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There are 19497 results for: content related to: HRAS1 Proto-Oncogene Polymorphism and Prostate Cancer

  1. You have free access to this content
    HRAS1 variable number of tandem repeats polymorphism and risk of bladder cancer

    International Journal of Cancer

    Volume 100, Issue 4, 1 August 2002, Pages: 414–418, Carla H. van Gils, Kathleen Conway, Yu Li and Jack A. Taylor

    Version of Record online : 12 JUN 2002, DOI: 10.1002/ijc.10497

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    Rare HRAS1 alleles are a risk factor for the development of brain tumors

    Cancer

    Volume 92, Issue 11, 1 December 2001, Pages: 2920–2926, Ana Vega, María J. Sobrido, Clara Ruiz-Ponte, Francisco Barros and Angel Carracedo

    Version of Record online : 27 NOV 2001, DOI: 10.1002/1097-0142(20011201)92:11<2920::AID-CNCR10110>3.0.CO;2-S

  3. An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences

    American Journal of Medical Genetics Part A

    Volume 167, Issue 9, September 2015, Pages: 2085–2097, Karen W. Gripp, Katia Sol-Church, Patroula Smpokou, Gail E. Graham, David A. Stevenson, Heather Hanson, David H. Viskochil, Laura C. Baker, Bridget Russo, Nick Gardner, Deborah L. Stabley, Verena Kolbe and Georg Rosenberger

    Version of Record online : 25 APR 2015, DOI: 10.1002/ajmg.a.37128

  4. You have full text access to this OnlineOpen article
    HRAS mutation prevalence and associated expression patterns in pheochromocytoma

    Genes, Chromosomes and Cancer

    Volume 55, Issue 5, May 2016, Pages: 452–459, Adam Stenman, Jenny Welander, Ida Gustavsson, Laurent Brunaud, Martin Bäckdahl, Peter Söderkvist, Oliver Gimm, C. Christofer Juhlin and Catharina Larsson

    Version of Record online : 23 FEB 2016, DOI: 10.1002/gcc.22347

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    Rare alleles at different VNTR loci among lung-cancer patients with microsatellite instability in tumours

    International Journal of Cancer

    Volume 70, Issue 4, 7 February 1997, Pages: 412–415, Bjørn-Arne Lindstedt, David Ryberg and Aage Haugen

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1097-0215(19970207)70:4<412::AID-IJC7>3.0.CO;2-Z

  6. A novel HRAS substitution (c.266C>G; p.S89C) resulting in decreased downstream signaling suggests a new dimension of RAS pathway dysregulation in human development

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2106–2118, Karen W. Gripp, Eugenia Bifeld, Deborah L. Stabley, Elizabeth Hopkins, Stefanie Meien, Kathy Vinette, Katia Sol-Church and Georg Rosenberger

    Version of Record online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35449

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    Inhibition of Ras oncogenic activity by Ras protooncogenes

    International Journal of Cancer

    Volume 113, Issue 2, 10 January 2005, Pages: 241–248, Roberto Diaz, Jeffrey Lue, Jeremy Mathews, Andrew Yoon, Daniel Ahn, Antonio Garcia-España, Peter Leonardi, Marcelo P. Vargas and Angel Pellicer

    Version of Record online : 13 SEP 2004, DOI: 10.1002/ijc.20563

  8. Molecular Genetics of Costello Syndrome

    Standard Article

    eLS

    Emma MM Burkitt Wright and Bronwyn Kerr

    Published Online : 15 SEP 2014, DOI: 10.1002/9780470015902.a0021471

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    Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1205–1217, Katherine A. Rauen, Erin Hefner, Kristin Carrillo, Jill Taylor, Laure Messier, Yoko Aoki, Karen W. Gripp, Yoichi Matsubara, Virginia K. Proud, Peter Hammond, Judith E. Allanson, Marie-Ange Delrue, Marni E. Axelrad, Angela E. Lin, Daniel A. Doyle, Bronwyn Kerr, John C. Carey, Frank McCormick, Alcino J. Silva, Mark W. Kieran, Aleksander Hinek, Tan T. Nguyen and Lisa Schoyer

    Version of Record online : 15 APR 2008, DOI: 10.1002/ajmg.a.32276

  10. Frequent activating HRAS mutations in trichilemmoma

    British Journal of Dermatology

    Volume 171, Issue 5, November 2014, Pages: 1073–1077, J.-H. Tsai, W.-C. Huang, J.-Y. Jhuang, Y.-M. Jeng, M.-L. Cheng, H.-Y. Chiu, K.-T. Kuo and J.-Y. Liau

    Version of Record online : 30 SEP 2014, DOI: 10.1111/bjd.13143

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    Thyroid nodules with KRAS mutations are different from nodules with NRAS and HRAS mutations with regard to cytopathologic and histopathologic outcome characteristics

    Cancer Cytopathology

    Volume 122, Issue 12, December 2014, Pages: 873–882, Lisa A. Radkay, Simion I. Chiosea, Raja R. Seethala, Steven P. Hodak, Shane O. LeBeau, Linwah Yip, Kelly L. McCoy, Sally E. Carty, Karen E. Schoedel, Marina N. Nikiforova, Yuri E. Nikiforov and N. Paul Ohori

    Version of Record online : 12 AUG 2014, DOI: 10.1002/cncy.21474

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    HRAS mutations in Costello syndrome: Detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 1, 1 January 2006, Pages: 8–16, Anne L. Estep, William E. Tidyman, Michael A. Teitell, Philip D. Cotter and Katherine A. Rauen

    Version of Record online : 13 DEC 2005, DOI: 10.1002/ajmg.a.31078

  13. Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1095–1101, Karen W. Gripp, Elizabeth Hopkins, Alvaro Serrano, Norma J. Leonard, Deborah L. Stabley and Katia Sol-Church

    Version of Record online : 9 APR 2012, DOI: 10.1002/ajmg.a.35294

  14. Minisatellite variant repeat (MVR) analysis of the HRAS1 minisatellite locus

    ELECTROPHORESIS

    Volume 19, Issue 18, December 1998, Pages: 3084–3089, Ana Vega, Francisco Barros, Susana Bellas and Dr. Angel Carracedo

    Version of Record online : 14 APR 2005, DOI: 10.1002/elps.1150191807

  15. Costello syndrome associated with novel germline HRAS mutations: An attenuated phenotype?

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 6, 15 March 2008, Pages: 683–690, Karen W. Gripp, A. Micheil Innes, Marni E. Axelrad, Tanya L. Gillan, Jillian S. Parboosingh, Christine Davies, Norma J. Leonard, Monique Lapointe, Daniel Doyle, Sarah Catalano, Linda Nicholson, Deborah L. Stabley and Katia Sol-Church

    Version of Record online : 4 FEB 2008, DOI: 10.1002/ajmg.a.32227

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    Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith–Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion

    American Journal of Medical Genetics Part A

    Volume 170, Issue 3, March 2016, Pages: 559–564, Karen W. Gripp, Katherine M. Robbins, Brandon S. Sheffield, Anna F. Lee, Millan S. Patel, Stephen Yip, Daniel Doyle, Deborah Stabley and Katia Sol-Church

    Version of Record online : 17 NOV 2015, DOI: 10.1002/ajmg.a.37471

  17. A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 125B, Issue 1, 15 February 2004, Pages: 112–119, Ging-Yuek R. Hsiung, Bonnie J. Kaplan, Tracey L. Petryshen, Shao Lu and L. Leigh Field

    Version of Record online : 25 AUG 2003, DOI: 10.1002/ajmg.b.20082

  18. The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy

    American Journal of Medical Genetics Part A

    Volume 170, Issue 6, June 2016, Pages: 1433–1438, Anita Hiippala, Catalina Vasilescu, Jonna Tallila, Tero-Pekka Alastalo, Anders Paetau, Tiina Tyni, Anu Suomalainen, Liliya Euro and Tiina Ojala

    Version of Record online : 17 FEB 2016, DOI: 10.1002/ajmg.a.37596

  19. Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome

    Clinical Genetics

    Volume 73, Issue 1, January 2008, Pages: 62–70, AL Schulz, B Albrecht, C Arici, I Van Der Burgt, A Buske, G Gillessen-Kaesbach, R Heller, D Horn, CA Hübner, GC Korenke, R König, W Kress, G Krüger, P Meinecke, J Mücke, B Plecko, E Rossier, A Schinzel, A Schulze, E Seemanova, H Seidel, S Spranger, B Tuysuz, S Uhrig, D Wieczorek, K Kutsche and M Zenker

    Version of Record online : 27 NOV 2007, DOI: 10.1111/j.1399-0004.2007.00931.x

  20. You have full text access to this Open Access content
    HRAS1 and LASS1 with APOE are associated with human longevity and healthy aging

    Aging Cell

    Volume 9, Issue 5, October 2010, Pages: 698–708, S. Michal Jazwinski, Sangkyu Kim, Jianliang Dai, Li Li, Xiuhua Bi, James C. Jiang, Jonathan Arnold, Mark A. Batzer, Jerilyn A. Walker, David A. Welsh, Christina M. Lefante, Julia Volaufova, Leann Myers, L. Joseph Su, Dorothy B. Hausman, Michael V. Miceli, Eric Ravussin, Leonard W. Poon, Katie E. Cherry, Michael A. Welsch and for the Georgia Centenarian Study and the Louisiana Healthy Aging Study

    Version of Record online : 21 JUN 2010, DOI: 10.1111/j.1474-9726.2010.00600.x