Related references
Note: Only part of the references are listed.The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis
Detina Zalli et al.
HUMAN MOLECULAR GENETICS (2012)
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways
Liyun Sang et al.
CELL (2011)
Nephrocystin-4 is required for pronephric duct-dependent cloaca formation in zebrafish
Krasimir Slanchev et al.
HUMAN MOLECULAR GENETICS (2011)
MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis
Corey L. Williams et al.
JOURNAL OF CELL BIOLOGY (2011)
Ciliogenesis: building the cell's antenna
Hiroaki Ishikawa et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2011)
Mechanisms of Disease: Ciliopathies
Friedhelm Hildebrandt et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Nephrocystin-3 is required for ciliary function in zebrafish embryos
Weibin Zhou et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2010)
Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region
Dai Shiba et al.
JOURNAL OF CELL SCIENCE (2009)
Nephronophthisis: Disease Mechanisms of a Ciliopathy
Friedhelm Hildebrandt et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2009)
The Tol2-mediated Gal4-UAS method for gene and enhancer trapping in zebrafish
Kazuhide Asakawa et al.
METHODS (2009)
Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants
Jessica Sullivan-Brown et al.
DEVELOPMENTAL BIOLOGY (2008)
Genetic and physical interaction between the NPHP5 and NPHP6 gene products
Tobias Schaefer et al.
HUMAN MOLECULAR GENETICS (2008)
NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis
Edgar A. Otto et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2008)
The zebrafish pronephros: A model to study nephron segmentation
R. A. Wingert et al.
KIDNEY INTERNATIONAL (2008)
Genetic dissection of neural circuits by Tol2 transposon-mediated Gal4 gene and enhancer trapping in zebrafish
Kazuhide Asakawa et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Kupffer's vesicle is a ciliated organ of asymmetry in the zebrafish embryo that initiates left-right development of the brain, heart and gut
JJ Essner et al.
DEVELOPMENT (2005)
The Cerberus/Dan-family protein Charon is a negative regulator of Nodal signaling during left-right patterning in zebrafish
H Hashimoto et al.
DEVELOPMENT (2004)
Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors
AJ Bowers et al.
GENE (2004)
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
EA Otto et al.
NATURE GENETICS (2003)
The zebrafish nodal-related gene southpaw is required for visceral and diencephalic left-right asymmetry
S Long et al.
DEVELOPMENT (2003)
Zebrafish pronephros: A model for understanding cystic kidney disease
CL Hostetter et al.
DEVELOPMENTAL DYNAMICS (2003)
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish
SM Liu et al.
DEVELOPMENT (2002)
Share Paper
