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

Yazar: Singh, Amrathlal Rabbind, Morin, Gilles, Rochette, Jacques
Yayımlandı Mol Genet Metab Rep (2015)

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

Yazar: Brigant, Benjamin, Metzinger-Le Meuth, Valérie, Rochette, Jacques, Metzinger, Laurent
Yayımlandı 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

Yazar: Shukla, Manish, Gupta, Rahul, Pandey, Vivek, Rochette, Jacques, Dhandapany, Perundurai S., Tiwari, Pramod Kumar, Amrathlal, Rabbind Singh
Yayımlandı Orthop J Sports Med (2020)

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

Yazar: Aguilar-Martinez, Patricia, Grandchamp, Bernard, Cunat, Séverine, Cadet, Estelle, Blanc, François, Nourrit, Marlène, Lassoued, Kaiss, Schved, Jean-François, Rochette, Jacques
Baskı/Yayın Bilgisi 2011

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

Yazar: 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
Baskı/Yayın Bilgisi 2013

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

Yazar: 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
Baskı/Yayın Bilgisi 2005

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

Yazar: 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
Baskı/Yayın Bilgisi 2001

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

Yazar: 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
Baskı/Yayın Bilgisi 2010

A new role of glutathione peroxidase 4 during human erythroblast enucleation

Yazar: 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
Yayımlandı Blood Adv (2020)

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

Yazar: 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
Yayımlandı Haematologica (2020)

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Yazar: 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
Baskı/Yayın Bilgisi 2012

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

Yazar: 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.
Baskı/Yayın Bilgisi 2011