Knockdown of bardet-biedl syndrome gene BBS9/PTHB1 leads to Cilia defects

PLoS ONE

Volumn 7, Issue 3, 2012, Pages

  Veleri, Shobi ^a   Bishop, Kevin ^b   Nogare, Damian E Dalle ^c   English, Milton A ^a,b   Foskett, Trevor J ^a   Chitnis, Ajay ^c   Sood, Raman ^b   Liu, Paul ^b   Swaroop, Anand ^a  

^a NATIONAL EYE INSTITUTE   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; MESSENGER RNA; MORPHOLINO OLIGONUCLEOTIDE; BBS9 PROTEIN, HUMAN; BBS9 PROTEIN, MOUSE; BBS9 PROTEIN, ZEBRAFISH; PROTEIN; TUMOR PROTEIN; ZEBRAFISH PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BARDET BIEDL SYNDROME; BBS9 GENE; CONTROLLED STUDY; EMBRYO; EUKARYOTIC FLAGELLUM; GENE EXPRESSION; GENE FUNCTION; GENE IDENTIFICATION; GENETIC CONSERVATION; HETEROZYGOSITY; HYDROCEPHALUS; KUPFFER CELL; MARKER GENE; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PTHB1 GENE; RETINOPATHY; ZEBRA FISH; ANIMAL; BRAIN; CELL LINE; CONGENITAL MALFORMATION; GENE SILENCING; GENETICS; HUMAN; METABOLISM; MOUSE; PATHOLOGY; PRENATAL DEVELOPMENT; RETINA;

DANIO RERIO; MAMMALIA;

ANIMALS; BARDET-BIEDL SYNDROME; BRAIN; CELL LINE; CILIA; GENE KNOCKDOWN TECHNIQUES; HUMANS; MICE; MORPHOLINOS; NEOPLASM PROTEINS; PROTEINS; RETINA; RNA, MESSENGER; ZEBRAFISH; ZEBRAFISH PROTEINS;

EID: 84859055138     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0034389     Document Type: Article

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