نتایج جستجو برای: l1 cells

تعداد نتایج: 1409324  

2017
Marie MacLennan Marta García-Cañadas Judith Reichmann Elena Khazina Gabriele Wagner Christopher J Playfoot Carmen Salvador-Palomeque Abigail R Mann Paula Peressini Laura Sanchez Karen Dobie David Read Chao-Chun Hung Ragnhild Eskeland Richard R Meehan Oliver Weichenrieder Jose Luis García-Pérez Ian R Adams

Mobilization of retrotransposons to new genomic locations is a significant driver of mammalian genome evolution, but these mutagenic events can also cause genetic disorders. In humans, retrotransposon mobilization is mediated primarily by proteins encoded by LINE-1 (L1) retrotransposons, which mobilize in pluripotent cells early in development. Here we show that TEX19.1, which is induced by dev...

2013
Constance Ciaudo Florence Jay Ikuhiro Okamoto Chong-Jian Chen Alexis Sarazin Nicolas Servant Emmanuel Barillot Edith Heard Olivier Voinnet

In most mouse tissues, long-interspersed elements-1 (L1s) are silenced via methylation of their 5'-untranslated regions (5'-UTR). A gradual loss-of-methylation in pre-implantation embryos coincides with L1 retrotransposition in blastocysts, generating potentially harmful mutations. Here, we show that Dicer- and Ago2-dependent RNAi restricts L1 accumulation and retrotransposition in undifferenti...

Journal: :Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research 1995
A M al-Katib R M Mohammad A Maki M R Smith

To identify potential effector molecules of human B-cell differentiation, the acute lymphoblastic leukemia cells (Reh) were induced to terminal differentiation in vitro using the phorbol ester, 12-O-tetradecanoylphorbol-13-acetate. Proteins of parent and differentiated Reh cells were mapped using powerful two-dimensional gel electrophoresis coupled with ultrasensitive silver stain. New protein ...

Journal: :Blood 2010
Don M Benson Courtney E Bakan Anjali Mishra Craig C Hofmeister Yvonne Efebera Brian Becknell Robert A Baiocchi Jianying Zhang Jianhua Yu Megan K Smith Carli N Greenfield Pierluigi Porcu Steven M Devine Rinat Rotem-Yehudar Gerard Lozanski John C Byrd Michael A Caligiuri

T-cell expression of programmed death receptor-1 (PD-1) down-regulates the immune response against malignancy by interacting with cognate ligands (eg, PD-L1) on tumor cells; however, little is known regarding PD-1 and natural killer (NK) cells. NK cells exert cytotoxicity against multiple myeloma (MM), an effect enhanced through novel therapies. We show that NK cells from MM patients express PD...

2017
Li-Yang Hu Xiao-Lu Xu Hui-Lan Rao Jie Chen Ren-Chun Lai Hui-Qiang Huang Wen-Qi Jiang Tong-Yu Lin Zhong-Jun Xia Qing-Qing Cai

BACKGROUND The programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) pathway inhibits the activation of T cells and plays a crucial role in the negative regulation of cellular and humoral immune responses. Diffuse large B-cell lymphoma (DLBCL) is the most common lymphoid malignancy in adults. In the present study, we aimed to detect the expression of PD-L1 in DLBCL and to analyz...

2016
Gustavo Dix Junqueira Pinto Luciano de Souza Viana Cristovam Scapulatempo Neto Sérgio Vicente Serrano

Lung cancer is the leading world cause of cancer-related death, in both genders, and smoking is the main etiological factor. The discovery of immune checkpoints corroborates the hypothesis that ligands presented in tumors modulate the mechanisms of carcinogenesis and the immune activity of tumor microenvironment. Among the most studied coregulatory molecules, PD-1 (programmed cell death 1) and ...

Journal: :Blood 2009
Long Zhang Thomas F Gajewski Justin Kline

Negative regulatory mechanisms within the solid tumor microenvironment inhibit antitumor T-cell function, leading to evasion from immune attack. One inhibitory mechanism is up-regulation of programmed death-ligand 1 (PD-L1) expressed on tumor or stromal cells which binds to programmed death-1 (PD-1) on activated T cells. PD-1/PD-L1 engagement results in diminished antitumor T-cell responses and...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2015
H R Ali S-E Glont F M Blows E Provenzano S-J Dawson B Liu L Hiller J Dunn C J Poole S Bowden H M Earl P D P Pharoah C Caldas

BACKGROUND Expression of programmed death ligand 1 (PD-L1) in solid tumours has been shown to predict whether patients are likely to respond to anti-PD-L1 therapies. To estimate the therapeutic potential of PD-L1 inhibition in breast cancer, we evaluated the prevalence and significance of PD-L1 protein expression in a large collection of breast tumours. PATIENTS AND METHODS Correlations betwe...

Journal: :Human molecular genetics 2003
Hitoshi Osaka Yu-Lai Wang Koji Takada Shuichi Takizawa Rieko Setsuie Hang Li Yae Sato Kaori Nishikawa Ying-Jie Sun Mikako Sakurai Takayuki Harada Yoko Hara Ichiro Kimura Shigeru Chiba Kazuhiko Namikawa Hiroshi Kiyama Mami Noda Shunsuke Aoki Keiji Wada

Mammalian neuronal cells abundantly express a deubiquitylating enzyme, ubiquitin carboxy-terminal hydrolase 1 (UCH L1). Mutations in UCH L1 are linked to Parkinson's disease as well as gracile axonal dystrophy (gad) in mice. In contrast to the UCH L3 isozyme that is universally expressed in all tissues, UCH L1 is expressed exclusively in neurons and testis/ovary. We found that UCH L1 associates...

Journal: :Cancer research 1992
P G Johnston C M Rondinone D Voeller C J Allegra

The 3T3-L1 cell line is a preadipocyte cell line derived from the Swiss 3T3 mouse fibroblast cell line. We have compared the effect of 3T3-L1 conditioned medium (3T3-L1 CM) and Swiss 3T3 conditioned medium (3T3 CM) on the growth of normal mouse mammary cells (NMMG) and the human MCF-7 breast carcinoma cell line. 3T3 CM increased the growth of both NMMG and MCF-7 cells by 19 +/- 2% (SD) and 24 +...

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