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Items: 1 to 20 of 253

1.
TIMP-1 is an activator of MHC-I expression in myeloid dendritic cells with implications for tumor immunogenicity
Miriam Langguth, Eleftheria Maranou, Saara A. Koskela, Oskar Elenius, Roosa E. Kallionpää, Eva-Maria Birkman, Otto I. Pulkkinen, Maria Sundvall, Marko Salmi, Carlos R. Figueiredo
Genes Immun. 2024; 25(3): 188–200. Published online 2024 May 22. doi: 10.1038/s41435-024-00274-7
PMCID:
PMC11178497
AbstractArticlePDF–3.9M
2.
HLA-B and TIMP1 as hub genes of the ventricular remodeling caused by hypertension
Gai-Feng Hu, Ling-Bing Meng, Jianyi Li, Jiapei Xu, Hong-Xuan Xu, De-Ping Liu
Aging (Albany NY) 2024 May 15; 16(9): 8260–8278. Published online 2024 May 9. doi: 10.18632/aging.205816
PMCID:
PMC11132017
AbstractArticlePDF–2.6M
3.
K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors
Anita Waltho, Oliver Popp, Christopher Lenz, Lukas Pluska, Mahil Lambert, Volker Dötsch, Philipp Mertins, Thomas Sommer
Life Sci Alliance. 2024 Aug; 7(8): e202402740. Published online 2024 May 21. doi: 10.26508/lsa.202402740
PMCID:
PMC11109483
AbstractArticlePDF–2.9M
4.
GnT-V-mediated aberrant N-glycosylation of TIMP-1 promotes diabetic retinopathy progression
Xiaoting Xi, Yanni Yang, Qianbo Chen, Jia Ma, Xuewei Wang, Yachun Deng, Xi Wang, Yan Li
Mol Biol Rep. 2024; 51(1): 428. Published online 2024 Mar 18. doi: 10.1007/s11033-024-09388-7
PMCID:
PMC10948582
AbstractArticlePDF–8.1M
5.
The role of sinusoidal endothelial cells and TIMP1 in the regulation of fibrosis in a novel human liver 3D NASH model
Sander van Riet, Anais Julien, Andrea Atanasov, Åsa Nordling, Magnus Ingelman-Sundberg
Hepatol Commun. 2024 Mar; 8(3): e0374. Published online 2024 Feb 14. doi: 10.1097/HC9.0000000000000374
PMCID:
PMC10871795
AbstractArticlePDF–1.6M
6.
Epigenetic-focused CRISPR/Cas9 screen identifies (absent, small, or homeotic)2-like protein (ASH2L) as a regulator of glioblastoma cell survival
Ezgi Ozyerli-Goknar, Ezgi Yagmur Kala, Ali Cenk Aksu, Ipek Bulut, Ahmet Cingöz, Sheikh Nizamuddin, Martin Biniossek, Fidan Seker-Polat, Tunc Morova, Can Aztekin, Sonia H. Y. Kung, Hamzah Syed, Nurcan Tuncbag, Mehmet Gönen, Martin Philpott, Adam P. Cribbs, Ceyda Acilan, Nathan A. Lack, Tamer T. Onder, H. T. Marc Timmers, Tugba Bagci-Onder
Cell Commun Signal. 2023; 21: 328. Published online 2023 Nov 16. doi: 10.1186/s12964-023-01335-6
PMCID:
PMC10652464
AbstractArticlePDF–8.0M
7.
Upregulated TIMP1 facilitates and coordinates myometrial contraction by decreasing collagens and cell adhesive capacity during human labor
Junjie Bao, Xiaodi Wang, Lina Chen, Bolun Wen, Qiu Gao, Xiuyu Pan, Yunshan Chen, Kaiyuan Ji, Huishu Liu
Mol Hum Reprod. 2023 Oct; 29(10): gaad034. Published online 2023 Sep 29. doi: 10.1093/molehr/gaad034
PMCID:
PMC10581194
AbstractArticlePDF–1.3M
8.
TIMP1 shapes an immunosuppressive microenvironment by regulating anoikis to promote the progression of clear cell renal cell carcinoma
Qiang Li, Kai Wei, Xi Zhang, Yang Lv, Miao Li, Chenchao Zhou, Shifeng Su, Daorong Hou, Jianquan Hou
Aging (Albany NY) 2023 Sep 15; 15(17): 8908–8929. Published online 2023 Sep 8. doi: 10.18632/aging.205005
PMCID:
PMC10522382
AbstractArticlePDF–3.7M
9.
Proteomics Identifies Circulating TIMP-1 as a Prognostic Biomarker for Diffuse Large B-Cell Lymphoma
Ning Lou, Guibin Wang, Yanrong Wang, Meng Xu, Yu Zhou, Qiaoyun Tan, Qiaofeng Zhong, Lei Zhang, Xiaomei Zhang, Shuxia Liu, Rongrong Luo, Shasha Wang, Le Tang, Jiarui Yao, Zhishang Zhang, Yuankai Shi, Xiaobo Yu, Xiaohong Han
Mol Cell Proteomics. 2023 Sep; 22(9): 100625. Published online 2023 Jul 26. doi: 10.1016/j.mcpro.2023.100625
PMCID:
PMC10470290
AbstractArticlePDF–5.1M
10.
The invariant chain CD74 protein is a cell surface binding partner of TIMP‐1 in breast cancer cells
Mikkel Høeberg, Julie Boertmann Noer, Mette Vixø Vistesen, Annette Bartels, Esben Matzen Bech, Sune Boris Nygård, Ulrik Lademann, Jan Stenvang, Siqi Liu, Anja Thoe Fuglsang, Nils Brünner, José Manuel Afonso Moreira
Mol Oncol. 2023 Aug; 17(8): 1595–1612. Published online 2023 Apr 28. doi: 10.1002/1878-0261.13436
PMCID:
PMC10399710
AbstractArticlePDF–7.8M
11.
Tissue Inhibitor of Matrix Metalloproteinases-1 (TIMP-1) and Pulmonary Involvement in COVID-19 Pneumonia
Maria Antonella Zingaropoli, Tiziana Latronico, Patrizia Pasculli, Giorgio Maria Masci, Roberta Merz, Federica Ciccone, Federica Dominelli, Cosmo Del Borgo, Miriam Lichtner, Franco Iafrate, Gioacchino Galardo, Francesco Pugliese, Valeria Panebianco, Paolo Ricci, Carlo Catalano, Maria Rosa Ciardi, Grazia Maria Liuzzi, Claudio Maria Mastroianni
Biomolecules. 2023 Jul; 13(7): 1040. Published online 2023 Jun 26. doi: 10.3390/biom13071040
PMCID:
PMC10377146
AbstractArticlePDF–2.7M
12.
CCR5 deficiency normalizes TIMP levels, working memory, and gamma oscillation power in APOE4 targeted replacement mice
Griffin A. Greco, Mitchell Rock, Matthew Amontree, Maria Fe Lanfranco, Holly Korthas, Sung Hyeok Hong, R. Scott Turner, G. William Rebeck, Katherine Conant
Neurobiol Dis. Author manuscript; available in PMC 2023 Jun 26.
Published in final edited form as: Neurobiol Dis. 2023 Apr; 179: 106057. Published online 2023 Mar 5. doi: 10.1016/j.nbd.2023.106057
PMCID:
PMC10291850
AbstractArticlePDF–1.4M
13.
siRNA-Mediated Timp1 Silencing Inhibited the Inflammatory Phenotype during Acute Lung Injury
Ivan V. Chernikov, Yaroslav Yu. Staroseletz, Irina S. Tatarnikova, Aleksandra V. Sen’kova, Innokenty A. Savin, Andrey V. Markov, Evgeniya B. Logashenko, Elena L. Chernolovskaya, Marina A. Zenkova, Valentin V. Vlassov
Int J Mol Sci. 2023 Jan; 24(2): 1641. Published online 2023 Jan 13. doi: 10.3390/ijms24021641
PMCID:
PMC9865963
AbstractArticlePDF–6.6M
14.
TIMP-1 is a novel ligand of Amyloid Precursor Protein and triggers a proinflammatory phenotype in human monocytes
Celina Eckfeld, Benjamin Schoeps, Daniel Häußler, Julian Frädrich, Felix Bayerl, Jan Philipp Böttcher, Percy Knolle, Simone Heisz, Olga Prokopchuk, Hans Hauner, Enkhtsetseg Munkhbaatar, Ihsan Ekin Demir, Chris D. Hermann, Achim Krüger
J Cell Biol. 2023 Feb 6; 222(2): e202206095. Published online 2023 Jan 11. doi: 10.1083/jcb.202206095
PMCID:
PMC9837626
AbstractArticlePDF–4.7M
15.
CST1 inhibits ferroptosis and promotes gastric cancer metastasis by regulating GPX4 protein stability via OTUB1
Dongbao Li, Yuhong Wang, Chao Dong, Tao Chen, Anqi Dong, Jiayu Ren, Weikang Li, Gege Shu, Jiaoyang Yang, Wenhao Shen, Lei Qin, Lin Hu, Jin Zhou
Oncogene. 2023; 42(2): 83–98. Published online 2022 Nov 12. doi: 10.1038/s41388-022-02537-x
PMCID:
PMC9816059
AbstractArticlePDF–7.6M
16.
TIMP1 promotes cell proliferation and invasion capability of right‐sided colon cancers via the FAK/Akt signaling pathway
Beibei Ma, Hiroyuki Ueda, Koichi Okamoto, Masahiro Bando, Shota Fujimoto, Yasuyuki Okada, Tomoyuki Kawaguchi, Hironori Wada, Hiroshi Miyamoto, Mitsuo Shimada, Yasushi Sato, Tetsuji Takayama
Cancer Sci. 2022 Dec; 113(12): 4244–4257. Published online 2022 Sep 21. doi: 10.1111/cas.15567
PMCID:
PMC9746056
AbstractArticlePDF–4.2M
17.
Aberrant TIMP-1 overexpression in tumor-associated fibroblasts drives tumor progression through CD63 in lung adenocarcinoma
Paula Duch, Natalia Díaz-Valdivia, Rafael Ikemori, Marta Gabasa, Evette S. Radisky, Marselina Arshakyan, Sabrina Gea-Sorlí, Anna Mateu-Bosch, Paloma Bragado, Josep Lluís Carrasco, Hidetoshi Mori, Josep Ramírez, Cristina Teixidó, Noemí Reguart, Cristina Fillat, Derek C. Radisky, Jordi Alcaraz
Matrix Biol. Author manuscript; available in PMC 2023 Aug 1.
Published in final edited form as: Matrix Biol. 2022 Aug; 111: 207–225. Published online 2022 Jul 2. doi: 10.1016/j.matbio.2022.06.009
PMCID:
PMC9667815
AbstractArticlePDF–2.3M
18.
TIMP-1 Dependent Modulation of Metabolic Profiles Impacts Chemoresistance in NSCLC
Wei Xiao, Pankaj Ahluwalia, Lan Wang, John Howard, Ravindra Kolhe, Amyn M. Rojiani, Mumtaz V. Rojiani
Cells. 2022 Oct; 11(19): 3036. Published online 2022 Sep 28. doi: 10.3390/cells11193036
PMCID:
PMC9562647
AbstractArticlePDF–4.8M
19.
SARS-CoV-2 Nsp6 damages Drosophila heart and mouse cardiomyocytes through MGA/MAX complex-mediated increased glycolysis
Jun-yi Zhu, Guanglei Wang, Xiaohu Huang, Hangnoh Lee, Jin-Gu Lee, Penghua Yang, Joyce van de Leemput, Weiliang Huang, Maureen A. Kane, Peixin Yang, Zhe Han
Commun Biol. 2022; 5: 1039. Published online 2022 Sep 30. doi: 10.1038/s42003-022-03986-6
PMCID:
PMC9523645
AbstractArticlePDF–3.9M
20.
The role of tissue inhibitor of metalloproteinases in the aetiology of inguinal and incisional hernias
Ugur Durukan, Orhan Agcaoglu, Emre Ozoran, Salih Nafiz Karahan, Ibrahim Ozata, Yigit Duzkoylu, Esra Pasaoglu, Acar Aren
Int Wound J. 2022 Oct; 19(6): 1502–1508. Published online 2022 Mar 11. doi: 10.1111/iwj.13746
PMCID:
PMC9493228
AbstractArticlePDF–1.2M

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