ライフサイエンスコーパス: CA repeat

1 utation due to the presence of uninterrupted CA repeats.

2 The MMP-9 microsatellite > or =24 CA repeat allele and the MMP-12-82 GG polymorphisms were

3 hat possess greater numbers of dinucleotide (CA) repeats also significantly associate with more sever

4 The STSs include 18 (CA) repeat and one tetranucleotide repeat marker that de

5 ons that shorten the length of uninterrupted CA repeat arrays; in contrast, all mutating alleles had

6 Because fewer d(CA) repeats associated with decreased MMP-9 expression i

7 ype clones demonstrated that the overall CpG-CA repeat composition of AD patients and controls is dis

8 In addition to the lack of CA repeats, differences include insertion of 42 base pai

9 on to extending understanding of mutation at CA repeat dinucleotide tracts, these findings have consi

10 ir-deficient lines had deletions of a single CA-repeat from the microsatellite sequence, whereas repa

11 r which one common allele (allele 2, with 12 CA repeats) has been shown to have a higher expression o

12 eles, containing from 13 to 20 copies of the CA repeats, have been detected.

13 (heterozygosity of 66 and 68%) and a complex CA repeat (heterozygosity of 78%) were isolated and char

14 regions within the MXI1 locus: a polymorphic CA repeat in the third intron and an AAAAC polymorphism

15 We report a role for CA repeats in the 3'-untranslated region (3'-UTR) in reg

16 characterized by a different length of the d(CA) repeat in the MMP-9 promoter and exhibit a significa

17 -9 promoter exhibits a decreased number of d(CA) repeats in the sclerosis-prone strain.

18 ranslation levels increased as the number of CA repeats increased; fewer multimers were required for

19 A polymorphic CA repeat is located in intron 4.

20 splicing regulated by hnRNP L and depends on CA repeat length at a specific site in intron 1.

21 of 403 AD patients and 444 controls for CpG-CA repeat length indicated shifted allelic frequency dis

22 ur estimates also suggest that most of these CA-repeat loci evolve according to multistep mutation mo

23 rosatellite D2S123 was studied as a paradigm CA repeat marker.

24 was sought by GENESCAN analysis of amplified CA repeat markers and indirectly by determining the numb

25 ls who were recombinants for HOXD8 or HOXD13-CA repeat markers.

26 wild type (hereafter referred as EKK), with CA-repeat markers as well as SSCP polymorphisms.

27 regions of the C32 strain are homozygous for CA-repeat markers in current stocks.

28 rains, C32 and SJD, we genotyped polymorphic CA-repeat markers randomly dispersed throughout the zebr

29 lex PCR allelic ladder standards and several CA-repeat markers were analyzed in > 100 runs.

30 within repeated sequence elements, including CA repeats, non-CA tandem repeats, and SINEs.

31 trace the evolution of length variation and CA repeat numbers.

32 A novel CA-repeat polymorphism identified within intron 2 of the

33 e 11p, we used 13 polymorphic microsatellite CA repeat primers to identify regions harboring potentia

34 rkers we present here, using microsatellite (CA) repeats, provides 1.2-cM average resolution.

35 insertion of two additional repeats within a CA repeat region of intron 53 of the sld genome enhances

36 eneous ribonucleoprotein L (hnRNP L) for a 6 CA repeat sequence (CA6) within intron 1.

37 Seven strains bearing haplotype 1 and a 21 CA repeat sequence at this position (CA21) express twice

38 tating alleles had relatively longer perfect CA repeat sequences.

39 occupied summits, and enrichment of GA- and CA-repeat sequences near Twist occupied summits.

40 phic markers (four diallelic markers and one CA repeat) spanning the PEX7 gene.

41 Cells containing frameshift mutations in the CA repeat that correct the reading frame of the neo gene

42 ream of this exon lies a stretch of intronic CA-repeats that proved to be polymorphic in two differen

43 Clones with insertions or deletions of CA-repeats that restored the normal reading frame of the

44 highly mucoid strain of E. coli K-12 ligates CA repeats to a significant proportion of lipopolysaccha

45 the frequency of frameshift mutations in the CA repeat tracts of the out-of-frame shuttle vector pZCA

46 rom this library suggests a preponderance of CA repeat tracts relative to their abundance in humans.

47 fied MLPS sample confirmed the presence of a CA repeat unit identical in carbohydrate sequence, but d

48 The ordering leads to a [-Ru-Ru-Ca-] repeat unit along each of the pseudocubic direction

49 e MMP-9 promoter in ROP MC contained fewer d(CA) repeats, which was associated with lower MMP-9 expre

50 p distal to an extensive region enriched for CA repeats with the potential to form Z-DNA.

51 Here we demonstrate that a CpG-CA repeat within the human ECE-1c promoter is highly pol