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Page 1
The stress of Arctic warming on polar bears.
Boonstra R, Bodner K, Bosson C, Delehanty B, Richardson ES, Lunn NJ, Derocher AE, Molnár PK. Boonstra R, et al. Among authors: bosson c. Glob Chang Biol. 2020 Aug;26(8):4197-4214. doi: 10.1111/gcb.15142. Epub 2020 Jun 10. Glob Chang Biol. 2020. PMID: 32364624
Variations in the TRPV1 gene are associated to exertional heat stroke.
Bosson C, Rendu J, Pelletier L, Abriat A, Chatagnon A, Brocard J, Brocard J, Figarella-Branger D, Ducreux S, van Coppenolle F, Sagui E, Marty I, Roux-Buisson N, Faure J. Bosson C, et al. J Sci Med Sport. 2020 Nov;23(11):1021-1027. doi: 10.1016/j.jsams.2020.04.018. Epub 2020 May 18. J Sci Med Sport. 2020. PMID: 32471784
Corrigendum to "22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd-7th October 2017" [Neuromuscular Disorders 27S2 (2017) S51-S270].
Rendu J, Bosson C, Roux-Buisson N, Chatagnon A, Bankole B, Rivier F, Durigneux J, Monges S, Stojkovic T, Romero N, Marty I, Fauré J. Rendu J, et al. Among authors: bosson c. Neuromuscul Disord. 2017 Nov;27(11):e1. doi: 10.1016/j.nmd.2017.09.014. Epub 2017 Oct 21. Neuromuscul Disord. 2017. PMID: 29033277 No abstract available.
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Le Tanno P, Breton J, Bidart M, Satre V, Harbuz R, Ray PF, Bosson C, Dieterich K, Jaillard S, Odent S, Poke G, Beddow R, Digilio MC, Novelli A, Bernardini L, Pisanti MA, Mackenroth L, Hackmann K, Vogel I, Christensen R, Fokstuen S, Béna F, Amblard F, Devillard F, Vieville G, Apostolou A, Jouk PS, Guebre-Egziabher F, Sartelet H, Coutton C. Le Tanno P, et al. Among authors: bosson c. J Med Genet. 2017 Jul;54(7):502-510. doi: 10.1136/jmedgenet-2016-104435. Epub 2017 Mar 7. J Med Genet. 2017. PMID: 28270404
Interpretation of the Elecsys Toxo IgG avidity results for very low and very high index: study on 741 sera with a determined date of toxoplasmosis.
Fricker-Hidalgo H, L'Ollivier C, Bosson C, Imbert S, Bailly S, Dard C, Piarroux R, Paris L, Pelloux H. Fricker-Hidalgo H, et al. Among authors: bosson c. Eur J Clin Microbiol Infect Dis. 2017 May;36(5):847-852. doi: 10.1007/s10096-016-2870-y. Epub 2016 Dec 19. Eur J Clin Microbiol Infect Dis. 2017. PMID: 27995345
Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic features.
Bidart M, El Atifi M, Miladi S, Rendu J, Satre V, Ray PF, Bosson C, Devillard F, Lehalle D, Malan V, Amiel J, Mencarelli MA, Baldassarri M, Renieri A, Clayton-Smith J, Vieville G, Thevenon J, Amblard F, Berger F, Jouk PS, Coutton C. Bidart M, et al. Among authors: bosson c. Genet Med. 2017 Jun;19(6):701-710. doi: 10.1038/gim.2016.180. Epub 2016 Dec 1. Genet Med. 2017. PMID: 27906199 Free article.
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