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There are 25983 results for: content related to: Forkhead box protein C2 contributes to invasion and metastasis of extrahepatic cholangiocarcinoma, resulting in a poor prognosis

  1. 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

  2. You have full text access to this OnlineOpen article
    miR-639 regulates transforming growth factor beta-induced epithelial–mesenchymal transition in human tongue cancer cells by targeting FOXC1

    Cancer Science

    Volume 105, Issue 10, October 2014, Pages: 1288–1298, Zhaoyu Lin, Lijuan Sun, Weiliang Chen, Bodu Liu, Youyuan Wang, Song Fan, Yilin Li and Jinsong Li

    Version of Record online : 29 SEP 2014, DOI: 10.1111/cas.12499

  3. Inorganic phosphate induces cancer cell mediated angiogenesis dependent on forkhead box protein C2 (FOXC2) regulated osteopontin expression

    Molecular Carcinogenesis

    Volume 54, Issue 9, September 2015, Pages: 926–934, Yiming Lin, Kelly E. McKinnon, Shin Woo Ha and George R. Beck Jr.

    Version of Record online : 2 APR 2014, DOI: 10.1002/mc.22153

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    Reduced PDE4 expression and activity contributes to enhanced catecholamine-induced cAMP accumulation in adipocytes from FOXC2 transgenic mice

    FEBS Letters

    Volume 580, Issue 17, July 24, 2006, Pages: 4126–4130, Line M. Grønning, George S. Baillie, Anna Cederberg, Martin J. Lynch, Miles D. Houslay, Sven Enerbäck and Kjetil Taskén

    Version of Record online : 30 JUN 2006, DOI: 10.1016/j.febslet.2006.06.058

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    Large-scale identification of genes implicated in kidney glomerulus development and function

    The EMBO Journal

    Volume 25, Issue 5, March 8, 2006, Pages: 1160–1174, Minoru Takemoto, Liqun He, Jenny Norlin, Jaakko Patrakka, Zhijie Xiao, Tatiana Petrova, Cecilia Bondjers, Julia Asp, Elisabet Wallgard, Ying Sun, Tore Samuelsson, Petter Mostad, Samuel Lundin, Naoyuki Miura, Yoshikazu Sado, Kari Alitalo, Susan E Quaggin, Karl Tryggvason and Christer Betsholtz

    Version of Record online : 23 FEB 2006, DOI: 10.1038/sj.emboj.7601014

  6. A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 3, 15 December 2004, Pages: 281–286, Cagri Yildirim-Toruner, Kavitha Subramanian, Lamya El Manjra, Emily Chen, Stanley Goldstein and Emilia Vitale

    Version of Record online : 2 NOV 2004, DOI: 10.1002/ajmg.a.30390

  7. The clinical significance of mesenchyme forkhead 1 (FoxC2) in gastric carcinoma

    Histopathology

    Volume 62, Issue 7, June 2013, Pages: 1038–1048, Jin-Liang Zhu, Yong-Xi Song, Zhen-Ning Wang, Peng Gao, Mei-Xian Wang, Yu-Lan Dong, Cheng-Zhong Xing and Hui-Mian Xu

    Version of Record online : 24 APR 2013, DOI: 10.1111/his.12132

  8. Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 839–849, Matthew G. Butler, Susan L. Dagenais, José L. Garcia-Perez, Pascal Brouillard, Miikka Vikkula, Peter Strouse, Jeffrey W. Innis and Thomas W. Glover

    Version of Record online : 9 MAR 2012, DOI: 10.1002/ajmg.a.35229

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    Expression of FoxC, FoxF, FoxL1, and FoxQ1 genes in the dogfish Scyliorhinus canicula defines ancient and derived roles for fox genes in vertebrate development

    Developmental Dynamics

    Volume 237, Issue 6, June 2008, Pages: 1590–1603, Karl R. Wotton, Françoise Mazet and Sebastian M. Shimeld

    Version of Record online : 22 MAY 2008, DOI: 10.1002/dvdy.21553

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    Overexpression of forkhead box C1 promotes tumor metastasis and indicates poor prognosis in hepatocellular carcinoma

    Hepatology

    Volume 57, Issue 2, February 2013, Pages: 610–624, Limin Xia, Wenjie Huang, Dean Tian, Hongwu Zhu, Xingshun Qi, Zheng Chen, Yongguo Zhang, Hao Hu, Daiming Fan, Yongzhan Nie and Kaichun Wu

    Version of Record online : 5 FEB 2013, DOI: 10.1002/hep.26029

  11. FGF8 regulates myogenesis and induces Runx2 expression and osteoblast differentiation in cultured cells

    Journal of Cellular Biochemistry

    Volume 106, Issue 4, 1 March 2009, Pages: 546–552, Kazuki Omoteyama and Minoru Takagi

    Version of Record online : 23 JAN 2009, DOI: 10.1002/jcb.22012

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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

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    The FOXC2 C-512T Polymorphism Is Associated with Obesity and Dyslipidemia

    Obesity Research

    Volume 12, Issue 11, November 2004, Pages: 1738–1743, Emma Carlsson, Peter Almgren, Johan Hoffstedt, Leif Groop and Martin Ridderstråle

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2004.215

  14. 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

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    Reduced Expression of FOXC2 and Brown Adipogenic Genes in Human Subjects with Insulin Resistance

    Obesity Research

    Volume 11, Issue 10, October 2003, Pages: 1182–1191, Xiaolin Yang, Sven Enerbäck and Ulf Smith

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2003.163

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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

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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

  18. c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 3, March 2010, Pages: 737–740, Pranoot Tanpaiboon, Piranit Kantaputra, Karn Wejathikul and Wirawit Piyamongkol

    Version of Record online : 22 FEB 2010, DOI: 10.1002/ajmg.a.33273

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    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

  20. FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate

    Clinical Genetics

    Volume 62, Issue 6, December 2002, Pages: 470–473, M Bahuau, C Houdayer, M Tredano, V Soupre, R Couderc and M-P Vazquez

    Version of Record online : 13 DEC 2002, DOI: 10.1034/j.1399-0004.2002.620608.x