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Heterogeneity in the progeny of single human muscle satellite cells Baroffio Barbier, Anne; Bochaton-Piallat, Marie-Luce; Gabbiani, Giulio; Bader, C. R. 1995
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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
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Major histocompatibility complex class II deficiency: a disease of gene regulation Steimle, Viktor; Reith, Walter; Mach, Bernard 1996
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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
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MHC class II deficiency: definition of a new complementation group Villard, Jean; Mach, Bernard; Reith, Walter 1997
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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
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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
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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
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Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity Blouin, Jean-Louis; Meeks, M.; Radhakrishna, U.; Sainsbury, A.; ... Antonarakis, Stylianos 2000
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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
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The bare lymphocyte syndrome and the regulation of MHC expression Reith, Walter; Mach, Bernard 2001
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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
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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
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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
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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
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Dissecting genetics of highly heterogeneous mendelian disorders: the example of Primary Ciliary Dyskinesia Blouin, Jean-Louis 2011
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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
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Clinical Relevance of Intra-Tumour Heterogeneity Borisch, Bettina; Stanta, Giorgio 2018