نتایج جستجو برای: lats2

تعداد نتایج: 211  

Journal: :Cancer research 2008
Peter Ouillette Harry Erba Lisa Kujawski Mark Kaminski Kerby Shedden Sami N Malek

Chronic lymphocytic leukemia (CLL) is a biologically heterogeneous illness with a variable clinical course. Loss of chromosomal material on chromosome 13 at cytoband 13q14 is the most frequent genetic abnormality in CLL, but the molecular aberrations underlying del13q14 in CLL remain incompletely characterized. We analyzed 171 CLL cases for loss of heterozygosity and subchromosomal copy loss on...

2012
MASARU KATOH

FAT1, FAT2, FAT3 and FAT4 are human homologs of Drosophila Fat, which is involved in tumor suppression and planar cell polarity (PCP). FAT1 and FAT4 undergo the first proteolytic cleavage by Furin and are predicted to undergo the second cleavage by γ‑secretase to release intracellular domain (ICD). Ena/VAPS‑binding to FAT1 induces actin polymeriza...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Xiaogang Tan Wenyan Qin Liang Zhang Jie Hang Baozhong Li Cuiyan Zhang Junting Wan Fang Zhou Kang Shao Yimin Sun Jianping Wu Xun Zhang Bin Qiu Ning Li Susheng Shi Xiaoli Feng Shouhua Zhao Zhen Wang Xiaohong Zhao Zhaoli Chen Keith Mitchelson Jing Cheng Yong Guo Jie He

PURPOSE Recent studies have suggested that microRNA biomarkers could be useful for stratifying lung cancer subtypes, but microRNA signatures varied between different populations. Squamous cell carcinoma (SCC) is one major subtype of lung cancer that urgently needs biomarkers to aid patient management. Here, we undertook the first comprehensive investigation on microRNA in Chinese SCC patients. ...

2008
Peter Ouillette Harry Erba Lisa Kujawski Mark Kaminski Kerby Shedden Sami N. Malek

Chronic lymphocytic leukemia (CLL) is a biologically heterogeneous illness with a variable clinical course. Loss of chromosomal material on chromosome 13 at cytoband 13q14 is the most frequent genetic abnormality in CLL, but the molecular aberrations underlying del13q14 in CLL remain incompletely characterized. We analyzed 171 CLL cases for loss of heterozygosity and subchromosomal copy loss on...

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