"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 |
|---|
| 1994 | 1 | 1 | 2 |
| 1995 | 2 | 2 | 4 |
| 1996 | 3 | 2 | 5 |
| 1997 | 3 | 1 | 4 |
| 1998 | 0 | 1 | 1 |
| 1999 | 5 | 4 | 9 |
| 2000 | 9 | 3 | 12 |
| 2001 | 3 | 6 | 9 |
| 2002 | 5 | 2 | 7 |
| 2003 | 6 | 4 | 10 |
| 2004 | 7 | 4 | 11 |
| 2005 | 9 | 8 | 17 |
| 2006 | 7 | 1 | 8 |
| 2007 | 4 | 2 | 6 |
| 2008 | 8 | 5 | 13 |
| 2009 | 6 | 3 | 9 |
| 2010 | 5 | 2 | 7 |
| 2011 | 1 | 1 | 2 |
| 2012 | 1 | 4 | 5 |
| 2013 | 4 | 1 | 5 |
| 2014 | 5 | 3 | 8 |
| 2015 | 4 | 1 | 5 |
| 2016 | 8 | 2 | 10 |
| 2017 | 1 | 1 | 2 |
| 2018 | 5 | 3 | 8 |
| 2019 | 1 | 1 | 2 |
| 2020 | 1 | 2 | 3 |
| 2021 | 1 | 3 | 4 |
| 2022 | 0 | 2 | 2 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Eye Proteins" by people in Profiles.
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Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss. Mol Genet Genomic Med. 2024 Feb; 12(2):e2404.
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Systematic assessment of the contribution of structural variants to inherited retinal diseases. Hum Mol Genet. 2023 06 05; 32(12):2005-2015.
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Exploring therapeutic strategies for infantile neuronal axonal dystrophy (INAD/PARK14). Elife. 2023 01 16; 12.
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Testis-specific serine kinase 3 is required for sperm morphogenesis and male fertility. Andrology. 2023 07; 11(5):826-839.
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Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical Results. Ophthalmol Retina. 2022 Dec; 6(12):1130-1144.
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Mutants of the white ABCG Transporter in Drosophila melanogaster Have Deficient Olfactory Learning and Cholesterol Homeostasis. Int J Mol Sci. 2021 Nov 30; 22(23).
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Transcript isoforms of Reep6 have distinct functions in the retina. Hum Mol Genet. 2021 10 13; 30(21):1907-1918.
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Missense mutation in the PAX6 gene can cause a complex mild variable phenotype predominated by concomitant strabismus. Ophthalmic Genet. 2022 02; 43(1):88-96.
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Single-Cell Transcriptomics Identifies a Unique Entity and Signature Markers of Transit-Amplifying Cells in Human Corneal Limbus. Invest Ophthalmol Vis Sci. 2021 07 01; 62(9):36.
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Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nat Commun. 2021 04 12; 12(1):2182.