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There are 1077 results for: content related to: Mutation screening of the EYA1, SIX1 , and SIX5 genes in an east asian cohort with branchio-oto-renal syndrome

  1. The AVR2–SIX5 gene pair is required to activate I-2-mediated immunity in tomato

    New Phytologist

    Volume 208, Issue 2, October 2015, Pages: 507–518, Lisong Ma, Petra M. Houterman, Fleur Gawehns, Lingxue Cao, Fabiano Sillo, Hanna Richter, Myriam J. Clavijo-Ortiz, Sarah M. Schmidt, Sjef Boeren, Jacques Vervoort, Ben J. C. Cornelissen, Martijn Rep and Frank L. W. Takken

    Article first published online : 13 MAY 2015, DOI: 10.1111/nph.13455

  2. You have free access to this content
    Dynamic expression of Six family genes in the dental mesenchyme and the epithelial ameloblast stem/progenitor cells during murine tooth development

    Journal of Anatomy

    Volume 216, Issue 1, January 2010, Pages: 80–91, Koji Nonomura, Masanori Takahashi, Yoshio Wakamatsu, Teruko Takano-Yamamoto and Noriko Osumi

    Article first published online : 9 NOV 2009, DOI: 10.1111/j.1469-7580.2009.01167.x

  3. Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations

    Human Mutation

    Volume 32, Issue 2, February 2011, Pages: 183–190, Pauline Krug, Vincent Morinière, Sandrine Marlin, Valérie Koubi, Heinz D. Gabriel, Estelle Colin, Dominique Bonneau, Rémi Salomon, Corinne Antignac and Laurence Heidet

    Article first published online : 28 JAN 2011, DOI: 10.1002/humu.21402

  4. Characterisation of the transcription factor, SIX5, using a new panel of monoclonal antibodies

    Journal of Cellular Biochemistry

    Volume 95, Issue 5, 1 August 2005, Pages: 990–1001, Y Chan N. Pham, Nguyen thi Man, Ian Holt, Caroline A. Sewry, Gurman Pall, Keith Johnson and Glenn E. Morris

    Article first published online : 16 JUN 2005, DOI: 10.1002/jcb.20454


    Standard Article

    Encyclopedia Of Molecular Medicine

    Sarah E. Harris and Keith J. Johnson

    Published Online : 15 JAN 2002, DOI: 10.1002/0471203076.emm0591

  6. A few more pieces of the DM puzzle

    Clinical Genetics

    Volume 59, Issue 3, March 2001, Pages: 150–152, Abigail S. Hackam

    Article first published online : 20 DEC 2001, DOI: 10.1034/j.1399-0004.2001.590302.x

  7. Myotonia and muscle contractile properties in mice with SIX5 deficiency

    Muscle & Nerve

    Volume 31, Issue 4, April 2005, Pages: 503–505, Kirkwood E. Personius, Joyti Nautiyal and Sita Reddy

    Article first published online : 9 NOV 2004, DOI: 10.1002/mus.20239

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    Branchio-oto-renal syndrome: Comprehensive review based on nationwide surveillance in Japan

    Pediatrics International

    Volume 56, Issue 3, June 2014, Pages: 309–314, Naoya Morisada, Kandai Nozu and Kazumoto Iijima

    Article first published online : 3 JUN 2014, DOI: 10.1111/ped.12357

  9. Genetic studies in congenital anterior midline cervical cleft

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 2021–2026, L.P. Jakobsen, P. Pfeiffer, M. Andersen, H. Eiberg, L. Hansen, Y. Mang, M. Bak, R.S. Møller, L.L. Klitten and N. Tommerup

    Article first published online : 11 JUL 2012, DOI: 10.1002/ajmg.a.35466

  10. You have full text access to this OnlineOpen article
    Identification of pathogenicity-related genes in Fusarium oxysporum f. sp. cepae

    Molecular Plant Pathology

    Andrew Taylor, Viktória Vágány, Alison C. Jackson, Richard J. Harrison, Alessandro Rainoni and John P. Clarkson

    Article first published online : 23 FEB 2016, DOI: 10.1111/mpp.12346

  11. Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genes

    Clinical Genetics

    Volume 73, Issue 3, March 2008, Pages: 262–267, L Olavarrieta, C Morales-Angulo, I Del Castillo, F Moreno and MA Moreno-Pelayo

    Article first published online : 30 DEC 2007, DOI: 10.1111/j.1399-0004.2007.00947.x

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    Identification and expression of six family genes in mouse retina

    FEBS Letters

    Volume 393, Issue 2-3, September 16, 1996, Pages: 259–263, Kiyoshi Kawakami, Hiromi Ohto, Toshihiro Takizawa and Takuma Saito

    Article first published online : 10 NOV 1999, DOI: 10.1016/0014-5793(96)00899-X

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    RNA steady-state defects in myotonic dystrophy are linked to nuclear exclusion of SHARP

    EMBO reports

    Volume 12, Issue 7, July 2011, Pages: 735–742, Warunee Dansithong, Sonali P Jog, Sharan Paul, Robabeh Mohammadzadeh, Stephanie Tring, Yukwah Kwok, Rebecca C Fry, Paul Marjoram, Lucio Comai and Sita Reddy

    Article first published online : 3 JUN 2011, DOI: 10.1038/embor.2011.86

  14. Six family genes—structure and function as transcription factors and their roles in development


    Volume 22, Issue 7, July 2000, Pages: 616–626, Kiyoshi Kawakami, Shigeru Sato, Hidenori Ozaki and Keiko Ikeda

    Article first published online : 23 JUN 2000, DOI: 10.1002/1521-1878(200007)22:7<616::AID-BIES4>3.0.CO;2-R

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    HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 976–985, Srirangan Sampath, Bronya J.B. Keats and Yves Lacassie

    Article first published online : 7 APR 2011, DOI: 10.1002/ajmg.a.33971

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    Effector gene screening allows unambiguous identification of Fusarium oxysporum f. sp. lycopersici races and discrimination from other formae speciales

    FEMS Microbiology Letters

    Volume 300, Issue 2, November 2009, Pages: 201–215, Bart Lievens, Petra M. Houterman and Martijn Rep

    Article first published online : 4 SEP 2009, DOI: 10.1111/j.1574-6968.2009.01783.x

  17. A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 396–402, Daniel R. Jensen, Donna M. Martin, Stephen Gebarski, Trilochan Sahoo, Ellen K. Brundage, A. Craig Chinault, Edgar A. Otto, Moumita Chaki, Friedhelm Hildebrandt, Sau Wai Cheung and Marci M. Lesperance

    Article first published online : 12 FEB 2009, DOI: 10.1002/ajmg.a.32691

  18. Molecular Genetic Basis of Myotonic Dystrophy

    Standard Article


    Jan Radvanszky and Ludevit Kadasi

    Published Online : 15 JAN 2013, DOI: 10.1002/9780470015902.a0023864

  19. Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle

    Muscle & Nerve

    Volume 23, Issue 9, September 2000, Pages: 1421–1426, Akira Inukai, Manabu Doyu, Takashi Kato, Yideng Liang, Satosi Kuru, Masahiko Yamamoto, Yasushi Kobayashi and Gen Sobue

    Article first published online : 15 AUG 2000, DOI: 10.1002/1097-4598(200009)23:9<1421::AID-MUS14>3.0.CO;2-Y

  20. A recurrent EYA1 mutation causing alternative RNA splicing in branchio-oto-renal syndrome: Implications for molecular diagnostics and disease mechanism

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 322–327, Tracy L. Stockley, Roberto Mendoza-Londono, Evan J. Propst, Sandi Sodhi, Lucie Dupuis and Blake C. Papsin

    Article first published online : 10 FEB 2009, DOI: 10.1002/ajmg.a.32679