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Showing 1 to 12 of 699 entries
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Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis.

Current respiratory medicine reviews

Moore BB, Thannickal VJ, Toews GB.
PMID: 27499722
Curr Respir Med Rev. 2005;1(1):69-76. doi: 10.2174/1573398052953613.

Progressive pulmonary fibrosis is characterized by failed alveolar reepithelialization and fibroblast/myofibroblast accumulation, with deposition of extracellular matrix. This results in loss of lung elasticity, alveolar collapse and fibrosis, impaired gas exchange and progressive decline in pulmonary function. Myofibroblasts represent...

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Moore BB, Thannickal VJ, Toews GB. Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis. Curr Respir Med Rev. 2005;1(1):69-76doi: 10.2174/1573398052953613.
Moore, B. B., Thannickal, V. J., & Toews, G. B. (2005). Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis. Current respiratory medicine reviews, 1(1), 69-76. https://doi.org/10.2174/1573398052953613
Moore, Bethany B, et al. "Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis." Current respiratory medicine reviews vol. 1,1 (2005): 69-76. doi: https://doi.org/10.2174/1573398052953613
Moore BB, Thannickal VJ, Toews GB. Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis. Curr Respir Med Rev. 2005;1(1):69-76. doi: 10.2174/1573398052953613. PMID: 27499722; PMCID: PMC4975536.
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TNFα in liver fibrosis.

Current pathobiology reports

Yang YM, Seki E.
PMID: 26726307
Curr Pathobiol Rep. 2015 Dec;3(4):253-261. doi: 10.1007/s40139-015-0093-z. Epub 2015 Sep 30.

Hepatocyte death, inflammation, and liver fibrosis are the hallmarks of chronic liver disease. Tumor necrosis factor-α (TNFα) is an inflammatory cytokine involved in liver inflammation and sustained liver inflammation leads to liver fibrosis. TNFα exerts inflammation, proliferation, and apoptosis....

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Yang YM, Seki E. TNFα in liver fibrosis. Curr Pathobiol Rep. 2015;3(4):253-261doi: 10.1007/s40139-015-0093-z.
Yang, Y. M., & Seki, E. (2015). TNFα in liver fibrosis. Current pathobiology reports, 3(4), 253-261. https://doi.org/10.1007/s40139-015-0093-z
Yang, Yoon Mee, and Seki, Ekihiro. "TNFα in liver fibrosis." Current pathobiology reports vol. 3,4 (2015): 253-261. doi: https://doi.org/10.1007/s40139-015-0093-z
Yang YM, Seki E. TNFα in liver fibrosis. Curr Pathobiol Rep. 2015 Dec;3(4):253-261. doi: 10.1007/s40139-015-0093-z. Epub 2015 Sep 30. PMID: 26726307; PMCID: PMC4693602.
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Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells.

Archives of medical science : AMS

Nakai K, Kawato T, Morita T, Yamazaki Y, Tanaka H, Tonogi M, Oki H, Maeno M.
PMID: 26170858
Arch Med Sci. 2015 Jun 19;11(3):628-37. doi: 10.5114/aoms.2015.52369.

INTRODUCTION: Angiotensin II (Ang II) not only regulates systemic blood pressure through a vasoconstrictive effect, but also promotes bone resorption. We recently reported that Ang II (10(-6) M) stimulated the production of matrix metalloproteinases via the AT1 receptor in...

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Nakai K, Kawato T, Morita T, et al. Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells. Arch Med Sci. 2015;11(3):628-37doi: 10.5114/aoms.2015.52369.
Nakai, K., Kawato, T., Morita, T., Yamazaki, Y., Tanaka, H., Tonogi, M., Oki, H., & Maeno, M. (2015). Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells. Archives of medical science : AMS, 11(3), 628-37. https://doi.org/10.5114/aoms.2015.52369
Nakai, Kumiko, et al. "Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells." Archives of medical science : AMS vol. 11,3 (2015): 628-37. doi: https://doi.org/10.5114/aoms.2015.52369
Nakai K, Kawato T, Morita T, Yamazaki Y, Tanaka H, Tonogi M, Oki H, Maeno M. Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells. Arch Med Sci. 2015 Jun 19;11(3):628-37. doi: 10.5114/aoms.2015.52369. PMID: 26170858; PMCID: PMC4495158.
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Analysis of co-assembly and co-localization of ameloblastin and amelogenin.

Frontiers in physiology

Mazumder P, Prajapati S, Lokappa SB, Gallon V, Moradian-Oldak J.
PMID: 25120489
Front Physiol. 2014 Jul 25;5:274. doi: 10.3389/fphys.2014.00274. eCollection 2014.

Epithelially-derived ameloblasts secrete extracellular matrix proteins including amelogenin, enamelin, and ameloblastin. Complex intermolecular interactions among these proteins are believed to be important in controlling enamel formation. Here we provide in vitro and in vivo evidence of co-assembly and co-localization...

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Mazumder P, Prajapati S, Lokappa SB, et al. Analysis of co-assembly and co-localization of ameloblastin and amelogenin. Front Physiol. 2014;5:274doi: 10.3389/fphys.2014.00274.
Mazumder, P., Prajapati, S., Lokappa, S. B., Gallon, V., & Moradian-Oldak, J. (2014). Analysis of co-assembly and co-localization of ameloblastin and amelogenin. Frontiers in physiology, 5274. https://doi.org/10.3389/fphys.2014.00274
Mazumder, Parichita, et al. "Analysis of co-assembly and co-localization of ameloblastin and amelogenin." Frontiers in physiology vol. 5 (2014): 274. doi: https://doi.org/10.3389/fphys.2014.00274
Mazumder P, Prajapati S, Lokappa SB, Gallon V, Moradian-Oldak J. Analysis of co-assembly and co-localization of ameloblastin and amelogenin. Front Physiol. 2014 Jul 25;5:274. doi: 10.3389/fphys.2014.00274. eCollection 2014. PMID: 25120489; PMCID: PMC4110739.
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Role of Neuropilin-1 in Diabetic Nephropathy.

Journal of clinical medicine

Bondeva T, Wolf G.
PMID: 26239560
J Clin Med. 2015 Jun 17;4(6):1293-311. doi: 10.3390/jcm4061293.

Diabetic nephropathy (DN) often develops in patients suffering from type 1 or type 2 diabetes mellitus. DN is characterized by renal injury resulting in proteinuria. Neuropilin-1 (NRP-1) is a single-pass transmembrane receptor protein devoid of enzymatic activity. Its large...

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Bondeva T, Wolf G. Role of Neuropilin-1 in Diabetic Nephropathy. J Clin Med. 2015;4(6):1293-311doi: 10.3390/jcm4061293.
Bondeva, T., & Wolf, G. (2015). Role of Neuropilin-1 in Diabetic Nephropathy. Journal of clinical medicine, 4(6), 1293-311. https://doi.org/10.3390/jcm4061293
Bondeva, Tzvetanka, and Wolf, Gunter. "Role of Neuropilin-1 in Diabetic Nephropathy." Journal of clinical medicine vol. 4,6 (2015): 1293-311. doi: https://doi.org/10.3390/jcm4061293
Bondeva T, Wolf G. Role of Neuropilin-1 in Diabetic Nephropathy. J Clin Med. 2015 Jun 17;4(6):1293-311. doi: 10.3390/jcm4061293. PMID: 26239560; PMCID: PMC4485001.
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Substrates for clinical applicability of stem cells.

World journal of stem cells

Enam S, Jin S.
PMID: 25815112
World J Stem Cells. 2015 Mar 26;7(2):243-52. doi: 10.4252/wjsc.v7.i2.243.

The capability of human pluripotent stem cells (hPSCs) to differentiate into a variety of cells in the human body holds great promise for regenerative medicine. Many substrates exist on which hPSCs can be self-renewed, maintained and expanded to further...

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Enam S, Jin S. Substrates for clinical applicability of stem cells. World J Stem Cells. 2015;7(2):243-52doi: 10.4252/wjsc.v7.i2.243.
Enam, S., & Jin, S. (2015). Substrates for clinical applicability of stem cells. World journal of stem cells, 7(2), 243-52. https://doi.org/10.4252/wjsc.v7.i2.243
Enam, Sanjar, and Jin, Sha. "Substrates for clinical applicability of stem cells." World journal of stem cells vol. 7,2 (2015): 243-52. doi: https://doi.org/10.4252/wjsc.v7.i2.243
Enam S, Jin S. Substrates for clinical applicability of stem cells. World J Stem Cells. 2015 Mar 26;7(2):243-52. doi: 10.4252/wjsc.v7.i2.243. PMID: 25815112; PMCID: PMC4369484.
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Republished: Importance of carcinoma-associated fibroblast-derived proteins in clinical oncology.

Postgraduate medical journal

Valcz G, Sipos F, Tulassay Z, Molnar B, Yagi Y.
PMID: 25976496
Postgrad Med J. 2015 May;91(1075):1026-31. doi: 10.1136/postgradmedj-2014-202561rep.

Carcinoma-associated fibroblast (CAF) as prominent cell type of the tumour microenvironment has complex interaction with both the cancer cells and other non-neoplastic surrounding cells. The CAF-derived regulators and extracellular matrix proteins can support cancer progression by providing a protective...

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Valcz G, Sipos F, Tulassay Z, et al. Republished: Importance of carcinoma-associated fibroblast-derived proteins in clinical oncology. Postgrad Med J. 2015;91(1075):1026-31doi: 10.1136/postgradmedj-2014-202561rep.
Valcz, G., Sipos, F., Tulassay, Z., Molnar, B., & Yagi, Y. (2015). Republished: Importance of carcinoma-associated fibroblast-derived proteins in clinical oncology. Postgraduate medical journal, 91(1075), 1026-31. https://doi.org/10.1136/postgradmedj-2014-202561rep
Valcz, Gabor, et al. "Republished: Importance of carcinoma-associated fibroblast-derived proteins in clinical oncology." Postgraduate medical journal vol. 91,1075 (2015): 1026-31. doi: https://doi.org/10.1136/postgradmedj-2014-202561rep
Valcz G, Sipos F, Tulassay Z, Molnar B, Yagi Y. Republished: Importance of carcinoma-associated fibroblast-derived proteins in clinical oncology. Postgrad Med J. 2015 May;91(1075):1026-31. doi: 10.1136/postgradmedj-2014-202561rep. PMID: 25976496.
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Microarray analysis of genes involved with shell strength in layer shell gland at the early stage of active calcification.

Asian-Australasian journal of animal sciences

Liu Z, Zheng Q, Zhang X, Lu L.
PMID: 25049830
Asian-Australas J Anim Sci. 2013 May;26(5):609-24. doi: 10.5713/ajas.2012.12398.

The objective of this study was to get a comprehensive understanding of how genes in chicken shell gland modulate eggshell strength at the early stage of active calcification. Four 32-week old of purebred Xianju hens with consistent high or...

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Liu Z, Zheng Q, Zhang X, et al. Microarray analysis of genes involved with shell strength in layer shell gland at the early stage of active calcification. Asian-Australas J Anim Sci. 2013;26(5):609-24doi: 10.5713/ajas.2012.12398.
Liu, Z., Zheng, Q., Zhang, X., & Lu, L. (2013). Microarray analysis of genes involved with shell strength in layer shell gland at the early stage of active calcification. Asian-Australasian journal of animal sciences, 26(5), 609-24. https://doi.org/10.5713/ajas.2012.12398
Liu, Zhangguo, et al. "Microarray analysis of genes involved with shell strength in layer shell gland at the early stage of active calcification." Asian-Australasian journal of animal sciences vol. 26,5 (2013): 609-24. doi: https://doi.org/10.5713/ajas.2012.12398
Liu Z, Zheng Q, Zhang X, Lu L. Microarray analysis of genes involved with shell strength in layer shell gland at the early stage of active calcification. Asian-Australas J Anim Sci. 2013 May;26(5):609-24. doi: 10.5713/ajas.2012.12398. PMID: 25049830; PMCID: PMC4093333.
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Chronic Kidney Disease and Fibrosis: The Role of Uremic Retention Solutes.

Frontiers in medicine

Mutsaers HA, Stribos EG, Glorieux G, Vanholder R, Olinga P.
PMID: 26380262
Front Med (Lausanne). 2015 Aug 31;2:60. doi: 10.3389/fmed.2015.00060. eCollection 2015.

Chronic kidney disease (CKD) is a major global health concern, and the uremic state is highly associated with fibrogenesis in several organs and tissues. Fibrosis is characterized by excessive production and deposition of extracellular matrix proteins with a detrimental...

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Mutsaers HA, Stribos EG, Glorieux G, et al. Chronic Kidney Disease and Fibrosis: The Role of Uremic Retention Solutes. Front Med (Lausanne). 2015;2:60doi: 10.3389/fmed.2015.00060.
Mutsaers, H. A., Stribos, E. G., Glorieux, G., Vanholder, R., & Olinga, P. (2015). Chronic Kidney Disease and Fibrosis: The Role of Uremic Retention Solutes. Frontiers in medicine, 260. https://doi.org/10.3389/fmed.2015.00060
Mutsaers, Henricus A M, et al. "Chronic Kidney Disease and Fibrosis: The Role of Uremic Retention Solutes." Frontiers in medicine vol. 2 (2015): 60. doi: https://doi.org/10.3389/fmed.2015.00060
Mutsaers HA, Stribos EG, Glorieux G, Vanholder R, Olinga P. Chronic Kidney Disease and Fibrosis: The Role of Uremic Retention Solutes. Front Med (Lausanne). 2015 Aug 31;2:60. doi: 10.3389/fmed.2015.00060. eCollection 2015. PMID: 26380262; PMCID: PMC4553389.
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Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes.

Stem cells international

Hogerheyde TA, Suzuki S, Walshe J, Bray LJ, Stephenson SA, Harkin DG, Richardson NA.
PMID: 27648078
Stem Cells Int. 2016;2016:8310127. doi: 10.1155/2016/8310127. Epub 2016 Aug 28.

Scaffolds prepared from silk fibroin derived from cocoons of the domesticated silkworm moth Bombyx mori have demonstrated potential to support the attachment and growth of human limbal epithelial (HLE) cells in vitro. In this study, we attempted to further...

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Hogerheyde TA, Suzuki S, Walshe J, et al. Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes. Stem Cells Int. 2016;2016:8310127doi: 10.1155/2016/8310127.
Hogerheyde, T. A., Suzuki, S., Walshe, J., Bray, L. J., Stephenson, S. A., Harkin, D. G., & Richardson, N. A. (2016). Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes. Stem cells international, 20168310127. https://doi.org/10.1155/2016/8310127
Hogerheyde, Thomas A, et al. "Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes." Stem cells international vol. 2016 (2016): 8310127. doi: https://doi.org/10.1155/2016/8310127
Hogerheyde TA, Suzuki S, Walshe J, Bray LJ, Stephenson SA, Harkin DG, Richardson NA. Optimization of Corneal Epithelial Progenitor Cell Growth on Bombyx mori Silk Fibroin Membranes. Stem Cells Int. 2016;2016:8310127. doi: 10.1155/2016/8310127. Epub 2016 Aug 28. PMID: 27648078; PMCID: PMC5018328.
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Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability.

Frontiers in aging neuroscience

Rodríguez MA, Del Rio Barquero LM, Ortez CI, Jou C, Vigo M, Medina J, Febrer A, Ramon-Krauel M, Diaz-Manera J, Olive M, González-Mera L, Nascimento A, Jimenez-Mallebrera C.
PMID: 28848425
Front Aging Neurosci. 2017 Aug 08;9:268. doi: 10.3389/fnagi.2017.00268. eCollection 2017.

Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and adults collectively termed collagen VI-related myopathies (COL6-RM) characterized by a varying degree of muscle weakness and joint contractures and which include Ullrich Congenital Muscular...

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Rodríguez MA, Del Rio Barquero LM, Ortez CI, et al. Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability. Front Aging Neurosci. 2017;9:268doi: 10.3389/fnagi.2017.00268.
Rodríguez, M. A., Del Rio Barquero, L. M., Ortez, C. I., Jou, C., Vigo, M., Medina, J., Febrer, A., Ramon-Krauel, M., Diaz-Manera, J., Olive, M., González-Mera, L., Nascimento, A., & Jimenez-Mallebrera, C. (2017). Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability. Frontiers in aging neuroscience, 9268. https://doi.org/10.3389/fnagi.2017.00268
Rodríguez, M A, et al. "Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability." Frontiers in aging neuroscience vol. 9 (2017): 268. doi: https://doi.org/10.3389/fnagi.2017.00268
Rodríguez MA, Del Rio Barquero LM, Ortez CI, Jou C, Vigo M, Medina J, Febrer A, Ramon-Krauel M, Diaz-Manera J, Olive M, González-Mera L, Nascimento A, Jimenez-Mallebrera C. Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability. Front Aging Neurosci. 2017 Aug 08;9:268. doi: 10.3389/fnagi.2017.00268. eCollection 2017. PMID: 28848425; PMCID: PMC5550692.
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Aortic Wall Extracellular Matrix Proteins Correlate with Syntax Score in Patients Undergoing Coronary Artery Bypass Surgery.

The open cardiovascular medicine journal

Chiong T, Cheow ES, Woo CC, Lin XY, Khin LW, Lee CN, Hartman M, Sze SK, Sorokin VA.
PMID: 27347220
Open Cardiovasc Med J. 2016 Apr 27;10:48-56. doi: 10.2174/1874192401610010048. eCollection 2016.

AIMS: The SYNTAX score correlate with major cardiovascular events post-revascularization, although the histopathological basis is unclear. We aim to evaluate the association between syntax score and extracellular matrix histological characteristics of aortic punch tissue obtained during coronary artery bypass...

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Chiong T, Cheow ES, Woo CC, et al. Aortic Wall Extracellular Matrix Proteins Correlate with Syntax Score in Patients Undergoing Coronary Artery Bypass Surgery. Open Cardiovasc Med J. 2016;10:48-56doi: 10.2174/1874192401610010048.
Chiong, T., Cheow, E. S., Woo, C. C., Lin, X. Y., Khin, L. W., Lee, C. N., Hartman, M., Sze, S. K., & Sorokin, V. A. (2016). Aortic Wall Extracellular Matrix Proteins Correlate with Syntax Score in Patients Undergoing Coronary Artery Bypass Surgery. The open cardiovascular medicine journal, 1048-56. https://doi.org/10.2174/1874192401610010048
Chiong, Terri, et al. "Aortic Wall Extracellular Matrix Proteins Correlate with Syntax Score in Patients Undergoing Coronary Artery Bypass Surgery." The open cardiovascular medicine journal vol. 10 (2016): 48-56. doi: https://doi.org/10.2174/1874192401610010048
Chiong T, Cheow ES, Woo CC, Lin XY, Khin LW, Lee CN, Hartman M, Sze SK, Sorokin VA. Aortic Wall Extracellular Matrix Proteins Correlate with Syntax Score in Patients Undergoing Coronary Artery Bypass Surgery. Open Cardiovasc Med J. 2016 Apr 27;10:48-56. doi: 10.2174/1874192401610010048. eCollection 2016. PMID: 27347220; PMCID: PMC4896997.
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Showing 1 to 12 of 699 entries