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There are 8144 results for: content related to: Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues

  1. Inactivation of the von Hippel–Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: Evidence for a VHL-independent pathway in clear cell renal tumourigenesis

    Genes, Chromosomes and Cancer

    Volume 22, Issue 3, July 1998, Pages: 200–209, Steven C. Clifford, Amanda H. Prowse, Nabeel A. Affara, Charles H. C. M. Buys and Eamonn R. Maher

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199807)22:3<200::AID-GCC5>3.0.CO;2-#

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    Tongue cancer patients have a high frequency of allelic loss at the von Hippel-Lindau gene and other loci on 3p

    Cancer

    Volume 112, Issue 3, 1 February 2008, Pages: 527–534, Takeshi Asakawa, Mariko Esumi, Sohei Endo, Akinori Kida and Minoru Ikeda

    Version of Record online : 10 DEC 2007, DOI: 10.1002/cncr.23200

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    Critical tumor-suppressor gene regions on chromosome 3P in major human epithelial malignancies: Allelotyping and quantitative real-time PCR

    International Journal of Cancer

    Volume 100, Issue 5, 10 August 2002, Pages: 534–541, Eleonora Braga, Vera Senchenko, Igor Bazov, Witaly Loginov, Jian Liu, Valeria Ermilova, Tatiana Kazubskaya, Raisa Garkavtseva, Natalia Mazurenko, Fedor Kisseljov, Michael I. Lerman, George Klein, Lev Kisselev and Eugene R. Zabarovsky

    Version of Record online : 19 JUN 2002, DOI: 10.1002/ijc.10511

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    Location of candidate tumour suppressor gene loci at chromosomes 3p, 8p and 9p for oral squamous cell carcinomas

    International Journal of Cancer

    Volume 83, Issue 3, 29 October 1999, Pages: 318–325, M. Partridge, G. Emilion, S. Pateromichelakis, E. Phillips and J. Langdon

    Version of Record online : 10 NOV 1999, DOI: 10.1002/(SICI)1097-0215(19991029)83:3<318::AID-IJC6>3.0.CO;2-V

  5. A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma

    Genes, Chromosomes and Cancer

    Volume 46, Issue 9, September 2007, Pages: 805–812, Kathryn S. Poland, Mohammed Azim, Matthew Folsom, Richard Goldfarb, Rizwan Naeem, Christopher Korch, Harry A. Drabkin, Robert M. Gemmill and Sharon E. Plon

    Version of Record online : 30 MAY 2007, DOI: 10.1002/gcc.20466

  6. Comparative analysis of loss of heterozygosity of specific chromosome 3, 13, 17, and X loci and TP53 mutations in human epithelial ovarian cancer

    Molecular Carcinogenesis

    Volume 34, Issue 2, 2002, Pages: 78–90, Emily N. Manderson, Nadège Presneau, Diane Provencher, Anne-Marie Mes-Masson and Patricia N. Tonin

    Version of Record online : 22 MAY 2002, DOI: 10.1002/mc.10051

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    Vascular endothelial growth factor overexpression is correlated with von Hippel-Lindau tumor suppressor gene inactivation in patients with sporadic renal cell carcinoma

    Cancer

    Volume 95, Issue 1, 1 July 2002, Pages: 47–53, Hiroshi Igarashi, Mariko Esumi, Hajime Ishida and Kiyoki Okada

    Version of Record online : 28 JUN 2002, DOI: 10.1002/cncr.10635

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    Molecular genetic analysis of the von Hippel-Lindau and human peroxisome proliferator–activated receptor γ tumor-suppressor genes in adenocarcinomas of the gastroesophageal junction

    International Journal of Cancer

    Volume 94, Issue 6, 15 December 2001, Pages: 891–895, Bas P.L. Wijnhoven, Eric Wim Lindstedt, Mustaffa Abbou, Ynske Ijzendoorn, Ronald R. de Krijger, Hugo W. Tilanus and Winand N.M. Dinjens

    Version of Record online : 23 SEP 2001, DOI: 10.1002/ijc.1559

  9. Frequent loss of heterozygosity at chromosome 3p14.2–3p21 in human pancreatic islet cell tumours

    Clinical Endocrinology

    Volume 51, Issue 1, July 1999, Pages: 27–33, Marina N. Nikiforova, Yuri E. Nikiforov, Paul Biddinger, Douglas R. Gnepp, Luis A. Grosembacher, Bernardo L. Wajchenberg, James A. Fagin and Robert M. Cohen

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2265.1999.00785.x

  10. Comprehensive mutational analysis of the VHL gene in sporadic renal cell carcinoma: Relationship to clinicopathological parameters

    Genes, Chromosomes and Cancer

    Volume 34, Issue 1, May 2002, Pages: 58–68, Keiichi Kondo, Masahiro Yao, Minoru Yoshida, Takeshi Kishida, Taro Shuin, Takeshi Miura, Masatoshi Moriyama, Kazuki Kobayashi, Naoki Sakai, Shigeki Kaneko, Satoshi Kawakami, Masaya Baba, Noboru Nakaigawa, Yoji Nagashima, Yukio Nakatani and Masahiko Hosaka

    Version of Record online : 7 FEB 2002, DOI: 10.1002/gcc.10054

  11. Somatic von Hippel–Lindau disease gene mutation in clear-cell renal carcinomas associated with end-stage renal disease/acquired cystic disease of the kidney

    Genes, Chromosomes and Cancer

    Volume 35, Issue 4, December 2002, Pages: 359–364, Minoru Yoshida, Masahiro Yao, Isao Ishikawa, Takeshi Kishida, Yoji Nagashima, Kei-ichi Kondo, Noboru Nakaigawa and Masahiko Hosaka

    Version of Record online : 15 SEP 2002, DOI: 10.1002/gcc.10123

  12. Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification

    Clinical Genetics

    Volume 72, Issue 2, August 2007, Pages: 122–129, FJ Hes, RB van der Luijt, ALW Janssen, RA Zewald, GJ de Jong, JW Lenders, TP Links, GPM Luyten, RH Sijmons, HJ Eussen, DJJ Halley, CJM Lips, PL Pearson, AMW van den Ouweland and DF Majoor-Krakauer

    Version of Record online : 4 JUL 2007, DOI: 10.1111/j.1399-0004.2007.00827.x

  13. Detailed deletion mapping of chromosome arm 3p in breast cancers: A 2-cM region on 3p14.3-21.1 and a 5-cM region on 3p24.3-25.1 commonly deleted in tumors

    Genes, Chromosomes and Cancer

    Volume 20, Issue 3, November 1997, Pages: 268–274, Satoshi Matsumoto, Fujio Kasumi, Goi Sakamoto, Masahiko Onda, Yusuke Nakamura and Mitsuru Emi

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199711)20:3<268::AID-GCC7>3.0.CO;2-0

  14. Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 15–26, Celeste Bento, Melanie J. Percy, Betty Gardie, Tabita Magalhães Maia, Richard van Wijk, Silverio Perrotta, Fulvio Della Ragione, Helena Almeida, Cedric Rossi, François Girodon, Maria Åström, Drorit Neumann, Susanne Schnittger, Britta Landin, Milen Minkov, Maria Luigia Randi, Stéphane Richard, Nicole Casadevall, William Vainchenker, Susana Rives, Sylvie Hermouet, M. Leticia Ribeiro, Mary Frances McMullin, Holger Cario, on behalf of ECE-Consortium, Aurelie Chauveau, Anne-Paule Gimenez-Roqueplo, Brigitte Bressac-de-Paillerets, Didem Altindirek, Felipe Lorenzo, Frederic Lambert, Harlev Dan, Sophie Gad-Lapiteau, Ana Catarina Oliveira, Cédric Rossi, Cristina Fraga, Gennadiy Taradin, Guillermo Martin-Nuñez, Helena Vitória, Herrera Diaz Aguado, Jan Palmblad, Julia Vidán, Luis Relvas, Maria Leticia Ribeiro, Maria Luigi Larocca, Maria Luigia Randi, Maria Pedro Silveira, Melanie Percy, Mor Gross, Ricardo Marques da Costa, Soheir Beshara, Tal Ben-Ami and Valérie Ugo

    Version of Record online : 22 OCT 2013, DOI: 10.1002/humu.22448

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    Hypoxia-inducible transcription factor 2α promotes steatohepatitis through augmenting lipid accumulation, inflammation, and fibrosis

    Hepatology

    Volume 54, Issue 2, August 2011, Pages: 472–483, Aijuan Qu, Matthew Taylor, Xiang Xue, Tsutomu Matsubara, Daniel Metzger, Pierre Chambon, Frank J. Gonzalez and Yatrik M. Shah

    Version of Record online : 26 JUN 2011, DOI: 10.1002/hep.24400

  16. Involvement of multiple loci on chromosome 3 in renal cell cancer development

    Genes, Chromosomes and Cancer

    Volume 19, Issue 2, June 1997, Pages: 59–76, Anke van den Berg and Charles H. C. M. Buys

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199706)19:2<59::AID-GCC1>3.0.CO;2-Z

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    Clinical response to therapy targeted at vascular endothelial growth factor in metastatic renal cell carcinoma: impact of patient characteristics and Von Hippel-Lindau gene status

    BJU International

    Volume 98, Issue 4, October 2006, Pages: 756–762, Brian I. Rini, Erich Jaeger, Vivian Weinberg, Nancy Sein, Karen Chew, Kristen Fong, Jeffery Simko, Eric J. Small and Frederic M. Waldman

    Version of Record online : 7 JUL 2006, DOI: 10.1111/j.1464-410X.2006.06376.x

  18. Expression of HGF/SF and Met protein is associated with genetic alterations of VHL gene in primary renal cell carcinomas

    APMIS

    Volume 110, Issue 3, March 2002, Pages: 229–238, Ro Ra Oh, Jik Young Park, Jong Heun Lee, Min Sun Shin, Hong Sug Kim, Sang Kyu Lee, Young Sil Kim, Sug Hyung Lee, Sie Nae Lee, Young Mok Yang, Nam Jin Yoo, Jung Young Lee and Won Sang Park

    Version of Record online : 20 JUN 2002, DOI: 10.1034/j.1600-0463.2002.100305.x

  19. Genotype–phenotype correlations in VHL exon deletions

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 10, October 2009, Pages: 2147–2151, Alisdair McNeill, Eleanor Rattenberry, Richard Barber, Pip Killick, Fiona MacDonald and Eamonn R. Maher

    Version of Record online : 16 SEP 2009, DOI: 10.1002/ajmg.a.33023

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    Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas

    International Journal of Cancer

    Volume 105, Issue 2, 10 June 2003, Pages: 190–195, Hilde Dannenberg, Ronald R. De Krijger, Erwin van der Harst, Mustaffa Abbou, Ynske IJzendoorn, Paul Komminoth and Winand N.M. Dinjens

    Version of Record online : 5 MAR 2003, DOI: 10.1002/ijc.11060