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1 he spontaneous spectrum or that derived from N-ethyl,N-nitrosourea.
2 mutation in the mouse Nell1 gene, induced by N-ethyl-N-nitrosourea.
3 ns after treatment with the powerful mutagen N-ethyl-N-nitrosourea.
4 y rat that had been treated with the mutagen N-ethyl-N-nitrosourea.
5 type cells was observed after treatment with N-ethyl-N-nitrosourea.
6 le-lethal mouse mutation that was induced by N-ethyl-N-nitrosourea.
7 rmates with a strong DNA-alkylating mutagen, N-ethyl-N-nitrosourea, 55% of transgenic mice developed
8 tically enhanced following administration of N-ethyl-N-nitrosourea, a carcinogen that induces DNA mut
10 ent, postnatally lethal mutations induced by N-ethyl-N-nitrosourea and mapped near Tyr are alleles of
11 vely resistant to DN, were mutagenized using N-ethyl-N-nitrosourea and screened for mutants that deve
12 outline mouse mutagenesis with the chemical N-ethyl-N-nitrosourea and the strategy used to instantan
13 tissue, treated with the chemical carcinogen N-ethyl-N-nitrosourea, and continuously passaged to yiel
14 Chinese hamster ovary cells were exposed to N-ethyl-N-nitrosourea, and the clearance of the damage f
15 nduced in the germline of C57BL/6J mice with N-ethyl-N-nitrosourea by measuring changes in the perfor
16 REM1 in the development of CDH comes from an N-ethyl-N-nitrosourea -derived mouse strain, eyes2, whic
17 trains postnatally exposed to the carcinogen N-ethyl-N-nitrosourea developed PTMCs, which closely res
20 etic response b (pob), was isolated using an N-ethyl N-nitrosourea (ENU)-based screening strategy des
22 a genome-wide, phenotype-driven, large-scale N-ethyl-N--nitrosourea (ENU) mutagenesis screen for domi
23 (e1500) was used to determine the utility of N-ethyl-N-nitrosourea (ENU) as a mutagen for genetic res
27 on of mouse mutations with the point mutagen N-ethyl-N-nitrosourea (ENU) is a key strategy for analys
29 mutations generated by the chemical mutagen n-ethyl-n-nitrosourea (ENU) mapped a new mutant locus (5
30 in (spontaneous inflammation) was induced by N-ethyl-N-nitrosourea (ENU) mutagenesis in C57BL/6J mice
32 y in both humans and mice, we established an N-ethyl-N-nitrosourea (ENU) mutagenesis screen to identi
36 utic intervention, we carried out a dominant N-ethyl-N-nitrosourea (ENU) mutagenesis suppressor scree
38 indirect ophthalmoscopy identified a line of N-ethyl-N-nitrosourea (ENU) mutagenized mice demonstrati
39 protocol for the production of mice carrying N-ethyl-N-nitrosourea (ENU) mutations and their screenin
40 ing bone marrow with the chemical carcinogen N-ethyl-N-nitrosourea (ENU) resulted in significantly ac
41 identified by five, independent mutations in N-ethyl-N-nitrosourea (ENU) saturation mutagenesis exper
42 conducted a second-generation (G2) dominant N-ethyl-N-nitrosourea (ENU) screen especially designed t
43 lin resistance has been used to sensitize an N-ethyl-N-nitrosourea (ENU) screen to identify novel mut
44 with dysfunctional IkappaBNS derived from an N-ethyl-N-nitrosourea (ENU) screen, named bumble, to inv
46 hemical mutagen of choice for mouse has been N-ethyl-N-nitrosourea (ENU), an alkylating agent that ma
47 a(TM)Mouse mice to benzo[a]pyrene (B[a]P) or N-ethyl-N-nitrosourea (ENU), daily for 28 consecutive da
48 g exposure to sublethal gamma-irradiation or N-ethyl-N-nitrosourea (ENU), MLL-CBP mice developed myel
49 or germline mutations induced by the mutagen N-ethyl-N-nitrosourea (ENU), numerous animals died under
50 treatment of mice with the alkylating agent, N-ethyl-N-nitrosourea (ENU), regardless of the levels of
51 males mutagenized with the germline mutagen N-ethyl-N-nitrosourea (ENU), we identified a recessive m
53 , 58% of aflatoxin B1 (AFB1)-induced, 14% of N-ethyl-N-nitrosourea (ENU)-induced and 12% of spontaneo
55 ed mice carrying homozygous and heterozygous N-ethyl-N-nitrosourea (ENU)-induced germline mutations f
56 s study, we developed protocols for creating N-ethyl-N-nitrosourea (ENU)-induced germline mutations i
60 e report the identification of a hyperactive N-ethyl-N-nitrosourea (ENU)-induced mouse mutant with ab
65 associated with and stabilized GPR89, and an N-ethyl-N-nitrosourea (ENU)-induced mutation (explorer)
72 ved substrains and used the panel to map two N-ethyl-N-nitrosourea (ENU)-induced mutations responsibl
73 In an ongoing forward genetic screen for N-ethyl-N-nitrosourea (ENU)-induced mutations that incre
76 man cancers and is mutationally activated in N-ethyl-N-nitrosourea (ENU)-induced rodent tumors of the
77 f magnetic resonance imaging (MRI)-localized N-ethyl-N-nitrosourea (ENU)-induced tumors in rat brains
79 s throughout Oceania, and A20 I325N, from an N-ethyl-N-nitrosourea (ENU)-mutagenized mouse strain.
89 and longer chain alkylating agents including N-ethyl-N-nitrosourea, ethyl methanesulfonate, N-propyl-
90 Genome-wide allelotyping of early passage N-ethyl-N-nitrosourea-exposed cell populations revealed
92 induced by the random germ line mutagen ENU (N-ethyl-N-nitrosourea), have disclosed key molecules in
95 mouse mutants, we identified ostes, a novel N-ethyl N-nitrosourea-induced mouse mutant with muscle a
97 n circadian timing in vivo, we exploited the N-ethyl-N-nitrosourea-induced afterhours mutant Fbxl3(Af
99 a null allele of the insulin receptor and an N-ethyl-N-nitrosourea-induced alternative splice mutatio
102 tion mutations in Herc2 in three independent N-ethyl-N-nitrosourea-induced jdf2 mutant alleles, each
106 unresponsive phenotype that results from an N-ethyl-N-nitrosourea-induced missense mutation in the T
107 describe the cleft secondary palate 1 (csp1) N-ethyl-N-nitrosourea-induced mouse model of non-syndrom
108 cilia genes, Dnah11 and Mks1, in independent N-ethyl-N-nitrosourea-induced mouse mutant lines with he
110 in iron-deficiency anemia, as revealed by an N-ethyl-N-nitrosourea-induced mouse phenotype called sub
117 have identified 'triple D' (3d), a recessive N-ethyl-N-nitrosourea-induced mutation and phenotype in
118 of inherited immunodeficiency revealed by an N-ethyl-N-nitrosourea-induced mutation called elektra.
119 viral infection was revealed by a recessive N-ethyl-N-nitrosourea-induced mutation called warmflash
120 27(+/-) and p27(-/-) mice displayed a higher N-ethyl-N-nitrosourea-induced mutation frequency in the
122 lymphoid lineages in mice, resulting from an N-ethyl-N-nitrosourea-induced mutation in the limb regio
125 In a forward genetic screen of mice with N-ethyl-N-nitrosourea-induced mutations for aberrant imm
126 In a forward genetic screen of mice with N-ethyl-N-nitrosourea-induced mutations for defects in a
127 (poly(I:C)) resulting from three independent N-ethyl-N-nitrosourea-induced mutations in host cell fac
129 uce a method for real-time identification of N-ethyl-N-nitrosourea-induced mutations that cause pheno
130 e carried out a genome-wide screen for novel N-ethyl-N-nitrosourea-induced mutations that give rise t
136 eport a novel zebrafish gata1 mutant with an N-ethyl-N-nitrosourea-induced point mutation in the C-fi
146 d out a forward genetic screen in mice using N-ethyl-N-nitrosourea mutagenesis to identify genetic mu
149 be the mutant mouse line 20884, generated by N-ethyl-N-nitrosourea mutagenesis, which is characterize
152 overy of another coronin 1A mutant during an N-ethyl-N-nitrosourea-mutagenesis screen for T cell-lymp
154 orn/fetal mice obtained from the breeding of N-ethyl-N-nitrosourea mutagenized mice were formalin-fix
156 invasive high frequency ultrasound to screen N-ethyl-N-nitrosourea mutagenized mouse fetuses for cong
159 generation germline mutant mice derived from N-ethyl-N-nitrosourea-mutagenized grandsires for intesti
163 less' (hdl) was detected in third-generation N-ethyl-N-nitrosourea-mutated mice that showed defective
165 nt of scid/scid mice with gamma radiation or N-ethyl-N-nitrosourea resulted in approximately 86% inci
167 nome-wide mutagenesis in C57BL/6J mice using N-ethyl-N-nitrosourea to identify mutations causing high
168 by sequencing in first-generation progeny of N-ethyl-N-nitrosourea-treated mice, involving 23 essenti