942 lines
53 KiB
Text
942 lines
53 KiB
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<div> <p>Thanks to the work of NEI scientists and grantees, we’re constantly learning new information about the causes and treatment of vision disorders. Get the latest updates about their work — along with other news about NEI.</p>
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48 items
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<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2020-06/cavefish_lo-res.jpg?itok=c4ztNu2o" width="200" height="200" alt="Surface-dwelling fish with an eye, and pale cave fish without eye" />
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|
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<a class="c-teaser__link" href="/about/news-and-events/news/gene-found-causes-eyes-wither-cavefish">
|
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Gene Found that Causes Eyes to Wither in Cavefish
|
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</a>
|
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</h2>
|
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<p class="c-teaser__date">
|
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<time datetime="2020-06-02T11:54:49-04:00">June 2, 2020</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
University of Maryland-led study identified the first gene responsible for eye loss in cavefish, revealing connection to a human vascular disease.
|
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</div>
|
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</div>
|
||
</div></div></div>
|
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<div class="c-sidebar-widget__list-item views-row">
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<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2019-11/Bardet-Biedel%20syndrome_horizontal_201910251941.jpg?itok=zAAUQKkv" width="200" height="200" alt="Rhesus macaque monkey" />
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<div class="c-teaser__content">
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|
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<a class="c-teaser__link" href="/about/news-and-events/news/discovery-monkeys-could-lead-treatment-blindness-causing-syndrome">
|
||
Discovery in monkeys could lead to treatment for blindness causing syndrome
|
||
</a>
|
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</h2>
|
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<p class="c-teaser__date">
|
||
<time datetime="2019-10-25T12:32:26-04:00">October 25, 2019</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
Oregon National Primate Research Center at OHSU reports first-ever nonhuman primate model for Bardet-Biedl Syndrome
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
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<div class="c-sidebar-widget__list-item views-row">
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<div class="field-content"><div class="c-teaser">
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<div class="c-teaser__image">
|
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|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2019-08/group_all%20copy.jpg?itok=4gRAXdS6" width="200" height="200" alt="7 men look at the camera in a group portrait" />
|
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|
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|
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|
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<div class="c-teaser__content">
|
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<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/nei-researchers-awarded-grants-knights-templar-eye-foundation">
|
||
NEI Researchers Awarded Grants by the Knights Templar Eye Foundation
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2019-07-11T18:19:35-04:00">July 11, 2019</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
The Knights Templar Eye Foundation has awarded two NEI scientists grants to research inherited retinal degenerations, diseases that can cause blindness in early childhood.
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
||
<div class="c-sidebar-widget__list-item views-row">
|
||
<div class="field-content"><div class="c-teaser">
|
||
<div class="c-teaser__image">
|
||
|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2021-03/S8L_Graphic_Sized_0.jpg?itok=WLnjUsP4" width="200" height="200" alt="Yellow, red and purple multi-colored mosaic" />
|
||
|
||
|
||
|
||
</div>
|
||
|
||
<div class="c-teaser__content">
|
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<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/imaging-method-reveals-long-lived-patterns-cells-eye">
|
||
Imaging Method Reveals Long-lived Patterns in Cells of the Eye
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2019-03-12T14:08:22-04:00">March 12, 2019</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
Cells of the retinal pigment epithelium (RPE) form unique patterns that can be used to track changes in this important layer of tissue in the back of the eye, researchers at the National Eye Institute (NEI) have found.
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
||
<div class="c-sidebar-widget__list-item views-row">
|
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<div class="field-content"><div class="c-teaser">
|
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<div class="c-teaser__image">
|
||
|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2021-04/Side-by-side_bl_6mo.jpg?itok=9Lrohhcq" width="200" height="200" alt="Side-by-side photos of trial participant before and after treatment" />
|
||
|
||
|
||
|
||
</div>
|
||
|
||
<div class="c-teaser__content">
|
||
<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/nitisinone-increases-melanin-people-albinism">
|
||
Nitisinone Increases Melanin in People With Albinism
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2019-02-20T00:00:00-05:00">February 20, 2019</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
A small pilot clinical study at the National Eye Institute (NEI) suggests that the drug nitisinone increases melanin production in some people with oculocutaneous albinism type 1B (OCA-1B), a rare genetic disease that causes pale skin and hair and poor vi
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
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<div class="c-sidebar-widget__list-item views-row">
|
||
<div class="field-content"><div class="c-teaser">
|
||
<div class="c-teaser__image">
|
||
|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/2019-05/News_Grantee_Placeholder.png?itok=CCnZ6UNM" width="200" height="200" alt="Grantee News" />
|
||
|
||
|
||
|
||
</div>
|
||
|
||
<div class="c-teaser__content">
|
||
<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/new-study-offers-hope-patients-suffering-rare-form-blindness">
|
||
New study offers hope for patients suffering from a rare form of blindness
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2018-10-31T11:19:45-04:00">October 31, 2018</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
A new form of therapy may halt or even reverse a form of progressive vision loss, spinocerebellar ataxia type 7 (SCA7). This new therapy has the potential to treat neurogenetic diseases effectively and with far fewer side effects than other medications.
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
||
<div class="c-sidebar-widget__list-item views-row">
|
||
<div class="field-content"><div class="c-teaser">
|
||
<div class="c-teaser__image">
|
||
|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/news/Cideciyan_pressrelease_v4.jpg?itok=QivVxNeK" width="200" height="200" alt="Illustration of icosahedral virus capsid, containing circular AAV vector. Arrows point from green and blue colored regions of the vector to shRNA and rhodopsin protein, respectively. " />
|
||
|
||
|
||
|
||
</div>
|
||
|
||
<div class="c-teaser__content">
|
||
<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/researchers-find-potential-new-gene-therapy-blinding-disease">
|
||
Researchers find potential new gene therapy for blinding disease
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2018-08-20T00:00:00-04:00">August 20, 2018</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
Scientists funded by the National Eye Institute (NEI) report a novel gene therapy that halts vision loss in a canine model of a blinding condition called autosomal dominant retinitis pigmentosa (adRP).
|
||
</div>
|
||
</div>
|
||
</div></div></div>
|
||
<div class="c-sidebar-widget__list-item views-row">
|
||
<div class="field-content"><div class="c-teaser">
|
||
<div class="c-teaser__image">
|
||
|
||
<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/news/KT_check_2018.jpg?itok=DJh7VYCY" width="200" height="200" alt="James Golladay and Aman George hold up grant award check" />
|
||
|
||
|
||
|
||
</div>
|
||
|
||
<div class="c-teaser__content">
|
||
<h2 class="c-teaser__header">
|
||
<a class="c-teaser__link" href="/about/news-and-events/news/knights-templar-eye-foundation-awards-research-grant-nei-scientist">
|
||
Knights Templar Eye Foundation awards research grant to NEI scientist
|
||
</a>
|
||
</h2>
|
||
<p class="c-teaser__date">
|
||
<time datetime="2018-06-21T00:00:00-04:00">June 21, 2018</time>
|
||
</p>
|
||
<div class="c-teaser__summary">
|
||
National Eye Institute (NEI) Postdoctoral Fellow Aman George, Ph.D., has received a $65,000 grant from the Knights Templar Eye Foundation to identify new drug treatments for vision impairment in children with a type of albinism.
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<img loading="lazy" src="/sites/default/files/styles/thumbnail/public/news/Fuchs.jpg?itok=2i7nft_v" width="200" height="200" alt="Corneal section from a person with Fuchs dystrophy shows the presence of ATP1B1 in the corneal endothelium." />
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NIH-funded team identifies genetic underpinnings of Fuchs dystrophy
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<time datetime="2017-03-30T00:00:00-04:00">March 30, 2017</time>
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|
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An international study of more than 5,417 people helps pinpoint the genetic risk factors associated with Fuchs endothelial corneal dystrophy, the most common disorder requiring corneal transplantation.
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NIH scientists identify disorder causing blindness, deafness, albinism and fragile bones
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Researchers at the National Eye Institute (NEI), part of the National Institutes of Health, have identified the genetic underpinnings of a rare disorder that causes children to be born with deafness, blindness, albinism and fragile bones.
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