TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome

Nature Cell Biology

Volumn 18, Issue 1, 2016, Pages 122-131

  Lambacher, Nils J ^a   Bruel, Ange Line ^b   Van Dam, Teunis J P ^c   Szymaska, Katarzyna ^d   Slaats, Gisela G ^e   Kuhns, Stefanie ^a   McManus, Gavin J ^f   Kennedy, Julie E ^a   Gaff, Karl ^a   Wu, Ka Man ^e   Van Der Lee, Robin ^c   Burglen, Lydie ^g,h   Doummar, Diane ^g   Rivière, Jean Baptiste ^b,i   Faivre, Laurence ^b,i   Attié Bitach, Tania ^j,k,l   Saunier, Sophie ^j,k,l   Curd, Alistair ^d   Peckham, Michelle ^d   Giles, Rachel H ^e   Johnson, Colin A ^d   Huynen, Martijn A ^c   Thauvin Robinet, Christel ^b,i   Blacque, Oliver E ^a   more..

^a UNIVERSITY COLLEGE DUBLIN   (Ireland)

^b UNIVERSITÉ DE BOURGOGNE   (France)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d UNIVERSITY OF LEEDS   (United Kingdom)

^e UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^f TRINITY COLLEGE DUBLIN   (Ireland)

^g ARMAND TROUSSEAU HOSPITAL   (France)

^h INSERM   (France)

ⁱ DIJON UNIVERSITY HOSPITAL   (France)

^j HÔPITAL NECKER ENFANTS MALADES   (France)

^k UNIVERSITÉ PARIS DESCARTES   (France)

^l IMAGINE INSTITUTE   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; JBTS 14 PROTEIN; MEMBRANE PROTEIN; MKS 1 PROTEIN; REGULATOR PROTEIN; TMEM 231 PROTEIN; TMEM107 PROTEIN; UNCLASSIFIED DRUG; CAENORHABDITIS ELEGANS PROTEIN; TMEM107 PROTEIN, MOUSE;

ARTICLE; BIOINFORMATICS; CAENORHABDITIS ELEGANS; CELL COMPOSITION; CELL DAMAGE; CELL MEMBRANE; CELL STRUCTURE; CILIARY TRANSITION ZONE; GENE; GENE EXPRESSION; GENE MUTATION; HUMAN; INSECT CELL; JOUBERT SYNDROME; MAMMAL CELL; MICROTUBULE; MOLECULAR DOCKING; MOLECULAR EVOLUTION; MOLECULAR PATHOLOGY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DETERMINATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; TRANSITION ZONE GENE; WORM; ANIMAL; CEREBELLUM; CONGENITAL MALFORMATION; EUKARYOTIC FLAGELLUM; EYE MALFORMATION; GENETICS; KIDNEY POLYCYSTIC DISEASE; METABOLISM; MULTIPLE MALFORMATION SYNDROME; RETINA;

ABNORMALITIES, MULTIPLE; ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; CEREBELLUM; CILIA; EYE ABNORMALITIES; HUMANS; KIDNEY DISEASES, CYSTIC; MEMBRANE PROTEINS; RETINA;

EID: 84952639414     PISSN: 14657392     EISSN: 14764679     Source Type: Journal    
DOI: 10.1038/ncb3273     Document Type: Article

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