Search Results - "Ravix, V"

A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjögren's syndrome: a preliminary report by Granel, B, Ravix, V, Pedeillier, K, Serratrice, J, Disdier, P, Voelckel, M A, Mattei, J F, Weiller, P J

“…Co-occurrent autoimmune disease and fragile X syndrome has been reported in the literature and we have therefore studied the expansion of…”
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PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase by Luciani, J.J, Depetris, D, Usson, Y, Metzler-Guillemain, C, Mignon-Ravix, C, Mitchell, M.J, Megarbane, A, Sarda, P, Sirma, H, Moncla, A, Feunteun, J, Mattei, M.-G

“…We have recently demonstrated that heterochromatin HP1 proteins are aberrantly distributed in lymphocytes of patients with immunodeficiency, centromeric…”
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Fragile X syndrome and 22q11.2 microdeletion in the same sibship by Missirian, Chantal, Moncla, Anne, Voelckel, Marie-Antoinette, Ravix, Valéry, Philip, Nicole

“…We present a family with an unusual association of two frequent genetic disorders, 22q11.2 microdeletion and fragile X syndrome, originating from the same…”
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