相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition
Kollu N. Rao et al.
SCIENTIFIC REPORTS (2015)
Wnt/β-catenin controls follistatin signalling to regulate satellite cell myogenic potential
Andrew E. Jones et al.
SKELETAL MUSCLE (2015)
Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina
Aiden Eblimit et al.
HUMAN MOLECULAR GENETICS (2015)
Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy
Susanne Roosing et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
N -methyl- N -nitrosourea-induced retinal degeneration in mice
Yuan-Yuan Chen et al.
EXPERIMENTAL EYE RESEARCH (2014)
OFD1 and Flotillins Are Integral Components of a Ciliary Signaling Protein Complex Organized by Polycystins in Renal Epithelia and Odontoblasts
Stephanie Jerman et al.
PLOS ONE (2014)
Nimodipine inhibits N-methyl-N-nitrosourea-induced retinalphotoreceptor apoptosis in vivo
Dan Wang et al.
INDIAN JOURNAL OF PHARMACOLOGY (2013)
Autophagy promotes primary ciliogenesis by removing OFD1 from centriolar satellites
Zaiming Tang et al.
NATURE (2013)
Wnt Signaling Promotes Muller Cell Proliferation and Survival after Injury
Bo Liu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2013)
FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies
Silvio Alessandro Di Gioia et al.
HUMAN MOLECULAR GENETICS (2012)
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)
Tom R. Webb et al.
HUMAN MOLECULAR GENETICS (2012)
Role of Oxidative Stress in Retinal Photoreceptor Cell Death in N-Methyl-N-nitrosourea-Treated Mice
Kazuhiro Tsuruma et al.
JOURNAL OF PHARMACOLOGICAL SCIENCES (2012)
Ofd1 Controls Dorso-Ventral Patterning and Axoneme Elongation during Embryonic Brain Development
Anna D'Angelo et al.
PLOS ONE (2012)
Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons
H. Patil et al.
CELL DEATH & DISEASE (2012)
Blue light stress in retinal neuronal (R28) cells is dependent on wavelength range and irradiance
Lilla Knels et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2011)
The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase
Karlien L. M. Coene et al.
HUMAN MOLECULAR GENETICS (2011)
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1
Carla A. M. Lopes et al.
JOURNAL OF CELL SCIENCE (2011)
The Ciliogenic Protein Oral-Facial-Digital 1 Regulates the Neuronal Differentiation of Embryonic Stem Cells
Julie Hunkapiller et al.
STEM CELLS AND DEVELOPMENT (2011)
Morphological and functional evaluation of an animal model for the retinal degeneration induced by N-methyl-N-nitrosourea
Eojin Jeong et al.
ANATOMY & CELL BIOLOGY (2011)
OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin
Karlien L. M. Coene et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
EARLY REMODELING IN AN INDUCIBLE ANIMAL MODEL OF RETINAL DEGENERATION
S. Nagar et al.
NEUROSCIENCE (2009)
Wnt-Signaling in Retinal Development and Disease
Eleonora M. Lad et al.
STEM CELLS AND DEVELOPMENT (2009)
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
Nicholas T. Gorden et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Cilia put a brake on Wnt signalling
Xi He
NATURE CELL BIOLOGY (2008)
Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms
Kevin C. Corbit et al.
NATURE CELL BIOLOGY (2008)
Functional characterization of the OFD1 protein reveals a nuclear localization and physical interaction with Subunits of a chromatin remodeling complex
Giovanna Giorgio et al.
MOLECULAR BIOLOGY OF THE CELL (2007)
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis
Anneke I. den Hollander et al.
NATURE GENETICS (2007)
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome
Bartlomiej Budny et al.
HUMAN GENETICS (2006)
Frizzled 5 signaling governs the neural potential of progenitors in the developing Xenopus retina
TJ Van Raay et al.
NEURON (2005)
Characterization of Wnt signaling components and activation of the Wnt canonical pathway in the murine retina
H Liu et al.
DEVELOPMENTAL DYNAMICS (2003)
Structural and functional protection of photoreceptors from MNU-induced retinal degeneration by the x-linked inhibitor of apoptosis
D Petrin et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2003)
The expression patterns of Wnts and their antagonists during avian eye development
EJ Jin et al.
MECHANISMS OF DEVELOPMENT (2002)
Identification of the gene for oral-facial-digital type I syndrome
MI Ferrante et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
A Gal et al.
NATURE GENETICS (2000)
Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat
PM D'Cruz et al.
HUMAN MOLECULAR GENETICS (2000)