| Title | Authors / Editors | Date |
unige:155608 |
Tau molecular diversity contributes to clinical heterogeneity in Alzheimer's disease |
Dujardin, Simon; Commins, Caitlin; Lathuiliere, Aurélien; Beerepoot, Pieter; ... Hyman, Bradley T |
2020 |
unige:127086 |
Clinical Relevance of Intra-Tumour Heterogeneity |
Borisch, Bettina; Stanta, Giorgio |
2018 |
unige:128423 |
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome |
Dorval, Guillaume; Gribouval, Olivier; Martinez-Barquero, Vanesa; Machuca, Eduardo; ... Boyer, Olivia |
2018 |
unige:95968 |
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy |
French Parkinson's Disease Genetics Study, International Parkinson's Disease Genomics Consortium |
2016 |
unige:16596 |
Dissecting genetics of highly heterogeneous mendelian disorders: the example of Primary Ciliary Dyskinesia |
Blouin, Jean-Louis |
2011 |
unige:55904 |
Treatment of chronic granulomatous disease with myeloablative conditioning and an unmodified hemopoietic allograft: a survey of the European experience, 1985-2000 |
Seger, Reinhard A; Gungor, Tayfun; Belohradsky, Bernd H; Blanche, Stephane; ... Fischer, Alain |
2002 |
unige:8658 |
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2 |
Buchet-Poyau, K.; Mehenni, H.; Radhakrishna, U.; Antonarakis, Stylianos |
2002 |
unige:8625 |
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia |
Bartoloni, Lucia; Blouin, Jean-Louis; Maiti, A. K.; Sainsbury, A.; ... Antonarakis, Stylianos |
2001 |
unige:11544 |
The bare lymphocyte syndrome and the regulation of MHC expression |
Reith, Walter; Mach, Bernard |
2001 |
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:26601 |
Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia |
Savioz, Armand; Kovari, Eniko Veronika; Anastasiu, R; Rossier, Colette; ... Leuba, G |
2000 |
unige:8649 |
Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity |
Blouin, Jean-Louis; Meeks, M.; Radhakrishna, U.; Sainsbury, A.; ... Antonarakis, Stylianos |
2000 |
unige:8974 |
Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes |
Pulver, A. E.; Mulle, J.; Nestadt, G.; Swartz, K. L.; ... McGrath, J. A. |
2000 |
unige:7706 |
Switch to unusual amino acids at codon 215 of the human immunodeficiency virus type 1 reverse transcriptase gene in seroconvertors infected with zidovudine-resistant variants |
Yerly Ferrillo, Sabine; Rakik, A.; De Loes, S. K.; Hirschel, Bernard; ... Perrin, Luc |
1998 |
unige:8891 |
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 |
unige:10995 |
MHC class II deficiency: definition of a new complementation group |
Villard, Jean; Mach, Bernard; Reith, Walter |
1997 |
unige:11593 |
Major histocompatibility complex class II deficiency: a disease of gene regulation |
Steimle, Viktor; Reith, Walter; Mach, Bernard |
1996 |
unige:8756 |
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22) |
Gill, M.; Vallada, H.; Collier, D.; Sham, P.; ... Read, C. M. |
1996 |
unige:11136 |
Heterogeneity in the progeny of single human muscle satellite cells |
Baroffio Barbier, Anne; Bochaton-Piallat, Marie-Luce; Gabbiani, Giulio; Bader, C. R. |
1995 |
unige:29869 |
T-cell-receptor repertoire in chronic plaque-stage psoriasis is restricted and lacks enrichment of superantigen-associated V beta regions |
Boehncke, Wolf-Henning; Dressel, Daniela; Manfras, B.; Zollner, Thomas Matthias; ... Sterry, Wolfram |
1995 |