PMC Links for Gene (Select 4148) - PMC

Zhu Guo, WeiLiang Su, RongYao Zhou, GuoQing Zhang, Shuai Yang, XiaoLin Wu, ChenSheng Qiu, WenBin Cong, Nana Shen, JianWei Guo, Chang Liu, Shang-You Yang, DongMing Xing, Yan Wang, BoHua Chen, HongFei Xiang

Oxid Med Cell Longev. 2021; 2021: 5542241. Published online 2021 May 27. doi: 10.1155/2021/5542241

PMCID:: PMC8175180

Abstract Article PDF–4.7M

Select item 71405484.

A novel p.A191D matrilin-3 variant in a Vietnamese family with multiple epiphyseal dysplasia: a case report

Thuong Thi Ho, Linh Huyen Tran, Lan Thu Hoang, Phuong Kim Thi Doan, Trang Thi Nguyen, Trang Hong Nguyen, Hoai Thu Tran, Ha Hoang, Ha Hoang Chu, Anh Lan Thi Luong

BMC Musculoskelet Disord. 2020; 21: 216. Published online 2020 Apr 7. doi: 10.1186/s12891-020-03222-4

PMCID:: PMC7140548

Abstract Article PDF–3.7M

Select item 61228465.

A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study

Jing Zhao, Weibo Xia, Min Nie, Xin Zheng, Qiuping Wang, Xiran Wang, Wenbo Wang, Zhiwei Ning, Wei Huang, Yan Jiang, Mei Li, Ou Wang, Xiaoping Xing, Yue Sun, Lianmei Luo, Shuli He, Wei Yu, Qiang Lin, Yu Pei, Fan Zhang, Youxia Han, Yanmin Tong, Ying Che, Ruixin Shen, Yingying Hu, Xueying Zhou, Qian Chen, Ling Xu

Bone. Author manuscript; available in PMC 2018 Sep 4.

Published in final edited form as: Bone. 2012 Apr; 50(4): 917–924. Published online 2012 Jan 16. doi: 10.1016/j.bone.2012.01.003

PMCID:: PMC6122846

Abstract Article PDF–546K

Select item 57843326.

Martrilin-3 (MATN3) Overexpression in Gastric Adenocarcinoma and its Prognostic Significance

Ping-Li Wu, Yi-Fu He, Han-Hui Yao, Bing Hu

Med Sci Monit. 2018; 24: 348–355. Published online 2018 Jan 18. doi: 10.12659/MSM.908447

PMCID:: PMC5784332

Abstract Article PDF–1.0M

Select item 34323537.

MATN3 Gene Polymorphism Is Associated with Osteoarthritis in Chinese Han Population: A Community-Based Case-Control Study

Jiaao Gu, Jiesheng Rong, Fulin Guan, Liying Jiang, Shuqing Tao, Guofa Guan, Tianzun Tao

ScientificWorldJournal. 2012; 2012: 656084. Published online 2012 Aug 22. doi: 10.1100/2012/656084

PMCID:: PMC3432353

Abstract Article PDF–498K

Select item 17572688.

Missense mutations in the ß strands of the single A-domain of matrilin-3 result in multiple epiphyseal dysplasia

G Jackson, F Barker, E Jakkula, M Czarny-Ratajczak, O Makitie, W Cole, M Wright, S Smithson, M Suri, P Rogala, G Mortier, C Baldock, A Wallace, R Elles, L Ala-Kokko, M Briggs

J Med Genet. 2004 Jan; 41(1): 52–59. doi: 10.1136/jmg.2003.011429

PMCID:: PMC1757268

Summary PDF–873K

Select item 17359389.

Matrilin-3 mutations that cause chondrodysplasias interfere with protein trafficking while a mutation associated with hand osteoarthritis does not

C Otten, R Wagener, M Paulsson, F Zaucke

J Med Genet. 2005 Oct; 42(10): 774–779. doi: 10.1136/jmg.2004.029462

PMCID:: PMC1735938

Summary PDF–256K

Select item 128823910.

Genome Scan for Predisposing Loci for Distal Interphalangeal Joint Osteoarthritis: Evidence for a Locus on 2q

Jenni Leppävuori, Urho Kujala, Jaakko Kinnunen, Jaakko Kaprio, Martti Nissilä, Markku Heliövaara, Nina Klinger, Jukka Partanen, Joseph D. Terwilliger, Leena Peltonen

Am J Hum Genet. 1999 Oct; 65(4): 1060–1067. Published online 1999 Sep 9. doi: 10.1086/302569

PMCID:: PMC1288239

Abstract Article PDF–283K

Select item 118030511.

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3

Stefán Einar Stefánsson, Helgi Jónsson, Thorvaldur Ingvarsson, Ileana Manolescu, Hjörtur H. Jónsson, Guðbjörg Ólafsdóttir, Ebba Pálsdóttir, Gerður Stefánsdóttir, Guðfinna Sveinbjörnsdóttir, Michael L. Frigge, Augustine Kong, Jeffrey R. Gulcher, Kári Stefánsson

Am J Hum Genet. 2003 Jun; 72(6): 1448–1459. Published online 2003 May 7. doi: 10.1086/375556

PMCID:: PMC1180305

Abstract Article PDF–487K

Select item 794025812.

Differentiation of Hypertrophic Chondrocytes from Human iPSCs for the In Vitro Modeling of Chondrodysplasias

Yann Pretemer, Shunsuke Kawai, Sanae Nagata, Megumi Nishio, Makoto Watanabe, Sakura Tamaki, Cantas Alev, Yoshihiro Yamanaka, Jing-Yi Xue, Zheng Wang, Kenichi Fukiage, Masako Tsukanaka, Tohru Futami, Shiro Ikegawa, Junya Toguchida

Stem Cell Reports. 2021 Mar 9; 16(3): 610–625. Published online 2021 Feb 25. doi: 10.1016/j.stemcr.2021.01.014

PMCID:: PMC7940258

Abstract Article PDF–6.6M

Select item 582445213.

Downregulation of microRNA-448 inhibits IL-1β-induced cartilage degradation in human chondrocytes via upregulation of matrilin-3

Hao Yang, Di Wu, Hua Li, Nan Chen, Yongjun Shang

Cell Mol Biol Lett. 2018; 23: 7. Published online 2018 Feb 22. doi: 10.1186/s11658-018-0072-6

PMCID:: PMC5824452

Abstract Article PDF–1.7M

Select item 358050714.

Matrilin-3 Induction of IL-1 receptor antagonist Is required for up-regulating collagen II and aggrecan and down-regulating ADAMTS-5 gene expression

Chathuraka T Jayasuriya, Mary B Goldring, Richard Terek, Qian Chen

Arthritis Res Ther. 2012; 14(5): R197. Published online 2012 Sep 11. doi: 10.1186/ar4033

PMCID:: PMC3580507

Abstract Article PDF–1.0M

Select item 272695615.

Multiple epiphyseal dysplasia mutations in MATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3

Sally L Cotterill, Gail C Jackson, Matthew P Leighton, Raimund Wagener, Outi Mäkitie, William G Cole, Michael D Briggs

Hum Mutat. 2005 Dec; 26(6): 557–565. doi: 10.1002/humu.20263

PMCID:: PMC2726956

Abstract Article PDF–333K

Select item 267423016.

Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutation

Matthew P. Leighton, Seema Nundlall, Tobias Starborg, Roger S. Meadows, Farhana Suleman, Lynette Knowles, Raimund Wagener, David J. Thornton, Karl E. Kadler, Raymond P. Boot-Handford, Michael D. Briggs

Hum Mol Genet. Author manuscript; available in PMC 2009 Apr 28.

Published in final edited form as: Hum Mol Genet. 2007 Jul 15; 16(14): 1728–1741. Published online 2007 May 21. doi: 10.1093/hmg/ddm121

PMCID:: PMC2674230

Abstract Article PDF–2.2M

Select item 267305517.

STRUCTURAL AND FUNCTIONAL CHARACTERISATION OF RECOMBINANT MATRILIN-3 A-DOMAIN AND IMPLICATIONS FOR HUMAN GENETIC BONE DISEASES

Maryline Fresquet, Thomas A. Jowitt, Joni Ylöstalo, Paul Coffey, Roger S. Meadows, Leena Ala-Kokko, David J. Thornton, Michael D. Briggs

J Biol Chem. Author manuscript; available in PMC 2009 Apr 24.

Published in final edited form as: J Biol Chem. 2007 Nov 30; 282(48): 34634–34643. Published online 2007 Sep 18. doi: 10.1074/jbc.M705301200

PMCID:: PMC2673055

Abstract Article PDF–1.3M

Select item 173576818.

Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMD

Z Borochowitz, D Scheffer, V Adir, N Dagoneau, A Munnich, V Cormier-Daire

J Med Genet. 2004 May; 41(5): 366–372. doi: 10.1136/jmg.2003.013342

PMCID:: PMC1735768

Summary PDF–512K

Select item 536318919.

Intra-articular Delivery of Antago-miR-483-5p Inhibits Osteoarthritis by Modulating Matrilin 3 and Tissue Inhibitor of Metalloproteinase 2

Hua Wang, Haiyan Zhang, Qiuyi Sun, Yun Wang, Jun Yang, Jincheng Yang, Tao Zhang, Shenqiu Luo, Liping Wang, Yu Jiang, Chun Zeng, Daozhang Cai, Xiaochun Bai

Mol Ther. 2017 Mar 1; 25(3): 715–727. Published online 2017 Jan 27. doi: 10.1016/j.ymthe.2016.12.020

PMCID:: PMC5363189

Abstract Article PDF–5.3M

Select item 327222020.

Pseudoachondroplasia and Multiple Epiphyseal Dysplasia: A 7-Year Comprehensive Analysis of the Known Disease Genes Identify Novel and Recurrent Mutations and Provides an Accurate Assessment of Their Relative Contribution

Gail C Jackson, Laureane Mittaz-Crettol, Jacqueline A Taylor, Geert R Mortier, Juergen Spranger, Bernhard Zabel, Martine Le Merrer, Valerie Cormier-Daire, Christine M Hall, Amaka Offiah, Michael J Wright, Ravi Savarirayan, Gen Nishimura, Simon C Ramsden, Rob Elles, Luisa Bonafe, Andrea Superti-Furga, Sheila Unger, Andreas Zankl, Michael D Briggs

Hum Mutat. 2012 Jan; 33(1): 144–157. Published online 2011 Sep 15. doi: 10.1002/humu.21611

PMCID:: PMC3272220

Abstract Article PDF–428K

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