Stormorken syndrome or York platelet syndrome: A clinician's dilemma

بواسطة Singh, Amrathlal Rabbind, Morin, Gilles, Rochette, Jacques
الحاوية / القاعدة Mol Genet Metab Rep (2015)

TRIMming down to TRIM37: Relevance to Inflammation, Cardiovascular Disorders, and Cancer in MULIBREY Nanism

بواسطة Brigant, Benjamin, Metzinger-Le Meuth, Valérie, Rochette, Jacques, Metzinger, Laurent
الحاوية / القاعدة Int J Mol Sci (2018)

VEGFA Promoter Polymorphisms rs699947 and rs35569394 Are Associated With the Risk of Anterior Cruciate Ligament Ruptures Among Indian Athletes: A Cross-sectional Study

بواسطة Shukla, Manish, Gupta, Rahul, Pandey, Vivek, Rochette, Jacques, Dhandapany, Perundurai S., Tiwari, Pramod Kumar, Amrathlal, Rabbind Singh
الحاوية / القاعدة Orthop J Sports Med (2020)

Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants

بواسطة Aguilar-Martinez, Patricia, Grandchamp, Bernard, Cunat, Séverine, Cadet, Estelle, Blanc, François, Nourrit, Marlène, Lassoued, Kaiss, Schved, Jean-François, Rochette, Jacques
منشور في 2011

Human pre-B cell receptor signal transduction: evidence for distinct roles of PI3kinase and MAP-kinase signalling pathways

بواسطة Anbazhagan, Kolandaswamy, Rabbind Singh, Amrathlal, Isabelle, Piec, Stella, Ibata, Céline, Alleaume-De Martel, Bissac, Eliane, Bertrand, Brassart, Rémy, Nyga, Naomi, Taylor, Vincent, Fuentes, Rochette, Jacques, Lassoued, Kaïss
منشور في 2013

PPARα inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16(INK4a)

بواسطة Gizard, Florence, Amant, Carole, Barbier, Olivier, Bellosta, Stefano, Robillard, Romain, Percevault, Frédéric, Sevestre, Henry, Krimpenfort, Paul, Corsini, Alberto, Rochette, Jacques, Glineur, Corine, Fruchart, Jean-Charles, Torpier, Gérard, Staels, Bart
منشور في 2005

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome

بواسطة Caraballo, Roberto, Pavek, Sylvana, Lemainque, Arnaud, Gastaldi, Marguerite, Echenne, Bernard, Motte, Jacques, Genton, Pierre, Cersósimo, Ricardo, Humbertclaude, Véronique, Fejerman, Natalio, Monaco, Anthony P., Lathrop, Mark G., Rochette, Jacques, Szepetowski, Pierre
منشور في 2001

Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11

بواسطة Roll, Patrice, Sanlaville, Damien, Cillario, Jennifer, Labalme, Audrey, Bruneau, Nadine, Massacrier, Annick, Délepine, Marc, Dessen, Philippe, Lazar, Vladimir, Robaglia-Schlupp, Andrée, Lesca, Gaëtan, Jouve, Elisabeth, Rudolf, Gabrielle, Rochette, Jacques, Lathrop, G. Mark, Szepetowski, Pierre
منشور في 2010

A new role of glutathione peroxidase 4 during human erythroblast enucleation

بواسطة Ouled-Haddou, Hakim, Messaoudi, Kahia, Demont, Yohann, Lopes dos Santos, Rogiéro, Carola, Candice, Caulier, Alexis, Vong, Pascal, Jankovsky, Nicolas, Lebon, Delphine, Willaume, Alexandre, Demagny, Julien, Boyer, Thomas, Marolleau, Jean-Pierre, Rochette, Jacques, Garçon, Loïc
الحاوية / القاعدة Blood Adv (2020)

PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells

بواسطة Caulier, Alexis, Jankovsky, Nicolas, Demont, Yohann, Ouled-Haddou, Hakim, Demagny, Julien, Guitton, Corinne, Merlusca, Lavinia, Lebon, Delphine, Vong, Pascal, Aubry, Aurélien, Lahary, Agnès, Rose, Christian, Gréaume, Sandrine, Cardon, Emilie, Platon, Jessica, Ouadid-Ahidouch, Halima, Rochette, Jacques, Marolleau, Jean-Pierre, Picard, Véronique, Garçon, Loïc
الحاوية / القاعدة Haematologica (2020)

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

بواسطة Cloarec, Robin, Bruneau, Nadine, Rudolf, Gabrielle, Massacrier, Annick, Salmi, Manal, Bataillard, Marc, Boulay, Clotilde, Caraballo, Roberto, Fejerman, Natalio, Genton, Pierre, Hirsch, Edouard, Hunter, Alasdair, Lesca, Gaetan, Motte, Jacques, Roubertie, Agathe, Sanlaville, Damien, Wong, Sau-Wei, Fu, Ying-Hui, Rochette, Jacques, Ptáček, Louis J., Szepetowski, Pierre
منشور في 2012

Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions

بواسطة Lee, Hsien-Yang, Huang, Yong, Bruneau, Nadine, Roll, Patrice, Roberson, Elisha D.O., Hermann, Mark, Quinn, Emily, Maas, James, Edwards, Robert, Ashizawa, Tetsuo, Baykan, Betul, Bhatia, Kailash, Bressman, Susan, Bruno, Michiko K., Brunt, Ewout R., Caraballo, Roberto, Echenne, Bernard, Fejerman, Natalio, Frucht, Steve, Gurnett, Christina A., Hirsch, Edouard, Houlden, Henry, Jankovic, Joseph, Lee, Wei-Ling, Lynch, David R., Mohamed, Shehla, Müller, Ulrich, Nespeca, Mark P., Renner, David, Rochette, Jacques, Rudolf, Gabrielle, Saiki, Shinji, Soong, Bing-Wen, Swoboda, Kathryn J., Tucker, Sam, Wood, Nicholas, Hanna, Michael, Bowcock, Anne, Szepetowski, Pierre, Fu, Ying-Hui, Ptáček, Louis J.
منشور في 2011