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2017 1
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2019 1
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2023 2
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Page 1
Class 3 PI3K coactivates the circadian clock to promote rhythmic de novo purine synthesis.
Alkhoury C, Henneman NF, Petrenko V, Shibayama Y, Segaloni A, Gadault A, Nemazanyy I, Le Guillou E, Wolide AD, Antoniadou K, Tong X, Tamaru T, Ozawa T, Girard M, Hnia K, Lutter D, Dibner C, Panasyuk G. Alkhoury C, et al. Among authors: le guillou e. Nat Cell Biol. 2023 Jul;25(7):975-988. doi: 10.1038/s41556-023-01171-3. Epub 2023 Jul 6. Nat Cell Biol. 2023. PMID: 37414850 Free PMC article.
[Second edition of the CoBioMe congress].
Janot C, Lefrère B, Michel M, Le Guillou E, Schell B. Janot C, et al. Among authors: le guillou e. Ann Biol Clin (Paris). 2019 Apr 1;77(2):233-240. doi: 10.1684/abc.2019.1435. Ann Biol Clin (Paris). 2019. PMID: 30998203 Free article. French. No abstract available.
[First edition of the CoBioMe congress].
Michel M, Le Guillou E, Schell B, Janot C. Michel M, et al. Among authors: le guillou e. Ann Biol Clin (Paris). 2018 Apr 1;76(2):205-216. doi: 10.1684/abc.2018.1341. Ann Biol Clin (Paris). 2018. PMID: 29623891 Free article. French. No abstract available.
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.
Huby T, Le Guillou E, Burin des Roziers C, Pacot L, Briand-Suleau A, Chansavang A, Toussaint A, Duchossoy V, Vaucouleur N, Benoit V, Lodé L, Molac C, North MO, Grotto S, Tsatsaris V, Jouinot A, Cochand-Priollet B, Paepegaey AC, Nectoux J, Groussin L, Pasmant E. Huby T, et al. Among authors: le guillou e. J Clin Endocrinol Metab. 2022 Mar 24;107(4):e1367-e1373. doi: 10.1210/clinem/dgab894. J Clin Endocrinol Metab. 2022. PMID: 34897474
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation.
Chartier S, Boutaud L, Le Guillou E, Alby C, Billon C, Millischer AE, Caillaud C, Galmiche L, Mechler C, Sonigo P, Boddaert N, Lyonnet S, Rondeau S, Bole-Feysot C, Masson C, Ville Y, Roth P, Desguerre I, Encha-Razavi F, Attie-Bitach T. Chartier S, et al. Among authors: le guillou e. Birth Defects Res. 2021 Nov;113(18):1324-1332. doi: 10.1002/bdr2.1950. Epub 2021 Sep 7. Birth Defects Res. 2021. PMID: 34491000
Troponin elevation in other conditions than acute coronary syndromes.
Masri W, Le Guillou E, Hamdi E, Ghazal K, Lebigot E, Cosson C, Cynober FB, Therond P. Masri W, et al. Among authors: le guillou e. Ann Biol Clin (Paris). 2017 Aug 1;75(4):411-419. doi: 10.1684/abc.2017.1262. Ann Biol Clin (Paris). 2017. PMID: 28751286 Free article. English.
Prenatal features and neonatal management of severe hyperparathyroidism caused by the heterozygous inactivating calcium-sensing receptor variant, Arg185Gln: A case report and review of the literature.
Aubert-Mucca M, Dubucs C, Groussolles M, Vial J, Le Guillou E, Porquet-Bordes V, Pasmant E, Salles JP, Edouard T. Aubert-Mucca M, et al. Among authors: le guillou e. Bone Rep. 2021 Jun 9;15:101097. doi: 10.1016/j.bonr.2021.101097. eCollection 2021 Dec. Bone Rep. 2021. PMID: 34169121 Free PMC article.