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There are 36512 results for: content related to: Deletion of MAP2K2/MEK2 : a novel mechanism for a RASopathy?

  1. You have full text access to this OnlineOpen article
    Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 510–520, D. Cragun, C. Radford, J.S. Dolinsky, M. Caldwell, E. Chao and T. Pal

    Version of Record online : 20 MAR 2014, DOI: 10.1111/cge.12359

  2. Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 539–544, AF Goodwin, S Oberoi, M Landan, C Charles, J Groth, A Martinez, C Fairley, LA Weiss, WE Tidyman, OD Klein and KA Rauen

    Version of Record online : 27 SEP 2012, DOI: 10.1111/cge.12005

  3. Hepatoma cell functions modulated by NEK2 are associated with liver cancer progression

    International Journal of Cancer

    Volume 140, Issue 7, 1 April 2017, Pages: 1581–1596, Sheng-Ming Wu, Syuan-Ling Lin, Kang-Yun Lee, Hsiao-Chi Chuang, Po-Hao Feng, Wan-Li Cheng, Chia-Jung Liao, Hsiang-Cheng Chi, Yang-Hsiang Lin, Chung-Ying Tsai, Wei-Jan Chen, Chau-Ting Yeh and Kwang-Huei Lin

    Version of Record online : 19 JAN 2017, DOI: 10.1002/ijc.30559

  4. You have full text access to this OnlineOpen article
    Use of panel tests in place of single gene tests in the cancer genetics clinic

    Clinical Genetics

    Volume 88, Issue 3, September 2015, Pages: 278–282, A. Yorczyk, L.S. Robinson and T.S. Ross

    Version of Record online : 16 OCT 2014, DOI: 10.1111/cge.12488

  5. Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland

    Clinical Genetics

    Volume 88, Issue 4, October 2015, Pages: 366–370, C. Cybulski, J. Lubiński, D. Wokołorczyk, W. Kuźniak, A. Kashyap, V. Sopik, T. Huzarski, J. Gronwald, T. Byrski, M. Szwiec, A. Jakubowska, B. Górski, T. Dębniak, S.A Narod and M.R Akbari

    Version of Record online : 13 NOV 2014, DOI: 10.1111/cge.12524

  6. You have full text access to this Open Access content
    Novel combination treatment for colorectal cancer using Nek2 siRNA and cisplatin

    Cancer Science

    Volume 101, Issue 5, May 2010, Pages: 1163–1169, Kazushi Suzuki, Toshio Kokuryo, Takeshi Senga, Yukihiro Yokoyama, Masato Nagino and Michinari Hamaguchi

    Version of Record online : 20 JAN 2010, DOI: 10.1111/j.1349-7006.2010.01504.x

  7. Malignancy in Noonan syndrome and related disorders

    Clinical Genetics

    Volume 88, Issue 6, December 2015, Pages: 516–522, P. Smpokou, D.J. Zand, K.N. Rosenbaum and M.L. Summar

    Version of Record online : 4 MAR 2015, DOI: 10.1111/cge.12568

  8. You have free access to this content
    Endosomal Targeting of MEK2 Requires RAF, MEK Kinase Activity and Clathrin-Dependent Endocytosis

    Traffic

    Volume 9, Issue 10, October 2008, Pages: 1776–1790, Emilia Galperin and Alexander Sorkin

    Version of Record online : 24 JUL 2008, DOI: 10.1111/j.1600-0854.2008.00788.x

  9. You have free access to this content
    Lung development requires an active ERK/MAPK pathway in the lung mesenchyme

    Developmental Dynamics

    Volume 246, Issue 1, January 2017, Pages: 72–82, Olivier Boucherat, Kim Landry-Truchon, Rifdat Aoidi, Nicolas Houde, Valérie Nadeau, Jean Charron and Lucie Jeannotte

    Version of Record online : 17 NOV 2016, DOI: 10.1002/dvdy.24464

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    Genetics of the corneal endothelial dystrophies: an evidence-based review

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 109–119, A J Aldave, J Han and R F Frausto

    Version of Record online : 10 JUN 2013, DOI: 10.1111/cge.12191

  11. You have full text access to this Open Access content
    Nek2 as a novel molecular target for the treatment of breast carcinoma

    Cancer Science

    Volume 100, Issue 1, January 2009, Pages: 111–116, Nobuyuki Tsunoda, Toshio Kokuryo, Koji Oda, Takeshi Senga, Yukihiro Yokoyama, Masato Nagino, Yuji Nimura and Michinari Hamaguchi

    Version of Record online : 27 NOV 2008, DOI: 10.1111/j.1349-7006.2008.01007.x

  12. You have free access to this content
    Genetics of primary ovarian insufficiency

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 183–198, R. Rossetti, I. Ferrari, M. Bonomi and L. Persani

    Version of Record online : 12 DEC 2016, DOI: 10.1111/cge.12921

  13. Overexpression of the Nek2 kinase in colorectal cancer correlates with beta-catenin relocalization and shortened cancer-specific survival

    Journal of Surgical Oncology

    Volume 110, Issue 7, December 1, 2014, Pages: 828–838, Christopher P. Neal, Andrew M. Fry, Catherine Moreman, Angus McGregor, Giuseppe Garcea, David P. Berry and Margaret M. Manson

    Version of Record online : 16 JUL 2014, DOI: 10.1002/jso.23717

  14. Abnormal expression of Nek2 and β-catenin in breast carcinoma: clinicopathological correlations

    Histopathology

    Volume 59, Issue 4, October 2011, Pages: 631–642, Shuling Wang, Weidong Li, Shuhua Lv, Yahong Wang, Ziyu Liu, Jing Zhang, Tieju Liu and Yun Niu

    Version of Record online : 20 OCT 2011, DOI: 10.1111/j.1365-2559.2011.03941.x

  15. Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

    Clinical Genetics

    C. Lintas and A.M. Persico

    Version of Record online : 1 MAR 2017, DOI: 10.1111/cge.12983

  16. You have full text access to this OnlineOpen article
    Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

    Clinical Genetics

    Maren F. Hansen, Jostein Johansen, Anna E. Sylvander, Inga Bjørnevoll, Bente A. Talseth-Palmer, Liss A. S. Lavik, Alexandre Xavier, Lars F. Engebretsen, Rodney J. Scott, Finn Drabløs and Wenche Sjursen

    Version of Record online : 22 MAR 2017, DOI: 10.1111/cge.12994

  17. (Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicine

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 403–415, A. Mussa, S. Russo, L. Larizza, A. Riccio and G.B. Ferrero

    Version of Record online : 30 JUL 2015, DOI: 10.1111/cge.12635

  18. Phenotype analysis impacts testing strategy in patients with Currarino syndrome

    Clinical Genetics

    Volume 89, Issue 1, January 2016, Pages: 109–114, G. Cuturilo, J.C. Hodge, C.K. Runke, E.C. Thorland, M.A. Al-Owain, J.W. Ellison and D. Babovic-Vuksanovic

    Version of Record online : 15 MAR 2015, DOI: 10.1111/cge.12572

  19. Homozygosity for a CHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype

    The Journal of Pathology

    Volume 206, Issue 2, June 2005, Pages: 198–204, Marjo van Puijenbroek, Christi J van Asperen, Anneke van Mil, Peter Devilee, Tom van Wezel and Hans Morreau

    Version of Record online : 8 APR 2005, DOI: 10.1002/path.1764

  20. Testing for CHEK2 in the cancer genetics clinic: ready for prime time?

    Clinical Genetics

    Volume 78, Issue 1, July 2010, Pages: 1–7, SA Narod

    Version of Record online : 23 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01402.x