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There are 37117 results for: content related to: Overexpression of forkhead box C1 promotes tumor metastasis and indicates poor prognosis in hepatocellular carcinoma

  1. You have free access to this content
    Foxc1 is required for early stage telencephalic vascular development

    Developmental Dynamics

    Volume 244, Issue 5, May 2015, Pages: 703–711, Thanit Prasitsak, Mya Nandar, Shigeru Okuhara, Shizuko Ichinose, Masato S. Ota and Sachiko Iseki

    Version of Record online : 8 APR 2015, DOI: 10.1002/dvdy.24269

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    Digenic inheritance of mutations in FOXC1 and PITX2 : Correlating transcription factor function and axenfeld-rieger disease severity

    Human Mutation

    Volume 32, Issue 10, October 2011, Pages: 1144–1152, Daniel Kelberman, Lily Islam, Susan E. Holder, Thomas S. Jacques, Patrick Calvas, Raoul C. Hennekam, Ken K. Nischal and Jane C. Sowden

    Version of Record online : 8 SEP 2011, DOI: 10.1002/humu.21550

  3. Generation of conditional alleles for Foxc1 and Foxc2 in mice

    genesis

    Volume 50, Issue 10, October 2012, Pages: 766–774, Amy Sasman, Carey Nassano-Miller, Kyoo Seok Shim, Hyun Young Koo, Ting Liu, Kathryn M. Schultz, Meredith Millay, Atsushi Nanano, Myengmo Kang, Takashi Suzuki and Tsutomu Kume

    Version of Record online : 14 MAY 2012, DOI: 10.1002/dvg.22036

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    Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice

    Congenital Anomalies

    Volume 54, Issue 3, August 2014, Pages: 172–177, Akihiko Machida, Shigeru Okuhara, Kiyoshi Harada and Sachiko Iseki

    Version of Record online : 21 AUG 2014, DOI: 10.1111/cga.12053

  5. Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis

    Clinical Genetics

    Volume 76, Issue 3, September 2009, Pages: 296–299, CD Fetterman, F Mirzayans and MA Walter

    Version of Record online : 24 SEP 2009, DOI: 10.1111/j.1399-0004.2009.01210.x

  6. A novel mutation in the FOXC1 gene in a family with Axenfeld–Rieger syndrome and Peters’ anomaly

    Clinical Genetics

    Volume 74, Issue 5, November 2008, Pages: 476–480, N Weisschuh, C Wolf, B Wissinger and E Gramer

    Version of Record online : 21 MAY 2008, DOI: 10.1111/j.1399-0004.2008.01025.x

  7. Cardiac anomalies in Axenfeld–Rieger syndrome due to a novel FOXC1 mutation

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 114–119, Karen W. Gripp, Elizabeth Hopkins, Kim Jenny, Deepika Thacker and Jonathan Salvin

    Version of Record online : 14 DEC 2012, DOI: 10.1002/ajmg.a.35697

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    A dicotyledon-specific glutaredoxin GRXC1 family with dimer-dependent redox regulation is functionally redundant with GRXC2

    Plant, Cell & Environment

    Volume 35, Issue 2, February 2012, Pages: 360–373, CHRISTOPHE RIONDET, JEAN PAUL DESOURIS, JOCELYNE GUILLEMINOT MONTOYA, YVETTE CHARTIER, YVES MEYER and JEAN-PHILIPPE REICHHELD

    Version of Record online : 19 JUL 2011, DOI: 10.1111/j.1365-3040.2011.02355.x

  9. Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2430–2438, Andrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean-Luc Alessandri, Marion Gérard, Pierre Bitoun, Julien Boumendil, Stéphanie Robin, Chan Huel, Romain Guilherme, Stéphane Serero, Pierre Gressens, Jacques Elion, Alain Verloes, Brigitte Benzacken, Anne-Lise Delezoide and Eva Pipiras

    Version of Record online : 17 AUG 2012, DOI: 10.1002/ajmg.a.35548

  10. FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 3, 30 January 2004, Pages: 280–287, Hui Z. Zhang, Peining Li, Dongmei Wang, Shannon Huff, Manjunath Nimmakayalu, Mazin Qumsiyeh and Barbara R. Pober

    Version of Record online : 31 JUL 2003, DOI: 10.1002/ajmg.a.20413

  11. Anirdia-like phenotype caused by 6p25 dosage aberrations

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 524–528, Karthikeyan Arcot Sadagopan, Grace T. Liu, Jenina E. Capasso, Wadakarn Wuthisiri, Rosanne B. Keep and Alex V. Levin

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36890

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    Identification of Tgfβ1i4 as a downstream target of Foxc1

    Development, Growth & Differentiation

    Volume 48, Issue 5, June 2006, Pages: 297–308, Paula Sommer, Hugh R. Napier, Brigid L. Hogan and Susan H. Kidson

    Version of Record online : 1 JUN 2006, DOI: 10.1111/j.1440-169X.2006.00866.x

  13. Foxc1 Expression in Early Osteogenic Differentiation Is Regulated by BMP4-SMAD Activity

    Journal of Cellular Biochemistry

    Volume 117, Issue 7, July 2016, Pages: 1707–1717, Alexander Hopkins, Freda Mirzayans and Fred Berry

    Version of Record online : 15 JAN 2016, DOI: 10.1002/jcb.25464

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    The role of FoxC1 in early Xenopus development

    Developmental Dynamics

    Volume 236, Issue 10, October 2007, Pages: 2731–2741, J.Y. Cha, B. Birsoy, M. Kofron, E. Mahoney, S. Lang, C. Wylie and J. Heasman

    Version of Record online : 17 AUG 2007, DOI: 10.1002/dvdy.21240

  15. Axenfeld–Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 4, 1 February 2005, Pages: 381–385, Kenneth Maclean, James Smith, Luke St. Heaps, Nicole Chia, Rebecca Williams, Gregory B. Peters, Ella Onikul, Tim McCrossin, Ordan J. Lehmann and Lesley C. Adès

    Version of Record online : 14 JAN 2005, DOI: 10.1002/ajmg.a.30274

  16. Foxc1 Regulates Early Cardiomyogenesis and Functional Properties of Embryonic Stem Cell Derived Cardiomyocytes

    STEM CELLS

    Volume 34, Issue 6, June 2016, Pages: 1487–1500, Erin Lambers, Baron Arnone, Anees Fatima, Gangjian Qin, J. Andrew Wasserstrom and Tsutomu Kume

    Version of Record online : 18 FEB 2016, DOI: 10.1002/stem.2301

  17. Renal complications in 6p duplication syndrome: Microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 592–601, Megumi Yoshimura-Furuhata, Akira Nishimura-Tadaki, Yoshiro Amano, Takashi Ehara, Yuko Hamasaki, Masaki Muramatsu, Seiichiro Shishido, Atsushi Aikawa, Riku Hamada, Kenji Ishikura, Hiroshi Hataya, Yoshihiko Hidaka, Shunsuke Noda, Kenichi Koike, Keiko Wakui, Yoshimitsu Fukushima, Naomichi Matsumoto, Midori Awazu, Noriko Miyake and Tomoki Kosho

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36942

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    Abstracts

    Congenital Anomalies

    Volume 53, Issue 4, December 2013, Pages: A1–A22,

    Version of Record online : 1 DEC 2013, DOI: 10.1111/cga.12033

  19. Deregulated FOX genes in Hodgkin lymphoma

    Genes, Chromosomes and Cancer

    Volume 53, Issue 11, November 2014, Pages: 917–933, Stefan Nagel, Corinna Meyer, Maren Kaufmann, Hans G. Drexler and Roderick A. F. MacLeod

    Version of Record online : 17 JUL 2014, DOI: 10.1002/gcc.22204

  20. Primary cellular meningeal defects cause neocortical dysplasia and dyslamination

    Annals of Neurology

    Volume 68, Issue 4, October 2010, Pages: 454–464, Jonathan H. Hecht, Julie A. Siegenthaler, Katelin P. Patterson and Samuel J. Pleasure

    Version of Record online : 25 OCT 2010, DOI: 10.1002/ana.22103