PubMed (OMIM) for id: 8626

Year	Number of Results
1968	1
1971	1
1972	1
1976	1
1981	1
1982	1
1985	1
1987	2
1988	2
1990	2
1991	2
1992	1
1993	2
1996	2
1997	1
1998	6
1999	4
2000	5
2001	3
2002	3
2003	6
2004	1
2005	4
2006	7
2007	3
2008	7
2009	9
2010	3
2011	3
2012	3
2013	1
2014	4
2015	3
2017	1
2018	2
2019	1
2020	1
2022	1
2023	1
2024	1

1

Editorial Expression of Concern: p63 and p73 are required for p53-dependent apoptosis in response to DNA damage.

Flores ER, Tsai KY, Crowley D, Sengupta S, Yang A, McKeon F, Jacks T. Flores ER, et al. Nature. 2024 Mar;627(8004):E10. doi: 10.1038/s41586-024-07223-4. Nature. 2024. PMID: 38418890 No abstract available.

2

TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosis.

Huang C, Zhao S, Yang Y, Guo T, Ke H, Mi X, Qin Y, Chen ZJ, Zhao S. Huang C, et al. J Clin Invest. 2023 Mar 1;133(5):e162315. doi: 10.1172/JCI162315. J Clin Invest. 2023. PMID: 36856110 Free PMC article.

3

Dominant TP63 missense variants lead to constitutive activation and premature ovarian insufficiency.

Tucker EJ, Gutfreund N, Belaud-Rotureau MA, Gilot D, Brun T, Kline BL, Bell KM, Domin-Bernhard M, Théard C, Touraine P, Robevska G, van van den Bergen J, Ayers KL, Sinclair AH, Dötsch V, Jaillard S. Tucker EJ, et al. Hum Mutat. 2022 Oct;43(10):1443-1453. doi: 10.1002/humu.24432. Epub 2022 Jul 29. Hum Mutat. 2022. PMID: 35801529 Free PMC article.

4

Novel phenotype of syndromic premature ovarian insufficiency associated with TP63 molecular defect.

Mathorne SW, Ravn P, Hansen D, Beck-Nielsen SS, Gjørup H, Sørensen KP, Fagerberg CR. Mathorne SW, et al. Clin Genet. 2020 May;97(5):779-784. doi: 10.1111/cge.13725. Epub 2020 Feb 24. Clin Genet. 2020. PMID: 32067224

5

TP63-truncating variants cause isolated premature ovarian insufficiency.

Tucker EJ, Jaillard S, Grover SR, van den Bergen J, Robevska G, Bell KM, Sadedin S, Hanna C, Dulon J, Touraine P, Sinclair AH. Tucker EJ, et al. Hum Mutat. 2019 Jul;40(7):886-892. doi: 10.1002/humu.23744. Epub 2019 Mar 29. Hum Mutat. 2019. PMID: 30924587

6

Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.

Basha M, Demeer B, Revencu N, Helaers R, Theys S, Bou Saba S, Boute O, Devauchelle B, Francois G, Bayet B, Vikkula M. Basha M, et al. J Med Genet. 2018 Jul;55(7):449-458. doi: 10.1136/jmedgenet-2017-105110. Epub 2018 Mar 2. J Med Genet. 2018. PMID: 29500247

7

Protein aggregation of the p63 transcription factor underlies severe skin fragility in AEC syndrome.

Russo C, Osterburg C, Sirico A, Antonini D, Ambrosio R, Würz JM, Rinnenthal J, Ferniani M, Kehrloesser S, Schäfer B, Güntert P, Sinha S, Dötsch V, Missero C. Russo C, et al. Proc Natl Acad Sci U S A. 2018 Jan 30;115(5):E906-E915. doi: 10.1073/pnas.1713773115. Epub 2018 Jan 16. Proc Natl Acad Sci U S A. 2018. PMID: 29339502 Free PMC article.

8

Genitourinary malformations: an under-recognized feature of ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome.

Hyder Z, Beale V, O'Connor R, Clayton-Smith J. Hyder Z, et al. Clin Dysmorphol. 2017 Apr;26(2):78-82. doi: 10.1097/MCD.0000000000000172. Clin Dysmorphol. 2017. PMID: 28166087

9

Lineage-negative progenitors mobilize to regenerate lung epithelium after major injury.

Vaughan AE, Brumwell AN, Xi Y, Gotts JE, Brownfield DG, Treutlein B, Tan K, Tan V, Liu FC, Looney MR, Matthay MA, Rock JR, Chapman HA. Vaughan AE, et al. Nature. 2015 Jan 29;517(7536):621-5. doi: 10.1038/nature14112. Epub 2014 Dec 24. Nature. 2015. PMID: 25533958 Free PMC article.

10

IAPP-driven metabolic reprogramming induces regression of p53-deficient tumours in vivo.

Venkatanarayan A, Raulji P, Norton W, Chakravarti D, Coarfa C, Su X, Sandur SK, Ramirez MS, Lee J, Kingsley CV, Sananikone EF, Rajapakshe K, Naff K, Parker-Thornburg J, Bankson JA, Tsai KY, Gunaratne PH, Flores ER. Venkatanarayan A, et al. Nature. 2015 Jan 29;517(7536):626-30. doi: 10.1038/nature13910. Epub 2014 Nov 17. Nature. 2015. PMID: 25409149 Free PMC article.

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