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There are 4186 results for: content related to: Induction, rapid fixation and retention of mutations in vegetatively propagated banana

  1. Infrequent genetic alterations of the tumor suppressor gene PTEN/MMAC1 in squamous cell carcinoma of the oral cavity

    Journal of Oral Pathology & Medicine

    Volume 31, Issue 5, May 2002, Pages: 270–276, A. Mavros, M. Hahn, I. Wieland, S. Koy, O. N. Koufaki, K. Strelocke, R. Koch, G. Haroske, H. K. Schackert and U. Eckelt

    Version of Record online : 21 JUN 2002, DOI: 10.1034/j.1600-0714.2002.310504.x

  2. Loss of expression of ZAC/LOT1 in squamous cell carcinomas of head and neck

    Head & Neck

    Volume 26, Issue 4, April 2004, Pages: 338–344, Susanne Koy, Martin Hauses, Hella Appelt, Katrin Friedrich, Hans K. Schackert and Uwe Eckelt

    Version of Record online : 10 MAR 2004, DOI: 10.1002/hed.10386

  3. 3p21, 5q21, and 9p21 allelic deletions are frequently found in normal bronchial cells adjacent to non-small-cell lung cancer, while they are unusual in patients with no evidence of malignancy

    The Journal of Pathology

    Volume 195, Issue 4, November 2001, Pages: 429–434, Julian Sanz-Ortega, Maria C. Saez, Elena Sierra, Antonio Torres, Jose L. Balibrea, Florentino Hernando, Julian Sanz-Esponera and Maria J. Merino

    Version of Record online : 19 OCT 2001, DOI: 10.1002/path.987

  4. Human mitochondrial transfer RNAs: Role of pathogenic mutation in disease

    Muscle & Nerve

    Volume 37, Issue 2, February 2008, Pages: 150–171, Fernando Scaglia and Lee-Jun C. Wong

    Version of Record online : 9 NOV 2007, DOI: 10.1002/mus.20917

  5. Genotype-phenotype Associations of Cytochrome P450 3A4 and 3A5 Polymorphism with Midazolam Clearance in Vivo

    Clinical Pharmacology & Therapeutics

    Volume 77, Issue 5, May 2005, Pages: 373–387, Ping He, Michael H. Court, David J. Greenblatt and Lisa L. von Moltke

    Version of Record online : 16 MAY 2005, DOI: 10.1016/j.clpt.2004.11.112

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    Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function

    Autism Research

    Volume 10, Issue 1, January 2017, Pages: 42–65, Thomas C. Jaramillo, Haley E. Speed, Zhong Xuan, Jeremy M. Reimers, Christine Ochoa Escamilla, Travis P. Weaver, Shunan Liu, Irina Filonova and Craig M. Powell

    Version of Record online : 5 AUG 2016, DOI: 10.1002/aur.1664

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    Cylindrical cell carcinomas of the paranasal sinuses do not show p53 alterations but loss of heterozygosity at 3p and 17p

    International Journal of Cancer

    Volume 85, Issue 5, 1 March 2000, Pages: 740–742, Karl Götte, Frank Riedel, Carsten Schäfer, Johannes Coy and Karl Hörmann

    Version of Record online : 2 MAR 2000, DOI: 10.1002/(SICI)1097-0215(20000301)85:5<740::AID-IJC23>3.0.CO;2-9

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    Large spinel grains in a CM chondrite (Acfer 331): Implications for reconstructions of ancient meteorite fluxes

    Meteoritics & Planetary Science

    Volume 48, Issue 2, February 2013, Pages: 180–194, Karolina Bjärnborg and Birger Schmitz

    Version of Record online : 7 FEB 2013, DOI: 10.1111/maps.12050

  9. Pathogenic mitochondrial DNA mutations in protein-coding genes

    Muscle & Nerve

    Volume 36, Issue 3, September 2007, Pages: 279–293, Lee-Jun C. Wong

    Version of Record online : 14 MAY 2007, DOI: 10.1002/mus.20807

  10. You have full text access to this OnlineOpen article
    The genetic risk of acute seizures in African children with falciparum malaria


    Volume 54, Issue 6, June 2013, Pages: 990–1001, Symon M. Kariuki, Kirk Rockett, Taane G. Clark, Hugh Reyburn, Tsiri Agbenyega, Terrie E. Taylor, Gretchen L. Birbeck, Thomas N. Williams and Charles R. J. C. Newton

    Version of Record online : 24 APR 2013, DOI: 10.1111/epi.12173

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    Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population

    British Journal of Dermatology

    Volume 169, Issue 4, October 2013, Pages: 804–811, J.A. Puig-Butillé, C. Carrera, R. Kumar, Z. Garcia-Casado, C. Badenas, P. Aguilera, J. Malvehy, E. Nagore and S. Puig

    Version of Record online : 10 OCT 2013, DOI: 10.1111/bjd.12418

  12. Frequent genetic alterations in flat urothelial hyperplasias and concomitant papillary bladder cancer as detected by CGH, LOH, and FISH analyses

    The Journal of Pathology

    Volume 199, Issue 1, January 2003, Pages: 50–57, EC Obermann, K Junker, R Stoehr, W Dietmaier, D Zaak, J Schubert, F Hofstaedter, R Knuechel and A Hartmann

    Version of Record online : 29 NOV 2002, DOI: 10.1002/path.1259

  13. Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis

    Genetic Epidemiology

    Volume 40, Issue 6, September 2016, Pages: 502–511, Longfei Wang, Sungyoung Lee, Jungsoo Gim, Dandi Qiao, Michael Cho, Robert C Elston, Edwin K Silverman and Sungho Won

    Version of Record online : 17 JUN 2016, DOI: 10.1002/gepi.21985


    Economic Inquiry

    Volume 54, Issue 2, April 2016, Pages: 1128–1149, Gerd Muehlheusser, Sandra Schneemann and Dirk Sliwka

    Version of Record online : 28 OCT 2015, DOI: 10.1111/ecin.12285

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    Assessment of microsatellite alterations in young patients with gastric adenocarcinoma


    Volume 79, Issue 4, 15 February 1997, Pages: 684–687, Jeremy D. Hayden, Lynn Cawkwell, Henry Sue-Ling, David Johnston, Michael F. Dixon, Philip Quirke and Iain G. Martin

    Version of Record online : 27 SEP 2000, DOI: 10.1002/(SICI)1097-0142(19970215)79:4<684::AID-CNCR4>3.0.CO;2-E

  16. Can Unknown Predisposition in Familial Breast Cancer be Family-Specific?

    The Breast Journal

    Volume 19, Issue 5, September/October 2013, Pages: 520–528, Henry Lynch, Hongxiu Wen, Yeong C. Kim, Carrie Snyder, Yulia Kinarsky, Pei Xian Chen, Fengxia Xiao, David Goldgar, Kenneth H. Cowan and San Ming Wang

    Version of Record online : 26 JUN 2013, DOI: 10.1111/tbj.12145

  17. Pincer nail deformity as the main manifestation of Clouston syndrome

    British Journal of Dermatology

    Volume 173, Issue 2, August 2015, Pages: 581–583, Y.-H. Hu, Y.-C. Lin, W.-L. Hwu and Y.-M. Lee

    Version of Record online : 19 JUN 2015, DOI: 10.1111/bjd.13703

  18. Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss

    Prenatal Diagnosis

    Volume 36, Issue 13, December 2016, Pages: 1233–1241, Ying Chen, Yiqian Liu, Benjing Wang, Jun Mao, Ting Wang, Kan Ye, Yanlin Ye, David S. Cram and Hong Li

    Version of Record online : 9 DEC 2016, DOI: 10.1002/pd.4962

  19. The MC1R melanoma risk variant p.R160W is associated with Parkinson disease

    Annals of Neurology

    Volume 77, Issue 5, May 2015, Pages: 889–894, Gemma Tell-Marti, Joan Anton Puig-Butille, Miriam Potrony, Celia Badenas, Montserrat Milà, Josep Malvehy, María José Martí, Mario Ezquerra, Rubén Fernández-Santiago and Susana Puig

    Version of Record online : 13 MAR 2015, DOI: 10.1002/ana.24373

  20. You have full text access to this OnlineOpen article
    TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasia

    The Journal of Pathology: Clinical Research

    Jenny Wegert, Christian Vokuhl, Barbara Ziegler, Karen Ernestus, Ivo Leuschner, Rhoikos Furtwängler, Norbert Graf and Manfred Gessler

    Version of Record online : 14 AUG 2017, DOI: 10.1002/cjp2.77