Show items per page
Elements: 11
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
TORC1 organized in inhibited domains (TOROIDs) regulate TORC1 activity Prouteau, Manoel; Desfosses, Ambroise; Sieben, Christian; Bourgoint, Clelia; ... Loewith, Robbie Joséph 2017
add to browser selection
Functional implications from the Cid1 poly(U) polymerase crystal structure Munoz Tello, Paola Andréa; Gabus, Caroline; Thore, Stéphane 2012
add to browser selection
It takes two to tango: defining an essential second active site in pyridoxal 5'-phosphate synthase Moccand, Cyril; Kaufmann, Markus; Fitzpatrick, Thérésa Bridget 2011
add to browser selection
Coordination of dual incision and repair synthesis in human nucleotide excision repair Staresincic, Lidija; Fagbemi, Adebanke F.; Enzlin, Jacqueline H.; Gourdin, Audrey M.; ... Scharer, Orlando D. 2009
add to browser selection
Genetic and biochemical analysis of yeast and human cap trimethylguanosine synthase: functional overlap of 2,2,7-trimethylguanosine caps, small nuclear ribonucleoprotein components, pre-mRNA splicing factors, and RNA decay pathways Hausmann, Stéphane; Zheng, Sushuang; Costanzo, Michael; Brost, Renee L.; ... Schwer, Beate 2008
add to browser selection
Phylogenetic distribution of catalase-peroxidases: are there patches of order in chaos? Passardi, Filippo; Zamocky, Marcel; Favet, Jocelyne; Jakopitsch, Christa; ... Dunand, Christophe 2007
add to browser selection
Vitamin B6 biosynthesis by the malaria parasite Plasmodium falciparum: biochemical and structural insights Gengenbacher, Martin; Fitzpatrick, Thérésa Bridget; Raschle, Thomas; Flicker, Karlheinz; ... Kappes, Barbara 2006
add to browser selection
Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency Germanos-Haddad, Myrna; De Moerloose, Philippe; Boehlen, Françoise; Peyvandi, Flora; Neerman Arbez, Marguerite 2005
add to browser selection
Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain De Moerloose, Philippe; Germanos-Haddad, Myrna; Boehlen, Françoise; Neerman Arbez, Marguerite 2004
add to browser selection
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients Wattenhofer, Marie; Di Iorio, M. V.; Rabionet, Raquel; Dougherty, Loretta; ... Antonarakis, Stylianos 2002
add to browser selection
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity Mehenni, H.; Gehrig, Corinne; Nezu, J.; Oku, A.; ... Antonarakis, Stylianos 1998