Show items per page
Elements: 43
Page 1 on 3
 TitleAuthors / EditorsDate
add to browser selection
Unique substrate specificity of anaplastic lymphoma kinase (ALK): development of phosphoacceptor peptides for the assay of ALK activity Donella-Deana, Arianna; Marin, Oriano; Cesaro, Luca; Gunby, Rosalind H.; ... Pinna, Lorenzo A. 2005
add to browser selection
The Swiss-Prot variant page and the ModSNP database: a resource for sequence and structure information on human protein variants Yip Sonderegger, Yum Lina; Scheib, Holger; Diemand, Alexander; Gattiker, Alexandre; ... Bairoch, Amos Marc 2004
add to browser selection
The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus Boda, Bernadett; Alberi, Stefano; Nikonenko, Irina; Nodé-Langlois, Roxanne; ... Muller, Dominique 2004
add to browser selection
The cytotoxic T lymphocyte protease granzyme A cleaves and inactivates poly(adenosine 5'-diphosphate-ribose) polymerase-1 Zhu, Pengcheng; Martinvalet, Denis; Chowdhury, Dipanjan; Zhang, Dong; ... Lieberman, Judy 2009
add to browser selection
Structural basis for polyadenosine-RNA binding by Nab2 Zn fingers and its function in mRNA nuclear export Brockmann, Christoph; Soucek, Sharon; Kuhlmann, Sonja I.; Mills-Lujan, Katherine; ... Stewart, Murray 2012
add to browser selection
Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations Ducamp, Sarah; Kannengiesser, Caroline; Touati, Mohamed; Garçon, Loïc; ... Grandchamp, Bernard 2011
add to browser selection
Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation Zdziarska, Joanna; Undas, Anetta; Basa, Joanna; Iwaniec, Teresa; ... Neerman Arbez, Marguerite 2009
add to browser selection
Sequence of a novel HLA-A2 allele in a haematopoietic stem cell donor of the international registry Kervaire, B.; Schmidt, A. H.; Villard, Jean; Tiercy, Jean-Marie 2009
add to browser selection
Screening of the THAP1 gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype Clot, Fabienne; Grabli, David; Burbaud, Pierre; Aya, Magali; ... Brice, Alexis 2011
add to browser selection
Sch9 is a major target of TORC1 in Saccharomyces cerevisiae Urban, Jörg; Soulard, Alexandre; Huber, Alexandre; Lippman, Soyeon; ... Loewith, Robbie 2007
add to browser selection
Residues in SRP9/14 essential for elongation arrest activity of the signal recognition particle define a positively charged functional domain on one side of the protein Mary, Camille; Scherrer, Anne Paule Marie; Huck, Laurent; Lakkaraju, Asvin Krishna Kumar; ... Strub, Katharina 2010
add to browser selection
Purifying selection in mammalian mitochondrial protein-coding genes is highly effective and congruent with evolution of nuclear genes Popadin, Konstantin; Nikolaev, Sergey Igorievich; Junier, Thomas; Baranova, Maria; Antonarakis, Stylianos 2013
add to browser selection
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with variation in vertebral bone mass, vertebral bone size, and stature in whites Ferrari, Serge Livio; Deutsch, Samuel; Choudhury, Urmila; Chevalley, Thierry; ... Antonarakis, Stylianos 2004
add to browser selection
Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia Ansari Djaberi, Marc Georges; Sauty, Géraldine; Labuda, Malgorzata; Gagné, Vincent; ... Krajinovic, Maja 2009
add to browser selection
Nomenclature for the description of human sequence variations den Dunnen, J. T.; Antonarakis, Stylianos 2001
add to browser selection
Mutations in GJB6 cause hidrotic ectodermal dysplasia Lamartine, J.; Munhoz Essenfelder, G.; Kibar, Z.; Lanneluc, I.; ... Waksman, G. 2000
add to browser selection
Modifier effects between regulatory and protein-coding variation Dimas, Antigone S.; Stranger, Barbara E.; Beazley, Claude; Finn, Robert D.; ... Dermitzakis, Emmanouil 2008
add to browser selection
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia Kannengiesser, Caroline; Sanchez, Mayka; Sweeney, Marion; Hetet, Gilles; ... May, Alison 2011
add to browser selection
LRP5 gene polymorphisms and idiopathic osteoporosis in men Ferrari, Serge Livio; Deutsch, Samuel; Baudoin, C.; Cohen-Solal, M.; ... de Vernejoul, M. C. 2005
add to browser selection
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt Perroud, N.; Courtet, P.; Vincze, Ilona; Jaussent, I.; ... Malafosse, Alain 2008
<< previous | 1 | 2 | 3 |