Genetic, environmental, and epigenetic factors involved in CAKUT, Nat. Rev. Nephrol, vol.11, pp.720-731, 2015. ,
, Ciliopathies. Cold Spring Harb. Perspect. Biol, vol.9, 2017.
Development of the Mammalian Kidney, Curr. Top. Dev. Biol, vol.117, pp.31-64, 2016. ,
A brief review of kidney development, maturation, developmental abnormalities, and drug toxicity: juvenile animal relevancy, J. Toxicol. Pathol, vol.30, pp.125-133, 2017. ,
Zebrafish kidney development, Methods Cell Biol, vol.134, pp.391-429, 2016. ,
Little fish, big catch: zebrafish as a model for kidney disease, Kidney Int, vol.89, pp.1204-1210, 2016. ,
Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract, J. Pediatr. Genet, vol.5, pp.51-60, 2016. ,
FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man, Dev. Cell, vol.22, pp.1191-1207, 2012. ,
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice, Am. J. Hum. Genet, vol.101, pp.803-814, 2017. ,
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans, Am. J. Hum. Genet, vol.94, pp.288-294, 2014. ,
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype, Clin. Genet, vol.86, pp.220-228, 2014. ,
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract, J. Am. Soc. Nephrol. JASN, vol.28, pp.2901-2914, 2017. ,
Neurogenesis during development of the vertebrate central nervous system, EMBO Rep, vol.15, pp.351-364, 2014. ,
Genetics and mechanisms leading to human cortical malformations, Semin. Cell Dev. Biol, vol.76, pp.33-75, 2018. ,
URL : https://hal.archives-ouvertes.fr/hal-01626222
Kinesin assembly and movement in cells, Annu. Rev. Biophys, vol.40, pp.267-288, 2011. ,
KIF14 Binds Tightly to Microtubules and Adopts a Rigor-Like Conformation, J. Mol. Biol, vol.426, pp.2997-3015, 2014. ,
RNA interference-mediated silencing of mitotic kinesin KIF14 disrupts cell cycle progression and induces cytokinesis failure, Mol. Cell. Biol, vol.26, pp.3853-3863, 2006. ,
KIF14 and citron kinase act together to promote efficient cytokinesis, J. Cell Biol, vol.172, pp.363-372, 2006. ,
Cytokinesis in animal cells, Cold Spring Harb. Perspect. Biol, vol.7, p.15834, 2015. ,
Citron kinase controls a molecular network required for midbody formation in cytokinesis, Proc. Natl. Acad. Sci. U. S. A, vol.110, pp.9782-9787, 2013. ,
Citron kinase mediates transition from constriction to abscission through its coiled-coil domain, J. Cell Sci, vol.126, pp.1773-1784, 2013. ,
Midbody: from cellular junk to regulator of cell polarity and cell fate, Curr. Opin. Cell Biol, vol.35, pp.51-58, 2015. ,
KIF14 negatively regulates Rap1a-Radil signaling during breast cancer progression, J. Cell Biol, vol.199, pp.951-967, 2012. ,
KLP38B: a mitotic kinesin-related protein that binds PP1, J. Cell Biol, vol.138, pp.395-409, 1997. ,
A chromatin-associated kinesin-related protein required for normal mitotic chromosome segregation in Drosophila, J. Cell Biol, vol.139, pp.1361-1371, 1997. ,
Mutation of a gene for a Drosophila kinesin-like protein, Klp38B, leads to failure of cytokinesis, J. Cell Sci, vol.110, pp.945-954, 1997. ,
A Drosophila kinesin-like protein, Klp38B, functions during meiosis, mitosis, and segmentation, Dev. Biol, vol.191, pp.284-296, 1997. ,
Kif14 mutation causes severe brain malformation and hypomyelination, PloS One, vol.8, p.53490, 2013. ,
Biallelic variants in KIF14 cause intellectual disability with microcephaly, Eur. J. Hum. Genet. EJHG, vol.26, pp.330-339, 2018. ,
Mutations of KIF14 cause primary microcephaly by impairing cytokinesis, Ann. Neurol, vol.82, pp.562-577, 2017. ,
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly, Hum. Genet, vol.135, pp.1199-1207, 2016. ,
Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons, Am. J. Hum. Genet, vol.99, pp.511-520, 2016. ,
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly, Am. J. Hum. Genet, vol.99, pp.501-510, 2016. ,
Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans, Hum. Genet, vol.135, pp.1191-1197, 2016. ,
Allele-specific activators and inhibitors for kinesin, Proc. Natl. Acad. Sci. U. S. A, vol.96, pp.9106-9111, 1999. ,
Luminal mitosis drives epithelial cell dispersal within the branching ureteric bud, Dev. Cell, vol.27, pp.319-330, 2013. ,
A systematic genome-wide analysis of zebrafish protein-coding gene function, Nature, vol.496, pp.494-497, 2013. ,
Initial formation of zebrafish brain ventricles occurs independently of circulation and requires the nagie oko and snakehead/atp1a1a.1 gene products, Dev. Camb. Engl, vol.132, pp.2057-2067, 2005. ,
Microcephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression, Open Biol, vol.3, pp.130065-130065, 2013. ,
Antennas of organ morphogenesis: the roles of cilia in vertebrate kidney development, vol.54, pp.457-469, 2000. ,
The Wilms tumor genes wt1a and wt1b control different steps during formation of the zebrafish pronephros, Dev. Biol, vol.309, pp.87-96, 2007. ,
Mechanisms of otoconia and otolith development, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.244, pp.239-253, 2015. ,
Vangl2 directs the posterior tilting and asymmetric localization of motile primary cilia, Nat. Cell Biol, vol.12, pp.407-412, 2010. ,
, Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization, vol.6, p.8666, 2015.
Control of the Wnt pathways by nephrocystin-4 is required for morphogenesis of the zebrafish pronephros, Hum. Mol. Genet, vol.20, pp.2611-2627, 2011. ,
Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis, 2013. ,
Chemokine signaling mediates self-organizing tissue migration in the zebrafish lateral line, Dev. Cell, vol.10, pp.673-680, 2006. ,
Mechanical stretch and PI3K signaling link cell migration and proliferation to coordinate epithelial tubule morphogenesis in the zebrafish pronephros, PloS One, vol.7, p.39992, 2012. ,
Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy, Am. J. Med. Genet, vol.47, pp.250-254, 1993. ,
Genetic basis of human congenital anomalies of the kidney and urinary tract, J. Clin. Invest, vol.128, pp.4-15, 2018. ,
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development, Hum. Mol. Genet, vol.27, pp.224-238, 2018. ,
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation, PLoS Genet, vol.12, p.1005894, 2016. ,
Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis, Am. J. Med. Genet. A, 2018. ,
Midbody and primary cilium of neural progenitors release extracellular membrane particles enriched in the stem cell marker prominin-1, J. Cell Biol, vol.176, pp.483-495, 2007. ,
Conserved and Divergent Features of Human and Mouse Kidney Organogenesis, J. Am. Soc. Nephrol. JASN, vol.29, pp.785-805, 2018. ,
Progressive Recruitment of Mesenchymal Progenitors Reveals a Time-Dependent Process of Cell Fate Acquisition in Mouse and Human Nephrogenesis, Dev. Cell, vol.45, pp.651-660, 2018. ,
Targeted disruption of Nphp1 causes male infertility due to defects in the later steps of sperm morphogenesis in mice, Hum. Mol. Genet, vol.17, pp.3368-3379, 2008. ,
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development, Hum. Mol. Genet, vol.20, pp.482-496, 2011. ,
Novel role for the midbody in primary ciliogenesis by polarized epithelial cells, J. Cell Biol, 2016. ,
The human genome browser at UCSC, Genome Res, vol.12, pp.996-1006, 2002. ,
, Nucleic Acids Res, vol.45, pp.635-642, 2017.
The actin-binding ERM protein Moesin binds to and stabilizes microtubules at the cell cortex, J. Cell Biol, vol.202, pp.251-260, 2013. ,
Genome engineering using the CRISPR-Cas9 system, Nat. Protoc, vol.8, pp.2281-2308, 2013. ,
, Phospho-histone H3 (PH3)