 Retinitis Pigmentosa
"Retinitis Pigmentosa" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field.
| Descriptor ID |
D012174
|
| MeSH Number(s) |
C11.270.684 C11.768.585.658.500 C16.320.290.684
|
| Concept/Terms |
Retinitis Pigmentosa- Retinitis Pigmentosa
- Cone-Rod Dystrophy
- Cone Rod Dystrophy
- Cone-Rod Dystrophies
- Dystrophies, Cone-Rod
- Dystrophy, Cone-Rod
- Cone-Rod Retinal Dystrophy
- Cone Rod Retinal Dystrophy
- Cone-Rod Retinal Dystrophies
- Dystrophies, Cone-Rod Retinal
- Dystrophy, Cone-Rod Retinal
- Retinal Dystrophies, Cone-Rod
- Retinal Dystrophy, Cone-Rod
- Tapetoretinal Degeneration
- Degeneration, Tapetoretinal
- Degenerations, Tapetoretinal
- Tapetoretinal Degenerations
- Retinal Cone-Rod Dystrophy
- Cone-Rod Dystrophies, Retinal
- Cone-Rod Dystrophy, Retinal
- Dystrophies, Retinal Cone-Rod
- Dystrophy, Retinal Cone-Rod
- Retinal Cone Rod Dystrophy
- Retinal Cone-Rod Dystrophies
- Rod Cone Dystrophies
- Dystrophies, Rod Cone
- Dystrophy, Rod Cone
- Rod Cone Dystrophy
- Rod-Cone Dystrophy
- Dystrophies, Rod-Cone
- Dystrophy, Rod-Cone
- Rod-Cone Dystrophies
- Cone-Rod Degenerations
- Cone Rod Degenerations
- Cone-Rod Degeneration
- Degeneration, Cone-Rod
- Degenerations, Cone-Rod
- Pigmentary Retinopathy
- Pigmentary Retinopathies
- Retinopathies, Pigmentary
- Retinopathy, Pigmentary
|
Below are MeSH descriptors whose meaning is more general than "Retinitis Pigmentosa".
Below are MeSH descriptors whose meaning is more specific than "Retinitis Pigmentosa".
This graph shows the total number of publications written about "Retinitis Pigmentosa" by people in this website by year, and whether "Retinitis Pigmentosa" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 1 | 0 | 1 | | 1995 | 0 | 1 | 1 | | 1996 | 1 | 0 | 1 | | 1997 | 0 | 1 | 1 | | 1998 | 1 | 0 | 1 | | 2000 | 1 | 0 | 1 | | 2003 | 1 | 1 | 2 | | 2005 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 | | 2008 | 1 | 0 | 1 | | 2009 | 2 | 0 | 2 | | 2010 | 2 | 0 | 2 | | 2014 | 1 | 1 | 2 | | 2015 | 2 | 1 | 3 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Retinitis Pigmentosa" by people in Profiles.
-
Conley SM, Stuck MW, Watson JN, Naash MI. Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa. Hum Mol Genet. 2017 Feb 01; 26(3):509-518.
-
Stuck MW, Conley SM, Naash MI. RDS Functional Domains and Dysfunction in Disease. Adv Exp Med Biol. 2016; 854:217-22.
-
Orhan E, Dalkara D, Neuillé M, Lechauve C, Michiels C, Picaud S, Léveillard T, Sahel JA, Naash MI, Lavail MM, Zeitz C, Audo I. Genotypic and phenotypic characterization of P23H line 1 rat model. PLoS One. 2015; 10(5):e0127319.
-
Han Z, Banworth MJ, Makkia R, Conley SM, Al-Ubaidi MR, Cooper MJ, Naash MI. Genomic DNA nanoparticles rescue rhodopsin-associated retinitis pigmentosa phenotype. FASEB J. 2015 Jun; 29(6):2535-44.
-
Murray AR, Vuong L, Brobst D, Fliesler SJ, Peachey NS, Gorbatyuk MS, Naash MI, Al-Ubaidi MR. Glycosylation of rhodopsin is necessary for its stability and incorporation into photoreceptor outer segment discs. Hum Mol Genet. 2015 May 15; 24(10):2709-23.
-
Conley SM, Naash MI. Gene therapy for PRPH2-associated ocular disease: challenges and prospects. Cold Spring Harb Perspect Med. 2014 Aug 28; 4(11):a017376.
-
Stuck MW, Conley SM, Naash MI. The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse. Hum Mol Genet. 2014 Dec 01; 23(23):6260-74.
-
Phillips MJ, Otteson DC, Sherry DM. Progression of neuronal and synaptic remodeling in the rd10 mouse model of retinitis pigmentosa. J Comp Neurol. 2010 Jun 01; 518(11):2071-89.
-
Cai X, Conley SM, Naash MI. Gene therapy in the Retinal Degeneration Slow model of retinitis pigmentosa. Adv Exp Med Biol. 2010; 664:611-9.
-
Cai X, Conley SM, Nash Z, Fliesler SJ, Cooper MJ, Naash MI. Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa. FASEB J. 2010 Apr; 24(4):1178-91.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|