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1 formation with CpG --> TpG mutations in the Apc gene.
2 gene and the mutation cluster region of the APC gene.
3 s with the D1822V [corrected] variant of the APC gene.
4 gene and the mutation cluster region of the APC gene.
5 tuses bearing a heterozygous mutation in the APC gene.
6 be shown to have truncating mutations of the APC gene.
7 r this disorder by genetically modifying the Apc gene.
8 310 kD and is encoded by exons 1 - 15 of the APC gene.
9 ed due to cancer-associated mutations in the APC gene.
10 AP) coli who have germ line mutations in the APC gene.
11 ht to be associated with a disruption in the APC gene.
12 es and thereby initiated CRC by mutating the APC gene.
13 Cre-mediated bi-allelic inactivation of the Apc gene.
14 nd because much is known about the causative APC gene.
15 iduals are heterozygous for mutations in the APC gene.
16 tudied in mice that inherit mutations in the Apc gene.
17 FAP is due to mutations in the APC gene.
18 d are negative for germline mutations in the APC gene.
19 to a thymine-adenine pair (G:C-->T:A) in the APC gene.
20 contribute to the specific targeting of the APC gene.
21 alterations in key regions of the K-ras and Apc genes.
22 mutations in the adenomatous polyposis coli (APC) gene.
23 ctivation of the adenomatous polyposis coli (APC) gene.
24 mutations in the Adenomatous polyposis coli (Apc) gene.
25 mutation in the adenomatous polyposis coli (APC) gene.
26 function of the Adenomatous polyposis coli (APC) gene.
27 ressors TP53 and adenomatous polyposis coli (APC) gene.
28 e product of the Adenomatous Polyposis Coli (APC) gene.
29 RC occurs in the adenomatous polyposis coli (APC) gene.
30 mutations to the adenomatous polyposis coli (Apc) gene.
31 mutation in the adenomatous polyposis coli (APC) gene.
32 mutations in the adenomatous polyposis coli (APC) gene.
33 mutations of the adenomatous polyposis coli (Apc) gene.
34 mutations in the adenomatous polyposis coli (APC) gene.
39 as no difference in the frequency of somatic APC gene alterations between FGPs with foveolar dysplasi
44 own that somatic adenomatous polyposis coli (APC) gene alterations are frequently present in FGPs ass
45 analyzed somatic adenomatous polyposis coli (APC) gene alterations in 41 FAP-associated FGPs (20 with
46 denomas that have homozygous mutation of the APC gene and also select against fetuses bearing a heter
47 from increased nuclear transcription of the APC gene and correlated with a concomitant increase in t
50 nt role for germ-line allele sequence in the APC gene and individual risk of metachronous adenomatous
51 cing and large rearrangement analysis of the APC gene and targeted sequence analysis for the 2 most c
52 hat have a chain-terminating mutation in the Apc gene and that were either wild-type for SCFA metabol
53 single-nucleotide polymorphisms (SNP) in the APC gene and the odds of developing metachronous colorec
54 C57BL/6J-Min/+ (Min/+) mouse bears a mutant Apc gene and therefore is an important in vivo model of
55 ification of the adenomatous polyposis coli (Apc) gene and are excellent models for familial cancer p
56 mutation in the adenomatous polyposis coli (Apc) gene and develop multiple adenomas throughout their
57 terations of the adenomatous polyposis coli (APC) gene and frequently demonstrate epithelial dysplasi
58 iciencies in the adenomatous polyposis coli (APC) gene and in cells stimulated with the Wnt3a ligand.
59 Mutations in the adenomatous polyposis coli (APC) gene and K-ras occur in the majority of human color
60 eficiency in the adenomatous polyposis coli (APC) gene and subsequent activation of beta-catenin lead
61 +/- mice that inherit a mutant allele of the Apc gene, and intermediate effects are seen if a single
62 oth are caused by inherited mutations in the APC gene, and management includes genetic testing, colon
63 vered in colon cancers that retain wild-type APC genes, and also in melanomas, medulloblastomas, pros
65 mutations in the adenomatous polyposis coli (APC) gene (APC) that are orthologous to those responsibl
69 Mutations in the adenomatous polyposis coli (APC) gene are associated with an early onset of colorect
70 ns of the human adenomatosis polyposis coli (APC) gene are associated with the development of familia
71 mutations in the Adenomatous Polyposis Coli (APC) gene are at increased risk of developing hepatoblas
72 terations of the adenomatous polyposis coli (APC) gene are common events in gastrointestinal tumor de
73 mutations of the adenomatous polyposis coli (APC) gene are initiating events in the majority of spora
74 Mutations in the adenomatous polyposis coli (APC) gene are linked to polyp formation in familial and
76 terations of the adenomatous polyposis coli (APC) gene are present in biliary tract cancers and the A
77 mutations in the adenomatous polyposis coli (APC) gene are thought to cause colon adenoma and carcino
78 ons in the human adenomatous polyposis coli (APC) gene are thought to initiate colorectal tumorigenes
79 mutations on the adenomatous polyposis coli (APC) gene as a model of FAP-related malignant cells.
81 ations at any of 15 sites on K-ras, p53, and APC genes; Bat-26, a microsatellite instability marker;
82 e germline mutation lay in the region of the APC gene between the first and second beta-catenin degra
88 hemistry to address barriers associated with APC gene delivery, which include cellular uptake and int
89 mutation in the adenomatous polyposis coli (Apc) gene, double heterozygous animals have increased nu
90 N-induced loss of heterozygosity, and indeed Apc gene editing was less efficient in tetraploid than i
95 Similarly, mice that contain a single mutant APC gene encoding a protein truncated at residue 716 (Ap
96 variants identified within the region of the APC gene examined, suggesting that any effect from this
97 n RNA interference showed that the wild-type APC gene expression is required for DNA methylation-indu
100 n the GI tract of these mice involve loss of Apc gene function in a manner very similar to that seen
102 utely transformed on in vivo deletion of the APC gene; however, the significance of this is unclear.
103 ine sequence alteration at codon 1307 of the APC gene (I1307K) has been reported in 6-7% of the Ashke
104 cently, a germ-line missense mutation in the APC gene, I1307K, was identified that may indirectly cau
108 he presence and patterns of mosaicism in the APC gene in patients with colon neoplasms not associated
109 activation of a gatekeeper gene, such as the APC gene in the colon and the CDKN2A gene in the pancrea
110 he mutation cluster region in exon 15 of the APC gene in those SPTs that did not harbor beta-catenin
115 mutation in the adenomatous polyposis coli (Apc) gene increased the tumor number in the GI tract and
116 ether this D1822V [corrected] variant of the APC gene is associated with colon cancer and whether its
120 In previous studies, we have shown that the APC gene is inducible and that the DNA damage-induced le
121 tant regulator in Wnt-signaling pathway, the APC gene is involved in apoptosis and cell cycle arrest.
123 hat the CaMKII-Cre used to delete the floxed APC gene is present in efferent olivocochlear (OC) neuro
125 ctivation of the adenomatous polyposis coli (APC) gene is a critical event in the development of huma
126 Mutation of the adenomatous polyposis coli (APC) gene is an early step in the development of colorec
127 Mutation of the adenomatous polyposis coli (APC) gene is an early step in the initiation of colon ca
131 mutation of the adenomatous polyposis coli (APC) gene, is characterized by development of colorectal
133 BER than the cell line expressing the mutant APC gene lacking the proliferating cell nuclear antigen-
134 g a fully penetrant dominant mutation in the Apc gene, leading to the development of gastrointestinal
137 In the patients with positive tests, mutant APC genes made up 0.4 to 14.1 percent of all APC genes i
139 re not functionally equivalent, and that the APC gene may have other tumor suppressor functions besid
140 crossed with mice bearing a mutation in the Apc gene (MIN mice), and the CEA.Tg/MIN progeny develope
141 y efficacious against CRC tumors carrying an APC gene mutation between the first and second 20-amino-
146 curs through induction of the Wnt pathway or APC gene mutations that cause familial adenomatous polyp
152 eas essentially never harbor beta-catenin or APC gene mutations, we have recently identified alterati
153 beta-catenin and adenomatous polyposis coli (APC) gene mutations are well established and are known t
155 ri infection and adenomatous polyposis coli (Apc) gene mutations have been linked to gastric cancer i
156 the role of adenomatous polyposis coli gene (Apc) gene mutations in the GI tumors of Mlh1 mutant mice
157 Mutations in the adenomatous polyposis coli (APC) gene occur in the vast majority of colorectal cance
158 a mutagen-induced nonsense allele of the rat Apc gene on an inbred F344/NTac (F344) genetic backgroun
159 ve mutational analysis in this region of the APC gene on DNA extracted from 240 Italian, Finnish, and
160 tumors that are either solely mutant in the Apc gene or in combination with another colon cancer-ass
161 rigenesis, mice with the min mutation of the APC gene or with the tm1 mutation of the p53 gene were c
162 mutations of the adenomatous polyposis coli (APC) gene or the beta-catenin gene that stabilize beta-c
163 esults indicate that somatic mutation of the APC gene plays an important role in the pathogenesis of
166 efore, C57Bl/6J(Min/+) mice with a truncated APC gene product were fed diets supplemented with cerami
169 ctivation of the adenomatous polyposis coli (APC) gene product, we examined protein levels and locali
171 (GSK-3beta), and adenomatous polyposis coli (APC) gene products interact to form a network that influ
174 thylation of the adenomatous polyposis coli (APC) gene promoter occurs in primary non-small cell lung
175 ting mutation of adenomatous polyposis coli (APC) gene reduces intestinal adenomatous polyposis via A
177 ic losses of 5q (adenomatous polyposis coli [APC] gene region) and 18q (deleted in colorectal cancer
181 omologues or the adenomatous polyposis coli (APC) gene, respectively, are important for the developme
183 Mutations in the adenomatous polyposis coli (APC) gene result in uncontrolled proliferation of intest
189 mutation of the adenomatous polyposis coli (APC) gene that causes colorectal cancer if prophylactic
190 mutations in the adenomatous polyposis coli (APC) gene that initiate colorectal tumors theoretically
191 ne allele of the adenomatous polyposis coli (Apc) gene that is similar to most mutations observed in
193 mutation in the adenomatous polyposis coli (APC) gene that results in the spontaneous development of
194 mutations in the adenomatous polyposis coli (APC) gene that underlies familial adenomatous polyposis.
195 dentified in the adenomatous polyposis coli (APC) gene that was suggested to increase cancer predispo
196 most adenomas have lost their WT copy of the Apc gene through loss of heterozygosity by homologous so
197 his alteration is believed to predispose the APC gene to a secondary mutation at the same locus, resu
199 ctivation of the adenomatous polyposis coli (Apc) gene to accelerate intestinal tumourigenesis using
200 efective for the adenomatous polyposis coli (APC) gene to reinvestigated the identity and importance
201 nderstanding to date of how mutations in the APC gene translate into changes at the protein level, wh
202 spectrum of DNA polymerase beta in the human APC gene under PCR conditions and compared it with the s
203 Mutations in the Adenomatous Polyposis Coli (APC) gene up-regulate Wnt signaling by stabilizing beta-
204 to detect chain-truncation mutations in the APC gene using DNA or RNA from cancer cell lines as well
206 on cancer cell line expressing the wild-type APC gene was more sensitive to a DNA-methylating agent d
207 urements showed that RNA expression from the APC gene was not significantly altered by the presence o
209 ngle nucleotide polymorphisms in the CRP and APCS genes was examined by application of family-based t
210 ations in the mutation cluster region of the APC gene were detected in the four JNAs without beta-cat
212 Furthermore, colorectal tumors with intact APC genes were found to contain activating mutations of
213 Microsatellites in human TGFBR2, PTEN and APC genes were placed in yeast vectors and analyzed in i
214 mutations in the adenomatous polyposis coli (APC) gene were demonstrated in 50% of dysplastic juvenil
215 heterozygous for a nonsense mutation in the Apc gene, were randomized at weaning to seven groups, in
216 cal onset group versus controls involved the APCS gene, whereas for late-onset cases, one APCS varian
217 Mutations in the adenomatous polyposis coli (APC) gene, which initiate almost all human colon cancers
218 mutation of the adenomatous polyposis coli (APC) gene, which leads to activation of the Wnt/beta-cat
219 mutations of the adenomatous polyposis coli (APC) gene, whose product is an important component of th
221 in allele of the adenomatous polyposis coli (Apc) gene with ethylnitrosourea (ENU) results in approxi
222 deletion of the adenomatous polyposis coli (Apc) gene within the adult bladder led rapidly to coinci
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