| | Title | Authors / Editors | Date |
|
unige:25139 |
Standardization of DNA isolation from low cell numbers for chimerism analysis by PCR of short tandem repeats |
van der Burg, M; Kreyenberg, H; Willasch, A; Barendregt, B H; ... van Dongen, J J M |
2011 |
|
unige:33527 |
The chloroplast transformation toolbox: selectable markers and marker removal |
Day, Anil; Goldschmidt-Clermont, Michel P. |
2011 |
|
unige:114066 |
The CST3 B haplotype is associated with frontotemporal lobar degeneration |
Benussi, L; Ghidoni, R; Galimberti, D; Boccardi, Marina; ... Binetti, G |
2010 |
|
unige:21051 |
New loci associated with kidney function and chronic kidney disease |
Kottgen, Anna; Pattaro, Cristian; Boger, Carsten A. |
2010 |
|
unige:19694 |
The matricellular protein periostin is required for sost inhibition and the anabolic response to mechanical loading and physical activity |
Bonnet, Nicolas; Standley, Kara N.; Bianchi, Estelle; Stadelmann, Vincent; ... Ferrari, Serge Livio |
2009 |
|
unige:2538 |
Candidate genes for temporal lobe epilepsy: a replication study |
Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain |
2008 |
|
unige:26597 |
Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22 |
Savioz, Armand; Riederer, Beat M; Heutink, Peter; Rizzu, Patrizia; ... Leuba, Geneviève |
2003 |
|
unige:8883 |
Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome |
Marneros, A. G.; Mehenni, H.; Reichenberger, E.; Antonarakis, Stylianos; ... Olsen, B. R. |
2001 |
|
unige:8688 |
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals |
Chrast, R.; Scott, Hamish Steele; Papasavvas, M. P.; Rossier, Colette; ... Antonarakis, Stylianos |
2000 |
|
unige:8857 |
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III |
Levinson, D. F.; Holmans, P.; Straub, R. E.; Owen, M. J.; ... Mallet, J. |
2000 |
|
unige:13238 |
Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study |
Quintana-Murci, L.; Semino, O.; Poloni, Estella S.; Liu, A.; ... Santachiara-Benerecetti, A S. |
1999 |
|
unige:8934 |
Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia |
Neerman Arbez, Marguerite; Honsberger, A.; Antonarakis, Stylianos; Morris, Michael Andréw |
1999 |
|
unige:13227 |
Human genetic affinities for Y-chromosome P49a,f/TaqI haplotypes show strong correspondence with linguistics |
Poloni, Estella S.; Semino, O.; Passarino, G.; Santachiara-Benerecetti, A S.; ... Excoffier, Laurent Georges Louis |
1997 |
Genetic Markers/genetics
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