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Items: 1 to 20 of 27

1.
A second chain of human CD8 is expressed on peripheral blood lymphocytes
J Exp Med. 1988 Dec 1; 168(6): 1993–2005. doi: 10.1084/jem.168.6.1993
PMCID:
PMC2189163
SummaryPDF–897K
2.
The human Lyt-3 molecule requires CD8 for cell surface expression.
J P DiSanto, R W Knowles, N Flomenberg
EMBO J. 1988 Nov; 7(11): 3465–3470. doi: 10.1002/j.1460-2075.1988.tb03221.x
PMCID:
PMC454846
SummaryPage BrowsePDF–1.3M
3.
Mycoplasma-associated multidrug resistance of hepatocarcinoma cells requires the interaction of P37 and Annexin A2
Danyang Liu, Yang Hu, Ying Guo, Zhu Zhu, Bingzheng Lu, Xuelan Wang, Yijun Huang
PLoS One. 2017; 12(10): e0184578. Published online 2017 Oct 4. doi: 10.1371/journal.pone.0184578
PMCID:
PMC5627893
AbstractArticlePDF–11M
4.
The Human CD8β M-4 Isoform Dominant in Effector Memory T Cells Has Distinct Cytoplasmic Motifs That Confer Unique Properties
Deepshi Thakral, Maria M. Coman, Arunima Bandyopadhyay, Sunil Martin, James L. Riley, Paula B. Kavathas
PLoS One. 2013; 8(3): e59374. Published online 2013 Mar 22. doi: 10.1371/journal.pone.0059374
PMCID:
PMC3606432
AbstractArticlePDF–1.2M
5.
A second subunit of CD8 is expressed in human T cells.
A M Norment, D R Littman
EMBO J. 1988 Nov; 7(11): 3433–3439. doi: 10.1002/j.1460-2075.1988.tb03217.x
PMCID:
PMC454842
SummaryPage BrowsePDF–1.4M
6.
A secreted form of the human lymphocyte cell surface molecule CD8 arises from alternative splicing.
P Giblin, J A Ledbetter, P Kavathas
Proc Natl Acad Sci U S A. 1989 Feb; 86(3): 998–1002. doi: 10.1073/pnas.86.3.998
PMCID:
PMC286608
SummaryPage BrowsePDF–1.2M
7.
Quantitative competitive reverse transcription polymerase chain reaction is not a useful method for quantification of CD4 and CD8 cell status during HIV infection
Heather B Jaspan, H Richard Gaumer, Robert F Garry
J Negat Results Biomed. 2003; 2: 2. Published online 2003 Mar 12. doi: 10.1186/1477-5751-2-2
PMCID:
PMC153544
AbstractArticlePDF–221K
8.
CD45RA, CD8β, and IFNγ Are Potential Immune Biomarkers of Human Cognitive Function
André J. Esgalhado, Débora Reste-Ferreira, Stephanie E. Albino, Adriana Sousa, Ana Paula Amaral, António Martinho, Isabel T. Oliveira, Ignacio Verde, Olga Lourenço, Ana M. Fonseca, Elsa M. Cardoso, Fernando A. Arosa
Front Immunol. 2020; 11: 592656. Published online 2020 Nov 25. doi: 10.3389/fimmu.2020.592656
PMCID:
PMC7723833
AbstractArticlePDF–3.3M
9.
cAMP-responsive Element Modulator α (CREMα) trans-Represses the Transmembrane Glycoprotein CD8 and Contributes to the Generation of CD3+CD4−CD8− T Cells in Health and Disease
Christian M. Hedrich, Thomas Rauen, Jose C. Crispin, Tomohiro Koga, Christina Ioannidis, Melissa Zajdel, Vasileios C. Kyttaris, George C. Tsokos
J Biol Chem. 2013 Nov 1; 288(44): 31880–31887. Published online 2013 Sep 18. doi: 10.1074/jbc.M113.508655
PMCID:
PMC3814780
AbstractArticlePDF–1.8M
10.
Non-stimulatory peptides contribute to antigen induced CD8-TCR interaction at the immunological synapse
Pia P. Yachi, Jeanette Ampudia, Nicholas R.J. Gascoigne, Tomasz Zal
Nat Immunol. Author manuscript; available in PMC 2006 Jan 27.
Published in final edited form as: Nat Immunol. 2005 Aug; 6(8): 785–792. Published online 2005 Jun 26. doi: 10.1038/ni1220
PMCID:
PMC1352171
AbstractArticlePDF–1.1M
11.
Experimental colitis promotes sustained, sex-dependent, T-cell-associated neuroinflammation and parkinsonian neuropathology
Madelyn C. Houser, W. Michael Caudle, Jianjun Chang, George T. Kannarkat, Yuan Yang, Sean D. Kelly, Danielle Oliver, Valerie Joers, Kathleen M. Shannon, Ali Keshavarzian, Malú Gámez Tansey
Acta Neuropathol Commun. 2021; 9: 139. Published online 2021 Aug 19. doi: 10.1186/s40478-021-01240-4
PMCID:
PMC8375080
AbstractArticlePDF–2.6M
12.
Down-Modulation of CD8αβ Is a Fundamental Activity of Primate Lentiviral Nef Proteins
Anke Heigele, Michael Schindler, Clement W. Gnanadurai, Jolie A. Leonard, Kathleen L. Collins, Frank Kirchhoff
J Virol. 2012 Jan; 86(1): 36–48. doi: 10.1128/JVI.00717-11
PMCID:
PMC3255914
AbstractArticlePDF–5.6M
13.
cAMP Responsive Element Modulator (CREM) α Mediates Chromatin Remodeling of CD8 during the Generation of CD3+CD4−CD8− T Cells
Christian M. Hedrich, José C. Crispín, Thomas Rauen, Christina Ioannidis, Tomohiro Koga, Noe Rodriguez Rodriguez, Sokratis A. Apostolidis, Vasileios C. Kyttaris, George C. Tsokos
J Biol Chem. 2014 Jan 24; 289(4): 2361–2370. Published online 2013 Dec 2. doi: 10.1074/jbc.M113.523605
PMCID:
PMC3900979
AbstractArticlePDF–2.9M
14.
Sequence and evolution of the human T-cell antigen receptor beta-chain genes.
A Tunnacliffe, R Kefford, C Milstein, A Forster, T H Rabbitts
Proc Natl Acad Sci U S A. 1985 Aug; 82(15): 5068–5072. doi: 10.1073/pnas.82.15.5068
PMCID:
PMC390500
SummaryPage BrowsePDF–1.0M
15.
Novel CD8+ Treg suppress EAE by TGF-β- and IFN-γ-dependent mechanisms
Mei-Ling Chen, Bo-Shiun Yan, Deneen Kozoriz, Howard L. Weiner
Eur J Immunol. Author manuscript; available in PMC 2010 Dec 1.
Published in final edited form as: Eur J Immunol. 2009 Dec; 39(12): 3423. doi: 10.1002/eji.200939441
PMCID:
PMC2814307
AbstractArticlePDF–2.3M
16.
Human Immunodeficiency Virus Nef Induces Rapid Internalization of the T-Cell Coreceptor CD8αβ
Veronique Stove, Inge Van de Walle, Evelien Naessens, Elisabeth Coene, Christophe Stove, Jean Plum, Bruno Verhasselt
J Virol. 2005 Sep; 79(17): 11422–11433. doi: 10.1128/JVI.79.17.11422-11433.2005
Correction in:
J Virol. 2005 Oct; 79(20): 13195.
PMCID:
PMC1193625
AbstractArticlePDF–852K
17.
HIV-1 Nef Disrupts Intracellular Trafficking of Major Histocompatibility Complex Class I, CD4, CD8, and CD28 by Distinct Pathways That Share Common Elements
Jolie A. Leonard, Tracy Filzen, Christoph C. Carter, Malinda Schaefer, Kathleen L. Collins
J Virol. 2011 Jul; 85(14): 6867–6881. doi: 10.1128/JVI.00229-11
PMCID:
PMC3126561
AbstractArticlePDF–4.8M
18.
Identification of common variants influencing risk of the tauopathy Progressive Supranuclear Palsy
Günter U. Höglinger, Nadine M. Melhem, Dennis W. Dickson, Patrick M.A. Sleiman, Li-San Wang, Lambertus Klei, Rosa Rademakers, Rohan de Silva, Irene Litvan, David E. Riley, John C. van Swieten, Peter Heutink, Zbigniew K. Wszolek, Ryan J. Uitti, Jana Vandrovcova, Howard I. Hurtig, Rachel G. Gross, Walter Maetzler, Stefano Goldwurm, Eduardo Tolosa, Barbara Borroni, Pau Pastor, PSP Genetics Study Group, Laura B. Cantwell, Mi Ryung Han, Allissa Dillman, Marcel P. van der Brug, J Raphael Gibbs, Mark R. Cookson, Dena G. Hernandez, Andrew B. Singleton, Matthew J. Farrer, Chang-En Yu, Lawrence I. Golbe, Tamas Revesz, John Hardy, Andrew J. Lees, Bernie Devlin, Hakon Hakonarson, Ulrich Müller, Gerard D. Schellenberg
Nat Genet. Author manuscript; available in PMC 2012 Jan 1.
Published in final edited form as: Nat Genet. 2011 Jul; 43(7): 699–705. Published online 2011 Jun 19. doi: 10.1038/ng.859
PMCID:
PMC3125476
AbstractArticlePDF–1.4M
19.
Viremic long-term nonprogressive HIV-1 infection is not associated with abnormalities in known Nef functions
Anke Heigele, David Camerini, Angélique B van’t Wout, Frank Kirchhoff
Retrovirology. 2014; 11: 13. Published online 2014 Feb 4. doi: 10.1186/1742-4690-11-13
PMCID:
PMC3927655
AbstractArticlePDF–821K
20.
Modulation of HIV pathogenesis and T-cell signaling by HIV-1 Nef
Shailendra K Saxena, Gaurav Shrivastava, Sneham Tiwari, ML Arvinda Swamy, Madhavan PN Nair
Future Virol. Author manuscript; available in PMC 2013 Apr 1.
Published in final edited form as: Future Virol. 2012 Jun 1; 7(6): 609–620. doi: 10.2217/FVL.12.42
PMCID:
PMC3404840
AbstractArticlePDF–1.4M

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