The meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity

Human Molecular Genetics

Volumn 22, Issue 10, 2013, Pages 2024-2040

  Leightner, Amanda C ^a   Hommerding, Cynthia J ^b   Peng, Ying ^a   Salisbury, Jeffrey L ^a   Gainullin, Vladimir G ^a   Czarnecki, Peter G ^b   Sussman, Caroline R ^c   Harris, Peter C ^a,b  

^a Department of Biochemistry and Molecular Biology ^*  (United States)

^b Division of Nephrology and Hypertension   (United States)

^c MAYO GRADUATE SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN D1; EPIDERMAL GROWTH FACTOR RECEPTOR; FIBRONECTIN; HERMES ANTIGEN; INSULIN RECEPTOR SUBSTRATE 1; KRUPPEL LIKE FACTOR 5; MECKELIN; MEMBRANE PROTEIN; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR; PLATELET DERIVED GROWTH FACTOR ALPHA RECEPTOR; PROTEIN C FOS; RHODOPSIN; TRANSFORMING GROWTH FACTOR BETA3; UNCLASSIFIED DRUG; WNT PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL FRACTIONATION; CELL JUNCTION; CELL POLARITY; COCHLEA; CONTROLLED STUDY; DISEASE SEVERITY; EUKARYOTIC FLAGELLUM; GENE DELETION; HAIR CELL; HENLE LOOP; KIDNEY PROXIMAL TUBULE; KINETOSOME; MECKEL SYNDROME; MOUSE; NONHUMAN; ONCOGENE MYC; PHENOTYPE; PHOTORECEPTOR CONNECTING CILIUM; PRIORITY JOURNAL; PROTEIN TRANSPORT; RETINA; RETINA DEGENERATION; SKELETON MALFORMATION; SURVIVAL; UPREGULATION; WNT SIGNALING PATHWAY; ZEBRA FISH;

ANIMALS; CELL POLARITY; CEREBELLAR DISEASES; CILIA; CILIARY MOTILITY DISORDERS; COCHLEA; DISEASE MODELS, ANIMAL; ENCEPHALOCELE; EYE ABNORMALITIES; HEK293 CELLS; HUMANS; KIDNEY DISEASES, CYSTIC; MEMBRANE PROTEINS; MICE; MICE, MUTANT STRAINS; POLYCYSTIC KIDNEY DISEASES; RETINA; WNT SIGNALING PATHWAY; ZEBRAFISH; ZEBRAFISH PROTEINS;

DANIO RERIO; VERTEBRATA;

EID: 84877018892     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt054     Document Type: Article

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