PubMed for id: 256764

Year	Number of Results
1993	1
1996	1
2002	1
2003	1
2004	2
2005	1
2006	1
2009	2
2010	7
2011	6
2012	3
2014	1
2016	1
2018	1
2019	3
2021	2
2022	2
2023	1
2024	0

1

WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis.

Zhang H, Koruyucu M, Seymen F, Kasimoglu Y, Kim JW, Tinawi S, Zhang C, Jacquemont ML, Vieira AR, Simmer JP, Hu JCC. Zhang H, et al. J Dent Res. 2019 May;98(5):541-548. doi: 10.1177/0022034518824571. Epub 2019 Feb 19. J Dent Res. 2019. PMID: 30779877 Free PMC article.

2

Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations.

Rungroj N, Nettuwakul C, Sawasdee N, Sangnual S, Deejai N, Misgar RA, Pasena A, Khositseth S, Kirdpon S, Sritippayawan S, Vasuvattakul S, Yenchitsomanus PT. Rungroj N, et al. Clin Genet. 2018 Nov;94(5):409-418. doi: 10.1111/cge.13418. Epub 2018 Aug 9. Clin Genet. 2018. PMID: 30028003

3

Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool.

Hentschel J, Tatun D, Parkhomchuk D, Kurth I, Schimmel B, Heinrich-Weltzien R, Bertzbach S, Peters H, Beetz C. Hentschel J, et al. Gene. 2016 Sep 15;590(1):1-4. doi: 10.1016/j.gene.2016.05.040. Epub 2016 May 31. Gene. 2016. PMID: 27259663

4

A Novel Homozygous WDR72 Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature.

Kuechler A, Hentschel J, Kurth I, Stephan B, Prott EC, Schweiger B, Schuster A, Wieczorek D, Lüdecke HJ. Kuechler A, et al. Mol Syndromol. 2012 Nov;3(5):223-9. doi: 10.1159/000343746. Epub 2012 Oct 19. Mol Syndromol. 2012. PMID: 23293580 Free PMC article.

5

Target gene analyses of 39 amelogenesis imperfecta kindreds.

Chan HC, Estrella NM, Milkovich RN, Kim JW, Simmer JP, Hu JC. Chan HC, et al. Eur J Oral Sci. 2011 Dec;119 Suppl 1(Suppl 1):311-23. doi: 10.1111/j.1600-0722.2011.00857.x. Eur J Oral Sci. 2011. PMID: 22243262 Free PMC article.

6

Amelogenesis imperfecta: genotype-phenotype studies in 71 families.

Wright JT, Torain M, Long K, Seow K, Crawford P, Aldred MJ, Hart PS, Hart TC. Wright JT, et al. Cells Tissues Organs. 2011;194(2-4):279-83. doi: 10.1159/000324339. Epub 2011 May 19. Cells Tissues Organs. 2011. PMID: 21597265 Free PMC article.

7

Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth.

El-Sayed W, Shore RC, Parry DA, Inglehearn CF, Mighell AJ. El-Sayed W, et al. Cells Tissues Organs. 2011;194(1):60-6. doi: 10.1159/000322036. Epub 2010 Dec 29. Cells Tissues Organs. 2011. PMID: 21196691 Free PMC article.

8

Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.

El-Sayed W, Parry DA, Shore RC, Ahmed M, Jafri H, Rashid Y, Al-Bahlani S, Al Harasi S, Kirkham J, Inglehearn CF, Mighell AJ. El-Sayed W, et al. Am J Hum Genet. 2009 Nov;85(5):699-705. doi: 10.1016/j.ajhg.2009.09.014. Epub 2009 Oct 22. Am J Hum Genet. 2009. PMID: 19853237 Free PMC article.

9

Identification of the C-terminal region in Amelogenesis Imperfecta causative protein WDR72 required for Golgi localization.

Husein D, Alamoudi A, Ohyama Y, Mochida H, Ritter B, Mochida Y. Husein D, et al. Sci Rep. 2022 Mar 17;12(1):4640. doi: 10.1038/s41598-022-08719-7. Sci Rep. 2022. PMID: 35301423 Free PMC article.

10

Novel WDR72 mutation and cytoplasmic localization.

Lee SK, Seymen F, Lee KE, Kang HY, Yildirim M, Tuna EB, Gencay K, Hwang YH, Nam KH, De La Garza RJ, Hu JC, Simmer JP, Kim JW. Lee SK, et al. J Dent Res. 2010 Dec;89(12):1378-82. doi: 10.1177/0022034510382117. Epub 2010 Oct 11. J Dent Res. 2010. PMID: 20938048 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

31 results

Results by year