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1 ontained within a single exon and includes a microsatellite repeat.
2 hat contained 8-bp deletions adjacent to the microsatellite repeat.
3 temic disease caused by expanded CTG or CCTG microsatellite repeats.
4 22 sites in regions immediately flanking the microsatellite repeats.
5 ancing our understanding of the evolution of microsatellite repeats.
6  provide an improved method for isolation of microsatellite repeats.
7 mosome 10 by analysis of loss of polymorphic microsatellite repeats.
8 seases are caused by pathogenic expansion of microsatellite repeats.
9                                Five distinct microsatellite repeats (2 dinucleotide, 2 trinucleotide,
10                               We studied the microsatellite repeats AAAG, ATAG, CAGT, and CA, as well
11 hisms located in the MIF gene, a -794CATT5-8 microsatellite repeat and a -173 G/C SNP.
12 pansion in SCA10 represents a novel class of microsatellite repeat and is one of the largest found to
13                                              Microsatellite repeat and single nucleotide polymorphism
14 n tumors leads to genome-wide instability of microsatellite repeats and a molecular phenotype referre
15 otide array that enables genotyping for both microsatellite repeats and SNPs in a single analysis.
16 tumors is accumulation of variants targeting microsatellite repeats and the potential for high tumor
17 plate polymerase chain reaction, polymorphic microsatellite repeats, and Southern blots.
18                              Two polymorphic microsatellite repeats are described, including one in i
19                                 In contrast, microsatellite repeats are functionally less characteriz
20                      Second, highly variable microsatellite repeats are not confined to prokaryotes a
21 kers for investigating mutation processes in microsatellite repeats as well as phylogenetic relations
22             We present a tool for genotyping microsatellite repeats called RepeatSeq, which uses Baye
23  an explanation for how and why unmethylated microsatellite repeats can be destabilized in cells with
24                                              Microsatellite repeats consisting of dinucleotide sequen
25 e observations suggest that transcription of microsatellite repeat-containing RNAs is more sensitive
26 or AVPR1A that varies in coding sequence and microsatellite repeat content relative to other primate
27 gical disorders, the study of these unstable microsatellite repeat disorders has provided insight int
28 ce data from human chromosome 22 and compare microsatellite repeat distributions with mitotic recombi
29 cific targeting and efficient elimination of microsatellite repeat expansion RNAs both when exogenous
30 herited human disorder that is caused by CTG microsatellite repeat expansions (MREs) in the 3' untran
31 al-dominant inherited disorder caused by CTG microsatellite repeat expansions (MREs) in the 3' untran
32 disease myotonic dystrophy (DM) is caused by microsatellite repeat expansions at two different genomi
33                           The discovery that microsatellite repeat expansions can cause clinical dise
34                                              Microsatellite repeat expansions in DNA produce pathogen
35                                              Microsatellite repeat expansions within genes contribute
36                              The presence of microsatellite repeat expansions within genes is associa
37 esigned to enrich simultaneously for various microsatellite repeats from a genomic clone.
38 this technique to isolate novel, polymorphic microsatellite repeats from clones containing the amelog
39                     The sequence contigs and microsatellite repeats from GenBank were ordered using t
40 zygous deletion, we isolated two polymorphic microsatellite repeats from genomic BAC clones containin
41       Using a newly described polymorphic CA microsatellite repeat in the third MXI1 intron, we show
42 lite repeats, including thousands of triplet microsatellite repeats in coding regions that apparently
43 ase chain reaction amplification of 17 (CA)n microsatellite repeats in mchr 6 A1-C3.
44 sorders are associated with the expansion of microsatellite repeats in noncoding regions that result
45 n of the resistance by analysing polymorphic microsatellite repeats in the flanking region of the dhf
46 ased assays to detect polymorphic alleles of microsatellite repeats in the human genome opens the pos
47           Somatic mutations in coding region microsatellite repeats in the TGFbetaIIR, IGFIIR, BAX, E
48 mined the number and length distributions of microsatellite repeats in vertebrate genomes over evolut
49 deum is known to have a very high density of microsatellite repeats, including thousands of triplet m
50 ) gene exhibit a predisposition to lymphoma, microsatellite repeat instability, and failure of sperma
51 pports a relationship between dNTP pools and microsatellite repeat instability.
52                    Transcription of expanded microsatellite repeats is associated with multiple human
53                    The dynamic mutability of microsatellite repeats is implicated in the modification
54                                   We assayed microsatellite repeat-length variation among 13 populati
55 tation rate is primarily a function of short microsatellite repeat lengths in the D. melanogaster gen
56        Alleles at NACP-Rep1, the polymorphic microsatellite repeat located approximately 10 kb upstre
57                          Fifteen polymorphic microsatellite repeat markers and 17 novel sequence-tagg
58 l of 61 clones (76%) exhibited LOH of linked microsatellite repeat markers at different locations on
59 resence or absence of LOH of proximal linked microsatellite repeat markers was used to divide the clo
60            A total of 177 highly polymorphic microsatellite repeat markers were used in locus-specifi
61 g the amount of template for genotyping with microsatellite repeat markers.
62       Determinants of instability at a given microsatellite repeat merits investigation in view of re
63  (PD) while certain polymorphic alleles at a microsatellite repeat, NACP-Rep1, located approximately
64  MIF transcription with selectivity for high microsatellite repeat number and correspondingly high ge
65 l insertions and deletions, and variation in microsatellite repeat number.
66 th abdominal pigmentation phenotypes, as are microsatellite repeat numbers in the region.
67 ase chain reaction amplification of 17 (CA)n microsatellite repeats on mouse chromosome (mchr) 6 A2-C
68 ome-wide search for LOH was undertaken using microsatellite repeat polymorphisms and a panel of 27 tu
69 encies at loci near a subset of dinucleotide microsatellite repeats (r = -0.55, P < 0.05), in particu
70                                   Of several microsatellite repeat regions identified within the Pitx
71    Sequence analyses of regions flanking the microsatellite repeat reveal considerable amounts of cry
72      Here we demonstrate that GGGGCC and CAG microsatellite repeat RNAs associated with C9orf72 in am
73 ter polymorphisms, a functional -794 CATT5-8 microsatellite repeat (rs5844572) and a -173 G/C single-
74 ymorphisms in the MIF gene, a -794 CATT(5-8) microsatellite repeat (rs5844572) and a -173 G/C single-
75                       Genetic instability of microsatellite repeat sequences [microsatellite instabil
76 itu hybridization and PCR analysis of canine microsatellite repeat sequences allowed selection of a p
77  detection reaction for the analysis of such microsatellite repeat sequences was investigated.
78 ontain mutations at hundreds of thousands of microsatellite repeat sequences.
79 utations in target genes that possess coding microsatellite repeats, such as the transforming growth
80                        Length alterations in microsatellite repeats, termed microsatellite instabilit
81 es with more transposable elements (TEs) and microsatellite repeats than noneusocial species.
82 in (GFP) in which a plasmid vector carries a microsatellite repeat that places the GFP sequence out o
83 h whether the genes containing coding region microsatellite repeats that are known to be disrupted in
84 ts on chromosome 17, we have used additional microsatellite repeats to examine patterns of allelic im
85 a certain probability of losing or gaining a microsatellite repeat unit during each PCR cycle.
86 locus containing a simple dinucleotide (CA)n microsatellite repeat were isolated by PCR-single-strand
87                     PCR primers flanking the microsatellite repeats were designed with one primer in
88 ic sequences, including a strong bias toward microsatellite repeats, which are predominantly enriched
89 rence between ska and wild-type mice is in a microsatellite repeat within intron 7.
90 systemic disorder caused by expansion of CTG microsatellite repeats within DMPK.
91 he allele sets of two new highly polymorphic microsatellite repeats within the PGL1 critical region.