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Did you mean ratio l[au] (31 results)?
A developmental component to Huntington's disease.
Ratié L, Humbert S. Ratié L, et al. Rev Neurol (Paris). 2024 Apr 12:S0035-3787(24)00487-9. doi: 10.1016/j.neurol.2024.04.001. Online ahead of print. Rev Neurol (Paris). 2024. PMID: 38614929 Free article. Review.
Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis.
Démurger F, Pasquier L, Dubourg C, Dupé V, Gicquel I, Evain C, Ratié L, Jaillard S, Beri M, Leheup B, Lespinasse J, Martin-Coignard D, Mercier S, Quelin C, Loget P, Marcorelles P, Laquerrière A, Bendavid C, Odent S, David V. Démurger F, et al. Among authors: ratie l. Mol Syndromol. 2013 Sep;4(6):267-72. doi: 10.1159/000353878. Epub 2013 Aug 1. Mol Syndromol. 2013. PMID: 24167461 Free PMC article.
DMRT5, DMRT3, and EMX2 Cooperatively Repress Gsx2 at the Pallium-Subpallium Boundary to Maintain Cortical Identity in Dorsal Telencephalic Progenitors.
Desmaris E, Keruzore M, Saulnier A, Ratié L, Assimacopoulos S, De Clercq S, Nan X, Roychoudhury K, Qin S, Kricha S, Chevalier C, Lingner T, Henningfeld KA, Zarkower D, Mallamaci A, Theil T, Campbell K, Pieler T, Li M, Grove EA, Bellefroid EJ. Desmaris E, et al. Among authors: ratie l. J Neurosci. 2018 Oct 17;38(42):9105-9121. doi: 10.1523/JNEUROSCI.0375-18.2018. Epub 2018 Aug 24. J Neurosci. 2018. PMID: 30143575 Free PMC article.
A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis.
Vezain M, Lecuyer M, Rubio M, Dupé V, Ratié L, David V, Pasquier L, Odent S, Coutant S, Tournier I, Trestard L, Adle-Biassette H, Vivien D, Frébourg T, Gonzalez BJ, Laquerrière A, Saugier-Veber P. Vezain M, et al. Among authors: ratie l. Acta Neuropathol Commun. 2018 Oct 19;6(1):109. doi: 10.1186/s40478-018-0610-5. Acta Neuropathol Commun. 2018. PMID: 30340542 Free PMC article.
11 results