|1.||Yamashima, Tetsumori: 7 articles (10/2014 - 12/2009)|
|2.||Seo, Jeong-Sun: 5 articles (11/2008 - 05/2002)|
|3.||Zhu, Hong: 3 articles (10/2014 - 02/2012)|
|4.||Oikawa, Shinji: 3 articles (06/2014 - 12/2009)|
|5.||Lee, Jae-Seon: 3 articles (06/2010 - 05/2002)|
|6.||Seo, J S: 3 articles (12/2001 - 06/2001)|
|7.||Yoshimoto, Tanihiro: 2 articles (10/2014 - 02/2012)|
|8.||Dazortsava, Maryia: 2 articles (06/2014 - 02/2012)|
|9.||Murata, Mariko: 2 articles (06/2014 - 04/2012)|
|10.||Kuramitsu, Yasuhiro: 2 articles (08/2005 - 12/2003)|
03/05/2015 - "Using the Hsp70.1/3(-/-)(Hsp70(-/-)) mouse model, we observed that tumor-derived HSP70 was neither required for cellular transformation nor for in vivo tumor growth. "
12/01/2001 - "Here we show that injection of rat hsp70.1 into mouse tumors in situ causes the complete eradication of tumors, and generates potent systemic antitumor immunity mediated by CD4+ and CD8+ T cells. "
12/01/2001 - "Induction of systemic antitumor immunity by gene transfer of mammalian heat shock protein 70.1 into tumors in situ."
12/01/2001 - "Unexpectedly, simultaneous gene transfer of hsp70.1 and B7.1 compromised the efficacy of hsp-mediated tumor rejection--a problem which could be partially overcome by the timed delivery of hsp70.1 and B7.1. Thus, gene transfer of hsp70 into tumors can be employed to generate potent systemic antitumor immunity, but further consideration is required if this approach is to be successfully combined with immunotherapies employing other T-cell costimulators."
04/15/2012 - "Immunoprecipitation and Western blot analyses of individual samples confirmed significantly greater carbonylation of serotransferrin, heat shock protein 70-kDa protein 1 (HSP70.1), and α1-antitrypsin (A1AT) in tumor tissues compared to normal tissues. "
08/01/2003 - "We conclude that inducible HSP70.1 and HSP70.3 are required for late-phase protection against infarction following IP in mice."
12/01/2001 - "The mean infarction volume was significantly larger in hsp70.1 knockout mice (92.5+/-8.3 mm(3)) than in the wild-type mice (59.3+/-8.9 mm,(3) P<0.001). "
12/01/2001 - "The expressions of hsp70.1 and hsp70.3 mRNAs and HSP70 protein were determined, and infarction volumes were measured and compared. "
12/01/2001 - "Targeted hsp70.1 disruption increases infarction volume after focal cerebral ischemia in mice."
07/01/2011 - "The present study aimed to investigate the association between inducible Hsp70.1 single nucleotide polymorphisms (SNPs) and heat shock (HS) response of peripheral blood mononuclear cells (PBMC) in dairy cows. "
11/01/2014 - "The expression of HSP genes (HSP18.2, HSP25.3, HSP70-1 and HSP83) was down-regulated in plc3 mutants and up-regulated in AtPLC3-overexpressing lines after heat shock. "
11/21/2008 - "However, heat shock-induced Hdac2 activation was blunted in the cardiomyocytes isolated from Hsp70.1(-/-) mice. "
09/01/2008 - "To determine whether Hsp70 is necessary for the protective effect of heat shock against aminoglycoside-induced hair cell death, we utilized utricles from Hsp70.1/3 (-/-) mice. "
12/01/2006 - "Heat shock released both mH2A1.1 and PARP-1 from the Hsp70.1 promoter and activated PARP-1 automodification activity. "
06/01/2001 - "The effect of oxygen on retinal degeneration in wild-type and hsp70.1 knockout neonatal retinal degeneration mice."
12/01/2001 - "The purposes of this study are to elucidate the retinal changes of heat shock protein 70.1 (hsp70.1) knockout mice and to compare them between in normal and in retinal degeneration (rd) mice. "
06/01/2001 - "The present study examined the effect of oxygen on photoreceptor degeneration in the retina of heat shock protein 70.1 (hsp70.1) knockout type and wild-type retinal degeneration (rd) mice. "
02/01/2012 - "We propose that the cascades underlying lysosomal stabilization and regulating NF-κB activation by Hsp70.1 may influence neuronal survival/death after the ischemia/reperfusion."
09/01/2004 - "hsp70.1 KO and WT mice underwent focal ischemia for 120 minutes. "
09/01/2004 - "To evaluate the role of HSP70.1 protein in ischemia, we analyzed the mitochondrial apoptotic pathway using hsp70.1 knockout (KO) mice and their wild-type (WT) mice. "
09/01/2013 - "Hsp70.1 KO and wild-type mice were divided into sham control (Sham), exercise preconditioning (Ex), renal ischemia-after-exercise (Ex+IR), and ischemia (IR) groups. "
02/01/2012 - "Recently, we found that calpain-mediated cleavage of carbonylated Hsp70.1 in the hippocampal cornu Ammonis1 (CA1) contributes to neuronal death after transient global ischemia. "
|1.||Heat-Shock Proteins (Heat-Shock Protein)
|2.||Transferrin (beta 2 Transferrin)
|3.||heat-shock protein 70.1
|5.||HSP70 Heat-Shock Proteins (Heat-Shock Protein 70)
|6.||heat shock transcription factor (heat shock transcription factors)
|7.||Molecular Chaperones (Chaperone, Molecular)
|8.||Reactive Oxygen Species (Oxygen Radicals)
|9.||NF-kappa B (NF-kB)
|10.||Transcription Factors (Transcription Factor)