corneal disease

Literature (7)

Literature for DOID 10124: corneal disease

Xenbase Articles Publications associated with this Disease Ontology entry or its descendants

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The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F,Hu W,Xian J,Ohnuma S,Brenton JD, Dev Biol. July 1, 2013; 379(1):1095-564X.
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL,Loganathan SK,Liu J,Riau AK,Young JD,Mehta JS,Vithana EN,Casey JR, Hum Mol Genet. November 15, 2013; 22(22):1460-2083.
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model., Pfirrmann T,Emmerich D,Ruokonen P,Quandt D,Buchen R,Fischer-Zirnsak B,Hecht J,Krawitz P,Meyer P,Klopocki E,Stricker S,Lausch E,Seliger B,Hollemann T,Reinhard T,Auw-Haedrich C,Zabel B,Hoffmann K,Villavicencio-Lorini P, Hum Mol Genet. June 1, 2015; 24(11):1460-2083.
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies., Loganathan SK,Schneider HP,Morgan PE,Deitmer JW,Casey JR, Am J Physiol Cell Physiol. November 1, 2016; 311(5):1522-1563.
Polymorphism of the LIG3 gene in keratoconus and Fuchs endothelial corneal dystrophy., Synowiec E,Wojcik KA,Izdebska J,Binczyk E,Szaflik J,Blasiak J,Szaflik JP, Cell Mol Biol (Noisy-le-grand). March 28, 2015; 61(1):0145-5680.
Understanding cornea homeostasis and wound healing using a novel model of stem cell deficiency in Xenopus., Adil MT,Simons CM,Sonam S,Henry JJ, Exp Eye Res. October 1, 2019; 187:0014-4835.
pH dependence of the Slc4a11-mediated H+ conductance is influenced by intracellular lysine residues and modified by disease-linked mutations., Quade BN,Marshall A,Parker MD, Am J Physiol Cell Physiol. August 1, 2020; 319(2):1522-1563.

The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F,Hu W,Xian J,Ohnuma S,Brenton JD, Dev Biol. July 1, 2013; 379(1):1095-564X.

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL,Loganathan SK,Liu J,Riau AK,Young JD,Mehta JS,Vithana EN,Casey JR, Hum Mol Genet. November 15, 2013; 22(22):1460-2083.

Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model., Pfirrmann T,Emmerich D,Ruokonen P,Quandt D,Buchen R,Fischer-Zirnsak B,Hecht J,Krawitz P,Meyer P,Klopocki E,Stricker S,Lausch E,Seliger B,Hollemann T,Reinhard T,Auw-Haedrich C,Zabel B,Hoffmann K,Villavicencio-Lorini P, Hum Mol Genet. June 1, 2015; 24(11):1460-2083.

Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies., Loganathan SK,Schneider HP,Morgan PE,Deitmer JW,Casey JR, Am J Physiol Cell Physiol. November 1, 2016; 311(5):1522-1563.

Polymorphism of the LIG3 gene in keratoconus and Fuchs endothelial corneal dystrophy., Synowiec E,Wojcik KA,Izdebska J,Binczyk E,Szaflik J,Blasiak J,Szaflik JP, Cell Mol Biol (Noisy-le-grand). March 28, 2015; 61(1):0145-5680.

Understanding cornea homeostasis and wound healing using a novel model of stem cell deficiency in Xenopus., Adil MT,Simons CM,Sonam S,Henry JJ, Exp Eye Res. October 1, 2019; 187:0014-4835.

pH dependence of the Slc4a11-mediated H+ conductance is influenced by intracellular lysine residues and modified by disease-linked mutations., Quade BN,Marshall A,Parker MD, Am J Physiol Cell Physiol. August 1, 2020; 319(2):1522-1563.