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There are 2078 results for: content related to: Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect

  1. CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 22, 15 November 2006, Pages: 2501–2505, Cheryl L. Maslen, Darcie Babcock, Susan W. Robinson, Lora J. H. Bean, Kenneth J. Dooley, Virginia L. Willour and Stephanie L. Sherman

    Article first published online : 11 OCT 2006, DOI: 10.1002/ajmg.a.31494

  2. Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)

    Clinical Genetics

    Volume 67, Issue 6, June 2005, Pages: 526–528, M Zatyka, M Priestley, E J Ladusans, A E Fryer, J Mason, F Latif and E R Maher

    Article first published online : 31 MAR 2005, DOI: 10.1111/j.1399-0004.2005.00435.x

  3. Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 2047–2049, Samaneh Zhian, John Belmont and Cheryl L. Maslen

    Article first published online : 27 JUN 2012, DOI: 10.1002/ajmg.a.35457

  4. You have free access to this content
    A key role for ALD1 in activation of local and systemic defenses in Arabidopsis

    The Plant Journal

    Volume 40, Issue 2, October 2004, Pages: 200–212, Jong Tae Song, Hua Lu, John M. McDowell and Jean T. Greenberg

    Article first published online : 24 AUG 2004, DOI: 10.1111/j.1365-313X.2004.02200.x

  5. Microarray based analysis of 3p25-p26 deletions (3p- syndrome)

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 10, October 2009, Pages: 2099–2105, Salwati Shuib, Dominic McMullan, Eleanor Rattenberry, Richard M. Barber, Fatimah Rahman, Malgosia Zatyka, Cyril Chapman, Fiona Macdonald, Farida Latif, Val Davison and Eamonn R. Maher

    Article first published online : 16 SEP 2009, DOI: 10.1002/ajmg.a.32824

  6. Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 2, 15 January 2008, Pages: 251–253, Maximilian G. Posch, Andreas Perrot, Katharina Schmitt, Sebastian Mittelhaus, Eva-Maria Esenwein, Brigitte Stiller, Christian Geier, Rainer Dietz, Reinhard Geßner, Cemil Özcelik and Felix Berger

    Article first published online : 12 DEC 2007, DOI: 10.1002/ajmg.a.32042

  7. You have full text access to this OnlineOpen article
    Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Pages: 1279–1284, James R. Priest, Santhosh Girirajan, Tiffany H. Vu, Aaron Olson, Evan E. Eichler and Michael A. Portman

    Article first published online : 23 APR 2012, DOI: 10.1002/ajmg.a.35315

  8. Atrioventricular Septal Defects

    Pediatric Cardiovascular Medicine, Second Edition

    Stuart Berger, Peter J. Bartz, David E. Saudek, John T. Hambrook, James S. Tweddell, Pages: 308–327, 2012

    Published Online : 13 JAN 2012, DOI: 10.1002/9781444398786.ch22

  9. Genetic aspects of atrioventricular septal defects

    American Journal of Medical Genetics

    Volume 97, Issue 4, Winter 2000, Pages: 289–296, Mary Ella M. Pierpont, Roger R. Markwald and Angela E. Lin

    Article first published online : 9 MAY 2001, DOI: 10.1002/1096-8628(200024)97:4<289::AID-AJMG1279>3.0.CO;2-U

  10. You have full text access to this Open Access content
    MARVELD1 inhibited cell proliferation and enhance chemosensitivity via increasing expression of p53 and p16 in hepatocellular carcinoma

    Cancer Science

    Volume 103, Issue 4, April 2012, Pages: 716–722, Youtao Yu, Yubao Zhang, Jianran Hu, Hao Zhang, Shan Wang, Fang Han, Lei Yue, Youpeng Qu, Yao Zhang, Hongjian Liang, Huan Nie and Yu Li

    Article first published online : 8 MAR 2012, DOI: 10.1111/j.1349-7006.2012.02220.x

  11. Genetic factors in non-syndromic congenital heart malformations

    Clinical Genetics

    Volume 78, Issue 2, August 2010, Pages: 103–123, MW Wessels and PJ Willems

    Article first published online : 17 MAY 2010, DOI: 10.1111/j.1399-0004.2010.01435.x

  12. You have free access to this content
    Clinical characteristics of pulmonary arterial hypertension associated with Down syndrome

    Pediatrics International

    Volume 56, Issue 3, June 2014, Pages: 297–303, Tsutomu Saji

    Article first published online : 3 JUN 2014, DOI: 10.1111/ped.12349

  13. Phospholipase D1 mediates lymphocyte adhesion and migration in experimental autoimmune encephalomyelitis

    European Journal of Immunology

    Volume 44, Issue 8, August 2014, Pages: 2295–2305, Kerstin Göbel, Michael K. Schuhmann, Susann Pankratz, David Stegner, Alexander M. Herrmann, Attila Braun, Johanna Breuer, Stefan Bittner, Tobias Ruck, Heinz Wiendl, Christoph Kleinschnitz, Bernhard Nieswandt and Sven G. Meuth

    Article first published online : 5 JUN 2014, DOI: 10.1002/eji.201344107

  14. Evaluation of Risk Factors for Prediction of Outcome in Fetal Spectrum of Atrioventricular Septal Defects

    Congenital Heart Disease

    Volume 9, Issue 4, July/August 2014, Pages: 286–293, Rima S. Bader, Rajesh Punn and Norman H. Silverman

    Article first published online : 19 SEP 2013, DOI: 10.1111/chd.12136

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    Sphingolipid Δ8 unsaturation is important for glucosylceramide biosynthesis and low-temperature performance in Arabidopsis

    The Plant Journal

    Volume 69, Issue 5, March 2012, Pages: 769–781, Ming Chen, Jonathan E. Markham and Edgar B. Cahoon

    Article first published online : 1 DEC 2011, DOI: 10.1111/j.1365-313X.2011.04829.x

  16. Atrioventricular septal defects: Possible etiologic differences between complete and partial defects


    Volume 63, Issue 2, February 2001, Pages: 87–93, Christopher A. Loffredo, Jeffrey Hirata, P. David Wilson, Charlotte Ferencz and Iosif W. Lurie

    Article first published online : 22 FEB 2001, DOI: 10.1002/1096-9926(200102)63:2<87::AID-TERA1014>3.0.CO;2-5

  17. Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development

    Congenital Heart Disease

    Volume 10, Issue 3, May/June 2015, Pages: 193–208, Thor Thorsson, William W. Russell, Nour El-Kashlan, Rachel Soemedi, Jonathan Levine, Sarah B. Geisler, Todd Ackley, Aoy Tomita-Mitchell, Jill A. Rosenfeld, Ana Töpf, Marwan Tayeh, Judith Goodship, Jeffrey W. Innis, Bernard Keavney and Mark W. Russell

    Article first published online : 11 APR 2014, DOI: 10.1111/chd.12179

  18. CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects

    American Journal of Medical Genetics Part A

    Volume 139A, Issue 3, 15 December 2005, Pages: 236–238, Anna Sarkozy, Giorgia Esposito, Emanuela Conti, Maria Cristina Digilio, Bruno Marino, Raffaele Calabrò, Antonio Pizzuti and Bruno Dallapiccola

    Article first published online : 8 NOV 2005, DOI: 10.1002/ajmg.a.31018

  19. You have free access to this content
    Redundant functions of phospholipases D1 and D2 in platelet α-granule release

    Journal of Thrombosis and Haemostasis

    Volume 10, Issue 11, November 2012, Pages: 2361–2372, I. THIELMANN, D. STEGNER, P. KRAFT, I. HAGEDORN, G. KROHNE, C. KLEINSCHNITZ, G. STOLL and B. NIESWANDT

    Article first published online : 30 OCT 2012, DOI: 10.1111/j.1538-7836.2012.04924.x

  20. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1661–1677, Margaret J. Wat, Oleg A. Shchelochkov, Ashley M. Holder, Amy M. Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T. Zori, Sau Wai Cheung, Daryl A. Scott and Sung-Hae Lee Kang

    Article first published online : 15 JUL 2009, DOI: 10.1002/ajmg.a.32896