authors: dumonceaux j. Neuromuscul Disord. 2023 Feb;33(2):196-198. doi: 10.1016/j.nmd.2022.12.005. Epub 2022 Dec 13. Neuromuscul Disord. 2023. PMID: 36682112 No abstract available.
Necroptosis mediates myofibre death in dystrophin-deficient mice.
Morgan JE, Prola A, Mariot V, Pini V, Meng J, Hourde C, Dumonceaux J, Conti F, Relaix F, Authier FJ, Tiret L, Muntoni F, Bencze M. Morgan JE, et al. Among authors: dumonceaux j. Nat Commun. 2018 Sep 7;9(1):3655. doi: 10.1038/s41467-018-06057-9. Nat Commun. 2018. PMID: 30194302 Free PMC article.
Meeting report: the 2020 FSHD International Research Congress.
Kyba M, Bloch RJ, Dumonceaux J, Harper SQ, van der Maarel SM, Sverdrup FM, Wagner KR, van Engelen B, Chen YW. Kyba M, et al. Among authors: dumonceaux j. Skelet Muscle. 2020 Dec 8;10(1):36. doi: 10.1186/s13395-020-00253-2. Skelet Muscle. 2020. PMID: 33292505 Free PMC article. No abstract available.
45 results