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Items: 1 to 20 of 48

1.
Activation of the TGFβ/SMAD Transcriptional Pathway Underlies a Novel Tumor Promoting Role of Sulfatase1 in Hepatocellular Carcinoma*
Renumathy Dhanasekaran, Ikuo Nakamura, Chunling Hu, Gang Chen, Abdul M. Oseini, Elif Sezin Seven, Alexander G Miamen, Catherine D Moser, Wei Zhou, Toin H. van Kuppevelt, Jan van Deursen, Taofic Mounajjed, Martin E. Fernandez-Zapico, Lewis R. Roberts
Hepatology. Author manuscript; available in PMC 2016 Apr 1.
Published in final edited form as: Hepatology. 2015 Apr; 61(4): 1269–1283. Published online 2015 Feb 13. doi: 10.1002/hep.27658
PMCID:
PMC4376661
AbstractArticlePDF–1.7M
2.
Expression of Heparan Sulfate Endosulfatases in the Adult Mouse Brain: Co-expression of Sulf1 and Dopamine D1/D2 Receptors
Ken Miya, Kazuko Keino-Masu, Takuya Okada, Kenta Kobayashi, Masayuki Masu
Front Neuroanat. 2021; 15: 726718. Published online 2021 Aug 20. doi: 10.3389/fnana.2021.726718
PMCID:
PMC8417564
AbstractArticlePDF–9.3M
3.
Abnormal Pyramidal Decussation and Bilateral Projection of the Corticospinal Tract Axons in Mice Lacking the Heparan Sulfate Endosulfatases, Sulf1 and Sulf2
Satoshi Aizawa, Takuya Okada, Kazuko Keino-Masu, Tri Huu Doan, Tadachika Koganezawa, Masahiro Akiyama, Akira Tamaoka, Masayuki Masu
Front Mol Neurosci. 2019; 12: 333. Published online 2020 Jan 21. doi: 10.3389/fnmol.2019.00333
PMCID:
PMC6985096
AbstractArticlePDF–7.8M
4.
Loss of endothelial sulfatase-1 after experimental sepsis attenuates subsequent pulmonary inflammatory responses
Kaori Oshima, Xiaorui Han, Yilan Ouyang, Rana El Masri, Yimu Yang, Sarah M. Haeger, Sarah A. McMurtry, Trevor C. Lane, Pavel Davizon-Castillo, Fuming Zhang, Xinping Yue, Romain R. Vivès, Robert J. Linhardt, Eric P. Schmidt
Am J Physiol Lung Cell Mol Physiol. 2019 Nov 1; 317(5): L667–L677. Published online 2019 Aug 28. doi: 10.1152/ajplung.00175.2019
PMCID:
PMC6879902
AbstractArticle
5.
Role of heparan sulfate 6-0 endosulfatases in intervertebral disc homeostasis
Shuhei Otsuki, Oscar Alvarez-Garcia, Martin K. Lotz, Masashi Neo
Histol Histopathol. Author manuscript; available in PMC 2020 Sep 1.
Published in final edited form as: Histol Histopathol. 2019 Sep; 34(9): 1051–1060. Published online 2019 Mar 29. doi: 10.14670/HH-18-107
PMCID:
PMC6742574
AbstractArticlePDF–1.3M
6.
Epithelial Deletion of Sulf2 Exacerbates Bleomycin-Induced Lung Injury, Inflammation, and Mortality
Xinping Yue
Am J Respir Cell Mol Biol. 2017 Nov; 57(5): 560–569. doi: 10.1165/rcmb.2016-0367OC
PMCID:
PMC5705905
AbstractArticlePDF–1.8M
7.
Overexpression of sulfatase-1 in murine hepatocarcinoma Hca-F cell line downregulates mesothelin and leads to reduction in lymphatic metastasis, both in vitro and in vivo
Salma Mahmoud, Mohammed Ibrahim, Ahmed Hago, Yuhong Huang, Yuanyi Wei, Jun Zhang, Qingqing Zhang, Yu Xiao, Jingwen Wang, Munkaila Adam, Yu Guo, Li Wang, Shuting Zhou, Boyi Xin, Wei Xuan, Jianwu Tang
Oncotarget. 2016 Nov 15; 7(46): 75052–75063. Published online 2016 Sep 10. doi: 10.18632/oncotarget.11933
PMCID:
PMC5342722
AbstractArticlePDF–6.1M
8.
Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions
Ina Kalus, Susanne Rohn, Tania M. Puvirajesinghe, Scott E. Guimond, Pieter J. Eyckerman-Kölln, Gerdy ten Dam, Toin H. van Kuppevelt, Jeremy E. Turnbull, Thomas Dierks
PLoS One. 2015; 10(10): e0139853. Published online 2015 Oct 8. doi: 10.1371/journal.pone.0139853
PMCID:
PMC4598108
AbstractArticlePDF–4.0M
9.
Organ-specific Sulfation Patterns of Heparan Sulfate Generated by Extracellular Sulfatases Sulf1 and Sulf2 in Mice
Satoshi Nagamine, Michiko Tamba, Hisako Ishimine, Kota Araki, Kensuke Shiomi, Takuya Okada, Tatsuyuki Ohto, Satoshi Kunita, Satoru Takahashi, Ronnie G. P. Wismans, Toin H. van Kuppevelt, Masayuki Masu, Kazuko Keino-Masu
J Biol Chem. 2012 Mar 16; 287(12): 9579–9590. Published online 2012 Feb 1. doi: 10.1074/jbc.M111.290262
PMCID:
PMC3308746
AbstractArticlePDF–3.3M
10.
Sulf1A and HGF regulate satellite-cell growth
Roop Gill, Laura Hitchins, Fenella Fletcher, Gurtej K. Dhoot
J Cell Sci. 2010 Jun 1; 123(11): 1873–1883. Published online 2010 May 4. doi: 10.1242/jcs.061242
PMCID:
PMC2873224
AbstractArticle
11.
Transforming Growth Factor-β1 Induces Heparan Sulfate 6-O-Endosulfatase 1 Expression in Vitro and in Vivo
Xinping Yue, Xian Li, Hong T. Nguyen, Dawn R. Chin, Deborah E. Sullivan, Joseph A. Lasky
J Biol Chem. 2008 Jul 18; 283(29): 20397–20407. doi: 10.1074/jbc.M802850200
PMCID:
PMC2459296
AbstractArticlePDF–646K
12.
Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity
William C. Lamanna, Rebecca J. Baldwin, Michael Padva, Ina Kalus, Gerdy ten Dam, Toin H. van Kuppevelt, John T. Gallagher, Kurt von Figura, Thomas Dierks, Catherine L. R. Merry
Biochem J. 2006 Nov 15; 400(Pt 1): 63–73. Prepublished online 2006 Aug 11. Published online 2006 Oct 27. doi: 10.1042/BJ20060848
PMCID:
PMC1635445
AbstractArticlePDF–812K
13.
Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticity
Ina Kalus, Benedikt Salmen, Christoph Viebahn, Kurt von Figura, Dietmar Schmitz, Rudi D'Hooge, Thomas Dierks
J Cell Mol Med. 2009 Nov-Dec; 13(11-12): 4505–4521. Published online 2008 Oct 16. doi: 10.1111/j.1582-4934.2008.00558.x
PMCID:
PMC4515066
AbstractArticlePDF–1.0M
14.
Heparan Sulfate 6-O-endosulfatases (Sulfs) Coordinate the Wnt Signaling Pathways to Regulate Myoblast Fusion during Skeletal Muscle Regeneration
Thanh H. Tran, Xiaofeng Shi, Joseph Zaia, Xingbin Ai
J Biol Chem. 2012 Sep 21; 287(39): 32651–32664. Published online 2012 Aug 3. doi: 10.1074/jbc.M112.353243
PMCID:
PMC3463311
AbstractArticlePDF–3.6M
15.
Gene Trap Disruption of the Mouse Heparan Sulfate 6-O-Endosulfatase Gene, Sulf2
David H. Lum, Jenille Tan, Steven D. Rosen, Zena Werb
Mol Cell Biol. 2007 Jan; 27(2): 678–688. Published online 2006 Nov 20. doi: 10.1128/MCB.01279-06
PMCID:
PMC1800820
AbstractArticlePDF–2.0M
16.
Desulfation of Heparan Sulfate by Sulf1 and Sulf2 Is Required for Corticospinal Tract Formation
Takuya Okada, Kazuko Keino-Masu, Satoshi Nagamine, Fuyuki Kametani, Tatsuyuki Ohto, Masato Hasegawa, Toin H. van Kuppevelt, Satoshi Kunita, Satoru Takahashi, Masayuki Masu
Sci Rep. 2017; 7: 13847. Published online 2017 Oct 23. doi: 10.1038/s41598-017-14185-3
PMCID:
PMC5653861
AbstractArticlePDF–5.0M
17.
The SULFs, Extracellular Sulfatases for Heparan Sulfate, Promote the Migration of Corneal Epithelial Cells during Wound Repair
Inna Maltseva, Matilda Chan, Ina Kalus, Thomas Dierks, Steven D. Rosen
PLoS One. 2013; 8(8): e69642. Published online 2013 Aug 8. doi: 10.1371/journal.pone.0069642
PMCID:
PMC3738537
AbstractArticlePDF–8.1M
18.
Distinct expression patterns of Sulf1 and Hs6st1 spatially regulate heparan sulfate sulfation during prostate development
Rita A. Buresh-Stiemke, Rita L. Malinowski, Kimberly P. Keil, Chad M. Vezina, Arie Oosterhof, Toin H. van Kuppevelt, Paul C. Marker
Dev Dyn. Author manuscript; available in PMC 2013 Dec 1.
Published in final edited form as: Dev Dyn. 2012 Dec; 241(12): 2005–2013. Published online 2012 Nov 5. doi: 10.1002/dvdy.23886
PMCID:
PMC3677568
AbstractArticlePDF–3.9M
19.
Roles of Heparan Sulfate Sulfation in Dentinogenesis
Satoru Hayano, Hiroshi Kurosaka, Takeshi Yanagita, Ina Kalus, Fabian Milz, Yoshihito Ishihara, Md. Nurul Islam, Noriaki Kawanabe, Masahiro Saito, Hiroshi Kamioka, Taiji Adachi, Thomas Dierks, Takashi Yamashiro
J Biol Chem. 2012 Apr 6; 287(15): 12217–12229. Published online 2012 Feb 20. doi: 10.1074/jbc.M111.332924
PMCID:
PMC3320973
AbstractArticlePDF–4.6M
20.
Expression regulation and function of heparan sulfate 6-O-endosulfatases in the spermatogonial stem cell niche
Aliete Langsdorf, Valerie Schumacher, Xiaofeng Shi, Thanh Tran, Joseph Zaia, Sanjay Jain, Mary Taglienti, Jordan A Kreidberg, Alan Fine, Xingbin Ai
Glycobiology. 2011 Feb; 21(2): 152–161. Published online 2010 Sep 20. doi: 10.1093/glycob/cwq133
PMCID:
PMC3031337
AbstractArticlePDF–458K

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