Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development

Organogenesis

Volumn 10, Issue 1, 2014, Pages 96-107

  Barker, Amy R ^a   Thomas, Rhys ^a   Dawe, Helen R ^a  

^a UNIVERSITY OF EXETER   (United Kingdom)

Author keywords

Brain; Cilia; Ciliopathy; Hedgehog; Joubert syndrome; Kidney; Meckel Gruber syndrome; Nephronophthisis; Signalling; Skeleton; Wnt

Indexed keywords

WNT PROTEIN;

BONE DEVELOPMENT; BRAIN MALFORMATION; CELL ORGANELLE; CELL POLARITY; CELL PROLIFERATION; CENTRAL NERVOUS SYSTEM; CILIOPATHY; CONGENITAL MALFORMATION; EUKARYOTIC FLAGELLUM; HEDGEHOG; HUMAN; KIDNEY DEVELOPMENT; MECKEL SYNDROME; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; REVIEW; WNT SIGNALING PATHWAY; BONE; CILIARY DYSKINESIA; CYTOLOGY; EMBRYOLOGY; ENCEPHALOCELE; ENZYMOLOGY; KIDNEY; KIDNEY DISEASE; KIDNEY POLYCYSTIC DISEASE; METABOLISM; PATHOPHYSIOLOGY;

BONE AND BONES; CENTRAL NERVOUS SYSTEM; CILIA; CILIARY MOTILITY DISORDERS; ENCEPHALOCELE; HUMANS; KIDNEY; KIDNEY DISEASES; POLYCYSTIC KIDNEY DISEASES;

EID: 84901455140     PISSN: 15476278     EISSN: 15558592     Source Type: Journal    
DOI: 10.4161/org.27375     Document Type: Review

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