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Type I and type II psoriasis show a similar usage of T-cell receptor variable regions Schmitt-Egenolf, M.; Boehncke, Wolf-Henning; Christophers, Enno; Stander, M.; Sterry, Wolfram 1991
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Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes Chen, H.; Lowther, W.; Avramopoulos, D.; Antonarakis, Stylianos 1994
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The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells Talbot, C. C.; Avramopoulos, D.; Gerken, S.; Chakravarti, A.; ... Antonarakis, Stylianos 1995
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Identification of regions interacting with ovoD mutations: potential new genes involved in germline sex determination or differentiation in Drosophila melanogaster Pauli, Daniel; Oliver, Brian Clay; Mahowald, Anthony P. 1995
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Nuclear DNA polymorphism in a Mandenka population from Senegal: comparison with eight other human populations Poloni, Estella S.; Excoffier, Laurent Georges Louis; Mountain, J.L.; Langaney, André; Cavalli-Sforza, LL. 1995
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Genetic linkage of IgG autoantibody production in relation to lupus nephritis in New Zealand hybrid mice Vyse, T. J.; Drake, C. G.; Rozzo, S. J.; Roper, E.; ... Kotzin, B. L. 1996
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Psoriasis and bacterial superantigens--formal or causal correlation? Boehncke, Wolf-Henning 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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prl mutations in the Escherichia coli secG gene Bost, S.; Belin, Dominique 1997
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Molecular characterization of HLA-C incompatibilities in HLA-ABDR-matched unrelated bone marrow donor-recipient pairs. Sequence of two new Cw alleles (Cw*02023 and Cw*0707) and recognition by cytotoxic T lymphocytes Grundschober, C; Rufer, Nathalie; Sanchez-Mazas, Alicia; Madrigal, A; ... Tiercy, Jean-Marie 1997
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Detection of polymorphisms in the human urokinase-type plasminogen activator gene Conne, Béatrice; Berczy, M.; Belin, Dominique 1997
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HLA class II DRB1, DQA1 and DQB1 polymorphisms in the Polish population from Wielkopolska Jungerman, M; Sanchez-Mazas, Alicia; Fichna, P; Ivanova, R; ... Djoulah, S 1997
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stand still, a Drosophila gene involved in the female germline for proper survival, sex determination and differentiation Pennetta, Giuseppa Léonarda; Pauli, Daniel 1997
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Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy Lalioti, M. D.; Scott, Hamish Steele; Buresi, C.; Rossier, Colette; ... Antonarakis, Stylianos 1997
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Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4 Mehenni, H.; Blouin, Jean-Louis; Radhakrishna, U.; Bhardwaj, S. S.; ... Antonarakis, Stylianos 1997
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Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee White, J. A.; McAlpine, P. J.; Antonarakis, Stylianos; Cann, H.; ... Povey, S. 1997
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Ligand specificity of the genetic variants of human alpha1-acid glycoprotein: generation of a three-dimensional quantitative structure-activity relationship model for drug binding to the A variant Herve, F.; Caron, Giulia; Duche, J. C.; Gaillard, Patrick; ... Testa, Bernard 1998
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HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area Izaabel, H; Garchon, H J; Caillat-Zucman, S; Beaurain, G; ... Sanchez-Mazas, Alicia 1998
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Identification of HLA-DR and -DQ alleles conferring susceptibility to pollen allergy and pollen associated food allergy Boehncke, Wolf-Henning; Loeliger, C.; Kuehnl, P.; Kalbacher, H.; ... Gall, H. 1998
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Genetic analysis of a conserved sequence in the HoxD complex: regulatory redundancy or limitations of the transgenic approach? Beckers, Johannes; Duboule, Denis 1998
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A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset Lalioti, M. D.; Scott, Hamish Steele; Genton, P.; Grid, D.; ... Antonarakis, Stylianos 1998
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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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Polymorphisms in the Cd22 gene of inbred mouse strains Lajaunias, Frédéric; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Chicheportiche, Yves; ... Izui, Shozo 1999
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Conditional gene targeting in macrophages and granulocytes using LysMcre mice Clausen, B. E.; Burkhardt, C.; Reith, Walter; Renkawitz, R.; Forster, I. 1999
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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
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Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G. 1999
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The genomic silencing of position-effect variegation in Drosophila melanogaster: interaction between the heterochromatin-associated proteins Su(var)3-7 and HP1 Delattre, Marion; Spierer-Royer, Anne; Tonka, Chia-Hwa; Spierer, Pierre 2000
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The molecular chaperone Cdc37 is required for Ste11 function and pheromone-induced cell cycle arrest Abbas-Terki, Toufik; Donze, Olivier; Picard, Didier 2000
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The TATA-binding protein-associated factor yTafII19p functionally interacts with components of the global transcriptional regulator Ccr4-Not complex and physically interacts with the Not5 subunit Lemaire, Marc; Collart, Martine 2000
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The essential function of Not1 lies within the Ccr4-Not complex Maillet, Laurent Jean Marie; Tu, Chi; Hong, Y K; Shuster, E O; Collart, Martine 2000
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Both transmembrane domains of SecG contribute to signal sequence recognition by the Escherichia coli protein export machinery Bost, S.; Silva, Filo; Rudaz, C.; Belin, Dominique 2000
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Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping Kibar, Z.; Dube, M. P.; Powell, J.; McCuaig, C.; ... Rouleau, G. A. 2000
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No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD) Maiti, A. K.; Bartoloni, Lucia; Mitchison, H. M.; Meeks, M.; ... Antonarakis, Stylianos 2000
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The molecular determination of HLA-Cw alleles in the Mandenka (West Africa) reveals a close genetic relationship between Africans and Europeans Sanchez-Mazas, Alicia; Steiner, Q G.; Grundschober, C.; Tiercy, Jean-Marie 2000
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Primary immunodeficiency mutation databases Vihinen, M.; Arredondo-Vega, F. X.; Casanova, J. L.; Etzioni, A.; ... Smith, C. I. 2001
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DNA sequence variability of IGHG3 alleles associated to the main G3m haplotypes in human populations Dard, Patricia; Lefranc, Marie-Paule; Osipova, Ludmilla; Sanchez-Mazas, Alicia 2001
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A study of Gm allotypes and immunoglobulin heavy gamma IGHG genes in Berbers, Arabs and sub-Saharan Africans from Jerba Island, Tunisia Loveslati, B Y.; Sanchez-Mazas, Alicia; Ennafaa, H.; Marrakchi, R.; ... Elgaaied, A B. 2001
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African diversity from the HLA point of view: influence of genetic drift, geography, linguistics, and natural selection Sanchez-Mazas, Alicia 2001
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The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
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An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos 2001
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Coupling of termination, 3' processing, and mRNA export Hammell, C M; Gross, Stefan; Zenklusen, Daniel; Heath, Catherine V; ... Cole, C N 2002
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Chronic graft dysfunction in renal transplant patients: potential role of plasminogen activator inhibitor type 1 Lahlou, Anis; Peraldi, Marie-Noelle; Thervet, Eric; Flahault, Antoine; ... Rondeau, Eric 2002
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Clinical characteristics of frontotemporal patients with symmetric brain atrophy Boccardi, Marina; Laakso, Mikko P; Bresciani, Lorena; Geroldi, Cristina; ... Frisoni, Giovanni 2002
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Formation of stable epialleles and their paramutation-like interaction in tetraploid Arabidopsis thaliana Mittelsten Scheid, Ortrun; Afsar, Karin; Paszkowski, Jerzy 2003
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Geographic patterns of functional categories of HLA-DRB1 alleles: a new approach to analyse associations between HLA-DRB1 and disease Gibert, M.; Sanchez-Mazas, Alicia 2003
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Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis 2003
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Genetic diversity in Tunisia: a study based on the GM polymorphism of human immunoglobulins Fadhlaoui-Zid, Karima; Dugoujon, Jean-Michel; Elgaaied, Amel; Ben Amor, Mohamed; ... Sanchez-Mazas, Alicia 2004
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Molecular biology of squamous cell carcinoma of the anus: a comparison of HIV-positive and HIV-negative patients Gervaz, Pascal; Hahnloser, Dieter; Wolff, Bruce G; Anderson, Sarah A; ... Thibodeau, Stephen N 2004
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APOE and modulation of Alzheimer's and frontotemporal dementia Boccardi, Marina; Sabattoli, F; Testa, C; Beltramello, A; ... Frisoni, Giovanni 2004
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Quantifiable cytotoxic T lymphocyte responses and HLA-related risk of progression to AIDS Scherer, Almut; Frater, A. John; Oxenius, Annette; Agudelo, Juliet; ... McLean, A. R. 2004
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