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Select item 31981351.

Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene

Franco Laccone, Katharina Schoner, Birgit Krabichler, Britta Kluge, Robin Schwerdtfeger, Bernt Schulze, Johannes Zschocke, Helga Rehder

Eur J Hum Genet. 2011 Nov; 19(11): 1133–1137. Published online 2011 Jun 8. doi: 10.1038/ejhg.2011.101

PMCID:: PMC3198135

Abstract Article PDF–294K

Select item 26479942.

Alteration of femoral bone morphology and density in COX-2−/− mice

Galen Robertson, Chao Xie, Di Chen, Hani Awad, Edward M. Schwarz, Regis J. O’Keefe, Robert E. Guldberg, Xinping Zhang

Bone. Author manuscript; available in PMC 2009 Feb 25.

Published in final edited form as: Bone. 2006 Oct; 39(4): 767–772. Published online 2006 May 30. doi: 10.1016/j.bone.2006.04.006

PMCID:: PMC2647994

Abstract Article PDF–903K

Select item 26846303.

Abnormalities in Osteoclastogenesis and Decreased Tumorigenesis in Mice Deficient for Ovarian Cancer G Protein-Coupled Receptor 1

Hui Li, Dongmei Wang, Lisam Shanjukumar Singh, Michael Berk, Haiyan Tan, Zhenwen Zhao, Rosemary Steinmetz, Kashif Kirmani, Gang Wei, Yan Xu

PLoS One. 2009; 4(5): e5705. Published online 2009 May 28. doi: 10.1371/journal.pone.0005705

Correction in:: PLoS One. 2015; 10(4): e0125463.

PMCID:: PMC2684630

Abstract Article PDF–1.6M

Select item 27682604.

Runx2, p53 and pRB status as diagnostic parameters for deregulation of osteoblast growth and differentiation in a new pre-chemotherapeutic osteosarcoma cell line (OS1)

Barry P. Pereira, Yefang Zhou, Anurag Gupta, David T. Leong, Khin Zarchi Aung, Ling Ling, Robert W. H. Pho, Mario Galindo, Manuel Salto-Tellez, Gary S. Stein, Simon M. Cool, Andre J. van Wijnen, Saminathan S. Nathan

J Cell Physiol. Author manuscript; available in PMC 2010 Dec 1.

Published in final edited form as: J Cell Physiol. 2009 Dec; 221(3): 778–788. doi: 10.1002/jcp.21921

PMCID:: PMC2768260

Abstract Article PDF–2.1M

Select item 28036785.

Radiographic Evaluation of Bones and Joints in Mucopolysaccharidosis I and VII Dogs After Neonatal Gene Therapy

Ramin Sedaghat Herati, Van W. Knox, Patricia O’Donnell, Marina D’Angelo, Mark E. Haskins, Katherine P. Ponder

Mol Genet Metab. Author manuscript; available in PMC 2010 Jan 8.

Published in final edited form as: Mol Genet Metab. 2008 Nov; 95(3): 142–151. Published online 2008 Aug 15. doi: 10.1016/j.ymgme.2008.07.003

PMCID:: PMC2803678

Abstract Article PDF–2.0M

Select item 29890946.

A histological and ultrastructural study of femoral head cartilage in a new type II collagenopathy

Peiqiang Su, Liangming Zhang, Yan Peng, Anjing Liang, Kaili Du, Dongsheng Huang

Int Orthop. 2010 Dec; 34(8): 1333–1339. Published online 2010 Mar 5. doi: 10.1007/s00264-010-0985-9

PMCID:: PMC2989094

Abstract Article PDF–602K

Select item 30056537.

Weismann-Netter-Stuhl Syndrome:A family report

Hayrullah Alp, Mehmet Emre Atabek, Özgür Pirgon

J Clin Res Pediatr Endocrinol. 2009 Jun; 1(4): 194–196. Published online 2010 Dec 8. doi: 10.4274/jcrpe.v1i4.45

PMCID:: PMC3005653

Abstract Article PDF–181K

Select item 30639878.

Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes

Shawna M. Pyott, Ulrike Schwarze, Helena E. Christiansen, Melanie G. Pepin, Dru F. Leistritz, Richard Dineen, Catharine Harris, Barbara K. Burton, Brad Angle, Katherine Kim, Michael D. Sussman, MaryAnn Weis, David R. Eyre, David W. Russell, Kevin J. McCarthy, Robert D. Steiner, Peter H. Byers

Hum Mol Genet. 2011 Apr 15; 20(8): 1595–1609. Published online 2011 Jan 31. doi: 10.1093/hmg/ddr037

PMCID:: PMC3063987

Abstract Article PDF–758K

Select item 30974269.

Material and mechanical properties of bones deficient for fibrillin-1 or fibrillin-2 microfibrils

Emilio Arteaga-Solis, Lee Sui-Arteaga, Minwook Kim, Mitchell B. Schaffler, Karl J. Jepsen, Nancy Pleshko, Francesco Ramirez

Matrix Biol. Author manuscript; available in PMC 2012 Apr 1.

Published in final edited form as: Matrix Biol. 2011 Apr; 30(3): 188–194. Published online 2011 Mar 29. doi: 10.1016/j.matbio.2011.03.004

PMCID:: PMC3097426

Abstract Article PDF–636K

Select item 312509510.

Research Resource: Haploinsufficiency of Receptor Activity-Modifying Protein-2 (Ramp2) Causes Reduced Fertility, Hyperprolactinemia, Skeletal Abnormalities, and Endocrine Dysfunction in Mice

Mahita Kadmiel, Kimberly Fritz-Six, Suruchi Pacharne, Gareth O. Richards, Manyu Li, Tim M. Skerry, Kathleen M. Caron

Mol Endocrinol. 2011 Jul; 25(7): 1244–1253. Published online 2011 May 12. doi: 10.1210/me.2010-0400

PMCID:: PMC3125095

Abstract Article

Select item 317932411.

Nell-1, a key Functional Mediator of Runx2, Partially Rescues Calvarial Defects in Runx2^+/− Mice

Xinli Zhang, Kang Ting, Catherine M Bessette, Cymbeline T Culiat, Sang Jin Sung, Haofu Lee, Feng Chen, Jia Shen, James J Wang, Shun'ichi Kuroda, Chia Soo

J Bone Miner Res. 2011 Apr; 26(4): 777–791. Published online 2010 Oct 11. doi: 10.1002/jbmr.267

PMCID:: PMC3179324

Abstract Article PDF–1.2M

Select item 259806112.

Schimke immuno‐osseous dysplasia: a clinicopathological correlation

J Marietta Clewing, Barbara C Antalfy, Thomas Lücke, Behzad Najafian, Katja M Marwedel, Akira Hori, Ralph M Powel, A F Safo Do, Lydia Najera, Karen SantaCruz, M John Hicks, Dawna L Armstrong

J Med Genet. 2007 Feb; 44(2): 122–130. doi: 10.1136/jmg.2006.044313

PMCID:: PMC2598061

Abstract Article PDF–5.4M

Select item 343517513.

Targeted deletion of Sost distal enhancer increases bone formation and bone mass

Nicole M. Collette, Damian C. Genetos, Aris N. Economides, LiQin Xie, Mohammad Shahnazari, Wei Yao, Nancy E. Lane, Richard M. Harland, Gabriela G. Loots

Proc Natl Acad Sci U S A. 2012 Aug 28; 109(35): 14092–14097. Published online 2012 Aug 10. doi: 10.1073/pnas.1207188109

PMCID:: PMC3435175

Abstract Article PDF–864K

Select item 349260914.

Hip Ontogenesis: How Evolution, Genes, and Load History Shape Hip Morphotype and Cartilotype

Tom Hogervorst, Wouter Eilander, Joost T. Fikkers, Ingrid Meulenbelt

Clin Orthop Relat Res. 2012 Dec; 470(12): 3284–3296. Published online 2012 Aug 28. doi: 10.1007/s11999-012-2511-4

PMCID:: PMC3492609

Abstract Article PDF–372K

Select item 366232415.

Severe congenital RYR1-associated myopathy: The expanding clinicopathologic and genetic spectrum

Diana Xerxes Bharucha-Goebel, Mariarita Santi, Līvija Medne, Kristin Zukosky, Jahannaz Dastgir, Perry B. Shieh, Thomas Winder, Gihan Tennekoon, Richard S. Finkel, James J. Dowling, Nicole Monnier, Carsten G. Bönnemann

Neurology. 2013 Apr 23; 80(17): 1584–1589. doi: 10.1212/WNL.0b013e3182900380

Correction in:: Neurology. 2013 May 28; 80(22): 2081.

PMCID:: PMC3662324

Abstract Article PDF–853K

Select item 369097416.

The Effect of Neonatal Gene Therapy on Skeletal Manifestations in Mucopolysaccharidosis VII Dogs after a Decade

Elizabeth M. Xing, Van W. Knox, Patricia A. O'Donnell, Tracey Sikura, Yuli Liu, Susan Wu, Margret L. Casal, Mark E. Haskins, Katherine P. Ponder

Mol Genet Metab. Author manuscript; available in PMC 2014 Jun 1.

Published in final edited form as: Mol Genet Metab. 2013 Jun; 109(2): 183–193. Published online 2013 Apr 6. doi: 10.1016/j.ymgme.2013.03.013

PMCID:: PMC3690974

Abstract Article PDF–5.3M

Select item 391363517.

Treatment with N- and C-Terminal Peptides of Parathyroid Hormone-Related Protein Partly Compensate the Skeletal Abnormalities in IGF-I Deficient Mice

Lourdes Rodríguez-de la Rosa, Ana López-Herradón, Sergio Portal-Núñez, Silvia Murillo-Cuesta, Daniel Lozano, Rafael Cediel, Isabel Varela-Nieto, Pedro Esbrit

PLoS One. 2014; 9(2): e87536. Published online 2014 Feb 4. doi: 10.1371/journal.pone.0087536

PMCID:: PMC3913635

Abstract Article PDF–1.9M

Select item 409022918.

The p38α MAPK Function in Osteoprecursors Is Required for Bone Formation and Bone Homeostasis in Adult Mice

Edgardo Rodríguez-Carballo, Beatriz Gámez, Lara Sedó-Cabezón, Manuela Sánchez-Feutrie, Antonio Zorzano, Cristina Manzanares-Céspedes, José Luis Rosa, Francesc Ventura

PLoS One. 2014; 9(7): e102032. Published online 2014 Jul 9. doi: 10.1371/journal.pone.0102032