PubMed for id: 322978

Year	Number of Results
1978	1
1997	1
2001	1
2002	1
2003	1
2004	2
2005	2
2007	3
2008	2
2009	2
2010	5
2012	1
2013	5
2014	4
2015	4
2016	5
2017	4
2018	1
2019	5
2020	1
2021	2
2022	3
2024	0

1

Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation.

Fernández-Gutiérrez E, Fernández-Pérez P, Boto-De-Los-Bueis A, García-Fernández L, Rodríguez-Solana P, Solís M, Vallespín E. Fernández-Gutiérrez E, et al. Int J Mol Sci. 2022 Dec 22;24(1):209. doi: 10.3390/ijms24010209. Int J Mol Sci. 2022. PMID: 36613650 Free PMC article.

2

Update on the genetics of corneal endothelial dystrophies.

Kannabiran C, Chaurasia S, Ramappa M, Mootha VV. Kannabiran C, et al. Indian J Ophthalmol. 2022 Jul;70(7):2239-2248. doi: 10.4103/ijo.IJO_992_22. Indian J Ophthalmol. 2022. PMID: 35791103 Free PMC article. Review.

3

Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy.

Liskova P, Hafford-Tear NJ, Skalicka P, Malinka F, Jedlickova J, Ďuďáková Ľ, Pontikos N, Davidson AE, Tuft S. Liskova P, et al. Acta Ophthalmol. 2022 Nov;100(7):e1426-e1430. doi: 10.1111/aos.15114. Epub 2022 Feb 17. Acta Ophthalmol. 2022. PMID: 35174971 Free article.

4

Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles.

Dudakova L, Stranecky V, Piherova L, Palecek T, Pontikos N, Kmoch S, Skalicka P, Vaneckova M, Davidson AE, Liskova P. Dudakova L, et al. Genes (Basel). 2021 Apr 30;12(5):677. doi: 10.3390/genes12050677. Genes (Basel). 2021. PMID: 33946386 Free PMC article.

5

Expression and Function of ZEB1 in the Cornea.

Zhang Y, Liu X, Liang W, Dean DC, Zhang L, Liu Y. Zhang Y, et al. Cells. 2021 Apr 16;10(4):925. doi: 10.3390/cells10040925. Cells. 2021. PMID: 33923743 Free PMC article. Review.

6

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. Exp Eye Res. 2019 Nov;188:107696. doi: 10.1016/j.exer.2019.107696. Epub 2019 Jun 21. Exp Eye Res. 2019. PMID: 31233731

7

CUGC for posterior polymorphous corneal dystrophy (PPCD).

Davidson AE, Hafford-Tear NJ, Dudakova L, Sadan AN, Pontikos N, Hardcastle AJ, Tuft SJ, Liskova P. Davidson AE, et al. Eur J Hum Genet. 2020 Jan;28(1):126-131. doi: 10.1038/s41431-019-0448-8. Epub 2019 Jun 14. Eur J Hum Genet. 2020. PMID: 31201376 Free PMC article.

8

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing.

Frausto RF, Chung DD, Boere PM, Swamy VS, Duong HNV, Kao L, Azimov R, Zhang W, Carrigan L, Wong D, Morselli M, Zakharevich M, Hanser EM, Kassels AC, Kurtz I, Pellegrini M, Aldave AJ. Frausto RF, et al. PLoS One. 2019 Jun 13;14(6):e0218279. doi: 10.1371/journal.pone.0218279. eCollection 2019. PLoS One. 2019. PMID: 31194824 Free PMC article.

9

Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3.

Dudakova L, Skalicka P, Davidson AE, Liskova P. Dudakova L, et al. Cornea. 2019 Jun;38(6):758-760. doi: 10.1097/ICO.0000000000001930. Cornea. 2019. PMID: 30950897

10

The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.

Dudakova L, Evans CJ, Pontikos N, Hafford-Tear NJ, Malinka F, Skalicka P, Horinek A, Munier FL, Voide N, Studeny P, Vanikova L, Kubena T, Rojas Lopez KE, Davidson AE, Hardcastle AJ, Tuft SJ, Liskova P. Dudakova L, et al. Exp Eye Res. 2019 May;182:160-166. doi: 10.1016/j.exer.2019.03.002. Epub 2019 Mar 7. Exp Eye Res. 2019. PMID: 30851240

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