| | Title | Authors / Editors | Date |
|
unige:8917 |
YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome |
Nadal, M.; Mila, M.; Pritchard, M.; Mur, A.; ... Estivill, X. |
1996 |
|
unige:25385 |
Whole-genome sequencing of Staphylococcus aureus strain RN4220, a key laboratory strain used in virulence research, identifies mutations that affect not only virulence factors but also the fitness of the strain |
Nair, Dhanalakshmi; Memmi, Guido; Hernandez, David; Bard, Jonathan; ... Cheung, Ambrose L |
2011 |
|
unige:8845 |
What is expanded in progressive myoclonus epilepsy? |
Lalioti, M. D.; Scott, Hamish Steele; Antonarakis, Stylianos |
1997 |
|
unige:89358 |
Vitamin deficiencies in humans: can plant science help? |
Fitzpatrick, Thérésa Bridget; Basset, Gilles J C; Borel, Patrick; Carrari, Fernando; ... Fernie, Alisdair R |
2012 |
|
unige:8772 |
Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codon |
Guipponi, Michel; Scott, Hamish Steele; Chen, H.; Schebesta, A.; ... Antonarakis, Stylianos |
1998 |
|
unige:11193 |
TWEAK, a new secreted ligand in the tumor necrosis factor family that weakly induces apoptosis |
Chicheportiche, Yves; Bourdon, P. R.; Xu, H.; Hsu, Y. M.; ... Browning, J. L. |
1997 |
|
unige:34646 |
Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes |
Cossec, Jack-Christophe; Lavaur, Jérémie; Berman, Diego E; Rivals, Isabelle; ... Potier, Marie-Claude |
2012 |
|
unige:8683 |
Trapping and sequence analysis of 1138 putative exons from human chromosome 18 |
Chen, H.; Wang, N.; Huo, Y.; Sklar, P.; ... McInnis, M. G. |
2003 |
|
unige:8699 |
Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome |
Dahmane, N.; Ghezala, G. A.; Gosset, P.; Chamoun, Z.; ... Delabar, J. M. |
1998 |
|
unige:1279 |
TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness |
Guipponi, Michel; Antonarakis, Stylianos; Scott, Hamish Steele |
2008 |
|
unige:5661 |
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma |
Gimelli, Stefania; Beri, Silvana; Drabkin, Harry A.; Gambini, Claudio; ... Gimelli, Giorgio |
2009 |
|
unige:90260 |
The transcriptome of equine peripheral blood mononuclear cells |
Pacholewska, Alicja; Drögemüller, Michaela; Klukowska-Rötzler, Jolanta; Lanz, Simone; ... Jagannathan, Vidhya |
2015 |
|
unige:9262 |
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells |
Talbot, C. C.; Avramopoulos, D.; Gerken, S.; Chakravarti, A.; ... Antonarakis, Stylianos |
1995 |
|
unige:8896 |
The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3 |
Merla, Giuseppe; Howald, Cedric; Antonarakis, Stylianos; Reymond, Alexandre |
2004 |
|
unige:38124 |
The short Sendai virus leader region controls induction of programmed cell death |
Garcin, Dominique; Taylor, G; Tanebayashi, K; Compans, R; Kolakofsky, Daniel |
1998 |
|
unige:9153 |
The SH3D1A gene maps to human chromosome 21q22.1-->q22.2 |
Chen, H.; Antonarakis, Stylianos |
1997 |
|
unige:8775 |
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family |
Guipponi, Michel; Tapparel, Caroline; Jousson, Olivier; Scamuffa, N.; ... Antonarakis, Stylianos |
2001 |
|
unige:8926 |
The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103 |
Neerman Arbez, Marguerite; Antonarakis, Stylianos; Blouin, Jean-Louis; Zeinali, S.; ... Tuddenham, E. G. |
1997 |
|
unige:9248 |
The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes |
Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L. |
1996 |
|
unige:90582 |
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study |
Winkler, Thomas W; Justice, Anne E; Graff, Mariaelisa; Barata, Llilda |
2015 |
|
unige:78421 |
The i5K Initiative: advancing arthropod genomics for knowledge, human health, agriculture, and the environment |
i5K Consortium |
2013 |
|
unige:9106 |
The human lanosterol synthase gene maps to chromosome 21q22.3 |
Young, M.; Chen, H.; Lalioti, M. D.; Antonarakis, Stylianos |
1996 |
|
unige:90438 |
The Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in Lepidoptera |
Lehtonen, Rainer; Waterhouse, Robert; Holm, Liisa; Auvinen, Petri; Frilander, Mikko J |
2014 |
|
unige:10960 |
The genes for MHC class II regulatory factors RFX1 and RFX2 are located on the short arm of chromosome 19 |
Pugliatti, L.; Derre, J.; Berger, R.; Ucla, C.; ... Mach, Bernard |
1992 |
|
unige:8976 |
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region |
Radhakrishna, U.; Blouin, Jean-Louis; Mehenni, H.; Mehta, T. Y.; ... Antonarakis, Stylianos |
1997 |
|
unige:30559 |
The ecoresponsive genome of Daphnia pulex |
Colbourne, John K |
2011 |
|
unige:9872 |
The dose of a putative ubiquitin-specific protease affects position-effect variegation in Drosophila melanogaster |
Henchoz, Sandra; De Rubertis, Francesco; Pauli, Daniel; Spierer, Pierre |
1996 |
|
unige:8796 |
The DNA sequence of human chromosome 21 |
Hattori, M. |
2000 |
|
unige:5598 |
The bovine lactation genome: insights into the evolution of mammalian milk |
Lemay, Danielle G.; Lynn, David J.; Martin, William F.; Neville, Margaret C.; ... Rijnkels, Monique |
2009 |
|
unige:8675 |
Single-minded and Down syndrome? |
Chen, H.; Chrast, R.; Rossier, Colette; Gos, A.; ... Minoshima, S. |
1995 |
|
unige:9854 |
Similar level of polyteny in bands and interbands of Drosophila giant chromosomes |
Spierer-Royer, Anne; Spierer, Pierre |
1984 |
|
unige:20744 |
Sequencing of Culex quinquefasciatus establishes a platform for mosquito comparative genomics |
Arensburger, Peter |
2010 |
|
unige:9164 |
Report of the Fourth International Workshop on Human Chromosome 21 |
Delabar, J. M.; Creau, N.; Sinet, P. M.; Ritter, O.; ... Patterson, D. |
1993 |
|
unige:25377 |
Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing |
Ratnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; ... Radhakrishna, Uppala |
2011 |
|
unige:8639 |
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region |
Berry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B. |
2000 |
|
unige:9259 |
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3 |
Scott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; ... Gal, A. |
2000 |
|
unige:8715 |
Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions |
Denoeud, France; Kapranov, Philipp; Ucla, Catherine; Frankish, Adam; ... Reymond, Alexandre |
2007 |
|
unige:10993 |
Primary immunodeficiency mutation databases |
Vihinen, M.; Arredondo-Vega, F. X.; Casanova, J. L.; Etzioni, A.; ... Smith, C. I. |
2001 |
|
unige:25386 |
Post genomic decade - the epigenome and exposome challenges |
Giacobino, Ariane |
2011 |
|
unige:7380 |
Positive control of the two-component RcsC/B signal transduction network by DjlA: a member of the DnaJ family of molecular chaperones in Escherichia coli |
Kelley, William; Georgopoulos, C. |
1997 |
|
unige:19879 |
Positional identification of variants of Adamts16 linked to inherited hypertension |
Joe, Bina; Saad, Yasser; Dhindaw, Seema; Lee, Norman H.; ... Bouchard, Claude |
2009 |
|
unige:11403 |
Polymorphisms in the Cd22 gene of inbred mouse strains |
Lajaunias, Frédéric; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Chicheportiche, Yves; ... Izui, Shozo |
1999 |
|
unige:8890 |
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 |
|
unige:8888 |
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness |
Masmoudi, S.; Antonarakis, Stylianos; Schwede, T.; Ghorbel, A. M.; ... Guipponi, Michel |
2001 |
|
unige:9263 |
New complete genome sequences of human rhinoviruses shed light on their phylogeny and genomic features |
Tapparel, Caroline; Junier, Thomas; Gerlach, Daniel; Cordey, Samuel; ... Kaiser, Laurent |
2007 |
|
unige:8626 |
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia |
Bartoloni, Lucia; Blouin, Jean-Louis; Pan, Yanzhen; Gehrig, Corinne; ... Antonarakis, Stylianos |
2002 |
|
unige:8849 |
Mutations in GJB6 cause hidrotic ectodermal dysplasia |
Lamartine, J.; Munhoz Essenfelder, G.; Kibar, Z.; Lanneluc, I.; ... Waksman, G. |
2000 |
|
unige:9850 |
Molecular mapping of genetic and chromomeric units in Drosophila melanogaster |
Spierer, Pierre; Spierer, Anne; Bender, W.; Hogness, D. S. |
1983 |
|
unige:9131 |
Molecular etiology of factor VIII deficiency in hemophilia A |
Antonarakis, Stylianos; Kazazian, H. H.; Tuddenham, E. G. |
1995 |
|
unige:41708 |
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 |
Chromosome mapping
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