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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells.
PLoS One. 2024 Jan 22;19(1):e0296928. doi: 10.1371/journal.pone.0296928. eCollection 2024.
PLoS One. 2024.
PMID: 38252645
Free PMC article.
Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish Patient.
Jatavallabhula K, Onyia O, Chung DD, Williams D, Wang K, Aldave AJ.
Jatavallabhula K, et al.
Cornea. 2024 Feb 1;43(2):253-256. doi: 10.1097/ICO.0000000000003399. Epub 2023 Oct 11.
Cornea. 2024.
PMID: 37823852
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Punctiform and Polychromatic Pre-Descemet Corneal Dystrophy: Clinical Evaluation and Identification of the Genetic Basis.
Alió Del Barrio JL, Chung DD, Al-Shymali O, Barrington A, Jatavallabhula K, Swamy VS, Yébana P, Angélica Henríquez-Recine M, Boto-de-Los-Bueis A, Alió JL, Aldave AJ.
Alió Del Barrio JL, et al. Among authors: jatavallabhula k.
Am J Ophthalmol. 2020 Apr;212:88-97. doi: 10.1016/j.ajo.2019.11.024. Epub 2019 Nov 27.
Am J Ophthalmol. 2020.
PMID: 31782998
Free PMC article.
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Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy.
Chung DD, Zhang W, Jatavallabhula K, Barrington A, Jung J, Aldave AJ.
Chung DD, et al. Among authors: jatavallabhula k.
Exp Eye Res. 2019 Nov;188:107696. doi: 10.1016/j.exer.2019.107696. Epub 2019 Jun 21.
Exp Eye Res. 2019.
PMID: 31233731
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