U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from MedGen

Items: 17

1.
Downregulation of collagen XI during late postnatal corneal development is followed by upregulation after injury
Mei Sun, Devon Cogswell, Sheila Adams, Yasmin Ayoubi, Ambuj Kumar, Tea Reljic, Marcel Y. Avila, Curtis E. Margo, Edgar M. Espana
J Cell Sci. 2022 Jan 1; 135(1): jcs258694. Published online 2022 Jan 12. doi: 10.1242/jcs.258694
PMCID:
PMC8767274
AbstractArticle
2.
Collagen V insufficiency in a mouse model for Ehlers Danlos-syndrome affects viscoelastic biomechanical properties explaining thin and brittle corneas
Sabine Kling, Emilio A. Torres-Netto, Hormoz Abdshahzadeh, Edgar M. Espana, Farhad Hafezi
Sci Rep. 2021; 11: 17362. Published online 2021 Aug 30. doi: 10.1038/s41598-021-96775-w
PMCID:
PMC8405695
AbstractArticlePDF–1.8M
3.
Morphometric analysis of cornea in the Slc39a13/Zip13-knockout mice
Takuya HIROSE, Ippei SUZUKI, Naoki TAKAHASHI, Toshiyuki FUKADA, Prasarn TANGKAWATTANA, Kazushige TAKEHANA
J Vet Med Sci. 2018 May; 80(5): 814–818. Published online 2018 Mar 22. doi: 10.1292/jvms.18-0019
PMCID:
PMC5989028
AbstractArticlePDF–2.0M
4.
Region-specific differential corneal and scleral mRNA expressions of MMP2, TIMP2, and TGFB2 in highly myopic-astigmatic chicks
Lisa Yan-yan Xi, Shea Ping Yip, Sze Wan Shan, Jody Summers-Rada, Chea-su Kee
Sci Rep. 2017; 7: 11423. Published online 2017 Sep 12. doi: 10.1038/s41598-017-08765-6
PMCID:
PMC5595952
AbstractArticlePDF–2.4M
5.
Genomic strategies to understand causes of keratoconus
Justyna A. Karolak, Marzena Gajecka
Mol Genet Genomics. 2017; 292(2): 251–269. Published online 2016 Dec 28. doi: 10.1007/s00438-016-1283-z
PMCID:
PMC5357269
AbstractArticlePDF–1.3M
6.
New histopathologic and ultrastructural findings in Reis-Bücklers corneal dystrophy caused by the Arg124Leu mutation of TGFBI gene
Wen-Ya Qiu, Li-Bin Zheng, Fei Pan, Bei-Bei Wang, Yu-Feng Yao
BMC Ophthalmol. 2016; 16(1): 158. Published online 2016 Sep 2. doi: 10.1186/s12886-016-0325-y
PMCID:
PMC5010699
AbstractArticlePDF–3.3M
7.
Rap1 GTPase is required for mouse lens epithelial maintenance and morphogenesis
Rupalatha Maddala, Tharkika Nagendran, Richard A. Lang, Alexei Morozov, Ponugoti V. Rao
Dev Biol. Author manuscript; available in PMC 2016 Oct 1.
Published in final edited form as: Dev Biol. 2015 Oct 1; 406(1): 74–91. Published online 2015 Jul 23. doi: 10.1016/j.ydbio.2015.06.022
PMCID:
PMC4587029
AbstractArticlePDF–1.6M
8.
Impact of Facial Conformation on Canine Health: Corneal Ulceration
Rowena M. A. Packer, Anke Hendricks, Charlotte C. Burn
PLoS One. 2015; 10(5): e0123827. Published online 2015 May 13. doi: 10.1371/journal.pone.0123827
PMCID:
PMC4430292
AbstractArticlePDF–1.5M
9.
The Role of crumbs Genes in the Vertebrate Cornea
Jill Beyer, Xinping C. Zhao, Richard Yee, Shagufta Khaliq, Timothy T. McMahon, Hongyu Ying, Beatrice Y. J. T. Yue, Jarema J. Malicki
Invest Ophthalmol Vis Sci. 2010 Sep; 51(9): 4549–4556. doi: 10.1167/iovs.09-4549
PMCID:
PMC2941173
AbstractArticlePDF–2.2M
10.
Ocular manifestations of branchio-oculo-facial syndrome: Report of a novel mutation and review of the literature
M.S. Al-Dosari, M. Almazyad, L. Al-Ebdi, J.Y. Mohamed, Saad Al-Dahmash, Hassan Al-Dhibi, Eman Al-Kahtani, Shahira Al-Turkmani, Hisham Alkuraya, B.D. Hall, F.S. Alkuraya
Mol Vis. 2010; 16: 813–818. Published online 2010 May 8.
PMCID:
PMC2866573
AbstractArticlePDF–902K
11.
Corneal dystrophies
Gordon K Klintworth
Orphanet J Rare Dis. 2009; 4: 7. Published online 2009 Feb 23. doi: 10.1186/1750-1172-4-7
PMCID:
PMC2695576
AbstractArticlePDF–16M
12.
IMMUNOHISTOCHEMISTRY AND ELECTRON MICROSCOPY OF EARLY-ONSET FUCHS CORNEAL DYSTROPHY IN THREE CASES WITH THE SAME L450W COL8A2 MUTATION
Cheng Zhang, W. Robert Bell, Olof H. Sundin, Zenaida De La Cruz, Walter J. Stark, W. Richard Green, John D. Gottsch
Trans Am Ophthalmol Soc. 2006 Dec; 104: 85–97.
PMCID:
PMC1809915
AbstractArticlePDF–1.6M
13.
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
K Kjaer, L Hansen, G Schwabe, A Marques-de-Faria, H Eiberg, S Mundlos, N Tommerup, T Rosenberg
J Med Genet. 2005 Apr; 42(4): 292–298. doi: 10.1136/jmg.2004.027821
PMCID:
PMC1736041
SummaryPDF–507K
14.
Severe Defects in Proliferation and Differentiation of Lens Cells in Foxe3 Null Mice
Olga Medina-Martinez, Isaac Brownell, Felipe Amaya-Manzanares, Qiyong Hu, Richard R. Behringer, Milan Jamrich
Mol Cell Biol. 2005 Oct; 25(20): 8854–8863. doi: 10.1128/MCB.25.20.8854-8863.2005
PMCID:
PMC1265778
AbstractArticlePDF–1.6M
15.
Xeroderma pigmentosum and band-shaped nodular corneal dystrophy.
J Freedman
Br J Ophthalmol. 1977 Feb; 61(2): 96–100. doi: 10.1136/bjo.61.2.96
PMCID:
PMC1042889
SummaryPage BrowsePDF–2.6M
16.
Iris Malformation and Anterior Segment Dysgenesis in Mice and Humans With a Mutation in PI 3-Kinase
Marie H. Solheim, Allen C. Clermont, Jonathon N. Winnay, Erlend Hallstensen, Anders Molven, Pål R. Njølstad, Eyvind Rødahl, C. Ronald Kahn
Invest Ophthalmol Vis Sci. 2017 Jul; 58(7): 3100–3106. doi: 10.1167/iovs.16-21347
PMCID:
PMC5482242
AbstractArticlePDF–1.0M
17.
Rapid, Accurate, and Non-Invasive Measurement of Zebrafish Axial Length and Other Eye Dimensions Using SD-OCT Allows Longitudinal Analysis of Myopia and Emmetropization
Ross F. Collery, Kerry N. Veth, Adam M. Dubis, Joseph Carroll, Brian A. Link
PLoS One. 2014; 9(10): e110699. Published online 2014 Oct 21. doi: 10.1371/journal.pone.0110699
Correction in:
PLoS One. 2015; 10(3): e0119779.
PMCID:
PMC4205002
AbstractArticlePDF–1.4M

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center