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Colette Rossier

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Anatomy

Chromosomes, Human, Pair 21

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Chemicals & Drugs

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Periklis Makrythanasis; Philipp Kapranov; Lucia Bartoloni; Alexandre Reymond; Samuel Deutsch; Roderic Guigó; France Denoeud; Jorg Drenkow; Colette Rossier; Francesca Ariani; Valeria Capra; Laurent Excoffier; Alessandra Renieri; Thomas Gingeras; Stylianos E Antonarakis
Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls.
Barbara D'haene; Catia Attanasio; Diane Beysen; Josée Dostie; Edmond Lemire; Philippe Bouchard; Michael Field; Kristie Jones; Birgit Lorenz; Björn Menten; Karen Buysse; Filip Pattyn; Marc Friedli; Catherine Ucla; Colette Rossier; Carine Wyss; Frank Speleman; Anne De Paepe; Job Dekker; Stylianos E Antonarakis; Elfride De Baere
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
M Failly; Lucia Bartoloni; A Letourneau; A Munoz; E Falconnet; Colette Rossier; Maria Margherita De Santi; Francesca Santamaria; O Sacco; Celia Delozier-Blanchet; Romain Lazor; Jean-Louis Blouin
Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia.

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All Publications

2009: Periklis Makrythanasis; Philipp Kapranov; Lucia Bartoloni; Alexandre Reymond; Samuel Deutsch; Roderic Guigó; France Denoeud; Jorg Drenkow; Colette Rossier; Francesca Ariani; Valeria Capra; Laurent Excoffier; Alessandra Renieri; Thomas Gingeras; Stylianos E Antonarakis
Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls.
Human mutation 2009;30(9):E866-79.
2009: Barbara D'haene; Catia Attanasio; Diane Beysen; Josée Dostie; Edmond Lemire; Philippe Bouchard; Michael Field; Kristie Jones; Birgit Lorenz; Björn Menten; Karen Buysse; Filip Pattyn; Marc Friedli; Catherine Ucla; Colette Rossier; Carine Wyss; Frank Speleman; Anne De Paepe; Job Dekker; Stylianos E Antonarakis; Elfride De Baere
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
PLoS genetics 2009;5(6):e1000522.
2009: M Failly; Lucia Bartoloni; A Letourneau; A Munoz; E Falconnet; Colette Rossier; Maria Margherita De Santi; Francesca Santamaria; O Sacco; Celia Delozier-Blanchet; Romain Lazor; Jean-Louis Blouin
Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia.
Journal of medical genetics 2009;46(4):281-6.
2008: Georg C Schwabe; Katrin Hoffmann; Niki Tomas Loges; Daniel Birker; Colette Rossier; Margherita M de Santi; Heike Olbrich; Manfred Fliegauf; Mike Failly; Uta Liebers; Mirella Collura; Gerhard Gaedicke; Stefan Mundlos; Ulrich Wahn; Jean-Louis Blouin; Bodo Niggemann; Heymut Omran; Stylianos E Antonarakis; Lucia Bartoloni
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations.
Human mutation 2008;29(2):289-98.
2008: Mike Failly; Alexandra Saitta; Analia Muñoz; Emilie Falconnet; Colette Rossier; Francesca Santamaria; Maria Margherita De Santi; Romain Lazor; Celia Delozier-Blanchet; Lucia Bartoloni; Jean-Louis Blouin
DNAI1 mutations explain only 2% of primary ciliary dykinesia.
Respiration; international review of thoracic diseases 2008;76(2):198-204.
2007: Hamid Mehenni; Nicoletta Resta; Ginevra Guanti; Luisa Mota-vieira; Aaron Lerner; Mohammed Peyman; Kim A Chong; Larbi Aissa; Ali Ince; Angel Cosme; Michael C Costanza; Colette Rossier; Uppala Radhakrishna; Randall W Burt; Didier Picard
Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
Digestive diseases and sciences 2007;52(8):1924-33.
2006: Jennifer Harrow; France Denoeud; Adam Frankish; Alexandre Reymond; Chao-Kung Chen; Jacqueline Chrast; Julien Lagarde; James G R Gilbert; Roy Storey; David Swarbreck; Colette Rossier; Catherine Ucla; Tim Hubbard; Stylianos E Antonarakis; Roderic Guigo
GENCODE: producing a reference annotation for ENCODE.
Genome biology 2006;7 Suppl 1():S4.1-9.
2003: Emmanouil T Dermitzakis; Alexandre Reymond; Nathalie Scamuffa; Catherine Ucla; Ewen F Kirkness; Colette Rossier; Stylianos E Antonarakis
Evolutionary discrimination of mammalian conserved non-genic sequences (CNGs).
Science (New York, N.Y.) 2003;302(5647):1033-5.
2002: Michel Guipponi; Grégoire Vuagniaux; Marie Wattenhofer; Kazunori Shibuya; Maria Vazquez; Loretta Dougherty; Nathalie Scamuffa; Elizabeth Guida; Michiyo Okui; Colette Rossier; Manuela Hancock; Karine Buchet; Alexandre Reymond; Edith Hummler; Phillip L Marzella; Jun Kudoh; Nobuyoshi Shimizu; Hamish Scott; Stylianos E Antonarakis; Bernard C Rossier
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro.
Human molecular genetics 2002;11(23):2829-36.
2002: Lucia Bartoloni; Jean-Louis Blouin; Yanzhen Pan; Corinne Gehrig; Amit K Maiti; Nathalie Scamuffa; Colette Rossier; Mark Jorissen; Miguel Armengot; Maggie Meeks; Hannah M Mitchison; Eddie M K Chung; Celia Delozier-Blanchet; William J Craigen; Stylianos E Antonarakis
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(16):10282-6.
2002: Alexandre Reymond; Anamaria A Camargo; Samuel Deutsch; Brian J Stevenson; Raphael B Parmigiani; Catherine Ucla; Fabiana Bettoni; Colette Rossier; Robert Lyle; Michel Guipponi; Sandro de Souza; Christian Iseli; Victor Jongeneel; Philipp Bucher; Andrew J G Simpson; Stylianos E Antonarakis
Nineteen additional unpredicted transcripts from human chromosome 21.
Genomics 2002;79(6):824-32.
2002: Joäelle Michaud; Feng Wu; Motomi Osato; Gregory M Cottles; Masatoshi Yanagida; Norio Asou; Shigesada Katsuya; Yoshiaki Ito; Kathleen F Benson; Wendy H Raskind; Colette Rossier; Stylianos E Antonarakis; Sara J Israels; Archibald McNicol; Harvey Weiss; Marshall Horwitz; Hamish Scott
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
Blood 2002;99(4):1364-72.
2002: Marie Wattenhofer; Mario Vincenzo Di Iorio; Raquel Rabionet; Loretta Dougherty; Andreas Pampanos; Torsten Schwede; Barbara Montserrat-Sentis; Maria Lourdes Arbones; Theophilos Iliades; Annamaria Pasquadibisceglie; Marcello D'Amelio; Sura Alwan; Colette Rossier; Hans-Henrik M Dahl; Michael B Petersen; Xavier Estivill; Paolo Gasparini; Hamish Scott; Stylianos E Antonarakis
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients.
Journal of molecular medicine (Berlin, Germany) 2002;80(2):124-31.
2001: Michel Guipponi; Caroline Tapparel; O Jousson; Nathalie Scamuffa; Christophe Mas; Colette Rossier; Pierre Hutter; Paolo Meda; Robert Lyle; Alexandre Reymond; Stylianos E Antonarakis
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family.
Human genetics 2001;109(6):569-75.
2001: Alexandre Reymond; Marc Friedli; Charlotte N Henrichsen; F Chapot; Samuel Deutsch; Catherine Ucla; Colette Rossier; Robert Lyle; Michel Guipponi; Stylianos E Antonarakis
From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map.
Genomics 2001;78(1-2):46-54.
2001: Saber Masmoudi; Stylianos E Antonarakis; Torsten Schwede; Ali Ghorbel; M Gratri; M P Pappasavas; Mohamed Drira; A Elgaied-Boulila; Marie Wattenhofer; Colette Rossier; Hamish Scott; Hammadi Ayadi; Michel Guipponi
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
Human mutation 2001;18(2):101-8.
2001: Ariane Paoloni-Giacobino; Colette Rossier; MP Papasavvas; Stylianos E Antonarakis
Frequency of replication/transcription errors in (A)/(T) runs of human genes.
Human genetics 2001;109(1):40-7.
2001: Lucia Bartoloni; Jean-Louis Blouin; Amit K Maiti; AJ Sainsbury; Colette Rossier; Corinne Gehrig; Jin-Xiong She; M P Marron; E S Lander; Maggie Meeks; E Chung; Miguel Armengot; Mark Jorissen; Hamish Scott; Celia Delozier-Blanchet; R Mark Gardiner; Stylianos E Antonarakis
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia.
Genomics 2001;72(1):21-33.
2001: Marie Wattenhofer; Kazunori Shibuya; Jun Kudoh; Robert Lyle; Joäelle Michaud; Colette Rossier; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; A Berry; Batsheva Bonne-Tamir; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains.
Human genetics 2001;108(2):140-7.
2001: Hamish Scott; Jun Kudoh; Marie Wattenhofer; Kazunori Shibuya; A Berry; R Chrast; Michel Guipponi; J Wang; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; F Younus; S Qasim Mehdi; Uppala Radhakrishna; MP Papasavvas; Corinne Gehrig; Colette Rossier; Michael Korostishevsky; A Gal; Nobuyoshi Shimizu; Batsheva Bonne-Tamir; Stylianos E Antonarakis
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
Nature genetics 2001;27(1):59-63.
2000: R Chrast; Hamish Scott; MP Papasavvas; Colette Rossier; E S Antonarakis; C Barras; Muriel T Davisson; C Schmidt; Xavier Estivill; Mara Dierssen; M Pritchard; Stylianos E Antonarakis
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals.
Genome research 2000;10(12):2006-21.
2000: Lucia Bartoloni; Marie Wattenhofer; Jun Kudoh; A Berry; Kazunori Shibuya; K Kawasaki; J Wang; Shuichi Asakawa; Ilana Talior; Batsheva Bonne-Tamir; Colette Rossier; Joäelle Michaud; Edward RB McCabe; Shinsei Minoshima; Nobuyoshi Shimizu; Hamish Scott; Stylianos E Antonarakis
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency.
Genomics 2000;70(2):190-200.
2000: Joäelle Michaud; Jun Kudoh; A Berry; Batsheva Bonne-Tamir; Maria D Lalioti; Colette Rossier; Kazunori Shibuya; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein.
Genomics 2000;68(1):71-9.
2000: Michel Guipponi; K Brunschwig; Z Chamoun; Hamish Scott; K Shibuya; Jun Kudoh; A L Delezoide; S El Samadi; Zoubida Chettouh; Colette Rossier; Nobuyoshi Shimizu; F Mueller; Jean-Maurice Delabar; Stylianos E Antonarakis
C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning.
Genomics 2000;68(1):30-40.
2000: A Berry; Hamish Scott; Jun Kudoh; Ilana Talior; Michael Korostishevsky; Marie Wattenhofer; Michel Guipponi; C Barras; Colette Rossier; Kazunori Shibuya; J Wang; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; Nobuyoshi Shimizu; Stylianos E Antonarakis; B Bonné-Tamir
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.
Genomics 2000;68(1):22-9.
2000: Marguerite Neerman-Arbez; P de Moerloose; C Bridel; A Honsberger; A Schönbörner; Colette Rossier; Kathelijne Peerlinck; S Claeyssens; D Di Michele; Roseline d'Oiron; M Dreyfus; M Laubriat-Bianchin; J Dieval; SE Antonarakis; Michael Morris
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
Blood 2000;96(1):149-52.
2000: Amit K Maiti; Lucia Bartoloni; Hannah M Mitchison; Maggie Meeks; E Chung; S Spiden; Corinne Gehrig; Colette Rossier; Celia Delozier-Blanchet; J Blouin; R Mark Gardiner; Stylianos E Antonarakis
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD).
Cytogenetics and cell genetics 2000;90(1-2):119-22.
2000: Armand Savioz; Enikö Kövari; R Anastasiu; Colette Rossier; Krishan D Saini; Constantin Bouras; Geneviève Leuba
Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia.
Experimental neurology 2000;161(1):330-5.
1999: Erich Roessler; L Mittaz; Y Du; Hamish Scott; J Chang; Colette Rossier; Michel Guipponi; S P Matsuda; Maximilian Muenke; Stylianos E Antonarakis
Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).
Human genetics 1999;105(5):489-95.
1999: H Chen; Colette Rossier; Michael Morris; Hamish Scott; A Gos; Amos Bairoch; Stylianos E Antonarakis
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.
Human genetics 1999;105(5):399-409.
1999: Armand Savioz; Geneviève Leuba; Charlotte Forsell; Lena Lilius; Colette Rossier; Krishan D Saini; Constantin Bouras; Lars Lannfelt
No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritance.
Dementia and geriatric cognitive disorders 1999;10(6):431-6.
1999: Uppala Radhakrishna; Dorothea Bornholdt; Hamish Scott; Uday C Patel; Colette Rossier; Hartmut Engel; Armand Bottani; D Chandal; Jean-Louis Blouin; Jitendra V Solanki; Karl-Heinz Grzeschik; Stylianos E Antonarakis
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
American journal of human genetics 1999;65(3):645-55.
1999: Marguerite Neerman-Arbez; K M Johnson; Michael Morris; J H McVey; Flora Peyvandi; William C Nichols; David Ginsburg; Colette Rossier; Stylianos E Antonarakis; Edward G D Tuddenham
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency.
Blood 1999;93(7):2253-60.
1999: L Mittaz; Colette Rossier; M Heino; Pärt Peterson; KJ Krohn; A Gos; Michael Morris; Jun Kudoh; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of the mouse Aire gene.
Biochemical and biophysical research communications 1999;255(2):483-90.
1999: M Heino; Hamish Scott; Q Chen; Pärt Peterson; U Mäebpää; MP Papasavvas; L Mittaz; C Barras; Colette Rossier; George Chrousos; Constantine Straturis; Kentaro Nagamine; Jun Kudoh; Nobuyoshi Shimizu; N Maclaren; Stylianos E Antonarakis; Kai Krohn
Mutation analyses of North American APS-1 patients.
Human mutation 1999;13(1):69-74.
1998: Hamid Mehenni; Corinne Gehrig; Jun-ichi Nezu; A Oku; Miyuki Shimane; Colette Rossier; N Guex; Jean-Louis Blouin; Hamish Scott; Stylianos E Antonarakis
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
American journal of human genetics 1998;63(6):1641-50.
1998: Michel Guipponi; Hamish Scott; H Chen; A Schebesta; Colette Rossier; Stylianos E Antonarakis
Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codon.
Genomics 1998;53(3):369-76.
1998: Michel Guipponi; Hamish Scott; Jun Kudoh; K Kawasaki; Kazunori Shibuya; A Shintani; Shuichi Asakawa; H Chen; Maria D Lalioti; Colette Rossier; Shinsei Minoshima; Nobuyoshi Shimizu; Stylianos E Antonarakis
Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence.
Human genetics 1998;103(4):386-92.
1998: Hamish Scott; M Heino; Pärt Peterson; L Mittaz; Maria D Lalioti; C Betterle; A Cohen; M Seri; M Lerone; Giovanni Romeo; P Collin; M Salo; Russell A Metcalfe; Anthony P Weetman; MP Papasavvas; Colette Rossier; Kentaro Nagamine; Jun Kudoh; Nobuyoshi Shimizu; KJ Krohn; Stylianos E Antonarakis
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins.
Molecular endocrinology (Baltimore, Md.) 1998;12(8):1112-9.
1998: Hamish Scott; Stylianos E Antonarakis; Maria D Lalioti; Colette Rossier; P A Silver; M F Henry
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2).
Genomics 1998;48(3):330-40.
1998: Jean-Louis Blouin; G Duriaux Saïl; Michel Guipponi; Colette Rossier; M P Pappasavas; Stylianos E Antonarakis
Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1.
Human genetics 1998;102(3):282-8.
1998: Hamish Scott; D S Kyriakou; Pärt Peterson; M Heino; M Tähtinen; Kai Krohn; H Chen; Colette Rossier; Maria D Lalioti; Stylianos E Antonarakis
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis.
Genomics 1998;47(1):64-70.
1997: Ariane Paoloni-Giacobino; Haiming Chen; Manuel Peitsch; Colette Rossier; Stylianos E Antonarakis
Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3.
Genomics 1997;44(3):309-20.
1997: R Chrast; Hamish Scott; Haiming Chen; Jun Kudoh; Colette Rossier; Shinsei Minoshima; Y Wang; Nobuyoshi Shimizu; Stylianos E Antonarakis
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.
Genome research 1997;7(6):615-24.
1997: Olivier Boss; Sonia Samec; Ariane Paoloni-Giacobino; Colette Rossier; Abdul G Dulloo; Josiane Seydoux; Patrick Muzzin; Jean-Paul Giacobino
Uncoupling protein-3: a new member of the mitochondrial carrier family with tissue-specific expression.
FEBS letters 1997;408(1):39-42.
1997: Hamish Scott; H Chen; Colette Rossier; Maria D Lalioti; Stylianos E Antonarakis
Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3.
Human genetics 1997;99(5):616-23.
1997: Maria D Lalioti; Hamish Scott; Catherine Buresi; Colette Rossier; Armand Bottani; Michael Morris; Alain Malafosse; Stylianos E Antonarakis
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy.
Nature 1997;386(6627):847-51.
1997: L Mittaz; Hamish Scott; Colette Rossier; P H Seeburg; M Higuchi; Stylianos E Antonarakis
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3.
Genomics 1997;41(2):210-7.
1997: H Chen; Colette Rossier; Y Nakamura; A Lynn; Aravinda Chakravarti; Stylianos E Antonarakis
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.
Genomics 1997;41(2):193-200.
1997: Maria D Lalioti; M Mirotsou; Catherine Buresi; Manuel Peitsch; Colette Rossier; Reda Ouazzani; Michel Baldy-Moulinier; Armand Bottani; Alain Malafosse; Stylianos E Antonarakis
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).
American journal of human genetics 1997;60(2):342-51.
1996: H Chen; Colette Rossier; Stylianos Antonarakis
Cloning of a human homolog of the Drosophila enhancer of zeste gene (EZH2) that maps to chromosome 21q22.2.
Genomics 1996;38(1):30-7.
1996: H Chen; R Chrast; Colette Rossier; Michael Morris; Maria D Lalioti; Stylianos Antonarakis
Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.
Genome research 1996;6(8):747-60.
1996: Maria D Lalioti; H Chen; Colette Rossier; R Shafaatian; J D Reid; Stylianos Antonarakis
Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3.
Genomics 1996;35(2):321-7.
1996: H Chen; Colette Rossier; Maria D Lalioti; A Lynn; Aravinda Chakravarti; G Perrin; Stylianos Antonarakis
Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.
American journal of human genetics 1996;59(1):66-75.
1996: J L Blouin; G Duriaux-Sail; Haiming Chen; A Gos; Michael Morris; Colette Rossier; Stylianos Antonarakis
Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21.
Genomics 1996;33(2):309-12.
1996: Maria D Lalioti; A Gos; M R Green; Colette Rossier; Michael Morris; Stylianos Antonarakis
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.
Genomics 1996;33(2):298-300.
1995: H Chen; Michael Morris; Colette Rossier; Jean-Louis Blouin; Stylianos Antonarakis
Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP5O) by exon trapping and mapping to chromosome 21q22.1-q22.2.
Genomics 1995;28(3):470-6.
1995: D Lucente; Haiming Chen; D Shea; Sonia Samec; M Rutter; R Chrast; Colette Rossier; AJ Buckler; Stylianos Antonarakis; M K McCormick
Localization of 102 exons to a 2.5 Mb region involved in Down syndrome.
Human molecular genetics 1995;4(8):1305-11.
1995: H Chen; R Chrast; Colette Rossier; A Gos; Stylianos Antonarakis; Jun Kudoh; A Yamaki; N Shindoh; H Maeda; Shinsei Minoshima
Single-minded and Down syndrome?
Nature genetics 1995;10(1):9-10.
1989: Colette Rossier; K Hoang-Van; G Turian
Secretion of an Mr 60000 protein by benomyl-treated cells of Neurospora crassa.
European journal of cell biology 1989;50(2):333-9.
1988: Colette Rossier; R Raju; Daniel Kolakofsky
LaCrosse virus gene expression in mammalian and mosquito cells.
Virology 1988;165(2):539-48.
1988: T C That; Colette Rossier; F Barja; G Turian; U P Roos
Induction of multiple germ tubes in Neurospora crassa by antitubulin agents.
European journal of cell biology 1988;46(1):68-79.
1985: Colette Rossier; A Pugin; G Turian
Genetic analysis of transformation in a microconidiating strain of Neurospora crassa.
Current genetics 1985;10(4):313-20.