ライフサイエンスコーパス: microsatellite repeat

1 ontained within a single exon and includes a microsatellite repeat.

2 hat contained 8-bp deletions adjacent to the microsatellite repeat.

3 22 sites in regions immediately flanking the microsatellite repeats.

4 ancing our understanding of the evolution of microsatellite repeats.

5 provide an improved method for isolation of microsatellite repeats.

6 mosome 10 by analysis of loss of polymorphic microsatellite repeats.

7 Five distinct microsatellite repeats (2 dinucleotide, 2 trinucleotide,

8 We studied the microsatellite repeats AAAG, ATAG, CAGT, and CA, as well

9 hisms located in the MIF gene, a -794CATT5-8 microsatellite repeat and a -173 G/C SNP.

10 pansion in SCA10 represents a novel class of microsatellite repeat and is one of the largest found to

11 Microsatellite repeat and single nucleotide polymorphism

12 n tumors leads to genome-wide instability of microsatellite repeats and a molecular phenotype referre

13 otide array that enables genotyping for both microsatellite repeats and SNPs in a single analysis.

14 plate polymerase chain reaction, polymorphic microsatellite repeats, and Southern blots.

15 Two polymorphic microsatellite repeats are described, including one in i

16 In contrast, microsatellite repeats are functionally less characteriz

17 Second, highly variable microsatellite repeats are not confined to prokaryotes a

18 kers for investigating mutation processes in microsatellite repeats as well as phylogenetic relations

19 We present a tool for genotyping microsatellite repeats called RepeatSeq, which uses Baye

20 an explanation for how and why unmethylated microsatellite repeats can be destabilized in cells with

21 Microsatellite repeats consisting of dinucleotide sequen

22 e observations suggest that transcription of microsatellite repeat-containing RNAs is more sensitive

23 or AVPR1A that varies in coding sequence and microsatellite repeat content relative to other primate

24 gical disorders, the study of these unstable microsatellite repeat disorders has provided insight int

25 ce data from human chromosome 22 and compare microsatellite repeat distributions with mitotic recombi

26 cific targeting and efficient elimination of microsatellite repeat expansion RNAs both when exogenous

27 disease myotonic dystrophy (DM) is caused by microsatellite repeat expansions at two different genomi

28 The discovery that microsatellite repeat expansions can cause clinical dise

29 Microsatellite repeat expansions in DNA produce pathogen

30 esigned to enrich simultaneously for various microsatellite repeats from a genomic clone.

31 this technique to isolate novel, polymorphic microsatellite repeats from clones containing the amelog

32 The sequence contigs and microsatellite repeats from GenBank were ordered using t

33 zygous deletion, we isolated two polymorphic microsatellite repeats from genomic BAC clones containin

34 Using a newly described polymorphic CA microsatellite repeat in the third MXI1 intron, we show

35 lite repeats, including thousands of triplet microsatellite repeats in coding regions that apparently

36 ase chain reaction amplification of 17 (CA)n microsatellite repeats in mchr 6 A1-C3.

37 sorders are associated with the expansion of microsatellite repeats in noncoding regions that result

38 n of the resistance by analysing polymorphic microsatellite repeats in the flanking region of the dhf

39 ased assays to detect polymorphic alleles of microsatellite repeats in the human genome opens the pos

40 Somatic mutations in coding region microsatellite repeats in the TGFbetaIIR, IGFIIR, BAX, E

41 mined the number and length distributions of microsatellite repeats in vertebrate genomes over evolut

42 deum is known to have a very high density of microsatellite repeats, including thousands of triplet m

43 ) gene exhibit a predisposition to lymphoma, microsatellite repeat instability, and failure of sperma

44 pports a relationship between dNTP pools and microsatellite repeat instability.

45 Transcription of expanded microsatellite repeats is associated with multiple human

46 The dynamic mutability of microsatellite repeats is implicated in the modification

47 We assayed microsatellite repeat-length variation among 13 populati

48 tation rate is primarily a function of short microsatellite repeat lengths in the D. melanogaster gen

49 Alleles at NACP-Rep1, the polymorphic microsatellite repeat located approximately 10 kb upstre

50 Fifteen polymorphic microsatellite repeat markers and 17 novel sequence-tagg

51 l of 61 clones (76%) exhibited LOH of linked microsatellite repeat markers at different locations on

52 resence or absence of LOH of proximal linked microsatellite repeat markers was used to divide the clo

53 A total of 177 highly polymorphic microsatellite repeat markers were used in locus-specifi

54 g the amount of template for genotyping with microsatellite repeat markers.

55 Determinants of instability at a given microsatellite repeat merits investigation in view of re

56 (PD) while certain polymorphic alleles at a microsatellite repeat, NACP-Rep1, located approximately

57 l insertions and deletions, and variation in microsatellite repeat number.

58 th abdominal pigmentation phenotypes, as are microsatellite repeat numbers in the region.

59 ase chain reaction amplification of 17 (CA)n microsatellite repeats on mouse chromosome (mchr) 6 A2-C

60 ome-wide search for LOH was undertaken using microsatellite repeat polymorphisms and a panel of 27 tu

61 encies at loci near a subset of dinucleotide microsatellite repeats (r = -0.55, P < 0.05), in particu

62 Of several microsatellite repeat regions identified within the Pitx

63 Sequence analyses of regions flanking the microsatellite repeat reveal considerable amounts of cry

64 Here we demonstrate that GGGGCC and CAG microsatellite repeat RNAs associated with C9orf72 in am

65 ymorphisms in the MIF gene, a -794 CATT(5-8) microsatellite repeat (rs5844572) and a -173 G/C single-

66 ter polymorphisms, a functional -794 CATT5-8 microsatellite repeat (rs5844572) and a -173 G/C single-

67 Genetic instability of microsatellite repeat sequences [microsatellite instabil

68 itu hybridization and PCR analysis of canine microsatellite repeat sequences allowed selection of a p

69 detection reaction for the analysis of such microsatellite repeat sequences was investigated.

70 ontain mutations at hundreds of thousands of microsatellite repeat sequences.

71 utations in target genes that possess coding microsatellite repeats, such as the transforming growth

72 Length alterations in microsatellite repeats, termed microsatellite instabilit

73 in (GFP) in which a plasmid vector carries a microsatellite repeat that places the GFP sequence out o

74 h whether the genes containing coding region microsatellite repeats that are known to be disrupted in

75 ts on chromosome 17, we have used additional microsatellite repeats to examine patterns of allelic im

76 a certain probability of losing or gaining a microsatellite repeat unit during each PCR cycle.

77 locus containing a simple dinucleotide (CA)n microsatellite repeat were isolated by PCR-single-strand

78 PCR primers flanking the microsatellite repeats were designed with one primer in

79 ic sequences, including a strong bias toward microsatellite repeats, which are predominantly enriched

80 rence between ska and wild-type mice is in a microsatellite repeat within intron 7.

81 he allele sets of two new highly polymorphic microsatellite repeats within the PGL1 critical region.