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1 is 97% made up of sequences from an apparent human endogenous retrovirus.
2 h homology to MMTV and low homology to known human endogenous retrovirus.
3 to be related to the LTR of an HERV-K class human endogenous retrovirus.
4 mislabeling, gross HTLV-I contamination, or human endogenous retroviruses.
5 ately 50 copies of the replication-defective human endogenous retrovirus 9 (ERV-9) and thousands of c
6 spersed nuclear element 1 (LINE-1 or L1) and human endogenous retrovirus, accompanies neoplastic tran
7 ribed from the LTR retrotransposons of ERV-9 human endogenous retrovirus activated transcription of k
9 xtinct 1918 strain of influenza virus and of human endogenous retroviruses and from the restructuring
10 se the pathogenesis of MS has been linked to human endogenous retroviruses, antiretroviral therapy fo
12 hip with the long terminal repeats (LTRs) of human endogenous retrovirus class K (HERV-K) as a mobile
13 akpoint was localized to an inverted pair of human endogenous retrovirus elements within the large, f
17 rovirus K (HERV-K)108--a betaretrovirus-like human endogenous retrovirus--for intersubunit bonding an
20 , express transcripts derived from the novel human endogenous retrovirus HERV-E (named CT-RCC HERV-E)
26 long interspersed nuclear element (LINE) or human endogenous retrovirus (HERV) repeats as a cause of
28 g this antigen were found to be derived from human endogenous retrovirus (HERV) type E and were expre
29 membrane proteins 1 and 2A), transactivate a human endogenous retrovirus (HERV), HERV-K18, in infecte
30 length and C-terminally truncated version of human endogenous retrovirus (HERV)-K10 protease were exp
31 viral sequence (IDDMK(1,2)22) similar to the human endogenous retrovirus (HERV)-K10/K18 subfamilies h
32 d and cloned an EBV-associated superantigen, human endogenous retrovirus (HERV)-K18 envelope protein
37 viously reported finding the RNA of a type K human endogenous retrovirus, HERV-K (HML-2), at high tit
43 yze the forces directing the accumulation of human endogenous retroviruses (HERVs) by comparing de no
55 t percent of the human genome is composed of human endogenous retroviruses (HERVs), which are thought
58 otransposon belonging to the ERV-9 family of human endogenous retroviruses in the apparent 5' boundar
59 solitary long terminal repeat (LTR) of ERV-9 human endogenous retrovirus is located upstream of the H
61 c and functional studies have implicated the human endogenous retrovirus K (HERV-K) dUTPase located w
63 ng related SAMHD1 to increased expression of human endogenous retrovirus K (HERV-K) in PAH versus con
67 e nucleotidohydrolase (dUTPase) encoded by a human endogenous retrovirus K (HERV-K) may be a candidat
69 he Env proteins of JSRV and MMTV, as well as human endogenous retrovirus K (HERV-K)108--a betaretrovi
73 us is 95% homologous to MMTV but only 57% to human endogenous retrovirus K10 in 3.5 kb of the gag and
74 al properties of the protease encoded by the human endogenous retrovirus, K10 (HERV-K), 213 amino aci
75 od mononuclear cells (PBMCs) were tested for human endogenous retrovirus-K18 (HERV-K18) env transcrip
78 we show that an LTR retrotransposon of ERV-9 human endogenous retrovirus located 40-70 kb upstream of
79 splicing into the long terminal repeat of a human endogenous retrovirus located between the last two
81 nsposon RNA transcripts, especially for some human endogenous retroviruses, such as LINE-1 and Alu re
82 is timely, however, to revisit the topic of human endogenous retroviruses-the subject of this articl
84 tein activates the overall expression of the human endogenous retrovirus type K (HERV-K) (HML-2), we
86 iruses, mouse mammary tumor virus (MMTV) and human endogenous retrovirus type K, encode analogous fac
89 e infections is attributed to members of the human endogenous retrovirus type-K (HERV-K) (HML-2) fami
90 ncoded by the antisense strand of the HRES-1 human endogenous retrovirus was isolated from peripheral
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