| | Title | Authors / Editors | Date |
|
unige:8600 |
10 years of Genomics, chromosome 21, and Down syndrome |
Antonarakis, Stylianos |
1998 |
|
unige:147447 |
A catalog of genetic loci associated with kidney function from analyses of a million individuals |
Wuttke, Matthias; Li, Yong; Li, Man; Sieber, Karsten B.; ... Pattaro, Cristian |
2019 |
|
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:9032 |
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 |
Sertie, A. L.; Quimby, M.; Moreira, E. S.; Murray, J.; ... Passos-Bueno, M. R. |
1996 |
|
unige:2014 |
A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families |
Sanchez-Mazas, Alicia; Djoulah, S.; Busson, M.; Le Monnier de Gouville, I.; ... Hors, J. |
2000 |
|
unige:20626 |
A map of open chromatin in human pancreatic islets |
Gaulton, Kyle J.; Nammo, Takao; Pasquali, Lorenzo; Simon, Jeremy M.; ... Ferrer, Jorge |
2010 |
|
unige:8645 |
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination |
Blouin, Jean-Louis; Christie, D. H.; Gos, A.; Lynn, A.; ... Antonarakis, Stylianos |
1995 |
|
unige:11165 |
A new genetic selection identifies essential residues in SecG, a component of the Escherichia coli protein export machinery |
Bost, S.; Belin, Dominique |
1995 |
|
unige:11551 |
A novel locus regulates both retroviral glycoprotein 70 and anti-glycoprotein 70 antibody production in New Zealand mice when crossed with BALB/c |
Rigby, R. J.; Rozzo, S. J.; Gill, Herpreet; Fernandez-Hart, Timothy; ... Vyse, T. J. |
2004 |
|
unige:31577 |
A novel regulatory element between the human FGA and FGG genes |
Fish, Richard; Neerman Arbez, Marguerite |
2012 |
|
unige:43381 |
A null mutation in a bZIP factor confers ABA-insensitivity in Arabidopsis thaliana |
Lopez Molina, Luis; Chua, N H |
2000 |
|
unige:40634 |
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study |
Peters, Ulrike; North, Kari E; Sethupathy, Praveen; Buyske, Steve; ... Kooperberg, Charles |
2013 |
|
unige:9037 |
A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects |
Spitz, François; Montavon, Thomas; Monso-Hinard, Christine; Morris, Michael Andréw; ... Duboule, Denis |
2002 |
|
unige:45068 |
A tale of two colons and two cancers. Distinct carcinogenesis and clinical outcome according to location proximal or distal to the splenic flexure |
Gervaz, Pascal; Buehler, Leo Hans; Scheiwiller, Andréas; Morel, Philippe |
2003 |
|
unige:8681 |
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y |
Chen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos |
1999 |
|
unige:37156 |
Activation in vivo of the minimal replication origin beta of plasmid R6K requires a small target sequence essential for DNA looping |
Kelley, William; Bastia, D |
1992 |
|
unige:90264 |
Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies |
Panousis, Nikolaos; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil; Lappalainen, Tuuli Emilia |
2014 |
|
unige:8981 |
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 |
|
unige:9076 |
Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency |
Villard, Jean; Reith, Walter; Barras, Emmanuele; Gos, A.; ... Mach, Bernard |
1997 |
|
unige:9043 |
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci |
Stratakis, C. A.; Kirschner, L. S.; Taymans, S. E.; Tomlinson, I. P.; ... Carney, J. A. |
1998 |
|
unige:46776 |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval |
Ducros, A; Nagy, T; Alamowitch, S; Nibbio, A; ... Tournier-Lasserve, E |
1996 |
|
unige:20946 |
Changing patterns of cancer incidence in the early- and late-HAART periods: the Swiss HIV Cohort Study |
Franceschi, S.; Lise, M.; Clifford, G. M.; Rickenbach, M.; ... Keiser, Olivia |
2010 |
|
unige:9264 |
Characterization and chromosomal localization of a human P2X receptor from the urinary bladder |
Valera, S.; Talabot, F.; Evans, R. J.; Gos, A.; ... Buell, G. N. |
1995 |
|
unige:9030 |
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis |
Scott, Hamish Steele; Kyriakou, D. S.; Peterson, P.; Heino, M.; ... Antonarakis, Stylianos |
1998 |
|
unige:9217 |
Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain |
Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. |
1995 |
|
unige:74429 |
Chimeric rhinoviruses obtained via genetic engineering or artificially induced recombination are viable only if the polyprotein coding sequence derives from the same species |
Schibler, Manuel; Piuz, Isabelle; Hao, Weidong; Tapparel, Caroline |
2015 |
|
unige:10963 |
Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse |
Rajput, B.; Marshall, A.; Killary, A. M.; Lalley, P. A.; ... Strickland, S. |
1987 |
|
unige:9852 |
Chromosomal walking and jumping to isolate DNA from the Ace and rosy loci and the bithorax complex in Drosophila melanogaster |
Bender, W.; Spierer, Pierre; Hogness, D. S. |
1983 |
|
unige:8611 |
Chromosome 21 and down syndrome: from genomics to pathophysiology |
Antonarakis, Stylianos; Lyle, Robert; Dermitzakis, Emmanouil; Reymond, Alexandre; Deutsch, Samuel |
2004 |
|
unige:8612 |
Chromosome 21: a small land of fascinating disorders with unknown pathophysiology |
Antonarakis, Stylianos; Lyle, Robert; Deutsch, Samuel; Reymond, Alexandre |
2002 |
|
unige:7172 |
Cloning and analysis of the K1 capsule biosynthesis genes of Escherichia coli: lack of homology with Neisseria meningitidis group B DNA sequences |
Echarti, C.; Hirschel, Bernard; Boulnois, G. J.; Varley, J. M.; ... Timmis, K. N. |
1983 |
|
unige:8676 |
Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping |
Chen, H.; Chrast, R.; Rossier, Colette; Morris, Michael Andréw; ... Antonarakis, Stylianos |
1996 |
|
unige:8679 |
Cloning of a human homolog of the Drosophila enhancer of zeste gene (EZH2) that maps to chromosome 21q22.2 |
Chen, H.; Rossier, Colette; Antonarakis, Stylianos |
1996 |
|
unige:8906 |
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3 |
Mittaz, L.; Scott, Hamish Steele; Rossier, Colette; Seeburg, P. H.; ... Antonarakis, Stylianos |
1997 |
|
unige:8682 |
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3 |
Chen, H.; Rossier, Colette; Nakamura, Y.; Lynn, A.; ... Antonarakis, Stylianos |
1997 |
|
unige:8952 |
Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndrome |
Giacobino, Ariane; Chen, H.; Antonarakis, Stylianos |
1997 |
|
unige:8674 |
Cloning of the cDNA for a human homolog of the rat PEP-19 gene and mapping to chromosome 21q22.2-q22.3 |
Chen, H.; Bouras, Constantin; Antonarakis, Stylianos |
1996 |
|
unige:8680 |
Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3 |
Chen, H.; Rossier, Colette; Lalioti, M. D.; Lynn, A.; ... Antonarakis, Stylianos |
1996 |
|
unige:8678 |
Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP5O) by exon trapping and mapping to chromosome 21q22.1-q22.2 |
Chen, H.; Morris, Michael Andréw; Rossier, Colette; Blouin, Jean-Louis; Antonarakis, Stylianos |
1995 |
|
unige:8953 |
Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3 |
Giacobino, Ariane; Chen, Haiming; Peitsch, M. C.; Rossier, Colette; Antonarakis, Stylianos |
1997 |
|
unige:8686 |
Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region |
Chrast, R.; Scott, Hamish Steele; Chen, H.; Kudoh, J.; ... Antonarakis, Stylianos |
1997 |
|
unige:8842 |
Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3 |
Lalioti, M. D.; Chen, H.; Rossier, Colette; Shafaatian, R.; ... Antonarakis, Stylianos |
1996 |
|
unige:8834 |
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 |
|
unige:20030 |
Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
Ehret, Georg Benedikt |
2009 |
|
unige:8717 |
Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment |
Dermitzakis, Emmanouil; Kirkness, Ewen; Schwarz, Scott; Birney, Ewan; ... Antonarakis, Stylianos |
2004 |
|
unige:6823 |
Compromised stability of DNA methylation and transposon immobilization in mosaic Arabidopsis epigenomes |
Reinders, Jon; Wulff, Brande B. H.; Mirouze, Marie; Marí-Ordóñez, Arturo; ... Paszkowski, Jerzy |
2009 |
|
unige:11627 |
Control of separate pathogenic autoantibody responses marks MHC gene contributions to murine lupus |
Vyse, T. J.; Halterman, R. K.; Rozzo, S. J.; Izui, Shozo; Kotzin, B. L. |
1999 |
|
unige:2191 |
De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer |
Hernandez, David; Francois, Patrice; Farinelli, Laurent Luca Denis; Osteras, Magne; Schrenzel, Jacques |
2008 |
|
unige:9231 |
Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing |
Nikolaev, S. I.; Iseli, Christian; Sharp, A. J.; Robyr, Daniel; ... Antonarakis, Stylianos |
2009 |
|
unige:9257 |
Dinucleotide repeat polymorphism within ERCC5 gene |
Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos |
1994 |
Chromosome mapping
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