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 romatin structure of breakpoint regions in a common fragile site.
2 essor gene, like FHIT and WWOX, located at a common fragile site.
3 cular demonstration of a germline break in a common fragile site.
4 kpoints of lost regions located in genes and common fragile sites.
5 demonstrate that OPT domains are enriched at common fragile sites.
6 s that resemble those of aphidicolin-induced common fragile sites.
7 ny characteristics similar to those in other common fragile sites.
8 nt known to result in chromosome breakage at common fragile sites.
9 and promotes replication of DNA lesions and common fragile sites.
10 inhibit DNA replication induce expression of common fragile sites.
11 ility regions are the most characteristic of common fragile sites.
12 n secondary structures that are hallmarks of common fragile sites.
13 it gene and asked whether it also contains a common fragile site and if it is unstable in mouse tumor
15 s evidence indicates that telomeres resemble common fragile sites and present a challenge for DNA rep
16 ty of ORC sites are strongly associated with common fragile sites and recurrent deletions in cancers.
17 toward understanding the genomic features of common fragile sites and the cellular processes that mon
18 14.2, is the most frequently expressed human common fragile site, and allelic losses at FRA3B have be
19 recessive cancer genes, 17 were of sequenced common fragile sites, and 178 were in genomic regions th
48 se cleaves late replication intermediates at common fragile sites (CFSs) during early mitosis to trig
49 n in cervical cancer and the position of the common fragile sites (CFSs) has been observed at both th
50 n in cervical cancer and the position of the common fragile sites (CFSs) has been observed at the cyt
52 from genomic deletions and duplications and common fragile sites (CFSs) seen as breaks on metaphase
53 ragile metaphase telomeres that resemble the common fragile sites (CFSs), and the association of sist
54 ol eta is also required for the stability of common fragile sites (CFSs), whose rearrangements are co
56 enomic regions, we assessed the stability of common fragile sites, chromosomal loci that are prone to
63 es of RET/PTC rearrangements, are located in common fragile sites FRA10C and FRA10G, and undergo DNA
64 ative tumor suppressor gene that maps to the common fragile site FRA16D on chromosome 16q23.3-24.1, i
65 the cloning of WWOX, a gene that maps to the common fragile site FRA16D region in chromosome 16q23.3-
69 omain containing oxidoreductase) gene at the common fragile site, FRA16D, is altered in many types of
73 e gaps and breaks and breaks at the specific common fragile sites FRA3B and FRA16D were significantly
75 One putative target, 3p14.2, contains the common fragile site, FRA3B, a hereditary renal carcinoma
76 tidine triad gene (FHIT) encompasses a human common fragile site, FRA3B, that is susceptible to envir
84 romosome structure, no biological effects of common fragile sites have been convincingly shown, altho
85 f cell cycle checkpoints and DNA repair, and common fragile sites have provided insight into understa
86 ntriguing component of chromosome structure, common fragile sites have taken on novel significance as
87 teresting component of chromosome structure, common fragile sites have taken on novel significance as
92 FRA3B at 3p14.2 is the most active of the common fragile sites in the human genome and is expresse
93 Parkin maps to FRA6E, one of the most active common fragile sites in the human genome, it represents
94 orts the role of DNA secondary structures in common fragile site instability, provides a systematic m
95 Thus, the physical relationship of Fhit to a common fragile site is similar to that observed with the
101 ues were associated with cancer breakpoints, common fragile sites, microRNA, and cancer-related genes
102 gene and is the most highly expressed of the common fragile sites observed when DNA replication is pe
103 t 3p14.2 is the most highly expressed of the common fragile sites observed when DNA replication is pe
104 3p14-p12 interval known to contain the most common fragile site of the human genome (FRA3B), the FHI
106 oxidoreductase (WWOX) spans the second most common fragile site of the human genome, FRA16D, located
113 dentification of a sequence element within a common fragile site that increases chromosome fragility.
114 ristics are possibly intrinsic properties of common fragile sites that may affect their replication a
115 mal abnormalities occurred preferentially at common fragile sites upon conditional Hus1 inactivation.
116 o learn about the general characteristics of common fragile sites, we investigated the chromatin stru
117 ngements in tumors are often associated with common fragile sites, which are specific genomic loci pr
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。