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There are 4574 results for: content related to: Distribution and molecular characterization of Corynespora cassiicola isolates resistant to boscalid

  1. You have free access to this content
    SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes

    Journal of Internal Medicine

    Volume 266, Issue 1, July 2009, Pages: 19–42, B. Pasini and C. A. Stratakis

    Version of Record online : 7 APR 2009, DOI: 10.1111/j.1365-2796.2009.02111.x

  2. High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands

    Clinical Genetics

    Volume 81, Issue 3, March 2012, Pages: 284–288, EF Hensen, N van Duinen, JC Jansen, EPM Corssmit, CMJ Tops, JA Romijn, AHJT Vriends, AGL van der Mey, CJ Cornelisse, P Devilee and JP Bayley

    Version of Record online : 15 MAR 2011, DOI: 10.1111/j.1399-0004.2011.01653.x

  3. You have free access to this content
    Characterization of mutations in the membrane-anchored subunits AaSDHC and AaSDHD of succinate dehydrogenase from Alternaria alternata isolates conferring field resistance to the fungicide boscalid

    Plant Pathology

    Volume 58, Issue 6, December 2009, Pages: 1134–1143, H. Avenot, A. Sellam and T. Michailides

    Version of Record online : 30 SEP 2009, DOI: 10.1111/j.1365-3059.2009.02154.x

  4. Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients

    Clinical Endocrinology

    Volume 75, Issue 5, November 2011, Pages: 650–655, E. F. Hensen, M. D. Siemers, J. C. Jansen, E. P. M. Corssmit, J. A. Romijn, C. M. J. Tops, A. G. L. van der Mey, P. Devilee, C. J. Cornelisse, J. P. Bayley and A. H. J. T. Vriends

    Version of Record online : 4 OCT 2011, DOI: 10.1111/j.1365-2265.2011.04097.x

  5. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility

    Clinical Endocrinology

    Volume 59, Issue 6, December 2003, Pages: 728–733, Dewi Astuti, Niki Hart-Holden, Farida Latif, Fiona Lalloo, Graeme C. Black, Caron Lim, Anthony Moran, Ashley B. Grossman, Shirley V. Hodgson, Anthony Freemont, Richard Ramsden, Charis Eng, D. Gareth R. Evans and Eamonn R. Maher

    Version of Record online : 20 NOV 2003, DOI: 10.1046/j.1365-2265.2003.01914.x

  6. You have free access to this content
    Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma

    Clinical Endocrinology

    Volume 78, Issue 6, June 2013, Pages: 898–906, Mariam Jafri, James Whitworth, Eleanor Rattenberry, Lindsey Vialard, Gail Kilby, Ajith V. Kumar, Louise Izatt, Fiona Lalloo, Paul Brennan, Jackie Cook, Patrick J. Morrison, Natalie Canham, Ruth Armstrong, Carole Brewer, Susan Tomkins, Alan Donaldson, Julian Barwell, Trevor R. Cole, A. Brew Atkinson, Simon Aylwin, Steve G. Ball, Umasuthan Srirangalingam, Shern L. Chew, Dafydd Gareth R Evans, Shirley V. Hodgson, Richard Irving, Emma Woodward, Fiona Macdonald and Eamonn R. Maher

    Version of Record online : 6 APR 2013, DOI: 10.1111/cen.12074

  7. Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 274–281, Peter E.M. Taschner, Jeroen C. Jansen, Bora E. Baysal, Anne Bosch, Efraim H. Rosenberg, Annette H.J.T. Bröcker-Vriends, Andel G.L. van der Mey, Gert-Jan B. van Ommen, Cees J. Cornelisse and Peter Devilee

    Version of Record online : 4 MAY 2001, DOI: 10.1002/gcc.1144

  8. You have full text access to this OnlineOpen article
    Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma

    Clinical Genetics

    A.S. Hoekstra, B. van den Ende, X.P. Julià, L. van Breemen, K. Scheurwater, C.M. Tops, A. Malinoc, P. Devilee, H.P.H. Neumann and J.-P. Bayley

    Version of Record online : 6 DEC 2016, DOI: 10.1111/cge.12843

  9. SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas

    Clinical Genetics

    Volume 66, Issue 5, November 2004, Pages: 461–466, AN Mhatre, Y Li, L Feng, A Gasperin and AK Lalwani

    Version of Record online : 11 OCT 2004, DOI: 10.1111/j.1399-0004.2004.00328.x

  10. Genomic imprinting and environment in hereditary paraganglioma

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 129C, Issue 1, 15 August 2004, Pages: 85–90, Bora E. Baysal

    Version of Record online : 1 JUL 2004, DOI: 10.1002/ajmg.c.30018

  11. Genetics of hereditary head and neck paragangliomas

    Head & Neck

    Volume 36, Issue 6, June 2014, Pages: 907–916, Carsten C. Boedeker, Erik F. Hensen, Hartmut P.H. Neumann, Wolfgang Maier, Francien H. van Nederveen, Carlos Suárez, Henricus P. Kunst, Juan P. Rodrigo, Robert P. Takes, Phillip K. Pellitteri, Alessandra Rinaldo and Alfio Ferlito

    Version of Record online : 30 NOV 2013, DOI: 10.1002/hed.23436

  12. A novel G106D alteration of the SDHD gene in a pedigree with familial paraganglioma

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 22, 15 November 2006, Pages: 2441–2446, Kazumi Ogawa, Kiyoto Shiga, Shigeru Saijo, Takenori Ogawa, Noriko Kimura and Akira Horii

    Version of Record online : 13 OCT 2006, DOI: 10.1002/ajmg.a.31444

  13. Risk assessment studies on succinate dehydrogenase inhibitors, the new weapons in the battle to control Septoria leaf blotch in wheat

    Molecular Plant Pathology

    Volume 13, Issue 3, April 2012, Pages: 263–275, BART A. FRAAIJE, CARLOS BAYON, SARAH ATKINS, HANS J. COOLS, JOHN A. LUCAS and MARCO W. FRAAIJE

    Version of Record online : 20 SEP 2011, DOI: 10.1111/j.1364-3703.2011.00746.x

  14. Mendelian genetics of rare—and not so rare—cancers

    Annals of the New York Academy of Sciences

    Volume 1214, Issue 1, December 2010, Pages: 70–82, Charis Eng

    Version of Record online : 28 SEP 2010, DOI: 10.1111/j.1749-6632.2010.05789.x

  15. No difference in phenotype of the main Dutch SDHD founder mutations

    Clinical Endocrinology

    Volume 79, Issue 6, December 2013, Pages: 824–831, L. T. van Hulsteijn, A. C. den Dulk, F. J. Hes, J. P. Bayley, J. C. Jansen and E. P. M. Corssmit

    Version of Record online : 11 MAY 2013, DOI: 10.1111/cen.12223

  16. A new point mutation in the iron–sulfur subunit of succinate dehydrogenase confers resistance to boscalid in Sclerotinia sclerotiorum

    Molecular Plant Pathology

    Volume 16, Issue 7, September 2015, Pages: 653–661, Yong Wang, Yabing Duan, Jianxin Wang and Mingguo Zhou

    Version of Record online : 29 JAN 2015, DOI: 10.1111/mpp.12222

  17. Cloning, mapping and association study with carcass traits of the porcine SDHD gene

    Animal Genetics

    Volume 36, Issue 3, June 2005, Pages: 191–195, Z. M. Zhu, J. B. Zhang, K. Li and S. H. Zhao

    Version of Record online : 28 APR 2005, DOI: 10.1111/j.1365-2052.2005.01270.x

  18. Genetic and Clinical Investigation of Pheochromocytoma

    Annals of the New York Academy of Sciences


    Version of Record online : 7 SEP 2006, DOI: 10.1196/annals.1353.013

  19. SNP discovery, expression and association analysis for the SDHD gene in pigs

    Journal of Animal Breeding and Genetics

    Volume 124, Issue 4, August 2007, Pages: 246–253, S.E.F. Guimaraes, M.F. Rothschild, D. Ciobanu, C.H. Stahl and S.M. Lonergan

    Version of Record online : 20 JUL 2007, DOI: 10.1111/j.1439-0388.2007.00667.x

  20. Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis

    International Journal of Andrology

    Volume 30, Issue 3, June 2007, Pages: 144–152, Sandra Bonache, Juanjo Martínez, Marlin Fernández, Lluís Bassas and Sara Larriba

    Version of Record online : 12 FEB 2007, DOI: 10.1111/j.1365-2605.2006.00730.x