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There are 46639 results for: content related to: Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density

  1. You have free access to this content
    Tooth root dentin mineralization defects in a mouse model of hypophosphatasia

    Journal of Bone and Mineral Research

    Volume 28, Issue 2, February 2013, Pages: 271–282, BL Foster, KJ Nagatomo, HW Tso, AB Tran, FH Nociti Jr, S Narisawa, MC Yadav, MD McKee, JL Millán and MJ Somerman

    Version of Record online : 15 JAN 2013, DOI: 10.1002/jbmr.1767

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    Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate Treatment

    Journal of Bone and Mineral Research

    Volume 30, Issue 9, September 2015, Pages: 1726–1737, Tim Cundy, Toshimi Michigami, Kanako Tachikawa, Michael Dray, John F Collins, Eleftherios P Paschalis, Sonja Gamsjaeger, Andreas Roschger, Nadja Fratzl-Zelman, Paul Roschger and Klaus Klaushofer

    Version of Record online : 17 AUG 2015, DOI: 10.1002/jbmr.2495

  3. Gene therapy improves dental manifestations in hypophosphatasia model mice

    Journal of Periodontal Research

    R. Okawa, O. Iijima, M. Kishino, H. Okawa, S. Toyosawa, H. Sugano-Tajima, T. Shimada, T. Okada, K. Ozono, T. Ooshima and K. Nakano

    Version of Record online : 26 AUG 2016, DOI: 10.1111/jre.12412

  4. Bone mineralization-dependent craniosynostosis and craniofacial shape abnormalities in the mouse model of infantile hypophosphatasia

    Developmental Dynamics

    Volume 245, Issue 2, February 2016, Pages: 175–182, John Durussel, Jin Liu, Cassandra Campbell, Hwa K. Nam and Nan E. Hatch

    Version of Record online : 28 DEC 2015, DOI: 10.1002/dvdy.24370

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    In Vivo Overexpression of Tissue-Nonspecific Alkaline Phosphatase Increases Skeletal Mineralization and Affects the Phosphorylation Status of Osteopontin

    Journal of Bone and Mineral Research

    Volume 28, Issue 7, July 2013, Pages: 1587–1598, Sonoko Narisawa, Manisha C Yadav and José Luis Millán

    Version of Record online : 18 JUN 2013, DOI: 10.1002/jbmr.1901

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    Enzyme replacement prevents enamel defects in hypophosphatasia mice

    Journal of Bone and Mineral Research

    Volume 27, Issue 8, August 2012, Pages: 1722–1734, Manisha C Yadav, Rodrigo Cardoso de Oliveira, Brian L Foster, Hanson Fong, Esther Cory, Sonoko Narisawa, Robert L Sah, Martha Somerman, Michael P Whyte and José Luis Millán

    Version of Record online : 17 JUL 2012, DOI: 10.1002/jbmr.1619

  7. Prenatal diagnosis of familial lethal hypophosphatasia using imaging, blood enzyme levels, chorionic villus sampling and archived fetal tissue

    Journal of Obstetrics and Gynaecology Research

    Volume 37, Issue 10, October 2011, Pages: 1470–1473, Nobuhiro Suzumori, Etienne Mornet, Eita Mizutani, Shintaro Obayashi, Yasuhiko Ozaki and Mayumi Sugiura-Ogasawara

    Version of Record online : 12 MAY 2011, DOI: 10.1111/j.1447-0756.2011.01526.x

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    The 2015 Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 39, Issue 7, November 2015, Pages: 529–599,

    Version of Record online : 14 SEP 2015, DOI: 10.1002/gepi.21916

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    “Atypical femoral fractures” during bisphosphonate exposure in adult hypophosphatasia

    Journal of Bone and Mineral Research

    Volume 27, Issue 5, May 2012, Pages: 987–994, Roger AL Sutton, Steven Mumm, Stephen P Coburn, Karen L Ericson and Michael P Whyte

    Version of Record online : 18 APR 2012, DOI: 10.1002/jbmr.1565

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    Chromatin Changes at the PPAR-γ2 Promoter During Bone Marrow-Derived Multipotent Stromal Cell Culture Correlate With Loss of Gene Activation Potential

    STEM CELLS

    Volume 33, Issue 7, July 2015, Pages: 2169–2181, Patrick J. Lynch, Elaine E. Thompson, Kathleen McGinnis, Yazmin I. Rovira Gonzalez, Jessica Lo Surdo, Steven R. Bauer and Deborah A. Hursh

    Version of Record online : 26 MAY 2015, DOI: 10.1002/stem.1967

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    2015 ACR/ARHP Annual Meeting Abstract Supplement

    Arthritis & Rheumatology

    Volume 67, Issue S10, October 2015, Pages: 1–4046,

    Version of Record online : 5 NOV 2015, DOI: 10.1002/art.39448

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    Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models

    Experimental Physiology

    Volume 94, Issue 4, April 2009, Pages: 412–421, Bernhard Aigner, Birgit Rathkolb, Matthias Klaften, Reinhard Sedlmeier, Martina Klempt, Sibylle Wagner, Dian Michel, Ulrike Mayer, Thomas Klopstock, Martin Hrabé de Angelis and Eckhard Wolf

    Version of Record online : 18 FEB 2009, DOI: 10.1113/expphysiol.2008.045864

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    Pathophysiological Role of Vascular Smooth Muscle Alkaline Phosphatase in Medial Artery Calcification

    Journal of Bone and Mineral Research

    Volume 30, Issue 5, May 2015, Pages: 824–836, Campbell R Sheen, Pia Kuss, Sonoko Narisawa, Manisha C Yadav, Jessica Nigro, Wei Wang, T Nicole Chhea, Eduard A Sergienko, Kapil Kapoor, Michael R Jackson, Marc F Hoylaerts, Anthony B Pinkerton, W Charles O'Neill and José Luis Millán

    Version of Record online : 16 APR 2015, DOI: 10.1002/jbmr.2420

  14. Wnt3a signaling induces murine dental follicle cells to differentiate into cementoblastic/osteoblastic cells via an osterix-dependent pathway

    Journal of Periodontal Research

    Volume 51, Issue 2, April 2016, Pages: 164–174, E. Nemoto, Y. Sakisaka, M. Tsuchiya, M. Tamura, T. Nakamura, S. Kanaya, M. Shimonishi and H. Shimauchi

    Version of Record online : 12 JUN 2015, DOI: 10.1111/jre.12294

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    ACR Meeting

    Arthritis & Rheumatism

    Volume 64, Issue S10, October 2012, Pages: S1–S1216,

    Version of Record online : 11 OCT 2012, DOI: 10.1002/art.37735

  16. You have full text access to this OnlineOpen article
    Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1–LGI1 signaling

    Molecular Genetics & Genomic Medicine

    Volume 4, Issue 4, July 2016, Pages: 447–456, Rhalena A. Thomas, Amirthagowri Ambalavanan, Guy A. Rouleau and Philip A. Barker

    Version of Record online : 11 MAR 2016, DOI: 10.1002/mgg3.215

  17. Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease

    Pacing and Clinical Electrophysiology

    Volume 34, Issue 6, June 2011, Pages: 742–749, TOMAS NOVOTNY, JITKA KADLECOVA, MARTINA RAUDENSKA, ALEXANDRA BITTNEROVA, IRENA ANDRSOVA, ALENA FLORIANOVA, ANNA VASKU, PETR NEUGEBAUER, MILAN KOZAK, MILAN SEPSI, LUBOMIR KRIVAN, RENATA GAILLYOVA and JINDRICH SPINAR

    Version of Record online : 16 MAR 2011, DOI: 10.1111/j.1540-8159.2011.03045.x

  18. LPL gene expression is associated with poor prognosis in CLL and closely related to NOTCH1 mutations

    European Journal of Haematology

    Volume 97, Issue 2, August 2016, Pages: 175–182, Louise Kristensen, Thomas Kristensen, Niels Abildgaard, Cristina Royo, Mikael Frederiksen, Torben Mourits-Andersen, Elias Campo and Michael Boe Møller

    Version of Record online : 17 DEC 2015, DOI: 10.1111/ejh.12700

  19. Uniaxial mechanical tension promoted osteogenic differentiation of rat tendon-derived stem cells (rTDSCs) via the Wnt5a-RhoA pathway

    Journal of Cellular Biochemistry

    Volume 113, Issue 10, October 2012, Pages: 3133–3142, Yu Shi, Yujie Fu, Wenxue Tong, Yiyun Geng, Pauline Po Yee Lui, Tingting Tang, Xiaoling Zhang and Kerong Dai

    Version of Record online : 9 AUG 2012, DOI: 10.1002/jcb.24190

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    Erv26p-Dependent Export of Alkaline Phosphatase from the ER Requires Lumenal Domain Recognition

    Traffic

    Volume 10, Issue 8, August 2009, Pages: 1006–1018, Julia Dancourt and Charles Barlowe

    Version of Record online : 29 APR 2009, DOI: 10.1111/j.1600-0854.2009.00936.x