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Select item 108029511.

Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

Doug D. Chung, Angela C. Chen, Charlene H. Choo, Wenlin Zhang, Dominic Williams, Christopher G. Griffis, Paul Bonezzi, Kavya Jatavallabhula, Alapakkam P. Sampath, Anthony J. Aldave

PLoS One. 2024; 19(1): e0296928. Published online 2024 Jan 22. doi: 10.1371/journal.pone.0296928

PMCID:: PMC10802951

Article PDF–3.6M

Select item 105990492.

12-year follow-up of the first endothelial keratoplasty without Descemet stripping in a 3-month newborn with Congenital Hereditary Endothelial Dystrophy (CHED)

Carlo Bellucci, Paolo Mora, Salvatore A. Tedesco, Stefano Gandolfi, Chiara Chierego, Roberto Bellucci

BMC Ophthalmol. 2023; 23: 433. Published online 2023 Oct 25. doi: 10.1186/s12886-023-03180-0

PMCID:: PMC10599049

Article PDF–1.7M

Select item 99564133.

Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma

Khazeema Yousaf, Sadaf Naz, Asma Mushtaq, Elizabeth Wohler, Nara Sobreira, Bo-Man Ho, Li-Jia Chen, Wai-Kit Chu, Rasheeda Bashir

Genes (Basel) 2023 Feb; 14(2): 310. Published online 2023 Jan 25. doi: 10.3390/genes14020310

PMCID:: PMC9956413

Article PDF–563K

Select item 79605594.

A Retrospective Study of Corneal Endothelial Dystrophy in Dogs (1991–2014)

Brian C. Leonard, Celine S. Kermanian, Sarah R. Michalak, Philip H. Kass, Steven R. Hollingsworth, Kathryn L. Good, David J. Maggs, Sara M. Thomasy

Cornea. Author manuscript; available in PMC 2021 May 1.

Published in final edited form as: Cornea. 2021 May 1; 40(5): 578–583. doi: 10.1097/ICO.0000000000002488

PMCID:: PMC7960559

Article PDF–676K

Select item 69004565.

Comparison of automated versus manual analysis of corneal endothelial cell density and morphology in normal and corneal endothelial dystrophy-affected dogs

Hidetaka Miyagi, Amelia A. Stanley, Tanvi J. Chokshi, Carina Y. Pasqualino, Alyssa L. Hoehn, Christopher J. Murphy, Sara M. Thomasy

Vet Ophthalmol. Author manuscript; available in PMC 2021 Jan 1.

Published in final edited form as: Vet Ophthalmol. 2020 Jan; 23(1): 44–51. Published online 2019 Jun 9. doi: 10.1111/vop.12682

PMCID:: PMC6900456

Article PDF–367K

Select item 66295006.

Imaging the Corneal Endothelium in Fuchs Corneal Endothelial Dystrophy

Stephan Ong Tone, Ula Jurkunas

Semin Ophthalmol. Author manuscript; available in PMC 2020 Jun 19.

Published in final edited form as: Semin Ophthalmol. 2019; 34(4): 340–346. Published online 2019 Jun 19. doi: 10.1080/08820538.2019.1632355

PMCID:: PMC6629500

Article PDF–472K

Select item 63893767.

R125H, W240S, C386R, and V507I SLC4A11 Mutations Associated with Corneal Endothelial Dystrophy Affect the Transporter Function but not Trafficking in PS120 cells

Shimin Li, Karmjot Singh Hundal, Xingjuan Chen, Moonjung Choi, Diego G. Ogando, Alexander G. Obukhov, Joseph A. Bonanno

Exp Eye Res. Author manuscript; available in PMC 2020 Mar 1.

Published in final edited form as: Exp Eye Res. 2019 Mar; 180: 86–91. Published online 2018 Dec 14. doi: 10.1016/j.exer.2018.12.003

PMCID:: PMC6389376

Article PDF–896K

Select item 45458548.

Descemet stripping automated endothelial keratoplasty in Fuchs’ corneal endothelial dystrophy: anterior segment optical coherence tomography and in vivo confocal microscopy analysis

Rita Mencucci, Eleonora Favuzza, Ruggero Tartaro, Massimo Busin, Gianni Virgili

BMC Ophthalmol. 2015; 15: 99. Published online 2015 Aug 8. doi: 10.1186/s12886-015-0096-x

PMCID:: PMC4545854

Article PDF–1011K

Select item 37293209.

Amyloid corneal deposition in corneal buttons of congenital hereditary endothelial dystrophy (CHED) – A clinical and histopathological case series

Abdulmajid Al-Shehah, Ali Al-Rajhi, Hind Alkatan

Saudi J Ophthalmol. 2010 Oct; 24(4): 111–118. Published online 2010 Oct 6. doi: 10.1016/j.sjopt.2010.06.001

PMCID:: PMC3729320

Article PDF–1.2M

Select item 351331910.

The Importance of the Interaction of CheD with CheC and the Chemoreceptors Compared to Its Enzymatic Activity during Chemotaxis in Bacillus subtilis

Wei Yuan, George D. Glekas, George M. Allen, Hanna E. Walukiewicz, Christopher V. Rao, George W. Ordal

PLoS One. 2012; 7(12): e50689. Published online 2012 Dec 3. doi: 10.1371/journal.pone.0050689

PMCID:: PMC3513319

Article PDF–522K

Select item 348097011.

Elucidation of the multiple roles of CheD in Bacillus subtilis chemotaxis

George D. Glekas, Matthew J. Plutz, Hanna E. Walukiewicz, George M. Allen, Christopher V. Rao, George W. Ordal

Mol Microbiol. Author manuscript; available in PMC 2013 Nov 1.

Published in final edited form as: Mol Microbiol. 2012 Nov; 86(3): 743–756. Published online 2012 Sep 20. doi: 10.1111/mmi.12015

PMCID:: PMC3480970

Article PDF–2.5M

Select item 313263312.

Functional Imaging of Pheochromocytoma with ⁶⁸Ga-DOTATOC and ⁶⁸C-HED in a Genetically Defined Rat Model of Multiple Endocrine Neoplasia

Matthias Miederer, Sara Molatore, Ilaria Marinoni, Aurel Perren, Christine Spitzweg, Sybille Reder, Hans-Jürgen Wester, Andreas K. Buck, Markus Schwaiger, Natalia S. Pellegata

Int J Mol Imaging. 2011; 2011: 175352. Published online 2011 Jun 8. doi: 10.1155/2011/175352

PMCID:: PMC3132633

Article PDF–1.9M

Select item 286320913.

SLC4A11 Prevents Osmotic Imbalance Leading to Corneal Endothelial Dystrophy, Deafness, and Polyuria

Nicole Gröger, Henning Fröhlich, Hannes Maier, Andrea Olbrich, Sawa Kostin, Thomas Braun, Thomas Boettger

J Biol Chem. 2010 May 7; 285(19): 14467–14474. Published online 2010 Feb 25. doi: 10.1074/jbc.M109.094680

PMCID:: PMC2863209

Article PDF–3.7M

Select item 259797914.

Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non‐syndromic corneal endothelial dystrophy

Julie Desir, Graciela Moya, Orit Reish, Nicole Van Regemorter, Hilde Deconinck, Karen L David, Françoise M Meire, Marc J Abramowicz

J Med Genet. 2007 May; 44(5): 322–326. Published online 2007 Jan 12. doi: 10.1136/jmg.2006.046904

PMCID:: PMC2597979

Article PDF–593K

Select item 259791415.

Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

Xiaodong Jiao, Afia Sultana, Prashant Garg, Balasubramanya Ramamurthy, Geeta K Vemuganti, Nibaran Gangopadhyay, J Fielding Hejtmancik, Chitra Kannabiran

J Med Genet. 2007 Jan; 44(1): 64–68. Published online 2006 Jul 6. doi: 10.1136/jmg.2006.044644