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Select item 108221911.

Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia

Yiting Liu, Jing Sun, Caiqi Zhang, Yi Wu, Siyuan Ma, Xuechun Li, Xiaoshan Wu, Qingping Gao

BMC Oral Health. 2024; 24: 136. Published online 2024 Jan 27. doi: 10.1186/s12903-024-03888-5

PMCID:: PMC10822191

Article PDF–5.4M

Select item 98752792.

Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites

Piranit Kantaputra, Peeranat Jatooratthawichot, Oranuch Tantachamroon, Kamonporn Nanekrungsan, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, James R. Ketudat Cairns

Int Dent J. 2023 Feb; 73(1): 79–86. Published online 2022 May 7. doi: 10.1016/j.identj.2022.04.006

PMCID:: PMC9875279

Article PDF–1.7M

Select item 81320003.

Transcriptomic and Immunohistochemical Analysis of Progressive Keratoconus Reveal Altered WNT10A in Epithelium and Bowman's Layer

James W. Foster, Rupin N. Parikh, Jiangxia Wang, Kraig S. Bower, Mario Matthaei, Shukti Chakravarti, Albert S. Jun, Charles G. Eberhart, Uri S. Soiberman

Invest Ophthalmol Vis Sci. 2021 May; 62(6): 16. Published online 2021 May 14. doi: 10.1167/iovs.62.6.16

PMCID:: PMC8132000

Article PDF–2.8M

Select item 51597584.

The association between WNT10A variants and dental development in patients with isolated oligodontia

Brunilda Dhamo, Willem Fennis, Marijn Créton, Strahinja Vucic, Marco Cune, Hans Kristian Ploos van Amstel, Eppo B Wolvius, Marie-José van den Boogaard, Edwin M Ongkosuwito

Eur J Hum Genet. 2017 Jan; 25(1): 59–65. Published online 2016 Sep 21. doi: 10.1038/ejhg.2016.117

PMCID:: PMC5159758

Article PDF–285K

Select item 51221545.

Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency

Birgitta Bergendal, Johanna Norderyd, Xiaolei Zhou, Joakim Klar, Niklas Dahl

BMC Med Genet. 2016; 17: 88. Published online 2016 Nov 24. doi: 10.1186/s12881-016-0349-4

PMCID:: PMC5122154

Article PDF–1.4M

Select item 41671666.

The WNT10A gene in Ectodermal Dysplasias and Selective Tooth Agenesis

Gabriele Mues, John Bonds, Lilin Xiang, Alexandre R. Vieira, Figen Seymen, Ophir Klein, Rena N. D’Souza

Am J Med Genet A. Author manuscript; available in PMC 2015 Oct 1.

Published in final edited form as: Am J Med Genet A. 2014 Oct; 164(10): 2455–2460. Published online 2014 Apr 3. doi: 10.1002/ajmg.a.36520

PMCID:: PMC4167166

Article PDF–624K

Select item 41084337.

Role of WNT10A-Expressing Kidney Fibroblasts in Acute Interstitial Nephritis

Akihiro Kuma, Sohsuke Yamada, Ke-Yong Wang, Noriaki Kitamura, Takahiro Yamaguchi, Yoshiko Iwai, Hiroto Izumi, Masahito Tamura, Yutaka Otsuji, Kimitoshi Kohno

PLoS One. 2014; 9(7): e103240. Published online 2014 Jul 23. doi: 10.1371/journal.pone.0103240

PMCID:: PMC4108433

Article PDF–10M

Select item 29870168.

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

Sadia Nawaz, Joakim Klar, Muhammad Wajid, Muhammad Aslam, Muhammad Tariq, Jens Schuster, Shahid Mahmood Baig, Niklas Dahl

Eur J Hum Genet. 2009 Dec; 17(12): 1600–1605. Published online 2009 May 27. doi: 10.1038/ejhg.2009.81

PMCID:: PMC2987016

Article PDF–306K

Select item 104203459.

The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients

Iago Ramirez, Christian Kirschneck, Alice Corrêa Silva-Sousa, Peter Proff, Leonardo S. Antunes, Marilisa C. L. Gabbardo, Daniela Silva Barroso de Oliveira, Manoel D. Sousa-Neto, Flares Baratto-Filho, Erika C. Küchler

PLoS One. 2023; 18(8): e0288782. Published online 2023 Aug 11. doi: 10.1371/journal.pone.0288782

PMCID:: PMC10420345

Article PDF–951K

Select item 449814810.

WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma

Apple Long, Véronique Giroux, Kelly A. Whelan, Kathryn E. Hamilton, Marie-Pier Tétreault, Koji Tanaka, Ju-Seog Lee, Andres J. Klein-Szanto, Hiroshi Nakagawa, Anil K. Rustgi

Carcinogenesis. 2015 May; 36(5): 598–606. Published online 2015 Mar 20. doi: 10.1093/carcin/bgv025

PMCID:: PMC4498148

Article PDF–3.8M

Select item 442979011.

Polymorphisms in WNT6 and WNT10A and Colorectal Adenoma Risk

Rachel L. Galbraith, Elizabeth M. Poole, David Duggan, Jill Muehling, Li Hsu, Karen Makar, Liren Xiao, John D. Potter, Cornelia M. Ulrich

Nutr Cancer. Author manuscript; available in PMC 2015 May 13.

Published in final edited form as: Nutr Cancer. 2011; 63(4): 558–564. doi: 10.1080/01635581.2011.542539

PMCID:: PMC4429790

Article PDF–224K

Select item 384238512.

Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese Population

Huiying He, Dong Han, Hailan Feng, Hong Qu, Shujuan Song, Baojing Bai, Zhenting Zhang

PLoS One. 2013; 8(11): e80393. Published online 2013 Nov 27. doi: 10.1371/journal.pone.0080393

PMCID:: PMC3842385

Article PDF–8.4M

Select item 347711713.

WNT10A Plays an Oncogenic Role in Renal Cell Carcinoma by Activating WNT/β-catenin Pathway

Ren-Jun Hsu, Jar-Yi Ho, Tai-Lung Cha, Dah-Shyong Yu, Chieh-Lin Wu, Wei-Ping Huang, Pauling Chu, Ying-Hsin Chen, Jiann-Torng Chen, Cheng-Ping Yu

PLoS One. 2012; 7(10): e47649. Published online 2012 Oct 19. doi: 10.1371/journal.pone.0047649

PMCID:: PMC3477117

Article PDF–1.5M

Select item 300972814.

Circadian Disruption Accelerates Tumor Growth and Angio/Stromagenesis through a Wnt Signaling Pathway

Yoshihiro Yasuniwa, Hiroto Izumi, Ke-Yong Wang, Shohei Shimajiri, Yasuyuki Sasaguri, Kazuaki Kawai, Hiroshi Kasai, Takashi Shimada, Koichi Miyake, Eiji Kashiwagi, Gen Hirano, Akihiko Kidani, Masaki Akiyama, Bin Han, Ying Wu, Ichiro Ieiri, Shun Higuchi, Kimitoshi Kohno

PLoS One. 2010; 5(12): e15330. Published online 2010 Dec 23. doi: 10.1371/journal.pone.0015330

PMCID:: PMC3009728

Article PDF–1.0M

Select item 270696215.

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

Axel Bohring, Thomas Stamm, Christiane Spaich, Claudia Haase, Kerstin Spree, Ute Hehr, Mandy Hoffmann, Susanne Ledig, Saadettin Sel, Peter Wieacker, Albrecht Röpke

Am J Hum Genet. 2009 Jul 10; 85(1): 97–105. doi: 10.1016/j.ajhg.2009.06.001

PMCID:: PMC2706962

Article PDF–451K

Select item 686226916.

Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations

Asia Parveen, Sher Alam Khan, Muhammad Usman Mirza, Hina Bashir, Fatima Arshad, Maria Iqbal, Waseem Ahmad, Ahsan Wahab, Amal Fiaz, Sidra Naz, Fareeha Ashraf, Tayyaba Mobeen, Salman Aziz, Syed Shoaib Ahmed, Noor Muhammad, Nehal F. Hassib, Mostafa I. Mostafa, Nagwa E. Gaboon, Roquyya Gul, Saadullah Khan, Matheus Froeyen, Muhammad Shoaib, Naveed Wasif

Int J Mol Sci. 2019 Nov; 20(21): 5282. Published online 2019 Oct 24. doi: 10.3390/ijms20215282

PMCID:: PMC6862269

Article PDF–3.1M

Select item 616567317.

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

Renqian Du, Nuriye Dinckan, Xiaofei Song, Zeynep Coban-Akdemir, Shalini N. Jhangiani, Yeliz Guven, Oya Aktoren, Hulya Kayserili, Lauren E. Petty, Donna M. Muzny, Jennifer E. Below, Eric Boerwinkle, Nan Wu, Richard A. Gibbs, Jennifer E. Posey, James R. Lupski, Ariadne Letra, Z. Oya Uyguner

Hum Genet. Author manuscript; available in PMC 2019 Sep 1.

Published in final edited form as: Hum Genet. 2018 Sep; 137(9): 689–703. Published online 2018 Jul 26. doi: 10.1007/s00439-018-1907-y

PMCID:: PMC6165673

Article PDF–942K

Select item 689219318.

EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population

María Carmen Martínez-Romero, María Juliana Ballesta-Martínez, Vanesa López-González, María José Sánchez-Soler, Ana Teresa Serrano-Antón, María Barreda-Sánchez, Lidya Rodriguez-Peña, María Teresa Martínez-Menchon, José Frías-Iniesta, Paloma Sánchez-Pedreño, Pablo Carbonell-Meseguer, Guillermo Glover-López, Encarna Guillén-Navarro, GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia)

Orphanet J Rare Dis. 2019; 14: 281. Published online 2019 Dec 3. doi: 10.1186/s13023-019-1251-x

PMCID:: PMC6892193

Article PDF–577K

Select item 197394419.

Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia

Lynn Adaimy, Eliane Chouery, Hala Mégarbané, Salman Mroueh, Valérie Delague, Elsa Nicolas, Hanen Belguith, Philippe de Mazancourt, André Mégarbané

Am J Hum Genet. 2007 Oct; 81(4): 821–828. Published online 2007 Aug 9. doi: 10.1086/520064

PMCID:: PMC1973944

Article PDF–391K

Select item 277582320.

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Sarah E. Medland, Dale R. Nyholt, Jodie N. Painter, Brian P. McEvoy, Allan F. McRae, Gu Zhu, Scott D. Gordon, Manuel A.R. Ferreira, Margaret J. Wright, Anjali K. Henders, Megan J. Campbell, David L. Duffy, Narelle K. Hansell, Stuart Macgregor, Wendy S. Slutske, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin

Am J Hum Genet. 2009 Nov 13; 85(5): 750–755. doi: 10.1016/j.ajhg.2009.10.009

PMCID:: PMC2775823

Article PDF–317K

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