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There are 10320 results for: content related to: Longitudinal evaluation of FGF23 changes and mineral metabolism abnormalities in a mouse model of chronic kidney disease

  1. Genotype–phenotype correlations in 17 Chinese patients with autosomal recessive Alport syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2188–2193, Yanqin Zhang, Fang Wang, Jie Ding, Hongwen Zhang, Dan Zhao, Lixia Yu, Huijie Xiao, Yong Yao, Xuhui Zhong and Suxia Wang

    Version of Record online : 6 AUG 2012, DOI: 10.1002/ajmg.a.35528

  2. Tumour necrosis factor-α drives Alport glomerulosclerosis in mice by promoting podocyte apoptosis

    The Journal of Pathology

    Volume 226, Issue 1, January 2012, Pages: 120–131, Mi Ryu, Shrikant R Mulay, Nicolai Miosge, Oliver Gross and Hans-Joachim Anders

    Version of Record online : 26 SEP 2011, DOI: 10.1002/path.2979

  3. You have free access to this content
    Elevated Fibroblast Growth Factor 23 Exerts Its Effects on Placenta and Regulates Vitamin D Metabolism in Pregnancy of Hyp Mice

    Journal of Bone and Mineral Research

    Volume 29, Issue 7, July 2014, Pages: 1627–1638, Yasuhisa Ohata, Miwa Yamazaki, Masanobu Kawai, Naoko Tsugawa, Kanako Tachikawa, Tomoko Koinuma, Kazuaki Miyagawa, Akihito Kimoto, Masahiro Nakayama, Noriyuki Namba, Hironori Yamamoto, Toshio Okano, Keiichi Ozono and Toshimi Michigami

    Version of Record online : 25 JUN 2014, DOI: 10.1002/jbmr.2186

  4. Collagen type IV-related nephropathies in Portugal: pathogenic COL4A3 and COL4A4 mutations and clinical characterization of 25 families

    Clinical Genetics

    Volume 88, Issue 5, November 2015, Pages: 456–461, M.J. Nabais Sá, H. Storey, F. Flinter, M. Nagel, S. Sampaio, R. Castro, J.A. Araújo, M.A. Gaspar, C. Soares, A. Oliveira, A.C. Henriques, A.G. da Costa, C.P. Abreu, P. Ponce, R. Alves, L. Pinho, S.E. Silva, C.P. de Moura, L. Mendonça, F. Carvalho, M. Pestana, S. Alves, F. Carvalho and J.P. Oliveira

    Version of Record online : 10 NOV 2014, DOI: 10.1111/cge.12521

  5. Conditional Deletion of Murine Fgf23: Interruption of the Normal Skeletal Responses to Phosphate Challenge and Rescue of Genetic Hypophosphatemia

    Journal of Bone and Mineral Research

    Volume 31, Issue 6, June 2016, Pages: 1247–1257, Erica L Clinkenbeard, Taryn A Cass, Pu Ni, Julia M Hum, Teresita Bellido, Matthew R Allen and Kenneth E White

    Version of Record online : 4 MAR 2016, DOI: 10.1002/jbmr.2792

  6. Bone mineralization is regulated by signaling cross talk between molecular factors of local and systemic origin: The role of fibroblast growth factor 23


    Volume 40, Issue 6, November/December 2014, Pages: 555–568, Rony Sapir-Koren and Gregory Livshits

    Version of Record online : 29 OCT 2014, DOI: 10.1002/biof.1186

  7. Plasma leakage through glomerular basement membrane ruptures triggers the proliferation of parietal epithelial cells and crescent formation in non-inflammatory glomerular injury

    The Journal of Pathology

    Volume 228, Issue 4, December 2012, Pages: 482–494, Mi Ryu, Adriana Migliorini, Nicolai Miosge, Oliver Gross, Stuart Shankland, Paul T Brinkkoetter, Henning Hagmann, Paola Romagnani, Helen Liapis and Hans-Joachim Anders

    Version of Record online : 26 JUL 2012, DOI: 10.1002/path.4046

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    Renal phosphate handling in human – what can we learn from hereditary hypophosphataemias?

    European Journal of Clinical Investigation

    Volume 40, Issue 6, June 2010, Pages: 552–560, Stefan Amatschek, Maria Haller and Rainer Oberbauer

    Version of Record online : 14 APR 2010, DOI: 10.1111/j.1365-2362.2010.02286.x

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    Mechanism of FGF23 processing in fibrous dysplasia

    Journal of Bone and Mineral Research

    Volume 27, Issue 5, May 2012, Pages: 1132–1141, Nisan Bhattacharyya, Malgorzata Wiench, Claudia Dumitrescu, Brian M Connolly, Thomas H Bugge, Himatkumar V Patel, Rachel I Gafni, Natasha Cherman, Monique Cho, Gordon L Hager and Michael T Collins

    Version of Record online : 18 APR 2012, DOI: 10.1002/jbmr.1546

  10. Ccl2/Mcp-1 blockade reduces glomerular and interstitial macrophages but does not ameliorate renal pathology in collagen4A3-deficient mice with autosomal recessive Alport nephropathy

    The Journal of Pathology

    Volume 218, Issue 1, May 2009, Pages: 40–47, Sebastian Clauss, Oliver Gross, Onkar Kulkarni, Alejandro Avila-Ferrufino, Ewa Radomska, Stephan Segerer, Dirk Eulberg, Sven Klussmann and Hans-Joachim Anders

    Version of Record online : 2 DEC 2008, DOI: 10.1002/path.2505

  11. Molecular Genetics of Inherited Hypophosphataemias

    Standard Article


    Armando Luis Negri

    Published Online : 15 DEC 2008, DOI: 10.1002/9780470015902.a0021465

  12. A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 155–160, B.D. Webb, T. Brandt, L. Liu, C. Jalas, J. Liao, A. Fedick, M.D. Linderman, G.A. Diaz, R. Kornreich, H. Trachtman, L. Mehta and L. Edelmann

    Version of Record online : 2 SEP 2013, DOI: 10.1111/cge.12247

  13. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 252–257, C. Fallerini, L. Dosa, R. Tita, D. Del Prete, S. Feriozzi, G. Gai, M. Clementi, A. La Manna, N. Miglietti, R. Mancini, G. Mandrile, G.M. Ghiggeri, G. Piaggio, F. Brancati, L. Diano, E. Frate, A.R. Pinciaroli, M. Giani, P. Castorina, E. Bresin, D. Giachino, M. De Marchi, F. Mari, M. Bruttini, A. Renieri and F. Ariani

    Version of Record online : 17 OCT 2013, DOI: 10.1111/cge.12258

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    A Phex mutation in a murine model of X-linked hypophosphatemia alters phosphate responsiveness of bone cells

    Journal of Bone and Mineral Research

    Volume 27, Issue 2, February 2012, Pages: 453–460, Shoji Ichikawa, Anthony M Austin, Amie K Gray and Michael J Econs

    Version of Record online : 23 JAN 2012, DOI: 10.1002/jbmr.544

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    ASBMR 29th Annual Meeting

    Journal of Bone and Mineral Research

    Volume 22, Issue S1, September 2007, Pages: s352–s401,

    Version of Record online : 4 MAR 2010, DOI: 10.1002/jbmr.5650221409

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    Characterization of the Genetic Basis for Autosomal Recessive Hereditary Nephropathy in the English Springer Spaniel

    Journal of Veterinary Internal Medicine

    Volume 26, Issue 2, March-April 2012, Pages: 294–301, K.L. Nowend, A.N. Starr-Moss, G.E. Lees, B.R. Berridge, F.J. Clubb, C.E. Kashtan, M.B. Nabity and K.E. Murphy

    Version of Record online : 28 FEB 2012, DOI: 10.1111/j.1939-1676.2012.00888.x

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    ASBMR 2010 Annual Meeting FR0005–FR0485

    Journal of Bone and Mineral Research

    Volume 25, Issue S1, 2010, Pages: S82–S135,

    Version of Record online : 16 JUN 2011, DOI: 10.1002/jbmr.5650251302

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    Serum FGF23 Levels in Normal and Disordered Phosphorus Homeostasis

    Journal of Bone and Mineral Research

    Volume 18, Issue 7, July 2003, Pages: 1227–1234, Thomas J Weber, Shiguang Liu, Olafur S Indridason and L Darryl Quarles

    Version of Record online : 1 JUL 2003, DOI: 10.1359/jbmr.2003.18.7.1227

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    Ablation of Systemic Phosphate-Regulating Gene Fibroblast Growth Factor 23 (Fgf23) Compromises the Dentoalveolar Complex

    The Anatomical Record

    Volume 293, Issue 7, July 2010, Pages: 1214–1226, E.Y. Chu, H. Fong, F.A. Blethen, K.A. Tompkins, B.L. Foster, K.D. Yeh, K.J. Nagatomo, D. Matsa-dunn, D. Sitara, B. Lanske, R.B. Rutherford and M.J. Somerman

    Version of Record online : 13 APR 2010, DOI: 10.1002/ar.21152

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    FGF23 Regulates Bone Mineralization in a 1,25(OH)2D3 and Klotho-Independent Manner

    Journal of Bone and Mineral Research

    Volume 31, Issue 1, January 2016, Pages: 129–142, Sathish Kumar Murali, Paul Roschger, Ute Zeitz, Klaus Klaushofer, Olena Andrukhova and Reinhold G Erben

    Version of Record online : 29 AUG 2015, DOI: 10.1002/jbmr.2606