About: Jean Weissenbach

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Weissenbach, Jean (1946-....) Weissenbach, Jean (1946-....) Weissenbach, Jean (1946-....) Weissenbach, Jean (1946-....) Weissenbach, Jean (1946-....)
Life Event	http://www.idref.fr/052460029/birth
bnf-onto:FRBNF	12646140(xsd:integer)
preferred label	Weissenbach, Jean (1946-....)
name	Jean Weissenbach
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000026582716
Given name	Jean
familyName	Weissenbach
note	Directeur de recherche au CNRS et directeur général de Génoscope-Centre national de séquençage (en 2000). Pharmacien et docteur ès sciences
is sameAs of	Weissenbach, Jean (1946-....)
is Thesis advisor of	http://www.sudoc.fr/059955686/id http://www.sudoc.fr/043914160/id http://www.sudoc.fr/119732408/id http://www.sudoc.fr/171625129/id http://www.sudoc.fr/114692467/id http://www.sudoc.fr/143337629/id http://www.sudoc.fr/144463431/id De la séquence à l’analyse de génomes procaryotes : application à l’étude de trois génomes du genre Acinetobacter sp. http://www.sudoc.fr/07339386X/id Elucidation du métabolisme des microorganismes par la modélisation et l'interprétation des données d'essentialités de gènes, application au métabolisme de la bactérie Acinetobacter baylyi ADP1 http://www.sudoc.fr/245834893/id Etude de la composante génétique de la maladie coeliaque, analyse des gènes HLA de susceptibilité et recherche d'autres facteurs de risque génétique DEVELOPPEMENT D'UNE METHODE D'ANALYSE DES MICROSATELLITES, APPLICATIONS A LA CARTOGRAPHIE DU CHROMOSOME 20 HUMAIN ET A L'ETUDE GENETIQUE DES PARAPLEGIES SPASTIQUES FAMILIALES VERS L'IDENTIFICATION D'UN SECOND GENE POUR LES ICHTYOSES LAMELLAIRES http://www.sudoc.fr/246965258/id http://www.sudoc.fr/24655083X/id Génétique des maladies dermatologiques avec l'exemple des kératodermies palmoplantaires, des ichtyoses récessives et du psoriasis http://www.sudoc.fr/246999659/id La séquence du génome de Tetraodon nigroviridis comme outil dans l’inventaire des gènes humains et dans l’analyse de l’évolution des chromosomes de vertébrés. http://www.sudoc.fr/246688335/id
is Narrator of	http://www.sudoc.fr/153801743/id
is Interviewer of	http://www.sudoc.fr/061179620/id
is Commentator of	http://www.sudoc.fr/060287608/id http://www.sudoc.fr/075850001/id
is Author of	http://www.sudoc.fr/001167510/id http://www.sudoc.fr/158663888/id http://www.sudoc.fr/092655041/id http://www.sudoc.fr/13203333X/id http://www.sudoc.fr/000706043/id http://www.sudoc.fr/024423076/id http://www.sudoc.fr/087525038/id Open science resources for the discovery and analysis of Tara Oceans data Eukaryotic plankton diversity in the sunlit ocean Metabolic diversity among main microorganisms inside an arsenic-rich ecosystem revealed by meta-and proteo-genomics http://www.sudoc.fr/241786436/id Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia The banana (Musa acuminata) genome and the evolution of monocotyledonous plants. Plasticity of animal genome architecture unmasked by rapid evolution of a pelagic tunicate Comparative genomics of protoploid Saccharomycetaceae Establishment of the marker order pter-NRAS-NGFB-D1S189-D1S252-D1S440-D1S453-D1S514-CEN-D1S442-D1S498-qter in relation to the centromere on human chromosome 1 Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2 The $Phaeodactylum$ genome reveals the evolutionary history of diatom genomes https://serval.unil.ch/notice/serval:BIB_2DC475008819#id https://serval.unil.ch/notice/serval:BIB_EA283A7C368E#id https://serval.unil.ch/notice/serval:BIB_D059AA26481D#id http://www.sudoc.fr/055377165/id Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval A tale of two oxidation states: bacterial colonization of arsenic-rich environments. https://serval.unil.ch/notice/serval:BIB_52502DBEA7E4#id A polymorphic DNA sequence from the terminal part of chromosome 12q [D12S37] Plankton networks driving carbon export in the oligotrophic ocean European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain. https://serval.unil.ch/notice/serval:BIB_7D33342D038F#id Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals Mutations in the gene encoding SLURP-1 in Mal de Meleda Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium Methylobacterium Genome Sequences: A Reference Blueprint to Investigate Microbial Metabolism of C1 Compounds from Natural and Industrial Sources Pichia sorbitophila, an Interspecies Yeast Hybrid, Reveals Early Steps of Genome Resolution After Polyploidization Structure and function of the global ocean microbiome Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome. Digital expression profiling of novel diatom transcripts provides insight into their biological functions. https://serval.unil.ch/notice/serval:BIB_79FBEDF1BD2E#id Proteome Adaptation to High Temperatures in the Ectothermic Hydrothermal Vent Pompeii Worm A high-density microsatellite map of the ataxia-telangiectasia locus Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Atlas of gene expression in the mouse kidney: new features of glomerular parietal cells http://www.calames.abes.fr/pub/#details?id=Calames-20151191114193654 Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma An interspersed repeated sequence specific for human subtelomeric regions. Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33 http://www.sudoc.fr/272048380/id https://serval.unil.ch/notice/serval:BIB_0FED258C5533#id Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13 Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization Development of genomic resources for <em>Medicago truncatula</em> and related legume crops Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1 Structure, function, and evolution of the Thiomonas spp. genome. A global ocean atlas of eukaryotic genes Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia. A polymorphic DNA sequence from the terminal part of chromosome 20q [D20S25] Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats Genome evolution in yeasts.

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