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1 penile shaft to 95.0% (kappa = 0.89) for the foreskin.
2 ible increased HIV-1 susceptibility of human foreskin.
3 important SIV-specific cellular immunity in foreskin.
4 ce potentially important immune responses in foreskin.
5 une responses to candidate HIV-1 vaccines in foreskin.
6 specific immune responses or inflammation in foreskin.
7 POT) assay in cell suspensions made from the foreskin.
8 dily found in cell suspensions made from the foreskin.
9 1.05) compared with sites more distal to the foreskin.
12 ong uncircumcised men, HPV prevalence in the foreskin (44%) was comparable to that in the glans/coron
13 we show that TLR3 expression was detected on foreskin, adult skin, and lung fibroblasts, and TLR3 lev
16 a complete population of immune cells in the foreskin and glans of normal RMs, although B cells were
20 or (TGF)B1-dependent transdifferentiation of foreskin and tongue, but not gingival fibroblasts into m
21 16 and HPV18 in organotypic raft cultures of foreskin and vaginal keratinocytes as determined by miRN
22 f cultured human keratinocytes from neonatal foreskins and cultured murine dermal papilla cells from
24 nvelopes prepared from human breast skin and foreskin, and from spontaneous and induced envelopes pre
25 nocyte cultures isolated from human neonatal foreskin, and human organotypic keratinocyte cultures.
26 abs were used to obtain penile shaft, glans, foreskin, and scrotum samples from 318 male university s
28 cific RNA in human fetal lung (HFL) or human foreskin (BJ) fibroblasts increased substantially after
29 vels of CRH-R1 and HDC as compared to normal foreskin, breast skin and cultured human keratinocytes.
30 of SIV-specific cellular immune responses in foreskin by adenovirus serotype 26 and 35 vaccine vector
33 n (108.8 vs 23.1 cells/mm(2); P < .001); but foreskin CD4 T-cell density was unchanged (43.0 vs 33.7/
39 s more readily detectable in facial skin and foreskin compared with skin from abdomen and breast.
42 e predominantly expressed spontaneously when foreskin-derived early-passage KCs undergo confluency-in
43 Under current culture conditions, neonatal foreskin-derived human keratinocytes possess a relativel
45 c dynein was identified in extracts of human foreskin epidermis and in isolated human keratinocytes.
46 median CD1a(+) dendritic cell density in the foreskin epidermis was significantly higher among males
49 ell clones derived from primary tonsillar or foreskin epithelia immortalized with HPV-16 genomes.
50 nd in HPV16- and 18-transformed cervical and foreskin epithelial cell lines showed that expression of
51 periments, human foreskin fibroblasts, human foreskin epithelial cells, and, to a lesser extent, HEp-
54 SG) expression, and CMV replication in human foreskin fibroblast (HFF) and peripheral blood mononucle
56 scular endothelial (HMVEC-d) cells and human foreskin fibroblast (HFF) cells in vitro by Kaposi's sar
57 scular endothelial (HMVEC-d) cells and human foreskin fibroblast (HFF) cells is characterized by the
58 rmal microvascular endothelial (HMVEC-d) and foreskin fibroblast (HFF) cells were examined by real-ti
59 hese spliced species occur in infected human foreskin fibroblast (HFF) cells, with accumulation kinet
63 low multiplicity of infection (MOI) in human foreskin fibroblast (HFF)- or NTera2-derived neuronal ce
64 lls (HMVECd)] and foreskin fibroblast [human foreskin fibroblast (HFF)] cells and human B cell line (
65 icrovascular endothelial cells (HMVECd)] and foreskin fibroblast [human foreskin fibroblast (HFF)] ce
66 f fibronectin are potent inhibitors of human foreskin fibroblast cell adhesion to fibronectin-coated
67 nanoUPLC-MS/MS to examine 500 mug of a human foreskin fibroblast cell lysate a total of 1,944 unique
68 class I molecules in B virus-infected human foreskin fibroblast cells and macaque kidney epithelial
69 -PMEG demonstrated increased uptake in human foreskin fibroblast cells and was readily converted in v
72 n numerous transfections of permissive human foreskin fibroblast cells with these three BAC DNA clone
74 r for the transcription of IE genes in human foreskin fibroblast cells, at lower MOIs, the murine CMV
75 n pAD/Cre was transfected into primary human foreskin fibroblast cells, Cre was expressed and mediate
76 n microvascular dermal endothelial and human foreskin fibroblast cells, they exhibited much lower vir
80 r compaction with these cells, whereas human foreskin fibroblast migration was positively correlated
84 ral growth by using human fibroblasts (human foreskin fibroblast-1) infected with the hCMV Towne stra
85 hat early during in vitro infection of human foreskin fibroblasts (2 to 4 h), HSV-1 induced the activ
86 s observed in different cell contexts: human foreskin fibroblasts (BJ), human colon and lung carcinom
87 tors by lovastatin treatment of normal human foreskin fibroblasts (FSF cells) resulted in an increase
88 5'-modified derivatives was greater in human foreskin fibroblasts (HFF cells) than in L1210 or KB tum
90 factor-3 (IRF-3) signaling in primary human foreskin fibroblasts (HFF) infected with herpes simplex
91 infection of beta-estradiol stimulated human foreskin fibroblasts (HFF) or HFF/DeltaB-Raf([FF]):ER (e
93 ritis synovial tissue (RASF), human neonatal foreskin fibroblasts (HFF), and the histiocytic cell lin
94 scular endothelial cells (HMVEC-d) and human foreskin fibroblasts (HFF), and these interactions are f
96 n decreased adherence of H. ducreyi to human foreskin fibroblasts (HFF); Flp1 and Flp2, the determina
98 irus was attenuated in primary human newborn foreskin fibroblasts (HFFs) and embryonic lung fibroblas
100 ilitates viral DNA synthesis in normal human foreskin fibroblasts (HFFs) but not in primary epithelia
101 sing rat dermal fibroblasts (RDFs) and human foreskin fibroblasts (HFFs) demonstrated that these cell
102 is showed induction of amyloid-beta in human foreskin fibroblasts (HFFs) infected with each of 3 clin
103 e investigated their relative roles in human foreskin fibroblasts (HFFs) infected with HSV or transfe
104 of resistance to Toxoplasma in primary human foreskin fibroblasts (HFFs) that does not depend on the
105 PS) cells and the fully differentiated human foreskin fibroblasts (HFFs) they were derived from.
106 The standard was prepared by infecting human foreskin fibroblasts (HFFs) with cytomegalovirus (CMV) s
107 -phase cell attachment assays in HSFs, human foreskin fibroblasts (HFFs), and human corneal stroma fi
108 d deltaTMgpK8.1A proteins bound to the human foreskin fibroblasts (HFFs), human dermal microvascular
109 ease of IFI16 protein levels in normal human foreskin fibroblasts (HFFs), normal oral keratinocytes (
110 were induced or inhibited in infected human foreskin fibroblasts (HFFs), T cells, and skin in respon
112 = 0.40-2.0 muM) and less toxic against human foreskin fibroblasts (IC(50) = 1.1-2.9 muM) and Vero cel
113 mphocytes in vivo as well as in normal human foreskin fibroblasts (NHFs) in vitro in normal (10%) ser
115 ved vimentin architecture in migrating human foreskin fibroblasts and found that network organization
116 l replication, telomerase-immortalized human foreskin fibroblasts and HEp-2 cells were transduced wit
117 sed an in vitro human skin model composed of foreskin fibroblasts and keratinocytes to examine host s
118 combinant TR1 induced proliferation of human foreskin fibroblasts and potentiated TNF-induced prolife
119 l mechanical properties in nonadherent human foreskin fibroblasts and THP-1 human monocytes before an
120 The three mutant strains adhered to human foreskin fibroblasts and to a human keratinocyte cell li
121 characterized molecular differences in human foreskin fibroblasts and WI-38 TRAIL-resistant cells and
122 cytoplasm of wild-type virus-infected human foreskin fibroblasts as early as 2 h and in HEp-2 cells
123 lls, foreskin fibroblasts, or LDLr-deficient foreskin fibroblasts at 4 degrees C by flow cytometry an
124 ary rat embryo fibroblasts (REF52) and human foreskin fibroblasts become senescent in tetraploid G1 a
126 Transient transfection experiments in human foreskin fibroblasts demonstrate that proteins binding t
127 pled receptors for bioactive lipids, whereas foreskin fibroblasts expressed Edg-2, Edg-3, and Edg-4.
128 size and length of focal adhesions of human foreskin fibroblasts gradually decreased from short to l
129 Cellular RNA extracted from quiescent human foreskin fibroblasts harvested at 1, 3, 7, or 12 h after
130 endogenous MMP-1 mRNA expression in 34 human foreskin fibroblasts homozygous or heterozygous for the
133 1P to human osteosarcoma MG63 cells or human foreskin fibroblasts increased cell-mediated binding and
135 levels from the early UL4 promoter in human foreskin fibroblasts infected by recombinant viruses wit
136 r changes, gene expression profiles of human foreskin fibroblasts infected with Toxoplasma were studi
137 inal epithelial cell lines, but not in human foreskin fibroblasts or in HT-1080 fibrosarcoma cells.
138 t wild-type levels with Shield-1 or in human foreskin fibroblasts overexpressing hemagglutinin (HA)-t
140 r purified plasma FBG with cultures of human foreskin fibroblasts resulted in FBG deposition in the E
142 abolic screen of VACV-infected primary human foreskin fibroblasts suggested that glutamine metabolism
143 reconstitution assay in HeLa cells and human foreskin fibroblasts to explore the processes by which E
145 6 increases the telomerase activity of human foreskin fibroblasts transduced with the hTERT gene, and
146 c AMP (-59/-53) regulatory elements in human foreskin fibroblasts treated with phorbol 12-myristate 1
147 onectin assembly by myrAkt1-expressing human foreskin fibroblasts was abolished by treatment with ant
149 ced collagen synthesis in both NRK and human foreskin fibroblasts was effectively blocked with specif
153 derived from healthy and diseased tissue and foreskin fibroblasts were grown to confluency, photograp
154 ects of VZV on this pathway, confluent human foreskin fibroblasts were infected with cell-associated
158 iled in MCF7 (breast cancer) and HFF1 (human foreskin fibroblasts) cell cultures, is less potent than
160 nously administered into HCMV-infected human foreskin fibroblasts, a reduction of about 80-90% in the
162 imary cell lines: aorta smooth muscle cells, foreskin fibroblasts, and umbilical vein endothelial cel
163 tingly, infectivity of tachyzoites for human foreskin fibroblasts, cells that are commonly used to gr
164 r, induced both E4-orf6/7 and TAp73 in human foreskin fibroblasts, emphasizing the importance of cell
168 ines with minimum growth inhibition in human foreskin fibroblasts, mouse fibroblasts, and immortalize
169 oteins, we assessed binding to MOLT-4 cells, foreskin fibroblasts, or LDLr-deficient foreskin fibrobl
170 8-fold higher in retinal endothelium than in foreskin fibroblasts, the cell subtype often used to inv
171 microvascular endothelium, as well as human foreskin fibroblasts, were grown to confluence in 24-wel
172 types, retinal pigment epithelial cells and foreskin fibroblasts, were transfected with vectors enco
173 essible genes, we identified a cDNA in human foreskin fibroblasts, which by GenBankTM DNA data base s
191 tants had reduced ability to attach to human foreskin fibroblasts; the defect correlated with reduced
192 e main agent of cervical cancer, using human foreskin fragments implanted in severe combined immunode
193 or extraction of infectious virus, and human foreskin fragments were incubated with the virus suspens
194 veloped from simultaneous infection of human foreskin fragments with HPV-11, -40, and -LVX82/MM7 viri
197 addition of EGF to COS-7 cells and to human foreskin Hs27 fibroblasts results in a rapid tyrosine ph
199 Abs capable of causing acantholysis of human foreskin in culture and blistering in neonatal mice.
203 nces of LMP2A expression in the normal human foreskin keratinocyte (HFK) cell line were investigated
205 A was transfected into an immortalized human foreskin keratinocyte cell line shown previously to supp
208 fic probe for TGX on Northern blots of human foreskin keratinocyte mRNA, indicating the presence of a
209 LMP2A expression induced migration in human foreskin keratinocytes (HFK) and HaCaT keratinocytes mea
210 amined markers of apoptosis in primary human foreskin keratinocytes (HFK) transduced with either a re
211 study a new cellular target in primary human foreskin keratinocytes (HFK), the serine/threonine kinas
215 nsufficient for the immortalization of human foreskin keratinocytes (HFKs) and human mammary epitheli
216 t genomes were transfected into normal human foreskin keratinocytes (HFKs) and selected for drug resi
219 retention of p27 and the migration of human foreskin keratinocytes (HFKs) in a phosphoinositide-3 ki
220 a integrin alpha(2)beta(1) by cultured human foreskin keratinocytes (HFKs) requires RhoGTP, a regulat
221 rotection assays in transduced primary human foreskin keratinocytes (HFKs) shows that the E6 gene (bu
222 ell lines with or without HPV16 and in human foreskin keratinocytes (HFKs) with or without HPV16 E6,
227 on single targeted individual primary human foreskin keratinocytes (PHFK) cells cultured and maintai
228 retroviruses, we acutely transduced neonatal foreskin keratinocytes (PHKs) with a lacZ reporter gene
229 were used to infect low-passage-number human foreskin keratinocytes and a variety of epithelial cell
231 E5 and E6 also induce koilocytosis in human foreskin keratinocytes but not in primate COS cells.
233 in experimental observations, pools of human foreskin keratinocytes from multiple sources were infect
235 mainly as a nuclear protein in primary human foreskin keratinocytes in monolayer cultures and their d
236 f cornified envelopes isolated from cultured foreskin keratinocytes releases several discrete involuc
237 g the high risk HPV-16 oncoprotein E7, human foreskin keratinocytes stably expressing E7 were treated
238 ubstratum, as in wound repair, enables human foreskin keratinocytes to interact via alpha(6)beta(4) a
239 religated, and transfected into normal human foreskin keratinocytes together with a neomycin-selectab
240 tion by pathogenic bacteria in both oral and foreskin keratinocytes was blocked by inhibitors of NF-k
243 n the other hand, infection of primary human foreskin keratinocytes with AAV2 resulted in upregulatio
245 emonstrated that lipofection of normal human foreskin keratinocytes with recircularized cloned HPV-31
248 Adherence to keratin types 1 and 10, human foreskin keratinocytes, and nasal epithelial cells was e
249 d its stability in HPV16 E6-expressing human foreskin keratinocytes, and NFX1-123 increased the stabi
250 duced by expression of viral oncoproteins in foreskin keratinocytes, and not seen in HPV-related prec
252 HPV-6 E7 (6E7G22D) and showed that, in human foreskin keratinocytes, HPV-6 E7G22D decreased the level
253 the elevated levels of p53 protein in human foreskin keratinocytes, relative to levels in dermal fib
263 characterized antiviral immune responses in foreskin of male rhesus macaques (RMs) inoculated with s
264 ) and CD8(+) T cells were also detectable in foreskin of SIV- and SHIV-infected animals and were at l
265 sured using immunohistochemistry analysis in foreskins of 79 males randomly selected from participant
266 s substantial influx of CD8 T-cells into the foreskins of HIV+ men (108.8 vs 23.1 cells/mm(2); P < .0
267 HIV-specific CD8 T cells were present in the foreskins of HIV+ men, although their frequency and func
268 mmunodeficiency virus (HIV) infection in the foreskin or glans of the human penis, although this is a
269 Envelopes prepared from human breast skin or foreskin, or spontaneous or induced envelopes prepared f
272 ision device causes ischemic necrosis of the foreskin, raising concerns of anaerobic overgrowth.
273 ing engraftment and vascularization of human foreskin resulted in marked CD3+ T cell infiltrates and
274 d CD8(+) T cell densities were quantified in foreskin samples obtained from medical circumcision in R
277 in the basal and suprabasal layer of newborn foreskins, suggesting that hTER expression is present bo
278 e of antiviral effector B and T cells in the foreskin suggests that vaccines may be able to elicit im
279 ke peripheral blood T cells, the majority of foreskin T cells exhibited transitional memory or effect
281 activated than peripheral blood T cells, but foreskin T cells were not further activated by vaccinati
282 d that HIV induces immune alterations in the foreskin that may impact the subsequent acquisition/clea
283 ecific CD4(+) and CD8(+) T cell responses in foreskin that were detectable for more than 1 year follo
290 r endothelial cells in placenta and neonatal foreskin, two tissues with ongoing growth of microvessel
291 membrane fraction was prepared from newborn foreskins using sucrose gradient centrifugation, followe
293 epidermal melanocytes isolated from neonatal foreskin were evaluated by similar techniques and served
294 derived from the same dark-skinned neonatal foreskins were seeded onto both acellular human dermis a
296 f 158 RAG-1 mice, grafted with human newborn foreskin, were separated into four groups and observed f
297 na, possibly because of its proximity to the foreskin, which may be particularly vulnerable to infect
298 ity is localized to the epidermis of newborn foreskin, which suggests that telomerase is expressed co
299 have genetically marked xenografts of human foreskin with a lentivirus encoding a fluorescent marker
300 resent in both the patient condyloma and the foreskin xenografts, and passage of both types was achie
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