An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology

Volumn 17, Issue 8, 2015, Pages 1074-1087

  Wheway, Gabrielle ^a   Schmidts, Miriam ^b,c,d,e   Mans, Dorus A ^c,d   Szymanska, Katarzyna ^a   Nguyen, Thanh Minh T ^c,d   Racher, Hilary ^f   Phelps, Ian G ^g   Toedt, Grischa ^h   Kennedy, Julie ⁱ   Wunderlich, Kirsten A ^j   Sorusch, Nasrin ^j   Abdelhamed, Zakia A ^a   Natarajan, Subaashini ^a   Herridge, Warren ^a   Van Reeuwijk, Jeroen ^c,d   Horn, Nicola ^k   Boldt, Karsten ^k   Parry, David A ^a   Letteboer, Stef J F ^c,d   Roosing, Susanne ^l   Adams, Matthew ^m   Bell, Sandra M ^m   Bond, Jacquelyn ^m   Higgins, Julie ^m   Morrison, Ewan E ^m   Tomlinson, Darren C ^m   Slaats, Gisela G ⁿ   Van Dam, Teunis J P ^c   Huang, Lijia ^o   Kessler, Kristin ^p   Giessl, Andreas ^p   Logan, Clare V ^a   Boyle, Evan A ^q   Shendure, Jay ^q   Anazi, Shamsa ^r   Aldahmesh, Mohammed ^r   Al Hazzaa, Selwa ^r,s   Hegele, Robert A ^t   Ober, Carole ^u   Frosk, Patrick ^v   Mhanni, Aizeddin A ^v   Chodirker, Bernard N ^v   Chudley, Albert E ^v   Lamont, Ryan ^f   Bernier, Francois P ^f   Beaulieu, Chandree L ^o   Gordon, Paul ^f   Pon, Richard T ^f   Donahue, Clem ^w   Barkovich, A James ^w   Wolf, Louis ^c   Toomes, Carmel ^a   Thiel, Christian T ^p   Boycott, Kym M ^o   McKibbin, Martin ^m   Inglehearn, Chris F ^a   Stewart, Fiona ^x   Omran, Heymut ^y   Huynen, Martijn A ^c   Sergouniotis, Panagiotis I ^z,aa   Alkuraya, Fowzan S ^r,s   Parboosingh, Jillian S ^f   Innes, A Micheil ^f   Willoughby, Colin E ^ab   Giles, Rachel H ⁿ   Webster, Andrew R ^z,aa   Ueffing, Marius ^k,ac   Blacque, Oliver ⁱ   Gleeson, Joseph G ^l   Wolfrum, Uwe ^j   Beales, Philip L ^b   Gibson, Toby ^h   Doherty, Dan ^g,q   Mitchison, Hannah M ^b   Roepman, Ronald ^c,d   Johnson, Colin A ^a   more..

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^e UNIVERSITY OF FREIBURG   (Germany)

^f ALBERTA CHILDREN S HOSPITAL RESEARCH INSTITUTE   (Canada)

^g UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^h EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

ⁱ UNIVERSITY COLLEGE DUBLIN   (Ireland)

^j JOHANNES GUTENBERG UNIVERSITY   (Germany)

^k UNIVERSITY OF TÜBINGEN   (Germany)

^l ROCKEFELLER UNIVERSITY   (United States)

^m ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

ⁿ UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^o CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^p UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^q UNIVERSITY OF WASHINGTON   (United States)

^r KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^s ALFAISAL UNIVERSITY   (Saudi Arabia)

^t ROBARTS RESEARCH INSTITUTE   (Canada)

^u UNIVERSITY OF CHICAGO   (United States)

^v UNIVERSITY OF MANITOBA   (Canada)

^w UNIVERSITY OF CALIFORNIA   (United States)

^x QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^y UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^z MOORFIELDS EYE HOSPITAL   (United Kingdom)

^aa UNIVERSITY COLLEGE LONDON   (United Kingdom)

^ab UNIVERSITY OF LIVERPOOL   (United Kingdom)

^ac INSTITUTE OF EPIDEMIOLOGY   (Germany)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 3; ANAPHASE PROMOTING COMPLEX SUBUNIT 3; GLUCOSE TRANSPORTER 2; GROWTH DIFFERENTIATION FACTOR 5; MYELOID LEUKEMIA FACTOR 1; NUCLEAR RECEPTOR NR1D1; POTASSIUM CHANNEL KCNQ1; SMALL INTERFERING RNA; C21ORF2 PROTEIN, HUMAN; GENETIC MARKER; MEMBRANE PROTEIN; PIBF1 PROTEIN, HUMAN; PIBF1 PROTEIN, MOUSE; PLACENTA PROTEIN; PROTEIN; SUPPRESSOR FACTOR; TMEM67 PROTEIN, MOUSE;

ADAMTS8 GENE; ADCK5 GENE; AFFINITY PROTEOMICS; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; ATF3 GENE; ATP6V0D2 GENE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA; B4GALT1 GENE; BIOCHEMISTRY; BIOINFORMATICS; C10ORF76 GENE; C14ORF149 GENE; C21ORF2 GENE; CBX5 GENE; CCDC41 GENE; CDC27 GENE; CDC73 GENE; CEP120 GENE; CHONDRODYSPLASIA; CONTROLLED STUDY; CRHR2 GENE; CTDSP1 GENE; ELOVL4 GENE; FEMALE; FUNCTIONAL GENOMICS; GALR2 GENE; GDF5 GENE; GENE; GENE IDENTIFICATION; GLIPR2 GENE; GPR173 GENE; GPR2 GENE; HADH GENE; HTR1B GENE; HUMAN; HUMAN CELL; HUWE1 GENE; IFIT3 GENE; JEUNE SYNDROME; JOUBERT SYNDROME; KANSL1 GENE; KANSL2 GENE; KCNQ1 GENE; KRT13 GENE; LMO1 GENE; LSM2 GENE; LSM5 GENE; MALE; MAP1A GENE; MAS1 GENE; MCRS1 GENE; MLF1 GENE; MOUSE; MT3 GENE; NONHUMAN; NR1D1 GENE; NRBP1A GENE; NUAK1 GENE; OFD1 GENE; OPN1MW GENE; OPN1SW GENE; OPRL1 GENE; OR2Z1 GENE; OR51M1 GENE; P2RY14 GENE; PCDHGA6 GENE; PIBF1 GENE; PLK4 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PRPF31 GENE; PRPF38A GENE; PRPF6 GENE; PRPF8 GENE; QUANTITATIVE ANALYSIS; RAB3IL1 GENE; RANGAP1 GENE; RAPSN GENE; RBX1 GENE; RETINITIS PIGMENTOSA; SLC17A8 GENE; SLC2A2 GENE; SRRT GENE; STOML2 GENE; SUMF2 GENE; TSC22D GENE; UBQLN1 GENE; USP3 GENE; WBP2NL GENE; WHOLE EXOME SEQUENCING; ABNORMALITIES; ANIMAL; C57BL MOUSE; CAENORHABDITIS ELEGANS; CEREBELLUM; CEREBELLUM DISEASE; CILIARY DYSKINESIA; DEFICIENCY; ELLIS VAN CREVELD SYNDROME; EUKARYOTIC FLAGELLUM; EYE MALFORMATION; GENETIC DATABASE; GENETIC MARKER; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETIC TRANSFECTION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HEK293 CELL LINE; HIGH THROUGHPUT SEQUENCING; KIDNEY POLYCYSTIC DISEASE; KNOCKOUT MOUSE; METABOLISM; MULTIPLE MALFORMATION SYNDROME; MUTATION; PATHOLOGY; PHENOTYPE; PHOTORECEPTOR CELL; PROCEDURES; REPRODUCIBILITY; RETINA; RNA INTERFERENCE; ULTRASTRUCTURE; ZEBRA FISH;

ABNORMALITIES, MULTIPLE; ANIMALS; CAENORHABDITIS ELEGANS; CEREBELLAR DISEASES; CEREBELLUM; CILIA; CILIARY MOTILITY DISORDERS; DATABASES, GENETIC; ELLIS-VAN CREVELD SYNDROME; EYE ABNORMALITIES; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HEK293 CELLS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; KIDNEY DISEASES, CYSTIC; MEMBRANE PROTEINS; MICE, INBRED C57BL; MICE, KNOCKOUT; MUTATION; PHENOTYPE; PHOTORECEPTOR CELLS; PREGNANCY PROTEINS; PROTEINS; REPRODUCIBILITY OF RESULTS; RETINA; RNA INTERFERENCE; SUPPRESSOR FACTORS, IMMUNOLOGIC; TRANSFECTION; ZEBRAFISH;

EID: 84938681395     PISSN: 14657392     EISSN: 14764679     Source Type: Journal    
DOI: 10.1038/ncb3201     Document Type: Article

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