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JOURNAL OF CELL SCIENCE, ISSN 0021-9533, 03/2011, Volume 124, Issue 5, pp. 718 - 726
Ciliopathies represent a newly emerging group of human diseases that share a common etiology resulting from dysfunction of the cilium or centrosome. The gene... 
NUCLEAR IMPORT | SIGNAL | EUKARYOTIC CILIUM | Retinitis pigmentosa | MEMBRANE | Importin | GTPASE RAN | PROTEIN RP2 | CELL BIOLOGY | RP2 | HNRNP A1 | MITOTIC-SPINDLE | INTRAFLAGELLAR TRANSPORT | Cilia | NUCLEOCYTOPLASMIC TRANSPORT
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1661-6596, 03/2019, Volume 20, Issue 6, p. 1518
X-linked retinitis pigmentosa (XLRP) is a type of severe retinal dystrophy, and female carriers of XLRP demonstrate markedly variable clinical severity. In... 
COMPREHENSIVE MOLECULAR DIAGNOSIS | NORTH-AMERICAN COHORT | FUNDUS AUTOFLUORESCENCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | RP2 GENE | IDENTIFICATION | CHEMISTRY, MULTIDISCIPLINARY | X-linked inheritance | RPGR | LEBER CONGENITAL AMAUROSIS | RP2 | FAMILIES | retinitis pigmentosa | MUTATIONS | visual function | genetic findings | Index Medicus
Journal Article
Journal of Cell Science, ISSN 0021-9533, 03/2011, Volume 124, Issue 5, pp. 718 - 726
Ciliopathies represent a newly emerging group of human diseases that share a common etiology resulting from dysfunction of the cilium or centrosome. The gene... 
Retinitis pigmentosa | RP2 | Importin | Cilia | s
Journal Article
FASEB Journal, ISSN 0892-6638, 03/2015, Volume 29, Issue 3, pp. 932 - 942
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 02/2019, Volume 198, pp. 111 - 123
This is a quantitative study of retinal structure, progression rates, and interocular symmetry in retinitis pigmentosa GTPase regulator gene ( )-associated... 
MUTATION ANALYSIS | BOUNDARIES | GENE | OPTICAL COHERENCE TOMOGRAPHY | RP2 | FAMILIES | DISEASE | OPHTHALMOLOGY | LINKED RETINITIS-PIGMENTOSA | Studies | Medical imaging | Mutation | Ophthalmology | Variance analysis | Age | Symmetry
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 04/2018, Volume 35, Issue 2, pp. 184 - 187
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 09/2018, Volume 59, Issue 11, pp. 4434 - 4440
Purpose: Mutations in the ORF15 region of RPGR account for approximately half of all X-linked retinitis pigmentosa cases. However, a robust high-throughput... 
ORF15 | Genetic testing | RPGR ORF15 | X-linked retinitis pigmentosa | RPGR | MUTATION ANALYSIS | DIAGNOSIS | EXON | GENE | RP2 | genetic testing | FAMILIES | DISEASE | OPHTHALMOLOGY | SPECTRUM | LINKED RETINITIS-PIGMENTOSA | Index Medicus
Journal Article
Gene, ISSN 0378-1119, 07/2019, Volume 707, pp. 86 - 92
Retinitis pigmentosa (RP) is the most common form of inherited retinal degenerative diseases. X-linked RP accounts for nearly 15% of all RP cases. In this... 
Protein stability | Mutation | Retinitis pigmentosa | RP2 | Proteasome | RETINAL DYSTROPHY | GENE | GENETICS & HEREDITY | MICE | PHOTORECEPTOR DEGENERATION | RPGR | Ubiquitin | Viral antibodies | Medical colleges | Biological products | Multiple myeloma | Carfilzomib | Antibodies | Genetic aspects | Tubulins | Index Medicus
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 01/2007, Volume 28, Issue 1, pp. 81 - 91
Journal Article