Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (Allemagne)

Index « Auteurs » - entrée « Habiba Chaabouni »
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Habiba Azab < Habiba Chaabouni < Habibolah Masoudi Farid  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 1.
Ident.Authors (with country if any)Title
002852 (2002) Thierry Bienvenu [France] ; Karine Poirier [France] ; Gaelle Friocourt [France] ; Nadia Bahi [France] ; Delphine Beaumont [France] ; Fabien Fauchereau [France] ; Lamia Ben Jeema [Tunisie] ; Ramzi Zemni [France] ; Marie-Claude Vinet [France] ; Fiona Francis [France] ; Philippe Couvert [France] ; Marie Gomot [France] ; Claude Moraine [France] ; Hans Van Bokhoven [Pays-Bas] ; Vera Kalscheuer [Allemagne] ; Suzanne Frints [Belgique] ; Josef Gecz [Australie] ; Kanae Ohzaki [Japon] ; Habiba Chaabouni [Tunisie] ; Jean-Pierre Fryns [Belgique] ; Vincent Desportes [France] ; Cherif Beldjord [France] ; Jamel Chelly [France]ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

List of associated KwdEn.i

Nombre de
documents
Descripteur
1Abnormal dhplc
1Adult brain
1Adult stages
1Amino
1Amino acid change
1Amino acid residues
1Amino acid sequence
1Aristaless
1Case study
1Cellular processes
1Cerebellum
1Cerebral cortex
1Coding exons
1Coding sequences
1Cognitive development
1Cortical plate
1Critical region
1Dhplc
1Different databases
1Different stages
1Direct sequencing
1Drosophila
1Drosophila melanogaster
1Embryo
1Exon
1Expression level
1Family family
1Family members
1Fetal
1Fetal brain
1Functional domains
1Genbank accession numbers
1Gene
1Gene expression
1Genet
1Genetic interval
1Genetic intervals
1Genetics
1Glial cells
1High level
1Hippocampus
1Homeobox gene
1Homeodomain
1Homeodomain proteins
1Homeotic gene
1Human
1Human genetics
1Hybridization
1Hybridization analysis
1Institut cochin
1Intermediate zone
1Linkage analysis
1Lymphoblastoid cell lines
1Marginal zone
1Mental retardation
1Missense
1Missense mutation
1Missense mutations
1Molecular genetics
1Monogenic causes
1Mouse embryos
1Mrna
1Mutation
1Nature genet
1Nervous system
1Neuronal
1Neuronal cells
1Neuronal morphogenesis
1Novel aristaless
1Novel gene
1Other genes
1Partington syndrome
1Phenotype
1Polyalanine
1Polyalanine expansions
1Polyalanine tract
1Polyalanine tracts
1Polyglutamine expansions
1Primary cultures
1Recherche medicale
1Retardation
1Santa clara
1Score values
1Sequencing
1Sex linked character
1Signal transduction pathways
1Skeletal muscle
1Small families
1Small insertion
1Spatial expression patterns
1Sporadic case
1Sporadic cases
1Standard procedures
1Syndrome
1Syndromic forms
1Telencephalon
1Thalamus
1Unpublished family
1Ventral
1Ventral thalamus

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EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/Allemagne/Analysis
HfdIndexSelect -h $EXPLOR_AREA/Data/Allemagne/Analysis/Author.i -k "Habiba Chaabouni" 
HfdIndexSelect -h $EXPLOR_AREA/Data/Allemagne/Analysis/Author.i  \
                -Sk "Habiba Chaabouni" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Allemagne/Analysis/biblio.hfd 

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   |clé=    Habiba Chaabouni
}}

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