✦ LIBER ✦

Role of cell cycle regulator E2F1 in regulating CD8 T cell responses during acute and chronic viral infection

✍ Scribed by Xiaoyan Gao; Kavita Tewari; John Svaren; M Suresh

Book ID: 113945937
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 638 KB
Volume: 324
Category: Article
ISSN: 0042-6822
DOI: 10.1016/j.virol.2004.04.012

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Role of cell cycle regulator p19ARF in r

Role of cell cycle regulator p19ARF in regulating T cell responses

✍ Xiaoyan Gao; John Svaren; M. Suresh 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 422 KB

Differential role of IL-2R signaling for

Differential role of IL-2R signaling for CD8+ T cell responses in acute and chronic viral infections

✍ Martin F. Bachmann; Petra Wolint; Senta Walton; Katrin Schwarz; Annette Oxenius 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 382 KB 👁 1 views

Regulation of apoptosis and replicative

Regulation of apoptosis and replicative senescence in CD8+ T cell following acute viral infection

✍ F. J. Plunkett; M. V. D. Soares; M. Salmon; A. N. Akbar 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 100 KB

Immunodominance of HIV-1-specific CD8+ T

Immunodominance of HIV-1-specific CD8+ T-cell responses in acute HIV-1 infection: at the crossroads of viral and host genetics

✍ Mathias Lichterfeld; Xu G. Yu; Sylvie Le Gall; Marcus Altfeld 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 129 KB

The Sentinel Role of CD8 T Cells in Regu

The Sentinel Role of CD8 T Cells in Regulating CD4 T Cell Responses to Proinsulin in β-Islet Cell Autoimmunity

✍ Vedran Batarelo; Ivana Durinovic-Belló 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 94 KB

Distinct roles for Sp1 and E2F sites in

Distinct roles for Sp1 and E2F sites in the growth/cell cycle regulation of the DHFR promoter

✍ David E. Jensen; Adrian R. Black; Andrew G. Swick; Jane Clifford Azizkhan 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 100 KB 👁 3 views

Dihydrofolate reductase activity is required for many biosynthetic pathways including nucleotide synthesis. Its expression is therefore central to cellular growth, and it has become a key target for cancer chemotherapy. Transcription of the dihydrofolate reductase gene is regulated with growth, bein