Search Results

There are 30583 results for: content related to: Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: Comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

  1. You have free access to this content
    Sp1 Family of Transcription Factors Regulates the Human α2 (XI) Collagen Gene (COL11A2) in Saos-2 Osteoblastic Cells

    Journal of Bone and Mineral Research

    Volume 21, Issue 5, May 2006, Pages: 661–673, Tomohiro Goto, Yoshito Matsui, Russell J Fernandes, Dennis A Hanson, Takahiro Kubo, Kiminori Yukata, Toshimi Michigami, Toshihisa Komori, Takashi Fujita, Liu Yang, David R Eyre and Natsuo Yasui

    Version of Record online : 20 FEB 2006, DOI: 10.1359/jbmr.020605

  2. Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 2, February 2012, Pages: 309–314, Stuart W. Tompson, Eissa Ali Faqeih, Leena Ala-Kokko, Jacqueline T. Hecht, Rika Miki, Tara Funari, Vincent A. Funari, Lisette Nevarez, Deborah Krakow and Daniel H. Cohn

    Version of Record online : 13 JAN 2012, DOI: 10.1002/ajmg.a.34406

  3. Posttranscriptional aspects of the biosynthesis of type 1 collagen pro-alpha chains: The effects of posttranslational modifications on synthesis pauses during elongation of the Pro α1(I) chain

    Journal of Cellular Biochemistry

    Volume 61, Issue 2, 1 May 1996, Pages: 194–215, Trisha Gura, Geng Hu and Arthur Veis

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4644(19960501)61:2<194::AID-JCB4>3.0.CO;2-P

  4. Involvement of neurotrophin-4/5 in regeneration of the periodontal Ruffini endings at the early stage

    Journal of Comparative Neurology

    Volume 501, Issue 3, 20 March 2007, Pages: 400–412, Shahiqul Jabbar, Fumiko Harada, Megumi Aita, Megumi Ohishi, Isao Saito, Yoshiro Kawano, Akiko Suzuki, Kayoko Nozawa-Inoue and Takeyasu Maeda

    Version of Record online : 23 JAN 2007, DOI: 10.1002/cne.21256

  5. Collagens: building blocks at the end of the development line

    Clinical Genetics

    Volume 58, Issue 4, October 2000, Pages: 270–279, PH Byers

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580404.x

  6. You have free access to this content
    Functional Impact of Human Collagen α2(XI) Gene Polymorphism in Pathogenesis of Ossification of the Posterior Longitudinal Ligament of the Spine

    Journal of Bone and Mineral Research

    Volume 16, Issue 5, May 2001, Pages: 948–957, Shingo Maeda, Yasuhiro Ishidou, Hiroaki Koga, Eiji Taketomi, Katsunori Ikari, Setsuro Komiya, Jun Takeda, Takashi Sakou and Ituro Inoue

    Version of Record online : 1 MAY 2001, DOI: 10.1359/jbmr.2001.16.5.948

  7. You have free access to this content
    Progenitors Systemically Transplanted into Neonatal Mice Localize to Areas of Active Bone Formation In Vivo: Implications of Cell Therapy for Skeletal Diseases


    Volume 24, Issue 8, August 2006, Pages: 1869–1878, Xujun Wang, Feng Li and Christopher Niyibizi

    Version of Record online : 4 MAY 2006, DOI: 10.1634/stemcells.2005-0430

  8. Brain iron uptake in hypotransferrinemic mice: Influence of systemic iron status

    Journal of Neuroscience Research

    Volume 79, Issue 1-2, 1 - 15 January 2005, Pages: 254–261, John L. Beard, Jason A. Wiesinger, Nan Li and James R. Connor

    Version of Record online : 2 DEC 2004, DOI: 10.1002/jnr.20324

  9. You have free access to this content
    Type V Collagen in Health, Disease, and Fibrosis

    The Anatomical Record

    Volume 299, Issue 5, May 2016, Pages: 613–629, Ki M. Mak, Chien Yi M. Png and Danielle J. Lee

    Version of Record online : 15 MAR 2016, DOI: 10.1002/ar.23330

  10. Collagen: Gene Structure

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Mon-Li Chu, Darwin J. Prockop, Pages: 223–248, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch2(ii)

  11. The Ehlers-Danlos Syndrome

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Beat Steinmann, Peter M. Royce, Andrea Superti-Furga, Pages: 431–523, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch9

  12. You have free access to this content
    Diversity in the processing events at the N-terminus of type-V collagen

    European Journal of Biochemistry

    Volume 221, Issue 3, May 1994, Pages: 987–995, Mahnaz MORADI-AMÉLI, Jean-Charles ROUSSEAU, Jean-Philippe KLEMAN, Marie-France CHAMPLIAUD, Marguerite-Marie BOUTILLON, Jacques BERNILLON, Jean WALLACH and Michel VAN DER REST

    Version of Record online : 3 MAR 2005, DOI: 10.1111/j.1432-1033.1994.tb18815.x

  13. You have free access to this content
    Differential responses to parathyroid hormone-related protein (PTHrP) deficiency in the various craniofacial cartilages

    The Anatomical Record

    Volume 255, Issue 4, 1 August 1999, Pages: 452–457, M. Ishii-Suzuki, N. Suda, K. Yamazaki, T. Kuroda, P.V. Senior, F. Beck and V. E. Hammond

    Version of Record online : 2 DEC 1999, DOI: 10.1002/(SICI)1097-0185(19990801)255:4<452::AID-AR10>3.0.CO;2-E

  14. Sulfatide decrease in myelin influences formation of the paranodal axo-glial junction and conduction velocity in the sciatic nerve


    Volume 61, Issue 4, April 2013, Pages: 466–474, Akiko Hayashi, Naoki Kaneko, Chiaki Tomihira and Hiroko Baba

    Version of Record online : 16 JAN 2013, DOI: 10.1002/glia.22447

  15. You have free access to this content
    Gene Expression of Bone Matrix Proteins and Endothelin Receptors in Endothelin-1–Deficient Mice Revealed by In Situ Hybridization

    Journal of Bone and Mineral Research

    Volume 13, Issue 2, February 1998, Pages: 237–244, Yukie Kitano, Hiroki Kurihara, Yukiko Kurihara, Koji Maemura, Yoshimi Ryo, Yoshio Yazaki and Kiyonori Harii

    Version of Record online : 1 FEB 1998, DOI: 10.1359/jbmr.1998.13.2.237

  16. Disruption of actin-binding domain-containing Dystonin protein causes dystonia musculorum in mice

    European Journal of Neuroscience

    Volume 40, Issue 10, November 2014, Pages: 3458–3471, Masao Horie, Keisuke Watanabe, Asim K. Bepari, Jun-ichiro Nashimoto, Kimi Araki, Hiromi Sano, Satomi Chiken, Atsushi Nambu, Katsuhiko Ono, Kazuhiro Ikenaka, Akiyoshi Kakita, Ken-ichi Yamamura and Hirohide Takebayashi

    Version of Record online : 6 SEP 2014, DOI: 10.1111/ejn.12711

  17. Spatial and temporal expression of fibril-forming minor collagen genes (types V and XI) during fracture healing

    Journal of Orthopaedic Research

    Volume 15, Issue 5, September 1997, Pages: 757–764, Masashi Yamazaki, Robert J. Majeska, Hidekatsu Yoshioka, Hideshige Moriya and Thomas A. Einhorn

    Version of Record online : 18 FEB 2005, DOI: 10.1002/jor.1100150519

  18. A mouse model of a human multiple GIST family with KIT-Asp820Tyr mutation generated by a knock-in strategy

    The Journal of Pathology

    Volume 214, Issue 3, February 2008, Pages: 302–311, N Nakai, T Ishikawa, A Nishitani, N-N Liu, M Shincho, H Hao, K Isozaki, T Kanda, T Nishida, J Fujimoto and S Hirota

    Version of Record online : 11 DEC 2007, DOI: 10.1002/path.2296

  19. Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations

    Clinical Genetics

    Volume 82, Issue 2, August 2012, Pages: 147–156, NA Akawi, L Al-Gazali and BR Ali

    Version of Record online : 18 JUL 2011, DOI: 10.1111/j.1399-0004.2011.01734.x

  20. Proteomic analysis of Col11a1-associated protein complexes


    Volume 11, Issue 24, December 2011, Pages: 4660–4676, Raquel J. Brown, Christopher Mallory, Owen M. McDougal and Julia Thom Oxford

    Version of Record online : 23 NOV 2011, DOI: 10.1002/pmic.201100058