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Items: 15

Select item 111627441.

Alterations of bone material properties in growing Ifitm5/BRIL p.S42 knock-in mice, a new model for atypical type VI osteogenesis imperfecta

Ghazal Hedjazi, Gali Guterman-Ram, Stéphane Blouin, Victoria Schemenz, Wolfgang Wagermaier, Peter Fratzl, Markus A. Hartmann, Jochen Zwerina, Nadja Fratzl-Zelman, Joan C. Marini

Bone. Author manuscript; available in PMC 2024 Jun 9.

Published in final edited form as: Bone. 2022 Sep; 162: 116451. Published online 2022 May 30. doi: 10.1016/j.bone.2022.116451

PMCID:: PMC11162744

Abstract Article PDF–3.2M

Select item 85769792.

Progressive pseudorheumatoid dysplasia misdiagnosed as juvenile idiopathic arthritis: a case report

Anjumanara Anver Omar, Salman Ahmed, John Chris Rodrigues, Allan Kayiza, Lawrence Owino

J Med Case Rep. 2021; 15: 551. Published online 2021 Nov 8. doi: 10.1186/s13256-021-03082-z

PMCID:: PMC8576979

Abstract Article PDF–1.1M

Select item 81270523.

Further phenotypic features and two novel POC1A variants in a patient with SOFT syndrome: A case report

Songting Li, Yan Zhong, Yongjia Yang, Siping He, Wenjuan He

Mol Med Rep. 2021 Jul; 24(1): 494. Published online 2021 May 5. doi: 10.3892/mmr.2021.12133

PMCID:: PMC8127052

Abstract Article PDF–1.8M

Select item 65844614.

LncRNA‐H19 Modulates Wnt/β‐catenin Signaling by Targeting Dkk4 in Hindlimb Unloaded Rat

Bing Li, Jun Liu, Jie Zhao, Jian‐xiong Ma, Hao‐bo Jia, Yang Zhang, Guo‐sheng Xing, Xin‐long Ma

Orthop Surg. 2017 Aug; 9(3): 319–327. Published online 2017 Apr 26. doi: 10.1111/os.12321

PMCID:: PMC6584461

Abstract Article PDF–2.7M

Select item 63441865.

X-linked dominant chondrodysplasia punctata with severe phenotype in a female fetus: A case report

Yan Liu, Li Wang, Bin Xu, Yike Yang, Dan Shan, Qingqing Wu

Medicine (Baltimore) 2019 Jan; 98(1): e13850. Published online 2019 Jan 4. doi: 10.1097/MD.0000000000013850

PMCID:: PMC6344186

Abstract Article PDF–918K

Select item 51032676.

Noscapine targets EGFR^p-Tyr1068 to suppress the proliferation and invasion of MG63 cells

Ming He, Linlin Jiang, Zhaozhou Ren, Guangbin Wang, Jiashi Wang

Sci Rep. 2016; 6: 37062. Published online 2016 Nov 10. doi: 10.1038/srep37062

PMCID:: PMC5103267

Abstract Article PDF–1.7M

Select item 47240827.

HDR syndrome in a Japanese girl with biliary atresia: a case report

Yousuke Higuchi, Kosei Hasegawa, Miho Yamashita, Yousuke Fujii, Hiroyuki Tanaka, Hirokazu Tsukahara

BMC Pediatr. 2016; 16: 14. Published online 2016 Jan 22. doi: 10.1186/s12887-016-0550-9

PMCID:: PMC4724082

Abstract Article PDF–619K

Select item 44559868.

Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia

Xunlun Sheng, Xue Chen, Bo Lei, Rui Chen, Hui Wang, Fangxia Zhang, Weining Rong, Ruoshui Ha, Yani Liu, Feng Zhao, Peizeng Yang, Chen Zhao

J Transl Med. 2015; 13: 179. Published online 2015 Jun 4. doi: 10.1186/s12967-015-0534-9

PMCID:: PMC4455986

Abstract Article PDF–1.7M

Select item 39136359.

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 327638610.

Long-Term Effects of Ovariectomy on Osteoporosis and Obesity in Estrogen-Receptor-β–Deleted Mice

Dana Seidlova-Wuttke, Ba Tiep Nguyen, Wolfgang Wuttke

Comp Med. 2012 Feb; 62(1): 8–13. Published online 2012 Feb.

PMCID:: PMC3276386

Abstract Article PDF–2.7M

Select item 264799411.

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 259803412.

The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type

Gen Nishimura, Eiji Nakashima, Yuichiro Hirose, Trevor Cole, Phillip Cox, Daniel H Cohn, David L Rimoin, Ralph S Lachman, Yoshinari Miyamoto, Bronwyn Kerr, Sheila Unger, Hirofumi Ohashi, Andrea Superti‐Furga, Shiro Ikegawa

J Med Genet. 2007 Apr; 44(4): e73. doi: 10.1136/jmg.2006.043869