FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Isabelle Creveaux

Research Profile

Anatomy

Chemicals & Drugs

Living Beings

Cattle

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Amino Acid Sequences

Procedures

Phenomena

Blotting, Northern

Co-author Network

Publications

TOP 3
Vincent José Soler; Elizabeth St Germain; Cyrielle Suarez; Khanh-Nhat Tran-Viet; Natalie A Afshari; Jean-Louis Arné; Patrick Calvas; Myriam Cassagne; Isabelle Creveaux; Pierre R Fournié; Stéphane D Galiacy; Céline Guillaud; Felicia Hawthorne; Bernadette Kantelip; Thomas Patrick Klemm; Vachiranee Limviphuvadh; Xiaoyan Luo; François Malecaze; Sebastian Maurer-Stroh; Weihua Meng; Steven G Rozen; Terri L Young
Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis.
Srinivasan Pugazhendhi; Srikanth Santhanam; Jayanthi Venkataraman; Isabelle Creveaux; Balakrishnan S Ramakrishna
NOD2 gene mutations associate weakly with ulcerative colitis but not with Crohn's disease in Indian patients with inflammatory bowel disease.
Radu Harbuz; James Lespinasse; Stéphanie Boulet; Christine Francannet; Isabelle Creveaux; Mariem Benkhelifa; Pierre-Simon Jouk; Joël Lunardi; Pierre F Ray
Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Isabelle Creveaux (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Vincent José Soler; Elizabeth St Germain; Cyrielle Suarez; Khanh-Nhat Tran-Viet; Natalie A Afshari; Jean-Louis Arné; Patrick Calvas; Myriam Cassagne; Isabelle Creveaux; Pierre R Fournié; Stéphane D Galiacy; Céline Guillaud; Felicia Hawthorne; Bernadette Kantelip; Thomas Patrick Klemm; Vachiranee Limviphuvadh; Xiaoyan Luo; François Malecaze; Sebastian Maurer-Stroh; Weihua Meng; Steven G Rozen; Terri L Young
Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis.
Journal of medical genetics 2013;50(4):246-54.
2013: Srinivasan Pugazhendhi; Srikanth Santhanam; Jayanthi Venkataraman; Isabelle Creveaux; Balakrishnan S Ramakrishna
NOD2 gene mutations associate weakly with ulcerative colitis but not with Crohn's disease in Indian patients with inflammatory bowel disease.
Gene 2013;512(2):309-13.
2010: Radu Harbuz; James Lespinasse; Stéphanie Boulet; Christine Francannet; Isabelle Creveaux; Mariem Benkhelifa; Pierre-Simon Jouk; Joël Lunardi; Pierre F Ray
Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.
Prenatal diagnosis 2010;30(11):1072-8.
2010: Marc F J André; Olivier Aumaître; Gilles Grateau; Mathias Chamaillard; Nathalie Costedoat-Chalumeau; Marie-Céleste Cardoso; Joëlle Henry-Berger; Balakrishnan S Ramakrishna; Marc Delpech; Jean-Charles Piette; Isabelle Creveaux
Longest form of CCTG microsatellite repeat in the promoter of the CD2BP1/PSTPIP1 gene is associated with aseptic abscesses and with Crohn disease in French patients.
Digestive diseases and sciences 2010;55(6):1681-8.
2009: Sylvie Tuffery-Giraud; Christophe Béroud; France Leturcq; Rabah Ben Yaou; dalil hamroun; Laurence Michel-Calemard; Marie-Pierre Moizard; Rafaëlle Bernard; Mireille Cossée; Pierre Boisseau; Martine Blayau; Isabelle Creveaux; Anne Guiochon-Mantel; Bérengère de Martinville; Christophe Philippe; Nicole Monnier; Eric Bieth; Philippe Khau Van Kien; François-Olivier Desmet; Véronique Humbertclaude; Jean-Claude Kaplan; Jamel Chelly; Mireille Claustres
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
Human mutation 2009;30(6):934-45.
2008: Nathalie Damon-Perriere; Patrice Menegon; Anne Olivier; Odile Boespflug-Tanguy; Florence Niel; Isabelle Creveaux; Vincent Dousset; Bruno Brochet; Cyril Goizet
Intra-familial phenotypic heterogeneity in adult onset vanishing white matter disease.
Clinical neurology and neurosurgery 2008;110(10):1068-71.
2008: Florence Brugnon; Frederic Bilan; Marie-Christine Heraud; Genevieve Grizard; Laurent Janny; Isabelle Creveaux
Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.
Fertility and sterility 2008;90(5):2004.e23-6.
2008: An C Jansen; Eva Andermann; Florence Niel; Isabelle Creveaux; Odile Boespflug-Tanguy; Frederick Andermann
Leucoencephalopathy with vanishing white matter may cause progressive myoclonus epilepsy.
Epilepsia 2008;49(5):910-3.
2008: Marc François Jean André; Olivier Aumaître; Jean-Charles Piette; Gilles Grateau; Marie-Céleste Cardoso; Lemlih Ouchchane; Jean-Louis Kémény; Bernard Dastugue; Marc Delpech; Isabelle Creveaux
Analysis of the NOD2/CARD15 gene in patients affected with the aseptic abscesses syndrome with or without inflammatory bowel disease.
Digestive diseases and sciences 2008;53(2):490-9.
2007: Christel Vache; Olivier Camares; Marie-Céleste Cardoso-Ferreira; Bernard Dastugue; Isabelle Creveaux; Chantal Vaury; Mahchid Bamdad
A potential genomic biomarker for the detection of polycyclic aromatic hydrocarbon pollutants: multidrug resistance gene 49 in Drosophila melanogaster.
Environmental toxicology and chemistry / SETAC 2007;26(7):1418-24.
2004: Gérard Tachdjian; Azzedine Aboura; Moncef Benkhalifa; Isabelle Creveaux; L Foix-Hélias; J F Gadisseux; Odile Boespflug-Tanguy; M Mohammed; Philippe Labrune
De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation pattern.
American journal of medical genetics. Part A 2004;131(3):273-80.
2004: Frédéric Chiambaretta; B Rozier; F Pilon; M Gérard; L M Coulangeon; Isabelle Creveaux; Danièle Rigal
[Phototherapeutic keratectomy in the treatment of lattice corneal dystrophy type I].
Journal français d'ophtalmologie 2004;27(7):747-53.
2004: Frédéric Chiambaretta; F Pilon; J-B Deriot; Max Gerard; M-L Couleangon; D F Schorderet; Jean-Louis Kemeny; Bernard Dastugue; Isabelle Creveaux; Danièle Rigal
[Early recurrence of Groenouw type I corneal dystrophy after phototherapeutic keratectomy. Molecular biology study suggests epithelial genesis].
Journal français d'ophtalmologie 2004;27(5):449-56.
2003: Catherine Vaurs-Barriere; Kondi Wong; Thais D Weibel; Mones Abu-Asab; Michael D Weiss; Christine R Kaneski; Tong-Hui Mixon; Simona Bonavita; Isabelle Creveaux; John D Heiss; Maria Tsokos; Ehud Goldin; Richard H Quarles; Odile Boespflug-Tanguy; Raphael Schiffmann
Insertion of mutant proteolipid protein results in missorting of myelin proteins.
Annals of neurology 2003;54(6):769-80.
2003: Nicolas Gonçalves-Mendes; Dominique Simon-Chazottes; Isabelle Creveaux; Annie Meiniel; Jean-Louis Guénet; Robert Meiniel
Mouse SCO-spondin, a gene of the thrombospondin type 1 repeat (TSR) superfamily expressed in the brain.
Gene 2003;312():263-70.
2003: Jérôme Solassol; Haíssam Rahil; Vincent Sapin; Didier Lemery; Bernard Dastugue; Odile Boespflug-Tanguy; Isabelle Creveaux
Detection of trisomy 21 by quantitative fluorescent-polymerase chain reaction in uncultured amniocytes.
Prenatal diagnosis 2003;23(4):287-91.
2003: Annie Meiniel; Robert Meiniel; Nicolas Gonçalves-Mendes; Isabelle Creveaux; Robert Didier; Bernard Dastugue
The thrombospondin type 1 repeat (TSR) and neuronal differentiation: roles of SCO-spondin oligopeptides on neuronal cell types and cell lines.
International review of cytology 2003;230():1-39.
2000: stéphane gobron; Isabelle Creveaux; Robert Meiniel; Robert Didier; A Herbet; Mahchid Bamdad; F El Bitar; Bernard Dastugue; Annie Meiniel
Subcommissural organ/Reissner's fiber complex: characterization of SCO-spondin, a glycoprotein with potent activity on neurite outgrowth.
Glia 2000;32(2):177-91.
2000: Robert Didier; Isabelle Creveaux; Robert Meiniel; A Herbet; Bernard Dastugue; Annie Meiniel
SCO-spondin and RF-GlyI: two designations for the same glycoprotein secreted by the subcommissural organ.
Journal of neuroscience research 2000;61(5):500-7.
1999: P Bouchard; V Ravet; Robert Meiniel; Isabelle Creveaux; Annie Meiniel; A Vellet; B Vigues
Use of a heterologous monoclonal antibody for cloning and detection of glial fibrillary acidic protein in the bovine ventricular ependyma.
Cell and tissue research 1999;298(2):207-16.
1999: Daniel Boucher; Isabelle Creveaux; Genevieve Grizard; C Jimenez; J Hermabessière; Bernard Dastugue
Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programme.
Molecular human reproduction 1999;5(6):587-93.
1999: stéphane gobron; Isabelle Creveaux; Robert Meiniel; Robert Didier; Bernard Dastugue; Annie Meiniel
SCO-spondin is evolutionarily conserved in the central nervous system of the chordate phylum.
Neuroscience 1999;88(2):655-64.
1998: Isabelle Creveaux; stéphane gobron; Robert Meiniel; Bernard Dastugue; Annie Meiniel
Complex expression pattern of the SCO-spondin gene in the bovine subcommissural organ: toward an explanation for Reissner's fiber complexity?
Brain research. Molecular brain research 1998;55(1):45-53.
1998: Isabelle Creveaux; Bernard Dastugue
[Apolipoprotein E and Alzheimer's disease].
Annales de biologie clinique 1998;56(2):130-1.
1997: C P Popescu; Hélène Hayes; Robert Meiniel; Isabelle Creveaux; Annie Meiniel
Localization of the SCO-spondin gene to cattle chromosome 4.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1997;5(4):276-7.
1996: stéphane gobron; H Monnerie; Robert Meiniel; Isabelle Creveaux; W Lehmann; D Lamalle; Bernard Dastugue; Annie Meiniel
SCO-spondin: a new member of the thrombospondin family secreted by the subcommissural organ is a candidate in the modulation of neuronal aggregation.
Journal of cell science 1996;109 ( Pt 5)():1053-61.
1996: Annie Meiniel; Robert Meiniel; R Didier; Isabelle Creveaux; stéphane gobron; H Monnerie; Bernard Dastugue
The subcommissural organ and Reissner's fiber complex. An enigma in the central nervous system?
Progress in histochemistry and cytochemistry 1996;30(2):1-66.
1995: Robert Meiniel; Isabelle Creveaux; Bernard Dastugue; Annie Meiniel
Specific transcripts analysed by in situ hybridization in the subcommissural organ of bovine embryos.
Cell and tissue research 1995;279(1):101-7.