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There are 37422 results for: content related to: Genetic and Epigenetic screening for gene alterations of the chromatin-remodeling factor, SMARCA4/BRG1, in lung tumors

  1. You have full text access to this OnlineOpen article
    Dual loss of the SWI/SNF complex ATPases SMARCA4/BRG1 and SMARCA2/BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type

    The Journal of Pathology

    Volume 238, Issue 3, February 2016, Pages: 389–400, Anthony N Karnezis, Yemin Wang, Pilar Ramos, William PD Hendricks, Esther Oliva, Emanuela D'Angelo, Jaime Prat, Marisa R Nucci, Torsten O Nielsen, Christine Chow, Samuel Leung, Friedrich Kommoss, Stefan Kommoss, Annacarolina Silva, Brigitte M Ronnett, Joseph T Rabban, David D Bowtell, Bernard E Weissman, Jeffrey M Trent, C Blake Gilks and David G Huntsman

    Version of Record online : 21 DEC 2015, DOI: 10.1002/path.4633

  2. You have free access to this content
    Retinal cone and rod photoreceptor cells exhibit differential susceptibility to light-induced damage

    Journal of Neurochemistry

    Volume 121, Issue 1, April 2012, Pages: 146–156, Kiichiro Okano, Akiko Maeda, Yu Chen, Vishal Chauhan, Johnny Tang, Grazyna Palczewska, Tsutomu Sakai, Hiroshi Tsuneoka, Krzysztof Palczewski and Tadao Maeda

    Version of Record online : 9 FEB 2012, DOI: 10.1111/j.1471-4159.2012.07647.x

  3. You have full text access to this OnlineOpen article
    Effective delivery of large genes to the retina by dual AAV vectors

    EMBO Molecular Medicine

    Volume 6, Issue 2, February 2014, Pages: 194–211, Ivana Trapani, Pasqualina Colella, Andrea Sommella, Carolina Iodice, Giulia Cesi, Sonia de Simone, Elena Marrocco, Settimio Rossi, Massimo Giunti, Arpad Palfi, Gwyneth J Farrar, Roman Polishchuk and Alberto Auricchio

    Version of Record online : 16 DEC 2013, DOI: 10.1002/emmm.201302948

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    Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation

    The Plant Journal

    Volume 70, Issue 2, April 2012, Pages: 292–302, Verena Kriechbaumer, Pengwei Wang, Chris Hawes and Ben M. Abell

    Version of Record online : 10 JAN 2012, DOI: 10.1111/j.1365-313X.2011.04866.x

  5. Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

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

    Volume 166, Issue 3, September 2014, Pages: 262–275, Tomoki Kosho, Nobuhiko Okamoto and Coffin-Siris Syndrome International Collaborators

    Version of Record online : 28 AUG 2014, DOI: 10.1002/ajmg.c.31407

  6. Retinol dehydrogenase 8 and ATP-binding cassette transporter 4 modulate dark adaptation of M-cones in mammalian retina

    The Journal of Physiology

    Volume 593, Issue 22, 15 November 2015, Pages: 4923–4941, Alexander V. Kolesnikov, Akiko Maeda, Peter H. Tang, Yoshikazu Imanishi, Krzysztof Palczewski and Vladimir J. Kefalov

    Version of Record online : 18 OCT 2015, DOI: 10.1113/JP271285

  7. Familial rhabdoid tumour 'avant la lettre'—from pathology review to exome sequencing and back again

    The Journal of Pathology

    Volume 231, Issue 1, September 2013, Pages: 35–43, Leora Witkowski, Emilie Lalonde, Jian Zhang, Steffen Albrecht, Nancy Hamel, Luca Cavallone, Sandra Thompson May, James C Nicholson, Nicholas Coleman, Matthew J Murray, Peter F Tauber, David G Huntsman, Stefan Schönberger, David Yandell, Martin Hasselblatt, Marc D Tischkowitz, Jacek Majewski and William D Foulkes

    Version of Record online : 6 AUG 2013, DOI: 10.1002/path.4225

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    The lipid translocase, ABCA4: seeing is believing

    The FEBS Journal

    Volume 278, Issue 18, September 2011, Pages: 3204–3214, Naomi Laura Pollock and Richard Callaghan

    Version of Record online : 13 JUN 2011, DOI: 10.1111/j.1742-4658.2011.08169.x

  9. Coffin–Siris syndrome is a SWI/SNF complex disorder

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 548–554, Y. Tsurusaki, N. Okamoto, H. Ohashi, S. Mizuno, N. Matsumoto, Y. Makita, M. Fukuda, B. Isidor, J. Perrier, S. Aggarwal, A.B. Dalal, A. Al-Kindy, J. Liebelt, D. Mowat, M. Nakashima, H. Saitsu, N. Miyake and N. Matsumoto

    Version of Record online : 23 JUL 2013, DOI: 10.1111/cge.12225

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    A metacaspase of Trypanosoma brucei causes loss of respiration competence and clonal death in the yeast Saccharomyces cerevisiae

    FEBS Letters

    Volume 517, Issue 1-3, April 24, 2002, Pages: 144–150, Alexander Szallies, Bruno K. Kubata and Michael Duszenko

    Version of Record online : 29 MAR 2002, DOI: 10.1016/S0014-5793(02)02608-X

  11. No small surprise – small cell carcinoma of the ovary, hypercalcaemic type, is a malignant rhabdoid tumour

    The Journal of Pathology

    Volume 233, Issue 3, July 2014, Pages: 209–214, William D Foulkes, Blaise A Clarke, Martin Hasselblatt, Jacek Majewski, Steffen Albrecht and W Glenn McCluggage

    Version of Record online : 20 MAY 2014, DOI: 10.1002/path.4362

  12. Coffin-Siris syndrome: Phenotypic evolution of a novel SMARCA4 mutation

    American Journal of Medical Genetics Part A

    Volume 164, Issue 7, July 2014, Pages: 1808–1814, Michael Tzeng, Christèle du Souich, Helen Wing-Hong Cheung and Cornelius F. Boerkoel

    Version of Record online : 3 APR 2014, DOI: 10.1002/ajmg.a.36533

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    p38 MAPK, but not ERK1/2, is critically involved in the cytotoxicity of the novel vascular disrupting agent combretastatin A4

    International Journal of Cancer

    Volume 122, Issue 8, 15 April 2008, Pages: 1730–1737, Haitian Quan, Yongping Xu and Liguang Lou

    Version of Record online : 11 DEC 2007, DOI: 10.1002/ijc.23262

  14. Clinical correlations of mutations affecting six components of the SWI/SNF complex: Detailed description of 21 patients and a review of the literature

    American Journal of Medical Genetics Part A

    Volume 161, Issue 6, June 2013, Pages: 1221–1237, Tomoki Kosho, Nobuhiko Okamoto, Hirofumi Ohashi, Yoshinori Tsurusaki, Yoko Imai, Yumiko Hibi-Ko, Hiroshi Kawame, Tomomi Homma, Saori Tanabe, Mitsuhiro Kato, Yoko Hiraki, Takanori Yamagata, Shoji Yano, Satoru Sakazume, Takuma Ishii, Toshiro Nagai, Tohru Ohta, Norio Niikawa, Seiji Mizuno, Tadashi Kaname, Kenji Naritomi, Yoko Narumi, Keiko Wakui, Yoshimitsu Fukushima, Satoko Miyatake, Takeshi Mizuguchi, Hirotomo Saitsu, Noriko Miyake and Naomichi Matsumoto

    Version of Record online : 1 MAY 2013, DOI: 10.1002/ajmg.a.35933

  15. Coffin–Siris Syndrome and the BAF Complex: Genotype–Phenotype Study in 63 Patients

    Human Mutation

    Volume 34, Issue 11, November 2013, Pages: 1519–1528, Gijs W.E. Santen, Emmelien Aten, Anneke T. Vulto-van Silfhout, Caroline Pottinger, Bregje W.M. van Bon, Ivonne J.H.M. van Minderhout, Ronelle Snowdowne, Christian A.C. van der Lans, Merel Boogaard, Margot M.L. Linssen, Linda Vijfhuizen, Michiel J.R. van der Wielen, M.J. (Ellen) Vollebregt, the Coffin-Siris consortium, Martijn H. Breuning, Marjolein Kriek, Arie van Haeringen, Johan T. den Dunnen, Alexander Hoischen, Jill Clayton-Smith, Bert B.A. de Vries, Raoul C.M. Hennekam, Martine J. van Belzen, Mariam Almureikhi, Anwar Baban, Mafalda Barbosa, Tawfeg Ben-Omran, Katherine Berry, Stefania Bigoni, Odile Boute, Louise Brueton, Ineke van der Burgt, Natalie Canham, Kate E. Chandler, Krystyna Chrzanowska, Amanda L. Collins, Teresa de Toni, John Dean, Nicolette S. den Hollander, Leigh Anne Flore, Alan Fryer, Alice Gardham, John M. Graham Jr., Victoria Harrison, Denise Horn, Marjolijn C. Jongmans, Dragana Josifova, Sarina G. Kant, Seema Kapoor, Helen Kingston, Usha Kini, Tjitske Kleefstra, Małgorzata Krajewska-Walasek, Nancy Kramer, Saskia M. Maas, Patricia Maciel, Grazia M.S. Mancini, Isabelle Maystadt, Shane McKee, Jeff M. Milunsky, Sheela Nampoothiri, Ruth Newbury-Ecob, Sarah M. Nikkel, Michael J. Parker, Luis A. Pérez-Jurado, Stephen P. Robertson, Caroline Rooryck, Debbie Shears, Margherita Silengo, Ankur Singh, Robert Smigiel, Gabriela Soares, Miranda Splitt, Helen Stewart, Elizabeth Sweeney, May Tassabehji, Beyhan Tuysuz, Albertien M. van Eerde, Catherine Vincent-Delorme, Louise C. Wilson and Gozde Yesil

    Version of Record online : 30 AUG 2013, DOI: 10.1002/humu.22394

  16. Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant

    Human Mutation

    Volume 36, Issue 1, January 2015, Pages: 43–47, Nathalie M. Bax, Riccardo Sangermano, Susanne Roosing, Alberta A.H.J. Thiadens, Lies H. Hoefsloot, L. Ingeborgh van den Born, Milan Phan, B. Jeroen Klevering, Carla Westeneng-van Haaften, Terry A. Braun, Marijke N. Zonneveld-Vrieling, Ilse de Wijs, Merve Mutlu, Edwin M. Stone, Anneke I. den Hollander, Caroline C.W. Klaver, Carel B. Hoyng and Frans P.M. Cremers

    Version of Record online : 30 DEC 2014, DOI: 10.1002/humu.22717

  17. You have free access to this content
    Retinal Photodamage Mediated by All-trans-retinal

    Photochemistry and Photobiology

    Volume 88, Issue 6, November/December 2012, Pages: 1309–1319, Tadao Maeda, Marcin Golczak and Akiko Maeda

    Version of Record online : 24 APR 2012, DOI: 10.1111/j.1751-1097.2012.01143.x

  18. A Tobacco etch virus NW isolate that overcomes pvr1 and pvr12 resistance in Capsicum sp.

    Plant Pathology

    Volume 63, Issue 3, June 2014, Pages: 675–683, N. Velasquez and J. F. Murphy

    Version of Record online : 26 AUG 2013, DOI: 10.1111/ppa.12121

  19. Biallelic somatic SMARCA4 mutations in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)

    Pediatric Blood & Cancer

    Volume 62, Issue 4, April 2015, Pages: 728–730, Shivani Bailey, Matthew J. Murray, Leora Witkowski, Elizabeth Hook, Martin Hasselblatt, Robin Crawford, William D. Foulkes, Marc Tischkowitz and James C. Nicholson

    Version of Record online : 12 OCT 2014, DOI: 10.1002/pbc.25279

  20. Distinct Phenotypes among Plasma Membrane Ca2+-ATPase Knockout Mice

    Annals of the New York Academy of Sciences

    Volume 1099, Issue 1, March 2007, Pages: 276–286, VIKRAM PRASAD, GBOLAHAN OKUNADE, LI LIU, RICHARD J. PAUL and GARY E. SHULL

    Version of Record online : 13 APR 2007, DOI: 10.1196/annals.1387.029