"Eye Proteins" 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.
PROTEINS derived from TISSUES of the EYE.
| Descriptor ID |
D005136
|
| MeSH Number(s) |
D12.776.306
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Eye Proteins".
Below are MeSH descriptors whose meaning is more specific than "Eye Proteins".
This graph shows the total number of publications written about "Eye Proteins" by people in this website by year, and whether "Eye Proteins" 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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2002 | 3 | 0 | 3 |
| 2003 | 2 | 0 | 2 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 2 | 3 |
| 2006 | 1 | 0 | 1 |
| 2007 | 0 | 1 | 1 |
| 2008 | 4 | 5 | 9 |
| 2009 | 4 | 3 | 7 |
| 2010 | 3 | 3 | 6 |
| 2011 | 3 | 2 | 5 |
| 2012 | 6 | 4 | 10 |
| 2013 | 4 | 5 | 9 |
| 2014 | 11 | 5 | 16 |
| 2015 | 5 | 1 | 6 |
| 2016 | 5 | 3 | 8 |
| 2017 | 3 | 2 | 5 |
| 2018 | 6 | 3 | 9 |
| 2019 | 3 | 1 | 4 |
| 2020 | 5 | 1 | 6 |
| 2021 | 2 | 0 | 2 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 2 | 3 |
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Below are the most recent publications written about "Eye Proteins" by people in Profiles.
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ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Elife. 2023 Nov 22; 12.
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A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report. Acta Neuropathol Commun. 2023 08 11; 11(1):131.
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Synapse-Specific Defects in Synaptic Transmission in the Cerebellum of W246G Mutant ELOVL4 Rats-a Model of Human SCA34. J Neurosci. 2023 Aug 16; 43(33):5963-5974.
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ELOVL4 Mutations That Cause Spinocerebellar Ataxia-34 Differentially Alter Very Long Chain Fatty Acid Biosynthesis. J Lipid Res. 2023 01; 64(1):100317.
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The interplay of environmental luminance and genetics in the retinal dystrophy induced by the dominant RPE65 mutation. Proc Natl Acad Sci U S A. 2022 03 15; 119(11):e2115202119.
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W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34. Mol Neurobiol. 2021 Oct; 58(10):4921-4943.
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Very long chain fatty acid-containing lipids: a decade of novel insights from the study of ELOVL4. J Lipid Res. 2021; 62:100030.
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Interphotoreceptor Retinol-Binding Protein Ameliorates Diabetes-Induced Retinal Dysfunction and Neurodegeneration Through Rhodopsin. Diabetes. 2021 03; 70(3):788-799.
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Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration. Int J Mol Sci. 2020 Oct 29; 21(21).
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Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1. Ophthalmic Genet. 2021 02; 42(1):15-22.