New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes

DMM Disease Models and Mechanisms

Volumn 10, Issue 4, 2017, Pages 463-474

  Abekhoukh, Sabiha ^a,b,c   Sahin, H Bahar ^d,e,f,g,r   Grossi, Mauro ^a,b,c   Zongaro, Samantha ^a,b,c   Maurin, Thomas ^a,b,c   Madrigal, Irene ^h,i,j   Kazue Sugioka, Daniele ^a,b,c,k   Raas Rothschild, Annick ^l   Doulazmi, Mohamed ^m   Carrera, Pilar ^d,e,f,g   Stachon, Andrea ^k   Scherer, Steven ⁿ   Drula Do Nascimento, Maria Rita ^k   Trembleau, Alain ^m   Arroyo, Ignacio ⁱ   Szatmari, Peter ⁿ   Smith, Isabel M ^o   Mila, Montserrat ^i,j   Smith, Adam C ^a,p   Giangrande, Angela ^d,e,f,g   Caillé, Isabelle ^m,q   Bardoni, Barbara ^a,b,c   more..

^a UNIVERSITÉ CÔTE D'AZUR   (France)

^b INSTITUT DE PHARMACOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^c CNRS LIA 'Neogenex'   (France)

^d INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^e CNRS   (France)

^f INSERM   (France)

^g UNIVERSITÉ DE STRASBOURG   (France)

^h HOSPITAL CLÍNIC   (Spain)

ⁱ CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^j INSTITUT D INVESTIGACIONS BIOMÈDIQUES AUGUST PI I SUNYER IDIBAPS   (Spain)

^k INSTITUTO DE PESQUISA PELÉ PEQUENO PRÍNCIPE   (Brazil)

^l SHEBA MEDICAL CENTER   (Israel)

^m SORBONNE UNIVERSITÉ   (France)

ⁿ HOSPITAL FOR SICK CHILDREN   (Canada)

^o IWK HEALTH CENTRE   (Canada)

^p UNIVERSITY HEALTH NETWORK   (Canada)

^q UNIVERSITÉ PARIS DESCARTES   (France)

^r KADIR HAS UNIVERSITY   (Turkey)

more..

Author keywords

Autism; BP1 BP2 deletion; CYFIP1; Fragile X; Intellectual disability

Indexed keywords

MESSENGER RNA; SHORT HAIRPIN RNA; CYFIP1 PROTEIN, MOUSE; DROSOPHILA PROTEIN; FRAGILE X MENTAL RETARDATION PROTEIN; MULTIPROTEIN COMPLEX; NERVE PROTEIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN; SRA-1 PROTEIN, DROSOPHILA; WISKOTT ALDRICH SYNDROME PROTEIN;

ADULT; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; CYTOPLASMIC FRAGILE X MENTAL RETARDATION PROTEIN INTERACTING PROTEIN 1 GENE; DROSOPHILA; FIBROBLAST; GENE; GENE EXPRESSION; GENE FUNCTION; GENE INTERACTION; GENE SILENCING; HOMOZYGOTE; IN VIVO STUDY; LOSS OF FUNCTION MUTATION; MORPHOLOGY; MOUSE; NERVE CELL; NERVE CELL DIFFERENTIATION; NERVE CELL PLASTICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROCESSING; SIGNAL TRANSDUCTION; SPINE; ANIMAL; C57BL MOUSE; CELL CULTURE; DROSOPHILA MELANOGASTER; EPISTASIS; GENE INACTIVATION; GENETICS; HUMAN; METABOLISM; OLFACTORY BULB;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; CELLS, CULTURED; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; EPISTASIS, GENETIC; FRAGILE X MENTAL RETARDATION PROTEIN; GENE KNOCKOUT TECHNIQUES; GENE SILENCING; HUMANS; MICE, INBRED C57BL; MULTIPROTEIN COMPLEXES; NERVE TISSUE PROTEINS; NEURONS; OLFACTORY BULB; RNA, MESSENGER; WISKOTT-ALDRICH SYNDROME PROTEIN FAMILY;

EID: 85017508335     PISSN: 17548403     EISSN: 17548411     Source Type: Journal    
DOI: 10.1242/dmm.025809     Document Type: Article

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