نتایج جستجو برای: tumor suppressor genes

تعداد نتایج: 823774  

Journal: :JNCI: Journal of the National Cancer Institute 1998

Hao Fu, Shunlin Qu, Tingting Tang Wenjing Fan, Wenke Song, Wenyi Deng Yufei Wang,

Objective(s): The stress-responsive genes of Sestrin family are recognized as new tumor suppressor genes in breast carcinoma, however, the function of Sestrin family in human prostate cancer is not clear. Ionizing radiation (IR) is known to induce Sestrin gene expression in breast cancer cells. However, the response of Sestrin to IR has not been reported in PC3 prostate cancer cells. Materials ...

Journal: :Journal of Clinical and Experimental Hematopathology 2002

Journal: :Cancer 2015
Luc G T Morris Timothy A Chan

Carcinogenesis is a multistep process attributable to both gain-of-function mutations in oncogenes and loss-of-function mutations in tumor suppressor genes. Currently, most molecular targeted therapies are inhibitors of oncogenes, because inactivated tumor suppressor genes have proven harder to "drug." Nevertheless, in cancers, tumor suppressor genes undergo alteration more frequently than do o...

Journal: :The Tohoku journal of experimental medicine 1992
M Koi L A Johnson A P Feinberg

To identify the tumor suppressor gene on human chromosome 11p15, we generated mouse microcell hybrids containing small transferable chromosome 11p15 fragments, which we have termed "DNA superfragments". These hybrids will be used to identify which fragments contain a tumor suppressor gene by direct transfer of the fragments to tumor cells via microcell fusion.

Journal: :Advances in genetics 1997
M A Brown

Preparing the books to read every day is enjoyable for many people. However, there are still many people who also don't like reading. This is a problem. But, when you can support others to start reading, it will be better. One of the books that can be recommended for new readers is tumor suppressor genes in human cancer. This book is not kind of difficult book to read. It can be read and unders...

Journal: :Genetics 2004
Yoh Iwasa Franziska Michor Martin A Nowak

We study a situation that arises in the somatic evolution of cancer. Consider a finite population of replicating cells and a sequence of mutations: type 0 can mutate to type 1, which can mutate to type 2. There is no back mutation. We start with a homogeneous population of type 0. Mutants of type 1 emerge and either become extinct or reach fixation. In both cases, they can generate type 2, whic...

Journal: :Blood 1995
G C Fraizer P Patmasiriwat X Zhang G F Saunders

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