Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Yousef G."'
Autor:
Reeves ME; Surgical Oncology Laboratory, Loma Linda VA Medical Center, Loma Linda, California, United States of America; Department of Surgery, Loma Linda University School of Medicine, Loma Linda, California, United States of America., Firek M; Surgical Oncology Laboratory, Loma Linda VA Medical Center, Loma Linda, California, United States of America., Chen ST; Musculoskeletal Disease Center, Loma Linda VA Medical Center, Loma Linda, California, United States of America., Amaar YG; Surgical Oncology Laboratory, Loma Linda VA Medical Center, Loma Linda, California, United States of America; Department of Surgery, Loma Linda University School of Medicine, Loma Linda, California, United States of America.
Publikováno v:
PloS one [PLoS One] 2014 Jul 09; Vol. 9 (7), pp. e101679. Date of Electronic Publication: 2014 Jul 09 (Print Publication: 2014).
Autor:
Shimizu-Okabe C; Department of Psychiatry and Behavioral Neurosciences, McMaster University, 1200 Main Street West, Hamilton, Ontario, L8N 3Z5, Canada., Yousef GM, Diamandis EP, Yoshida S, Shiosaka S, Fahnestock M
Publikováno v:
Neuroreport [Neuroreport] 2001 Aug 28; Vol. 12 (12), pp. 2747-51.
Akademický článek
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Autor:
Yousef G. Amaar, Mark E. Reeves
Publikováno v:
Current Issues in Molecular Biology
Volume 45
Issue 2
Pages: 1113-1126
Volume 45
Issue 2
Pages: 1113-1126
The tumor microenvironment (TME) plays a vital role in tumor invasion and metastasis and provides a rich environment for identifying novel therapeutic targets. The TME landscape consists of an extracellular matrix (ECM) and stromal cells. ECM is a ma
Autor:
Mark E. Reeves, Yousef G. Amaar
Publikováno v:
Oncotarget
Introduction Recently we have identified a novel RASSF1C-PIWIL1-piRNA pathway that promotes lung cancer cell progression and migration. PIWI-like proteins interact with piRNAs to form complexes that regulate gene expression at the transcriptional and
Autor:
Marlon G. Minera, Mark E. Reeves, Subburaman Mohan, Donna D. Strong, Yousef G. Amaar, Laurice K. Hatran
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 291:L1185-L1190
Recently, the Ras association domain family 1 gene ( RASSF1) has been identified as a Ras effector encoding two major mRNA forms, RASSF1A and RASSF1C, derived by alternative promoter selection and alternative mRNA splicing. RASSF1A is a tumor suppres
Autor:
Melissa L Baldwin, Shin-Tai Chen, Xin-Min Li, Robert Aragon, Yousef G. Amaar, Subburaman Mohan, Scott W. Baldwin, Mark E. Reeves
Publikováno v:
BMC Research Notes, Vol 5, Iss 1, p 239 (2012)
BMC Research Notes
BMC Research Notes
Background RASSF1A and RASSF1C are two major isoforms encoded by the Ras association domain family 1 (RASSF1) gene through alternative promoter selection and mRNA splicing. RASSF1A is a well established tumor suppressor gene. Unlike RASSF1A, RASSF1C
Publikováno v:
Cancer Research. 75:2146-2146
Introduction: RASSF1C is emerging as an important oncoprotein in lung cancer cell growth. We have shown that RASSF1C promotes lung cancer cell proliferation and migration; and RASSF1C up-regulates important genes in lung cancer cell growth that inclu
Publikováno v:
Cancer Research. 74:2454-2454
Introduction: We have previously shown that RASSF1C promotes cell proliferation, migration and attenuates apoptosis in cancer cells. We have also shown that RASSF1C is significantly up-regulated in breast and lung cancer tissues compared to normal ti
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101679 (2014)
PLoS ONE
PLoS ONE
RASSF1C is a major isoform of the RASSF1 gene, and is emerging as an oncogene. This is in contradistinction to the RASSF1A isoform, which is an established tumor suppressor. We have previously shown that RASSF1C promotes lung cancer cell proliferatio