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There are 3878 results for: content related to: Genetic modifier to chromatin may contribute to 22q11 deletion/VCF/DiGeorge syndrome variability

  1. 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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    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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    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

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    Tbx1 is regulated by forkhead proteins in the secondary heart field

    Developmental Dynamics

    Volume 235, Issue 3, March 2006, Pages: 701–710, Jun Maeda, Hiroyuki Yamagishi, John McAnally, Chihiro Yamagishi and Deepak Srivastava

    Version of Record online : 27 JAN 2006, DOI: 10.1002/dvdy.20686

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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

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    Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm

    Developmental Dynamics

    Volume 236, Issue 2, February 2007, Pages: 353–363, Akbar Dastjerdi, Lesley Robson, Rebecca Walker, Julia Hadley, Zhen Zhang, Marc Rodriguez-Niedenführ, Paris Ataliotis, Antonio Baldini, Peter Scambler and Philippa Francis-West

    Version of Record online : 20 NOV 2006, DOI: 10.1002/dvdy.21010

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    Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos

    Developmental Dynamics

    Volume 237, Issue 10, October 2008, Pages: 3071–3078, Raphälle Grifone, Thérèse Jarry, Mathieu Dandonneau, Julien Grenier, Delphine Duprez and Robert G. Kelly

    Version of Record online : 24 SEP 2008, DOI: 10.1002/dvdy.21718

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    Visualization of outflow tract development in the absence of Tbx1 using an FgF10 enhancer trap transgene

    Developmental Dynamics

    Volume 236, Issue 3, March 2007, Pages: 821–828, Robert G. Kelly and Virginia E. Papaioannou

    Version of Record online : 19 JAN 2007, DOI: 10.1002/dvdy.21063

  9. 22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development

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    Amelie Calmont and Peter Scambler

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

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    Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis

    Developmental Dynamics

    Volume 243, Issue 9, September 2014, Pages: 1143–1151, Abigail Jackson, Sahrunizam Kasah, Suzanne L. Mansour, Bernice Morrow and M. Albert Basson

    Version of Record online : 12 JUN 2014, DOI: 10.1002/dvdy.24147

  11. Coronary stem development in wild-type and Tbx1 null mouse hearts

    Developmental Dynamics

    Volume 245, Issue 4, April 2016, Pages: 445–459, Magali Théveniau-Ruissy, José-Maria Pérez-Pomares, Pauline Parisot, Antonio Baldini, Lucile Miquerol and Robert G. Kelly

    Version of Record online : 19 JAN 2016, DOI: 10.1002/dvdy.24380

  12. Pharyngeal arch deficiencies affect taste bud development in the circumvallate papilla with aberrant glossopharyngeal nerve formation

    Developmental Dynamics

    Volume 244, Issue 7, July 2015, Pages: 874–887, Tadashi Okubo and Shinji Takada

    Version of Record online : 18 JUN 2015, DOI: 10.1002/dvdy.24289

  13. 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

  14. A novel role for the T-box transcription factor Tbx1 as a negative regulator of tumor cell growth in mice

    Molecular Carcinogenesis

    Volume 50, Issue 12, December 2011, Pages: 981–991, Carol S. Trempus, Sung-Jen Wei, Margaret M. Humble, Hong Dang, Carl D. Bortner, Maria I. Sifre, Grace E. Kissling, Jeffrey A. Sunman, Steven K. Akiyama, John D. Roberts, Charles J. Tucker, Kyung-Soo Chun, Raymond W. Tennant and Robert Langenbach

    Version of Record online : 22 MAR 2011, DOI: 10.1002/mc.20768

  15. 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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    Absence of the vagus nerve in the stomach of Tbx1−/− mutant mice

    Neurogastroenterology & Motility

    Volume 23, Issue 2, February 2011, Pages: 125–130, A. Calmont, N. Thapar, P. J. Scambler and A. J. Burns

    Version of Record online : 11 OCT 2010, DOI: 10.1111/j.1365-2982.2010.01615.x

  17. 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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    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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    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

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    Tbx1 is required for second heart field proliferation in zebrafish

    Developmental Dynamics

    Volume 242, Issue 5, May 2013, Pages: 550–559, Kathleen Nevis, Pablo Obregon, Conor Walsh, Burcu Guner-Ataman, C. Geoffrey Burns and Caroline E. Burns

    Version of Record online : 6 MAR 2013, DOI: 10.1002/dvdy.23928