| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2016PLoSO..1155860W |
| P356 | DOI | 10.1371/JOURNAL.PONE.0155860 |
| P3181 | OpenCitations bibliographic resource ID | 1500908 |
| P932 | PMC publication ID | 4873209 |
| P698 | PubMed publication ID | 27196396 |
| P2093 | author name string | Xin Chen | |
| Peng Li | |||
| Fang Wang | |||
| Juan Wang | |||
| Jieping Zhang | |||
| Guo-Tong Xu | |||
| Jingying Xu | |||
| Haibin Tian | |||
| Zongyi Li | |||
| Lixia Lu | |||
| Jingfa Zhang | |||
| Weiye Li | |||
| Furong Gao | |||
| Caixia Jin | |||
| P2860 | cites work | FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies | Q24297877 |
| Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy | Q24300726 | ||
| Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina | Q24306695 | ||
| OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin | Q24320320 | ||
| Autophagy promotes primary ciliogenesis by removing OFD1 from centriolar satellites | Q24337670 | ||
| Identification of the gene for oral-facial-digital type I syndrome | Q24536160 | ||
| CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290 | Q24644138 | ||
| OFD1 and flotillins are integral components of a ciliary signaling protein complex organized by polycystins in renal epithelia and odontoblasts | Q27313336 | ||
| Functional characterization of the OFD1 protein reveals a nuclear localization and physical interaction with subunits of a chromatin remodeling complex | Q28118131 | ||
| Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa | Q28142917 | ||
| Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat | Q28145723 | ||
| Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition | Q28263322 | ||
| ARPE-19, a human retinal pigment epithelial cell line with differentiated properties | Q28283979 | ||
| Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms | Q29614613 | ||
| A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome | Q34539684 | ||
| Ofd1 controls dorso-ventral patterning and axoneme elongation during embryonic brain development | Q34541428 | ||
| Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1. | Q34541509 | ||
| Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis | Q34633991 | ||
| Wnt-signaling in retinal development and disease | Q34806242 | ||
| Frizzled 5 signaling governs the neural potential of progenitors in the developing Xenopus retina. | Q52052842 | ||
| A modified histoimmunochemistry-assisted method for in situ RPE evaluation. | Q53782138 | ||
| Influence of eye pigmentation and light deprivation on inherited retinal dystrophy in the rat | Q67273988 | ||
| Photoreceptor characteristics in congenic strains of RCS rats | Q70728892 | ||
| N-methyl-N-nitrosourea-induced photoreceptor apoptosis in the mouse retina | Q71741199 | ||
| Pigmentary degeneration induced by N-methyl-N-nitrosourea and the fate of pigment epithelial cells in the rat retina | Q71906488 | ||
| Retinal degeneration induced by N-methyl-N-nitrosourea in Syrian golden hamsters | Q77444459 | ||
| The Royal College of Surgeons rat: an animal model for inherited retinal degeneration with a still unknown genetic defect | Q77610298 | ||
| Role of oxidative stress in diabetic complications: a new perspective on an old paradigm | Q77804864 | ||
| Caspaselike proteases activated in apoptotic photoreceptors of Royal College of Surgeons rats | Q77958683 | ||
| Cilia put a brake on Wnt signalling | Q80439010 | ||
| [Correlation between primary cilium and Wnt signaling pathway] | Q86953784 | ||
| Senior- loken syndrome - a ciliopathy | Q34910105 | ||
| The Ciliogenic Protein Oral-Facial-Digital 1 Regulates the Neuronal Differentiation of Embryonic Stem Cells | Q35084114 | ||
| Wnt/β-catenin controls follistatin signalling to regulate satellite cell myogenic potential. | Q35575301 | ||
| Morphological and functional evaluation of an animal model for the retinal degeneration induced by N-methyl-N-nitrosourea | Q35663757 | ||
| Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons | Q36121779 | ||
| Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) | Q36122430 | ||
| Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis | Q36499349 | ||
| Nimodipine inhibits N-methyl-N-nitrosourea-induced retinal photoreceptor apoptosis in vivo | Q36865449 | ||
| The retinal ciliopathies. | Q36951820 | ||
| Photoreceptor sensory cilia and inherited retinal degeneration | Q37711181 | ||
| FAM161A, a novel centrosomal-ciliary protein implicated in autosomal recessive retinitis pigmentosa | Q38199020 | ||
| Bardet-Biedl syndrome: Is it only cilia dysfunction? | Q38558495 | ||
| Role of oxidative stress in retinal photoreceptor cell death in N-methyl-N-nitrosourea-treated mice | Q39391046 | ||
| Blue light stress in retinal neuronal (R28) cells is dependent on wavelength range and irradiance | Q39502414 | ||
| The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. | Q39522092 | ||
| Establishment and characterization of a retinal Müller cell line. | Q41071402 | ||
| Structural and functional protection of photoreceptors from MNU-induced retinal degeneration by the X-linked inhibitor of apoptosis | Q44453160 | ||
| Characterization of Wnt signaling components and activation of the Wnt canonical pathway in the murine retina. | Q44483726 | ||
| Wnt signaling promotes Müller cell proliferation and survival after injury. | Q45133272 | ||
| Early remodeling in an inducible animal model of retinal degeneration. | Q46094681 | ||
| The expression patterns of Wnts and their antagonists during avian eye development | Q46843599 | ||
| N -methyl- N -nitrosourea-induced retinal degeneration in mice | Q47607742 | ||
| Expression of Frizzled genes in the developing chick eye. | Q48228579 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | photoreceptor protein | Q7187894 |
| P304 | page(s) | e0155860 | |
| P577 | publication date | 2016-01-01 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | OFD1, as a Ciliary Protein, Exhibits Neuroprotective Function in Photoreceptor Degeneration Models | |
| P478 | volume | 11 |
| Q55003204 | Distinct mutations with different inheritance mode caused similar retinal dystrophies in one family: a demonstration of the importance of genetic annotations in complicated pedigrees. |
| Q37566005 | Isolation and characterization of antimutagenic components of Glycyrrhiza aspera against N-methyl-N-nitrosourea |
| Q36231506 | Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing |
| Q89668382 | OFD1 mutation induced renal failure and polycystic kidney disease in a pair of childhood male twins in China |
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