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There are 10523 results for: content related to: ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus

  1. ARVCF expression is significantly correlated with the malignant phenotype of non-small cell lung cancer

    Molecular Carcinogenesis

    Volume 54, Issue S1, July 2015, Pages: E185–E191, Di Zhang, Na Tang, Yang Liu and En-Hua Wang

    Version of Record online : 14 FEB 2015, DOI: 10.1002/mc.22281

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    Inhibition of cell adhesion by xARVCF indicates a regulatory function at the plasma membrane

    Developmental Dynamics

    Volume 237, Issue 9, September 2008, Pages: 2328–2341, Wolfgang E. Reintsch, Craig A. Mandato, Pierre D. McCrea and François Fagotto

    Version of Record online : 26 AUG 2008, DOI: 10.1002/dvdy.21651

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    Kazrin, and its binding partners ARVCF- and delta-catenin, are required for Xenopus laevis craniofacial development

    Developmental Dynamics

    Volume 240, Issue 12, December 2011, Pages: 2601–2612, Kyucheol Cho, Moonsup Lee, Dongmin Gu, William A. Munoz, Hong Ji, Malgorzata Kloc and Pierre D. McCrea

    Version of Record online : 25 OCT 2011, DOI: 10.1002/dvdy.22721

  4. A functional variant provided further evidence for the association of ARVCF with schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 5, July 2010, Pages: 1052–1059, Sergi Mas, Miquel Bernardo, Patricia Gassó, Santi Álvarez, Clemente Garcia-Rizo, Miquel Bioque, Brian Kirkpatrick and Amalia Lafuente

    Version of Record online : 23 MAR 2010, DOI: 10.1002/ajmg.b.31073

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    Retinoic acid down-regulates Tbx1 expression in vivo and in vitro

    Developmental Dynamics

    Volume 232, Issue 4, April 2005, Pages: 928–938, Catherine Roberts, Sarah M. Ivins, Chela T. James and Peter J. Scambler

    Version of Record online : 25 FEB 2005, DOI: 10.1002/dvdy.20268

  6. The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 3, May/June 2013, Pages: 393–403, Irinna Papangeli and Peter Scambler

    Version of Record online : 19 JUN 2012, DOI: 10.1002/wdev.75

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    Cdc42 GTPase and Rac1 GTPase act downstream of p120 catenin and require GTP exchange during gastrulation of zebrafish mesoderm

    Developmental Dynamics

    Volume 241, Issue 10, October 2012, Pages: 1545–1561, Cynthia L. Hsu, Claire P. Muerdter, Abhay D. Knickerbocker, Ryan M. Walsh, Martha A. Zepeda-Rivera, Kevin H. Depner, Maya Sangesland, Trinidad B. Cisneros, Ju Youn Kim, Patricia Sanchez-Vazquez, Lidia Cherezova, Rainy D. Regan, Nadia M. Bahrami, Elizabeth A. Gray, Andrew Y. Chan, Terry Chen, Milly Y. Rao and Merrill B. Hille

    Version of Record online : 4 SEP 2012, DOI: 10.1002/dvdy.23847

  8. Cellular and molecular events during early thymus development

    Immunological Reviews

    Volume 209, Issue 1, February 2006, Pages: 28–46, Georg Holländer, Jason Gill, Saulius Zuklys, Norimasa Iwanami, Cunlan Liu and Yousuke Takahama

    Version of Record online : 31 JAN 2006, DOI: 10.1111/j.0105-2896.2006.00357.x

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    Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle

    Developmental Dynamics

    Volume 239, Issue 6, June 2010, Pages: 1708–1722, Laina Freyer and Bernice E. Morrow

    Version of Record online : 12 MAY 2010, DOI: 10.1002/dvdy.22308

  10. Changing the Business Model: Effects of Venture Capital Firms and Outside CEOs on Portfolio Company Performance

    Strategic Entrepreneurship Journal

    Volume 9, Issue 1, March 2015, Pages: 79–98, Violetta Gerasymenko, Dirk De Clercq and Harry J. Sapienza

    Version of Record online : 8 DEC 2014, DOI: 10.1002/sej.1189

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    Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization

    Ultrasound in Obstetrics & Gynecology

    Volume 43, Issue 4, April 2014, Pages: 396–403, M. Chen, Y.-S. Yang, J.-C. Shih, W.-H. Lin, D.-J. Lee, Y.-S. Lin, C.-H. Chou, A. D. Cameron, N. A. Ginsberg, C.-A. Chen, M.-L. Lee and G.-C. Ma

    Version of Record online : 26 DEC 2013, DOI: 10.1002/uog.12550

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    Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

    Developmental Dynamics

    Volume 241, Issue 8, August 2012, Pages: 1310–1324, Subreena Simrick, Dorota Szumska, Jennifer R. Gardiner, Kieran Jones, Karun Sagar, Bernice Morrow, Shoumo Bhattacharya and M. Albert Basson

    Version of Record online : 26 JUN 2012, DOI: 10.1002/dvdy.23812

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    Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development

    Developmental Dynamics

    Volume 241, Issue 3, March 2012, Pages: 563–573, Dennis C. Monks and Bernice E. Morrow

    Version of Record online : 1 FEB 2012, DOI: 10.1002/dvdy.23731

  14. 22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development

    Standard Article

    eLS

    Amelie Calmont and Peter Scambler

    Published Online : 15 SEP 2010, DOI: 10.1002/9780470015902.a0006074.pub2

  15. Taking a Second Look in a Warped Crystal Ball: Explaining the Accuracy of Revised Forecasts

    Journal of Management Studies

    Volume 53, Issue 8, December 2016, Pages: 1292–1319, Violetta Bacon-Gerasymenko, Russell Coff and Rodolphe Durand

    Version of Record online : 6 MAY 2016, DOI: 10.1111/joms.12207

  16. Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 139B, Issue 1, 5 November 2005, Pages: 45–50, Elena Michaelovsky, Amos Frisch, Shani Leor, Daniel Stein, Yardena Danziger, Cynthia Carel, Silvana Fennig, Marc Mimouni, Sabine M. Klauck, Axel Benner, Annemarie Poustka, Alan Apter and Abraham Weizman

    Version of Record online : 23 AUG 2005, DOI: 10.1002/ajmg.b.30230

  17. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients

    Human Mutation

    Volume 32, Issue 11, November 2011, Pages: 1278–1289, Tingwei Guo, Donna McDonald-McGinn, Anna Blonska, Alan Shanske, Anne S. Bassett, Eva Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, Maria C. Digilio, Bruno Marino, Bruno Dallapiccola, Courtney Carpenter, Xin Zheng, Jacob Johnson, Jonathan Chung, Anne Marie Higgins, Nicole Philip, Tony J. Simon, Karlene Coleman, Damian Heine-Suner, Jordi Rosell, Wendy Kates, Marcella Devoto, Elizabeth Goldmuntz, Elaine Zackai, Tao Wang, Robert Shprintzen, Beverly Emanuel, Bernice Morrow and The International Chromosome 22q11.2 Consortium

    Version of Record online : 16 SEP 2011, DOI: 10.1002/humu.21568

  18. Firm and Group Influences on Venture Capital Firms’ Involvement in New Ventures

    Journal of Management Studies

    Volume 45, Issue 7, November 2008, Pages: 1169–1194, Dirk De Clercq, Harry J. Sapienza and Akbar Zaheer

    Version of Record online : 21 FEB 2008, DOI: 10.1111/j.1467-6486.2007.00764.x

  19. Developmental perspectives on copy number abnormalities of the 22q11.2 region

    Clinical Genetics

    Volume 78, Issue 3, September 2010, Pages: 201–218, TY Tan, CT Gordon, DJ Amor and PG Farlie

    Version of Record online : 23 APR 2010, DOI: 10.1111/j.1399-0004.2010.01456.x

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    vcfr: a package to manipulate and visualize variant call format data in R

    Molecular Ecology Resources

    Volume 17, Issue 1, January 2017, Pages: 44–53, Brian J. Knaus and Niklaus J. Grünwald

    Version of Record online : 12 JUL 2016, DOI: 10.1111/1755-0998.12549