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Items: 1 to 20 of 33

1.
Dual role of GRHL3 in bladder carcinogenesis depending on histological subtypes
Franziska C. Lammert, Julia Pannhausen, Erik Noetzel, Florian Friedland, Julia Wirtz, Yannick Herfs, Sophie Leypold, Lin Gan, Ralf Weiskirchen, Tician Schnitzler, Ruth Knüchel, Jochen Maurer, Danny D. Jonigk, Michael Rose, Nadine T. Gaisa
Mol Oncol. 2024 Jun; 18(6): 1397–1416. Published online 2024 Mar 2. doi: 10.1002/1878-0261.13623
PMCID:
PMC11164254
AbstractArticlePDF–7.3M
2.
Novel GRHL3 variants in a South African cohort with cleft lip palate
Thirona Naicker, Chinyere Adeleke, Azeez Alade, Peter A. Mossey, Waheed A. Awotoye, Tamara Busch, Mary Li, Joy Olotu, Lord J. J. Gowans, Colleen Aldous, Azeez Butali
Cleft Palate Craniofac J. Author manuscript; available in PMC 2023 Sep 1.
Published in final edited form as: Cleft Palate Craniofac J. 2022 Sep; 59(9): 1125–1130. Published online 2021 Aug 30. doi: 10.1177/10556656211038453
PMCID:
PMC9790085
AbstractArticlePDF–372K
3.
GRHL3 Promotes Tumor Growth and Metastasis via the MEK Pathway in Colorectal Cancer
Lin Tan, Weiming Qu, Dajun Wu, Minji Liu, Qian Wang, Qiongjia Ai, Hongsai Hu, Min Chen, Weishun Chen, Hongbing Zhou
Anal Cell Pathol (Amst) 2021; 2021: 6004821. Published online 2021 Nov 30. doi: 10.1155/2021/6004821
PMCID:
PMC8651427
AbstractArticlePDF–2.1M
4.
Grainyhead-Like 3 Influences Migration and Invasion of Urothelial Carcinoma Cells
Felix Wezel, Johannes Lustig, Anca Azoitei, Junnan Liu, Sabine Meessen, Gregoire Najjar, Viktor Zehe, Philipp Faustmann, Friedemann Zengerling, Axel John, Thomas Martini, Christian Bolenz, Cagatay Günes
Int J Mol Sci. 2021 Mar; 22(6): 2959. Published online 2021 Mar 15. doi: 10.3390/ijms22062959
PMCID:
PMC8000182
AbstractArticlePDF–4.0M
5.
Hypomethylation of GRHL3 gene is associated with the occurrence of neural tube defects
Tian Tian, Linlin Wang, Yan Shen, Bo Zhang, Richard H Finnell, Aiguo Ren
Epigenomics. 2018 Jul; 10(7): 891–901. Published online 2018 Mar 28. doi: 10.2217/epi-2018-0016
PMCID:
PMC6077761
AbstractArticlePDF–4.8M
6.
GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
Rachel Herndon Klein, Ziguang Lin, Amelia Soto Hopkin, William Gordon, Lam C. Tsoi, Yun Liang, Johann E. Gudjonsson, Bogi Andersen
PLoS Genet. 2017 Apr; 13(4): e1006745. Published online 2017 Apr 26. doi: 10.1371/journal.pgen.1006745
PMCID:
PMC5425218
AbstractArticlePDF–22M
7.
Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population
Miao He, Zhuan Bian
PLoS One. 2016; 11(7): e0159940. Published online 2016 Jul 26. doi: 10.1371/journal.pone.0159940
PMCID:
PMC4961390
AbstractArticlePDF–178K
8.
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
Elisabeth Mangold, Anne C. Böhmer, Nina Ishorst, Ann-Kathrin Hoebel, Pinar Gültepe, Hannah Schuenke, Johanna Klamt, Andrea Hofmann, Lina Gölz, Ruth Raff, Peter Tessmann, Stefanie Nowak, Heiko Reutter, Alexander Hemprich, Thomas Kreusch, Franz-Josef Kramer, Bert Braumann, Rudolf Reich, Gül Schmidt, Andreas Jäger, Rudolf Reiter, Sibylle Brosch, Janis Stavusis, Miho Ishida, Rimante Seselgyte, Gudrun E. Moore, Markus M. Nöthen, Guntram Borck, Khalid A. Aldhorae, Baiba Lace, Philip Stanier, Michael Knapp, Kerstin U. Ludwig
Am J Hum Genet. 2016 Apr 7; 98(4): 755–762. Published online 2016 Mar 24. doi: 10.1016/j.ajhg.2016.02.013
PMCID:
PMC4833214
AbstractArticlePDF–447K
9.
The functional GRHL3-filaggrin axis maintains a tumor differentiation potential and influences drug sensitivity
Yuchen Bai, Zixuan Zhao, Jarryd Boath, Bryce J. van Denderen, Charbel Darido
Mol Ther. 2021 Aug 4; 29(8): 2571–2582. Published online 2021 Mar 26. doi: 10.1016/j.ymthe.2021.03.016
PMCID:
PMC8353142
AbstractArticlePDF–2.9M
10.
Grhl3 induces human epithelial tumor cell migration and invasion via downregulation of E-cadherin
Pan Zhao, Sijia Guo, Zhenzhen Tu, Lijun Di, Xiaojun Zha, Haisheng Zhou, Xuejun Zhang
Acta Biochim Biophys Sin (Shanghai) 2016 Mar; 48(3): 266–274. Published online 2016 Feb 1. doi: 10.1093/abbs/gmw001
PMCID:
PMC4885135
AbstractArticlePDF–629K
11.
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22
Lara Slavec, Ksenija Geršak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
Int J Mol Sci. 2023 Mar; 24(5): 4262. Published online 2023 Feb 21. doi: 10.3390/ijms24054262
PMCID:
PMC10002089
AbstractArticlePDF–1.5M
12.
Coordinated expression and genetic polymorphisms in Grainyhead-like genes in human non-melanoma skin cancers
Agnieszka Kikulska, Tobias Rausch, Ewa Krzywinska, Magdalena Pawlak, Bartek Wilczynski, Vladimir Benes, Piotr Rutkowski, Tomasz Wilanowski
BMC Cancer. 2018; 18: 23. Published online 2018 Jan 4. doi: 10.1186/s12885-017-3943-8
PMCID:
PMC5755140
AbstractArticlePDF–806K
13.
Recent discoveries concerning the involvement of transcription factors from the Grainyhead-like family in cancer
Michal Mlacki, Agnieszka Kikulska, Ewa Krzywinska, Magdalena Pawlak, Tomasz Wilanowski
Exp Biol Med (Maywood) 2015 Nov; 240(11): 1396–1401. doi: 10.1177/1535370215588924
PMCID:
PMC4935299
AbstractArticlePDF–86K
14.
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J. Leslie, Huan Liu, Jenna C. Carlson, John R. Shaffer, Eleanor Feingold, George Wehby, Cecelia A. Laurie, Deepti Jain, Cathy C. Laurie, Kimberly F. Doheny, Toby McHenry, Judith Resick, Carla Sanchez, Jennifer Jacobs, Beth Emanuele, Alexandre R. Vieira, Katherine Neiswanger, Jennifer Standley, Andrew E. Czeizel, Frederic Deleyiannis, Kaare Christensen, Ronald G. Munger, Rolv T. Lie, Allen Wilcox, Paul A. Romitti, L. Leigh Field, Carmencita D. Padilla, Eva Maria C. Cutiongco-de la Paz, Andrew C. Lidral, Luz Consuelo Valencia-Ramirez, Ana Maria Lopez-Palacio, Dora Rivera Valencia, Mauricio Arcos-Burgos, Eduardo E. Castilla, Juan C. Mereb, Fernando A. Poletta, Iêda M. Orioli, Flavia M. Carvalho, Jacqueline T. Hecht, Susan H. Blanton, Carmen J. Buxó, Azeez Butali, Peter A. Mossey, Wasiu L. Adeyemo, Olutayo James, Ramat O. Braimah, Babatunde S. Aregbesola, Mekonen A. Eshete, Milliard Deribew, Mine Koruyucu, Figen Seymen, Lian Ma, Javier Enríquez de Salamanca, Seth M. Weinberg, Lina Moreno, Robert A. Cornell, Jeffrey C. Murray, Mary L. Marazita
Am J Hum Genet. 2016 Apr 7; 98(4): 744–754. Published online 2016 Mar 24. doi: 10.1016/j.ajhg.2016.02.014
PMCID:
PMC4833215
AbstractArticlePDF–1023K
15.
GRHL3/GET1 and Trithorax Group Members Collaborate to Activate the Epidermal Progenitor Differentiation Program
Amelia Soto Hopkin, William Gordon, Rachel Herndon Klein, Francisco Espitia, Kenneth Daily, Michael Zeller, Pierre Baldi, Bogi Andersen
PLoS Genet. 2012 Jul; 8(7): e1002829. Published online 2012 Jul 19. doi: 10.1371/journal.pgen.1002829
PMCID:
PMC3400561
AbstractArticlePDF–943K
16.
The identification and characterization of human Sister-of-Mammalian Grainyhead (SOM) expands the grainyhead-like family of developmental transcription factors.
Stephen B Ting, Tomasz Wilanowski, Loretta Cerruti, Lin-Lin Zhao, John M Cunningham, Stephen M Jane
Biochem J. 2003 Mar 15; 370(Pt 3): 953–962. doi: 10.1042/BJ20021476
PMCID:
PMC1223248
SummaryPDF–437K
17.
Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis
Lara Slavec, Nataša Karas Kuželički, Igor Locatelli, Ksenija Geršak
Sci Rep. 2022; 12: 1214. Published online 2022 Jan 24. doi: 10.1038/s41598-021-02159-5
PMCID:
PMC8786890
AbstractArticlePDF–1.9M
18.
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate
M.A. Eshete, H. Liu, M. Li, W.L. Adeyemo, L.J.J Gowans, P.A. Mossey, T. Busch, W. Deressa, P. Donkor, P.B. Olaitan, B.S. Aregbesola, R.O. Braimah, G.O. Oseni, F. Oginni, R. Audu, C. Onwuamah, O. James, E. Augustine-Akpan, L.A. Rahman, M.O. Ogunlewe, F.K.N. Arthur, S.A. Bello, P. Agbenorku, P. Twumasi, F. Abate, T. Hailu, Y. Demissie, A. Hailu, G. Plange-Rhule, S. Obiri-Yeboah, M.M. Dunnwald, P.E. Gravem, M.L. Marazita, A.A. Adeyemo, J.C. Murray, R.A. Cornell, A. Butali
J Dent Res. 2018 Jan; 97(1): 41–48. Published online 2017 Sep 8. doi: 10.1177/0022034517729819
PMCID:
PMC5755809
AbstractArticlePDF–956K
19.
Loss of GRHL3 leads to TARC/CCL17-mediated keratinocyte proliferation in the epidermis
Stephen J. Goldie, Denny L. Cottle, Fiona H. Tan, Suraya Roslan, Seema Srivastava, Rhys Brady, Darren D. Partridge, Alana Auden, Ian M. Smyth, Stephen M. Jane, Sebastian Dworkin, Charbel Darido
Cell Death Dis. 2018 Nov; 9(11): 1072. Published online 2018 Oct 19. doi: 10.1038/s41419-018-0901-6
PMCID:
PMC6195598
AbstractArticlePDF–22M
20.
Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
Myriam Peyrard-Janvid, Elizabeth J. Leslie, Youssef A. Kousa, Tiffany L. Smith, Martine Dunnwald, Måns Magnusson, Brian A. Lentz, Per Unneberg, Ingegerd Fransson, Hannele K. Koillinen, Jorma Rautio, Marie Pegelow, Agneta Karsten, Lina Basel-Vanagaite, William Gordon, Bogi Andersen, Thomas Svensson, Jeffrey C. Murray, Robert A. Cornell, Juha Kere, Brian C. Schutte
Am J Hum Genet. 2014 Jan 2; 94(1): 23–32. doi: 10.1016/j.ajhg.2013.11.009
PMCID:
PMC3882735
AbstractArticlePDF–3.4M

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