戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 sequence length polymorphic markers in an F2 intercross.
2 F(2) rats generated from an SR/JrHsd x SHRSP intercross.
3 h some unexpected differences from the B x A intercross.
4 geny from an Itgb2(tm1Bay) (PL/J x C57BL/6J) intercross.
5 r's yeast from a multiparent 12th generation intercross.
6 ession data from a cohort of F2 female mouse intercross.
7 ntified in a B6-Tulp1(tm1Pjn/tm1Pjn) x AKR/J intercross.
8  at this block on albumin excretion in an F2 intercross.
9 re accurately than is possible with standard intercrosses.
10 re generated from Aqp11 +/sjds and Aqp11 +/- intercrosses.
11 e 2 congenic strains and three additional F2 intercrosses.
12 correlated with body weight in two of the F2 intercrosses.
13 to analyze individual embryos from Asah1 +/- intercrosses.
14 pressure QTLs detected in equivalent genetic intercrosses.
15 ood pressure QTLs in equivalent (Dahl S x R)-intercrosses.
16 ygous offspring were observed from PINCH1+/- intercrosses.
17 more than do conventional backcrosses and F2 intercrosses.
18 sis occurs in the F2 generation following F1 intercrosses.
19 allelic chimeric mice without further strain intercrossing.
20 utcrossing to C57BL/10J, and backcrossing or intercrossing.
21 an that of Apob(38.9/38.9) from Apob(38.9/+) intercrosses (1.8% versus 12%).
22                                Here, we have intercrossed 129S1/SvImJ, which carries the Xce(a) allel
23 ncreasingly complex genetic structure: an F2 intercross, a heterogeneous stock (HS) formed by crossin
24 g the F(10) generation of the LG,SM advanced intercross (AI) line.
25 te-selective Smad2/Smad3 double knockouts by intercrossing AlbCre/Smad2(f/f) (S2HeKO) and Smad3-defic
26  expression between sexes, and the use of an intercross allowed analysis of the genetic control of se
27 e through application to a set of four mouse intercrosses among five inbred strains, with data on HDL
28 will facilitate transfer of useful genes and intercrossing among the beans.
29 linkage analyses on the progeny of a B6CBAF1 intercross and a CBAxB6CBAF1 backcross were performed.
30 ved (avg. spacing 1.77 cM) in a single large intercross and anchored in the rat genomic sequence (avg
31                      We compared a classical intercross and three CSS intercrosses to examine the gen
32 g chromosomes with no significant QTL in the intercross and, in some cases (CSS-1, CSS-17), effects t
33  status of suckling offspring from LFKO(-/-) intercrosses and from wild-type (WT) intercrosses showed
34 arbitrary sequence of selfing, backcrossing, intercrossing and haploid-doubling steps that includes m
35 on as new allelic combinations arose through intercrossing and inbreeding to create new stable geneti
36 over multigenotype crosses, such as the F(2) intercross, and multiple QTL models.
37 the major loci previously identified in this intercross, and with SSLPs covering chromosomes 12 and 1
38 gregating populations including backcrosses, intercrosses, and natural populations.
39 clinically affected are 90% greater for F(2) intercross animals injected in the summercompared to tho
40 ock-out, and knock-in mouse models and their intercrosses are more recent developments that mirror de
41                 Furthermore, we used genetic intercrosses as well as pharmacological agents to link t
42 generated from G alpha(12)+/- G alpha(13)+/- intercrosses, at least one intact G alpha(12) allele is
43 using C57Bl/6 (B6), 129S6/SvEvTac (129), and intercross (B6 x 129)F2 mice on a low- or high-fat diet.
44                       Linkage analysis in F2 intercross (B6 x MSM) progeny identified several MSM loc
45 mouse population from a C57BL/6J and CASA/Rk intercross (B6CASAF2).
46 d a humanized mouse model of HD, Hu97/18, by intercrossing BACHD and YAC18 mice with knockout of the
47                                           An intercross between atherosclerosis susceptible (C57BL/6J
48 bility locus on chromosome 19 revealed in an intercross between atherosclerosis-susceptible C57BL6 an
49 ale F(2) mice (n=266) were generated from an intercross between B6.Apoe(-/-) and BALB.Apoe(-/-) mice
50 HC) was performed in wan/wan mice from an F2 intercross between C3H/HeJ(+/wan) and CAST/Ei(+/+) F1 hy
51 FeJ strain, F2 Eya1(bor/bor) mutants from an intercross between C3HeB/FeJ-Eya1(bor/+) and C57BL/6J sh
52                                     Using an intercross between C57BL/6J (B6) and C3H/HeJ (C3H) apoE(
53       A team led by Hopi Hoekstra studied an intercross between deer mice and old-field mice that dif
54                                        In an intercross between F1(BBDP x F344) rats, we identified a
55                                  Using an F2 intercross between H. cydno and H. pachinus, we first ma
56  somatic tissues of 334 mice derived from an intercross between inbred mouse strains C57BL/6J and C3H
57 inants and mechanisms underlying MetS, an F2 intercross between Lyon hypertensive and Lyon normotensi
58 cross with QTL identified in a previous F(2) intercross between M. m. musculus and M. m. domesticus a
59 uivalent to the Kauai population-an advanced intercross between Red Junglefowl and domestic layer bir
60 e expression and metabolic traits in a mouse intercross between strains C57BL/6J and C3H/HeJ.
61 t locus (QTL) analysis of schooling in an F2 intercross between strongly schooling marine and weakly
62 and validation of network connections: an F2 intercross between the C57BL/6 J and C3H/HeJ mouse strai
63 position traits in the F(3) generation of an intercross between the Large (LG/J) and Small (SM/J) inb
64 F(2) (n = 1181) population resulting from an intercross between the M16 and ICR lines of mice.
65                                     Using an intercross between the two divergent chicken lines, 16 a
66 titative trait locus (QTL) analysis using an intercross between the two strains carrying the apoE-/-
67                                We created an intercross between these lines, and in the F2 progeny, w
68                   F2 male mice created by an intercross between these two strains exhibit a 60% incid
69 s performed with 8-month-old progeny from an intercross between these two strains.
70 mice in the F(2) generation produced from an intercross between two inbred strains (C57BL/6J and AKR/
71 ntified that underlie serum IGF-I in a mouse intercross between two inbred strains.
72 solation in house mice, we conducted an F(2) intercross between wild-derived inbred strains from Mus
73 key reproductive barrier, we conducted an F2 intercross between wild-derived inbred strains from two
74 veying viability of Egfrtm1Mag mutants using intercrosses between 129S6/SvEvTAC-Egfrtm1Mag and nine S
75                                    Moreover, intercrosses between Atmin(Gpg6/+) and Vangl2(Lp/+) mice
76                                              Intercrosses between B and three CSSs (CSS-3, CSS-11, an
77               By analysis of backcrosses and intercrosses between C3H or CBA and resistant B6 mice, w
78 c linkage maps constructed from experimental intercrosses between closely related house mouse subspec
79                            F1 offspring from intercrosses between F0 animals that carry embryonic let
80         We use genetic mapping in large F(2) intercrosses between Gough Island mice and WSB/EiJ to id
81                                              Intercrosses between inbred lines provide a traditional
82                                Using genetic intercrosses between Nf1 +/- and class I (A)-PI-3K-defic
83 on-complementation of aganglionosis in mouse intercrosses between Ret null and the Ednrb hypomorphic
84 nduced pituitary tumorigenesis in reciprocal intercrosses between the genetically related ACI and Cop
85 ote mutations that reduce the probability of intercrossing between populations carrying different rea
86                                              Intercrossing between wild-type and Faah-/- mice rescued
87               We investigated the effects of intercross breeding designs on the utility of such lines
88                                 Heterozygous intercross breeding of the mutant mice yielded the expec
89  found among progeny of A1cf and Ago2 mutant intercrosses but not in backcrosses and without fetal lo
90 assic complement pathway in atherogenesis by intercrossing C1q-deficient mice (C1qa-/-) with low-dens
91  through only four (backcross case) or nine (intercross case) independent standard normal random vari
92 g 2-deficient (Gcm2-deficient) background by intercrossing CasR- and Gcm2-deficient mice.
93 d into a single strain by "endoreduplication intercross." Chemically synthesized genomes like Sc2.0 a
94                                          The intercross data reveal locus heterogeneity of the En1 mo
95 approach is illustrated through a mouse F(2) intercross data set.
96 fied by other network analyses of this mouse intercross data-set, but all have been previously associ
97 tal parasite infections of advanced mosquito intercrosses demonstrated a strong association between t
98 chromosome 19 in a leptin-deficient obese F2 intercross derived from C57BL/6 (B6) and BTBR T+ tf/J (B
99                                We found that intercrossing Dnd1+/KO heterozygotes to generate a compl
100 MHC genes controlling EBA susceptibility, we intercrossed EBA-susceptible MRL/MpJ with EBA-resistant
101     In this article, motivated by a mosquito intercross experiment involving two selected lines that
102 es are further illustrated with data from an intercross experiment to identify QTL contributing to va
103                                              Intercross experiments demonstrate that susceptibility i
104 gly, although diabetes was evident in the F1 intercross expressing rat insulin promoter (RIP)-TNF, of
105    The AR trial phenotype of BALB/cJ x SWR/J intercross F(1) and F(2) mice was consistent with BALB/c
106        Genome-wide mapping conducted with 60 intercross F(2) animals linked two loci to the number of
107 9(+/-) mice were generated, but heterozygous intercrosses failed to yield Mrad9(-/-) pups, since embr
108                                           We intercrossed female and male F(1) adult control (C) and
109  specks revealed a compact network of highly intercrossed filaments, whereas pyrin domain (PYD) or ca
110  to hepcidin independently of each other, we intercrossed Hjv(-/-) and Bmp6(-/-) mice and compared th
111 sis were determined in C57BL/6J, BALB/cJ, F1 intercross identical with C57BL/6J X 129S3/SvIM, and 129
112 s analysis performed on F2 C57; Eln(+/-)x129 intercrosses identified highly significant peaks on chro
113 onents of this autoimmune disorder, we first intercrossed IL-2-deficient mice with mice lacking CD28
114 binant inbred lines derived from an advanced intercross, in which multiple generations of mating have
115                              By studying two intercrosses, in which the DCC trait segregates, a singl
116 ption and preference in F2 rats generated by intercrossing inbred P and nonpreferring rats.
117 ng power calculations for backcross and F(2) intercross incorporating selective genotyping and marker
118 uantitative trait locus (QTL) analysis of an intercross involving the inbred mouse strains NZB/BlNJ a
119 he JNK2 isoform in metabolic homeostasis, we intercrossed Jnk1(-/-) and Jnk2(-/-) mice and examined b
120 n this family segregated either in 1:2:1 (F2 intercross-like segregation) or 1:1 ratio (backcross-lik
121 fixed effects model using simulated advanced intercross line (AIL) data.
122 econd was the 10th generation of an advanced intercross line (AIL) derived from a broiler-layer cross
123  in mice, we used a 34th generation advanced intercross line (AIL) derived from two inbred strains (S
124      We generated a large (n = 815) advanced intercross line of mice (G(4)) derived from a line selec
125                              An F34 advanced intercross line of mice (Wustl:LG,SM-G34) was generated
126 position in a large (n = 645) mouse advanced intercross line originating from a cross between C57BL/6
127 n of this four-way autoimmune-prone advanced intercross line were immunized with a fragment of murine
128  Ae. aegypti were mapped in an F(3) advanced intercross line.
129 ed in the F(2) and again in an F(5) advanced intercross line.
130  and a more highly recombinant F(8) advanced intercross line.
131 ly developed F(11) generation mouse advanced intercross lines (AIL) to fine map Pas1-3 quantitative t
132 ly detected in this vector using F6 advanced intercross lines (AIL).
133               The novel approach of advanced intercross lines (AILs) generates many more recombinatio
134  derived from inbred lines, such as advanced intercross lines and heterogeneous stocks, can be used t
135 is thaliana (multiparent advanced generation intercross lines) in controlled conditions simulating fo
136 lectron transfer dissociation (ETD)-MS/MS of intercross-linked peptides (two peptides connected with
137                    We conclude that, in this intercross, loci of atherosclerosis susceptibility are i
138 sis thaliana multiparent advanced generation intercross (MAGIC) lines.
139 sions of the multiparent advanced generation intercross (MAGIC) population showed that significant na
140 al stiffness in six-week old F2 (Dahl S x R)-intercross male and female rats characterized for abdomi
141               Genome-wide analysis of 200 F2-intercross male rats detects two QTLs with highly signif
142  groups have developed multi-parent advanced intercross mapping panels in different model organisms i
143 on Resource (DSPR), a multiparental advanced intercross mapping population.
144 to, rather than a replacement for, classical intercross mapping.
145                                              Intercross matings show that hem6 can suppress the porph
146  modifier screen through F1 backcross and F1 intercross matings.
147 er loss of Mbd2 increases lymphomagenesis by intercrossing Mbd2 deficient mice with p53 deficient and
148 were found to be different in female BS x BS intercross mice as compared with females from the three
149       We therefore surmise that LG/J by SM/J intercross mice can be used to dissect the genetic basis
150 ion restricted cohorts of (B10.S x SJL/J) F2 intercross mice in an effort to identify such linkages.
151 n the susceptibility of (B10.S x SJL/J) F(2) intercross mice to experimental allergic encephalomyelit
152 s deleted in macrophages and neutrophils, we intercrossed mice carrying a loxP-flanked (floxed) IL-4R
153                                           We intercrossed mice heterozygous for a (7.18) Rb transloca
154                                           We intercrossed mice heterozygous for a (7.18) Robertsonian
155 that were preserved in the iWAT of B6x129 F1-intercrossed mice, with an imbalance favoring the 129-de
156 ficient) CaR(-/-) mice (Pth(-/-)CaR(-/-)) by intercrossing mice heterozygous for the null CaR allele
157 analysis on F2 (B6.Rag1(-/-) x NOD.Rag1(-/-) intercross) mice.
158                                           We intercrossed mouse mammary tumor virus (MMTV)-c-neu tran
159 ogy was rescued and viable mice generated by intercrossing MRTF-B mutants with mice expressing Cre re
160                          We analyzed an F(2) intercross (n = 282 mice) between mouse strains resistan
161  were detected in the F(2) generation of the intercross (n = 510), where no maternal genetic effect v
162 rive from 8 founder inbred strains by serial intercrossing (n>60), resulting in fine-grained genetic
163 atically pair the recombinant gametes of two intercrossed natural genomes into an array of diploid hy
164                                              Intercrossing Nf1(+/-) mice and mice deficient in class
165                 Similar to the Swiss-derived intercrosses, nine congenic strains, derived from 129S6/
166  hscy, 1,160 F(2) mice were produced from an intercross of (C57BL/6-hscy x CAST/EiJ) F(1) hybrids, an
167                                           An intercross of 2 transgenic lines produced offspring with
168 ls could also be recovered following a blind intercross of G1 progeny, yielding several new white-eye
169                                          The intercross of hR120GCryAB cardiomyopathic animals with m
170 ns affecting mouse skeletal morphology in an intercross of LG/J and SM/J inbred strains (N = 1040), u
171 our methods to data on gut length in a large intercross of mice carrying the Sox10Dom mutation, a mod
172 or an ordinal trait, dead fetuses, in a F(2) intercross of mice.
173 congenic WF.iddm4 rats and report that in an intercross of N5 generation WF.iddm4 rats, approximately
174                                     Using an intercross of Pak 1(-/-) mice with Nf1(+/-) mice, we det
175 a quantitative trait locus analysis using an intercross of PERA/Ei and I/LnJ inbred strains of mice.
176 otyped >3100 hearts from a second-generation intercross of the inbred mouse strains C57BL/6 and FVB/N
177 exes in a population of mice derived from an intercross of the Large and Small inbred strains.
178  F(3) population of mice originating from an intercross of the LG/J (Large) and SM/J (Small) inbred s
179 arly growth in mice using a three-generation intercross of the Small (SM/J) and Large (LG/J) inbred m
180 nic mouse strains by performing a reciprocal intercross of the strains HcB-8 and HcB-23, phenotyped f
181          Through linkage analysis of a cross-intercross of these two parental strains, this trait was
182                       Here, we studied an F2 intercross of two outbred lines of rats selected for tam
183  library of an F2 population derived from an intercross of var. hallii and filipes.
184                 Using F(2) population of the intercross of wild-type and chr15 consomic strain, we co
185 rabidopsis thaliana individuals derived from intercrosses of 30 parents in a half diallel mating sche
186 apoB-27.6 homozygotes (Apob(27.6/27.6)) from intercrosses of Apob(27.6/+) was 7-fold lower than that
187      Homozygous null mice were produced from intercrosses of heterozygous null mice at the expected M
188                      Successive generational intercrosses of mTerc(-/-)MMT mice produced cohorts with
189                                              Intercrosses of Nmt1+/- mice yielded no viable homozygot
190                                              Intercrosses of Pol epsilon-, Pol delta-, and mismatch r
191 rdbp(+/-)) mice are fertile and healthy, but intercrosses of Tardbp(+/-) mice yielded no viable homoz
192 Interval mapping in the F(2) generation from intercrosses of the LG/J and SM/J strains revealed 33 QT
193 nant inbred line population derived from the intercrossing of 19 accessions.
194                                              Intercrossing of heterozygous TAFI mice produced offspri
195 n embryonic stem cells and/or time-consuming intercrossing of mice with a single mutation.
196 a(-/-) embryonic stem (ES) cells through the intercrossing of p38alpha(+/-) mice.
197                                          The intercrossing of Par-1a(-/-) with Par-1b(-/-) mice revea
198                  Arthritic male (DA x ACI)F2 intercross offspring (n = 143) were analyzed separately
199 tides of RNA-seq reads from the livers of F2 intercross offspring and parental rats.
200                                              Intercross offspring were genotyped, and linkage analysi
201 P overexpression, so FVBxF1 backcross and F2 intercross offspring were produced.
202 imately 30% smaller than that from GPR4(+/+) intercrosses on N3 and N5 C57BL/6 genetic backgrounds.
203 in the second generation (F2) of the F1 X F1 intercross or backcrosses to the parental strains.
204 ) is a newly developed multifounder advanced intercross panel consisting of >1600 recombinant inbred
205 om the same parental cross: the IBM advanced intercross population and a conventional recombinant inb
206  gene expression data from an MRL/MpJ x SM/J intercross population and predicted a previously unchara
207 e Panel (DGRP) and a large outbred, advanced intercross population derived from 40 DGRP lines (Flylan
208 ative trait locus GWA on an outbred advanced intercross population derived from extreme DGRP lines, a
209 squito Aedes albopictus and examined an F(1) intercross population for quantitative trait loci (QTL)
210 e mandibular molars in house mice from an F2 intercross population generated from crossing the Large
211 he DGRP and a DGRP-derived outbred, advanced intercross population identified candidate genes and gen
212            A multiparent advanced-generation intercross population of maize has been developed to hel
213 otypes derived from a multiparental advanced-intercross population, mapping three moderate-effect loc
214  data from a multiparent advanced generation intercross population.
215  are opposite to those observed in the B x A intercross population.
216 uantitative trait variation in a large yeast intercross population.
217 eference Panel (DGRP) and replicate advanced intercross populations derived from the most and least a
218 thanol/sucrose in the F2 offspring of a B6D2 intercross positively correlates with Ucn immunoreactivi
219 ob(27.6/38.9) offspring, but Apob(27.6/27.6) intercrosses produced no offspring.
220                    Additional analysis of F2 intercross progeny confirms a highly significant effect
221 n effects influence EAE, using reciprocal F2 intercross progeny generated between EAE-susceptible SJL
222                    QTL mapping using 87 F(2) intercross progeny identified two significant chromosome
223 lionosis as a quantitative trait in Sox10Dom intercross progeny to investigate the contribution of st
224 ymorphism-based genome scan in Sox10Dom/+ F1 intercross progeny.
225 n-MHC locations by analysis of backcross and intercross progeny.
226                                      We have intercrossed Rassf1a-knockout mice with mice lacking the
227 random mating, we constructed a new advanced intercross recombinant inbred line (RIL) population deri
228 ted B73 x Mo17 (IBM) population, an advanced intercross recombinant inbred line population derived fr
229        Using QTL mapping with a new advanced intercross-recombinant inbred line (AI-RIL) population,
230 t of early 2-cell embryos from the Asah1 +/- intercrosses rescued Asah1-/- embryos, and enabled their
231 tlSl-20J mice display a white belly spot and intercrossing results in an embryonic lethal phenotype i
232                                           We intercrossed Ret and Sema3d double null heterozygotes to
233                      Analysis of a Ggcx(+/-) intercross revealed a partial developmental block with o
234                                    The B x A intercross revealed significant quantitative trait loci
235                                           An intercross revealed that Mom2R encodes a recessive embry
236 r 150 offspring or embryos from heterozygous intercrosses revealed an absence of Asah1(-/-) individua
237                                     Directed intercrosses revealed that these phenotypes are heritabl
238 be a new approach, called recombinant inbred intercross (RIX) mapping, that extends the power of reco
239                       The recombinant inbred intercrosses (RIX) generated from CC recombinant inbred
240 er, total genome-analysis of an F2[Dahl RxS]-intercross selected for contrasting parental strain susc
241 KO(-/-) intercrosses and from wild-type (WT) intercrosses showed that lactoferrin is not essential fo
242 en after genetic background is controlled by intercrossing strains.
243  the design and analysis of traditional F(2) intercross studies allows high-confidence prediction of
244 ed test in a real data set collected from F2 intercross studies of inbred mouse strains.
245                                  The present intercross study was executed to replicate the earlier f
246  Our inability to predict the results of CSS intercrosses suggests that additional complexity will be
247                                           We intercrossed SwissOF1-En1+/- and C57Bl/6 mice to obtain
248  test for a possible genetic interaction, we intercrossed Tbx1(+/-) and Pitx2(+/-) mice.
249                                              Intercrossing TFPI(+/-)/mTF(+/-)/hTF+/- mice generated c
250                                           By intercrossing the congenic lines to create hybrid F1 emb
251 nd the doubly deficient CA IV/XIV KO mice by intercrossing the individual null mice.
252 the chromosome 10 locus in F2 mice from this intercross, the observations now reported suggest that p
253 research in these two areas and propose that intercrossing them and increasing funding to guide resea
254                                     A single intercross then produces homozygous mutant offspring.
255 ertional mutagenesis screen was performed by intercrossing these mice with those carrying a Sleeping
256                                           By intercrossing these mutants, we show that the stabilitie
257 finding significant differences in RD, an F1 intercross to determine rd3 QTLs that influence this inh
258 n of IFN signature genes in NZW, as shown by intercross to mice with an Ifnar1 knockout.
259 6.NODc1t mice carrying Idd5 were crossed and intercrossed to generate a C57BL/6.NODc3.NODc1t mouse li
260 and fibromodulin-null heterozygous mice were intercrossed to obtain wild-type (Lum(+/+)Fmod(+/+)), lu
261      The late-generation Tert(+/-) mice were intercrossed to produce genotypically wild-type Tert(+/+
262  backcrosses produced N10F1 rats, which were intercrossed to produce rats that were homozygous for GH
263  x 129)F1 x 129 backcross 1 mice, which were intercrossed to select for homozygosity of particular re
264        Heterozygous Lbr and Dhcr14 mice were intercrossed to test for a digenic phenotype.
265 ompared a classical intercross and three CSS intercrosses to examine the genetic architecture underly
266 plications have extended beyond experimental intercrosses to outbred populations by exploiting long-r
267 nase using biolistics, lentivirus or genetic intercrosses triggered heterologous expression of TRPV1
268                                           We intercrossed two closely related species of monkeyflower
269 t consists of 32 BXD strains of mice made by intercrossing two progenitor strains--C57BL/6J and DBA/2
270 ltiple generations, and the breeding scheme (intercrossing vs. outcrossing) drastically affected the
271 thyroidism-induced hearing impairment, an F1 intercross was generated between DW/J-Pou1f1dw/+ carrier
272 ld-type to Asah1(+/-) individuals from these intercrosses was 1:2.
273       The average litter size from GPR4(-/-) intercrosses was approximately 30% smaller than that fro
274 eny from a CAST.B6 Mom1(R/S) x B6 Apc(Min/+) intercross were 110 or 200 days of age and screened for
275  mice from a B6-Tulp1(tm1Pjn/tm1Pjn) x AKR/J intercross were genotyped with a panel of single nucleot
276 ifferences in the ONL, F2 progeny from an F1 intercross were measured for ONL thickness.
277 srupted La gene, and the offspring from La+/-intercrosses were analyzed.
278               Embryos from Arhgap29(K326X/+) intercrosses were harvested at various time points.
279      Offspring of LSL-KRAS(G12D) x PDX-1-Cre intercrosses were randomly allocated to a diet supplemen
280 and linkage analysis in a large F2(DA x PVG) intercross, which identified quantitative trait loci reg
281 erneurons evident in NCAM-EC transgenic mice intercrossed with a reporter line expressing green fluor
282    Floxed beta-catenin (exons 2-6) mice were intercrossed with Albumin-Cre recombinase transgenic mic
283                                   These were intercrossed with C57BL/6.lpr/lpr and MRL/Mp-lpr/lpr str
284                             Nf1+/- mice were intercrossed with conditional Rac1(flox/flox)Mxcre+ (Rac
285  report here that when Foxo1(KR/KR) mice are intercrossed with low density lipoprotein receptor knock
286 rsion of tcfap2a which has subsequently been intercrossed with mice expressing Cre recombinase under
287 ment in vivo, TgE-LMP2A-transgenic mice were intercrossed with mice expressing loxP-flanked Notch1 ge
288 homozygous for a conditional Apc allele were intercrossed with mice transgenic for Cre recombinase un
289                                         When intercrossed with obese, insulin-resistant, and diabetic
290 al cells (LPCs; IKKalpha/beta(LPC-KO) ) were intercrossed with RIPK1(LPC-KO) or RIPK3(-/-) mice to ex
291 54) exhibit a mild disorder, whereas animals intercrossed with SJL/J mice (F1.Q54) have a severe phen
292                   When susceptible mice were intercrossed with specific immune knockout mice, a criti
293  of another CD1-defective strain, as well as intercrosses with C57BL/6 mice, indicated that the impai
294 PPP family phosphatases (e.g. PP2A and PP4), intercrosses with mouse lines that ubiquitously express
295                                   Successive intercrossing with mice bearing a conditional Nf1 allele
296 ion of this gene in any tissue of choice, by intercrossing with mice in which Cre-recombinase express
297                                     Notably, intercrossing with p53-deficient mice completely rescued
298 ow generated a companion model, Hu128/21, by intercrossing YAC128 and BAC21 mice on the Hdh-/- backgr
299 y variable in F2 XY gonads from B6 and 129S1 intercrosses, yet strong correlations emerged.
300               Blastocysts derived from La+/- intercrosses yielded 38 La+/+ and La+/- embryonic stem (

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top