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Select item 111670831.

Single-cell RNA sequencing reveals different chondrocyte states in femoral cartilage between osteoarthritis and healthy individuals

Zewen Sun, Mingyue Yan, Junjie Wang, Haoyun Zhang, Xiaobin Ji, Yujing Xiao, Tianrui Wang, Tengbo Yu

Front Immunol. 2024; 15: 1407679. Published online 2024 May 29. doi: 10.3389/fimmu.2024.1407679

PMCID:: PMC11167083

Abstract Article PDF–10M

Select item 110082682.

Deficiency of Cbfβ in articular cartilage leads to osteoarthritis-like phenotype through Hippo/Yap, TGFβ, and Wnt/β-catenin signaling pathways

Yan Zhang, Huiwen Chen, Jinjin Wu, Abigail McVicar, Yilin Chen, Jiacan Su, Yi-Ping Li, Wei Chen

Int J Biol Sci. 2024; 20(6): 1965–1977. Published online 2024 Mar 11. doi: 10.7150/ijbs.90250

PMCID:: PMC11008268

Abstract Article PDF–16M

Select item 107978363.

A new phenotype of EVEN‐PLUS syndrome in a Chinese family and literature review

Ming Liu, Huanhuan Li, Shuhong Ren, Changhong Ding

Mol Genet Genomic Med. 2024 Jan; 12(1): e2335. Published online 2024 Jan 19. doi: 10.1002/mgg3.2335

PMCID:: PMC10797836

Abstract Article PDF–2.2M

Select item 94229174.

Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey

Emine Kartal Baykan, Ayberk Türkyılmaz

J Clin Res Pediatr Endocrinol. 2022 Sep; 14(3): 350–355. Published online 2022 Aug 25. doi: 10.4274/jcrpe.galenos.2021.2020.0301

PMCID:: PMC9422917

Abstract Article PDF–1.0M

Select item 93588905.

Anatomical characteristics and potential gene mutation sites of a familial recurrent patellar dislocation

Qi-hao Zhang, Yan Zhang, Rui-xuan He, Han-ming Guo, Xin-guang Wang

BMC Med Genomics. 2022; 15: 176. Published online 2022 Aug 7. doi: 10.1186/s12920-022-01330-9

PMCID:: PMC9358890

Abstract Article PDF–1.2M

Select item 91846636.

Somatic TEK variant with intraarticular venous malformation and knee hemarthrosis treated with rapamycin

Salma Adham, Nicole Revencu, Sandrine Mestre, Monira Nou‐Howaldt, Hélène Vernhet‐Kovacsik, Isabelle Quéré

Mol Genet Genomic Med. 2022 Jun; 10(6): e1931. Published online 2022 Apr 15. doi: 10.1002/mgg3.1931

PMCID:: PMC9184663

Abstract Article PDF–736K

Select item 83692567.

Histone deacetylase 4 deletion results in abnormal chondrocyte hypertrophy and premature ossification from collagen type 2α1-expressing cells

Guoqing Du, Chuan Xiang, Xiaowen Sang, Xiang Wang, Ying Shi, Nan Wang, Shaowei Wang, Pengcui Li, Xiaochun Wei, Min Zhang, Lilan Gao, Hongsheng Zhan, Lei Wei

Mol Med Rep. 2020 Nov; 22(5): 4031–4040. Published online 2020 Aug 27. doi: 10.3892/mmr.2020.11465

PMCID:: PMC8369256

Abstract Article PDF–948K

Select item 69131548.

Novel in-frame FLNB deletion causes Larsen syndrome in a three-generation pedigree

Scott E. Hickey, Daniel C. Koboldt, Theresa Mihalic Mosher, Patrick Brennan, Beth A. Schmalz, Erin Crist, Kim L. McBride, Brent H. Adler, Peter White, Richard K. Wilson

Cold Spring Harb Mol Case Stud. 2019 Dec; 5(6): a004176. doi: 10.1101/mcs.a004176

PMCID:: PMC6913154

Abstract Article PDF–1.7M

Select item 68846889.

PRMT5 is necessary to form distinct cartilage identities in the knee and long bone

Janani Ramachandran, Zhaoyang Liu, Ryan S. Gray, Steven A. Vokes

Dev Biol. Author manuscript; available in PMC 2020 Dec 15.

Published in final edited form as: Dev Biol. 2019 Dec 15; 456(2): 154–163. Published online 2019 Aug 20. doi: 10.1016/j.ydbio.2019.08.012

PMCID:: PMC6884688

Abstract Article PDF–3.4M

Select item 608386810.

MICE HARBORING A HAJDU CHENEY SYNDROME MUTATION ARE SENSITIZED TO OSTEOARTHRITIS

S. Zanotti, J. Yu, D. Bridgewater, J.M. Wolf, E. Canalis

Bone. Author manuscript; available in PMC 2019 Sep 1.

Published in final edited form as: Bone. 2018 Sep; 114: 198–205. Published online 2018 Jun 22. doi: 10.1016/j.bone.2018.06.020

PMCID:: PMC6083868

Abstract Article PDF–999K

Select item 557779011.

Fibroma of tendon sheath around large joints: clinical characteristics and literature review

Kayo Suzuki, Taketoshi Yasuda, Shun Suzawa, Kenta Watanabe, Masahiko Kanamori, Tomoatsu Kimura

BMC Musculoskelet Disord. 2017; 18: 376. Published online 2017 Aug 30. doi: 10.1186/s12891-017-1736-5

PMCID:: PMC5577790

Abstract Article PDF–1.2M

Select item 483070112.

Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies

Uluç Yis, Figen Baydan, Mert Karakaya, Semra Hız Kurul, Sebahattin Cirak

Biomed Res Int. 2016; 2016: 3128735. Published online 2016 Mar 31. doi: 10.1155/2016/3128735

PMCID:: PMC4830701

Abstract Article PDF–1.5M

Select item 464275913.

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Yichuan Liu, Yun Li, Michael E. March, Nguyen Kenny, Kexiang Xu, Fengxiang Wang, Yiran Guo, Brendan Keating, Joseph Glessner, Jiankang Li, Theodore J. Ganley, Jianguo Zhang, Matthew A. Deardorff, Xun Xu, Hakon Hakonarson

Hum Genomics. 2015; 9: 31. Published online 2015 Nov 11. doi: 10.1186/s40246-015-0053-z

Correction in:: Hum Genomics. 2016; 10: 5.

PMCID:: PMC4642759

Abstract Article PDF–1.7M

Select item 404603014.

Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in flat-coated retrievers

Ineke C M Lavrijsen, Peter A J Leegwater, Chalika Wangdee, Frank G van Steenbeek, Monique Schwencke, Gert J Breur, Freek J Meutstege, Isaac J Nijman, Edwin Cuppen, Henri C M Heuven, Herman A W Hazewinkel

BMC Genet. 2014; 15: 64. Published online 2014 May 28. doi: 10.1186/1471-2156-15-64