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There are 7678 results for: content related to: Differential PERP regulation by TP63 mutants provides insight into AEC pathogenesis

  1. You have free access to this content
    International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) Syndrome

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 1885–1893, Mary Fete, Hans vanBokhoven, Suzanne E. Clements, Frank McKeon, Dennis R. Roop, Maranke I. Koster, Caterina Missero, Laura D. Attardi, Vivian A. Lombillo, Edward Ratovitski, Meena Julapalli, Derek Ruths, Virginia P. Sybert, Elaine C. Siegfried and Alanna F. Bree

    Version of Record online : 7 APR 2009, DOI: 10.1002/ajmg.a.32761

  2. EEC- and ADULT-Associated TP63 Mutations Exhibit Functional Heterogeneity Toward P63 Responsive Sequences

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 894–904, Paola Monti, Debora Russo, Renata Bocciardi, Giorgia Foggetti, Paola Menichini, Maria T. Divizia, Margherita Lerone, Claudio Graziano, Anita Wischmeijer, Hector Viadiu, Roberto Ravazzolo, Alberto Inga and Gilberto Fronza

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22304

  3. You have full text access to this OnlineOpen article
    PERP, a host tetraspanning membrane protein, is required for Salmonella-induced inflammation

    Cellular Microbiology

    Volume 17, Issue 6, June 2015, Pages: 843–859, Kelly N. Hallstrom, C. V. Srikanth, Terence A. Agbor, Christopher M. Dumont, Kristen N. Peters, Luminita Paraoan, James E. Casanova, Erik J. Boll and Beth A. McCormick

    Version of Record online : 24 JAN 2015, DOI: 10.1111/cmi.12406

  4. You have full text access to this Open Access content
    P53 apoptosis mediator PERP: localization, function and caspase activation in uveal melanoma

    Journal of Cellular and Molecular Medicine

    Volume 13, Issue 8b, August 2009, Pages: 1995–2007, Lyndsay Davies, Donna Gray, Dave Spiller, Mike R. H. White, Bertil Damato, Ian Grierson and Luminita Paraoan

    Version of Record online : 18 NOV 2008, DOI: 10.1111/j.1582-4934.2008.00590.x

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    The scaffolding and signalling functions of a localization factor impact polar development

    Molecular Microbiology

    Volume 84, Issue 4, May 2012, Pages: 712–735, Patrick D. Curtis, Ellen M. Quardokus, Melanie L. Lawler, Xiaoyun Guo, David Klein, Joseph C. Chen, Randy J. Arnold and Yves V. Brun

    Version of Record online : 19 APR 2012, DOI: 10.1111/j.1365-2958.2012.08055.x

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    How the TP53 Family Proteins TP63 and TP73 Contribute to Tumorigenesis: Regulators and Effectors

    Human Mutation

    Volume 35, Issue 6, June 2014, Pages: 702–714, Eleonora Candi, Massimiliano Agostini, Gerry Melino and Francesca Bernassola

    Version of Record online : 7 MAR 2014, DOI: 10.1002/humu.22523

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    Pro-apoptotic TP53 homolog TAp63 is repressed via epigenetic silencing and B-cell receptor signalling in chronic lymphocytic leukaemia

    British Journal of Haematology

    Volume 163, Issue 5, December 2013, Pages: 590–602, Leigh A. Humphries, J. Claire Godbersen, Olga V. Danilova, Prabhjot Kaur, Brock C. Christensen and Alexey V. Danilov

    Version of Record online : 30 SEP 2013, DOI: 10.1111/bjh.12580

  8. Modeling AEC—New approaches to study rare genetic disorders

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2443–2454, Peter J. Koch, Jason Dinella, Mary Fete, Elaine C. Siegfried and Maranke I. Koster

    Version of Record online : 24 MAR 2014, DOI: 10.1002/ajmg.a.36455

  9. Theory of Direct Photoisomerization of Stilbene

    Annalen der Physik

    Volume 491, Issue 2, 1979, Pages: 81–90, H. Paerschke, K.-E. Süsse and D.-G. Welsch

    Version of Record online : 16 MAR 2006, DOI: 10.1002/andp.19794910202

  10. Functional and molecular studies in primary carnitine deficiency

    Human Mutation

    Volume 38, Issue 12, December 2017, Pages: 1684–1699, Marta Frigeni, Bijina Balakrishnan, Xue Yin, Fernanda R.O. Calderon, Rong Mao, Marzia Pasquali and Nicola Longo

    Version of Record online : 14 SEP 2017, DOI: 10.1002/humu.23315

  11. A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families

    Human Mutation

    Volume 39, Issue 2, February 2018, Pages: 237–254, Danielle C. Kimble, Francis P. Lach, Siobhan Q. Gregg, Frank X. Donovan, Elizabeth K. Flynn, Aparna Kamat, Alice Young, Meghana Vemulapalli, James W. Thomas, James C. Mullikin, Arleen D. Auerbach, Agata Smogorzewska and Settara C. Chandrasekharappa

    Version of Record online : 22 NOV 2017, DOI: 10.1002/humu.23366

  12. The first solvation shell of magnesium ion in a model protein environment with formate, water, and X-NH3, H2S, imidazole, formaldehyde, and chloride as ligands: An ab initio study

    Proteins: Structure, Function, and Bioinformatics

    Volume 21, Issue 3, March 1995, Pages: 244–255, David W. Deerfield II, Douglas J. Fox, Martin Head-Gordon, Richard G. Hiskey and Lee G. Pedersen

    Version of Record online : 3 FEB 2004, DOI: 10.1002/prot.340210307

  13. A memory and decision model for eyewitness identification

    Applied Cognitive Psychology

    Volume 17, Issue 6, September 2003, Pages: 629–654, Steven E. Clark

    Version of Record online : 1 SEP 2003, DOI: 10.1002/acp.891

  14. Ectodermal Dysplasias

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Yuka Asai, Alan D. Irvine, Pages: 127.1–127.104, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch127

  15. Nucleophilic attack on ketene, 6-methylene-2,4-cyclohexadienylideneketene, 6-oxo-2,4-cyclohexadienylideneketene and 4-oxo-2,5-cyclohexadienylideneketene: an ab initio study

    Journal of Physical Organic Chemistry

    Volume 17, Issue 12, December 2004, Pages: 1075–1083, James R. Keeffe

    Version of Record online : 14 JUN 2004, DOI: 10.1002/poc.784

  16. Rapp–Hodgkin and Hay–Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder

    British Journal of Dermatology

    Volume 163, Issue 3, September 2010, Pages: 624–629, S.E. Clements, T. Techanukul, S.T. Holden, J.E. Mellerio, H. Dorkins, F. Escande and J.A. McGrath

    Version of Record online : 20 MAY 2010, DOI: 10.1111/j.1365-2133.2010.09859.x

  17. On the Importance of Decarbonylation as a Side-Reaction in the Ruthenium-Catalysed Dehydrogenation of Alcohols: A Combined Experimental and Density Functional Study

    Chemistry - A European Journal

    Volume 20, Issue 14, April 1, 2014, Pages: 4141–4155, Dr. Nicolas Sieffert, Romain Réocreux, Patrizia Lorusso, Prof. Dr. David J. Cole-Hamilton and Prof. Dr. Michael Bühl

    Version of Record online : 5 MAR 2014, DOI: 10.1002/chem.201303722

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    A functional variant in TP63 at 3q28 associated with bladder cancer risk by creating an miR-140-5p binding site

    International Journal of Cancer

    Volume 139, Issue 1, 1 July 2016, Pages: 65–74, Meilin Wang, Mulong Du, Lan Ma, Haiyan Chu, Qiang Lv, Dingwei Ye, Jianming Guo, Chengyuan Gu, Guowei Xia, Yao Zhu, Qiang Ding, Lin Yuan, Guangbo Fu, Na Tong, Chao Qin, Changjun Yin, Jianfeng Xu and Zhengdong Zhang

    Version of Record online : 18 JAN 2016, DOI: 10.1002/ijc.29978

  19. CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

    Human Mutation

    Volume 38, Issue 11, November 2017, Pages: 1579–1591, Anja K. Mayer, Caroline Van Cauwenbergh, Christine Rother, Britta Baumann, Peggy Reuter, Elfride De Baere, Bernd Wissinger, Susanne Kohl and ACHM Study Group

    Version of Record online : 28 AUG 2017, DOI: 10.1002/humu.23311

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    CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants

    Human Mutation

    Volume 39, Issue 1, January 2018, Pages: 5–22, Leandro Simonetti, Carlos D. Bruque, Cecilia S. Fernández, Belén Benavides-Mori, Marisol Delea, Jorge E. Kolomenski, Lucía D. Espeche, Noemí D. Buzzalino, Alejandro D. Nadra and Liliana Dain

    Version of Record online : 6 NOV 2017, DOI: 10.1002/humu.23351