ライフサイエンスコーパス: microsatellite polymorphism

1 influenced by an interaction with the TNFa6 microsatellite polymorphism.

2 C polymorphism, and 13% had the short-allele microsatellite polymorphism.

3 of these linkage groups contain at least one microsatellite polymorphism.

4 carcinoma in each patient was compared using microsatellite polymorphisms.

5 tern Spain are associated with different TNF microsatellite polymorphisms.

6 iomyomas by polymerase chain reaction for 26 microsatellite polymorphisms.

7 ge groups (2n = 80) from the analysis of 288 microsatellite polymorphisms, 13 allozyme markers, and p

8 , surface maker expression, DNA content, and microsatellite polymorphisms, 74 had disease.

9 The MIF promoter contains a 4-nucleotide microsatellite polymorphism (-794 CATT) that repeats 5 t

10 lymorphism (alleles SacI+ or SacI-) and a CT microsatellite polymorphism (alleles CT+ or CT-).

11 losses affecting the gene were evaluated by microsatellite polymorphism analysis and genomic alterat

12 ations were observed between any single TNFa microsatellite polymorphism and disease severity, althou

13 /2J, C57BL/6J, and BALB/cJ, the frequency of microsatellite polymorphisms appears to be strain specif

14 e to tobacco and that gene amplification and microsatellite polymorphism are evolutionary drivers in

15 siblings using both the ACE D/I marker and a microsatellite polymorphism at the neighboring locus for

16 t allele (designated allele 86) of the Ctla4 microsatellite polymorphism (AT)n located in the 3'-untr

17 Polymerase chain reaction (PCR) analysis of microsatellite polymorphisms corresponding to four loci

18 Three families shared microsatellite polymorphisms covering at most 19 cM, whe

19 ; GenBank no. L34155), and on three flanking microsatellite polymorphism (D18S45, D18S478, and D18S48

20 A microsatellite polymorphism, D2S1788, mapped to chromoso

21 Two new microsatellite polymorphisms, D8S1991 and D8S1992, also

22 llelic loss of chromosome 9p, as assessed by microsatellite polymorphisms flanking the CDKN2/p16 regi

23 We present a genetic map based on microsatellite polymorphisms for the African human malar

24 We have also used a microsatellite polymorphism from within the Fmn gene to

25 ventories from 2,082 worldwide languages and microsatellite polymorphisms from 246 worldwide populati

26 on studies, and the level of simple-sequence microsatellite polymorphisms has important implications

27 We found a significant excess of microsatellite polymorphisms having a repeat unit length

28 Repeat length of the CAG microsatellite polymorphism in exon 1 of the androgen re

29 y comparing recombination rate and levels of microsatellite polymorphism in humans.

30 ngle nucleotide polymorphisms (SNPs) and one microsatellite polymorphism in MMP genes MMP-1, MMP-2, M

31 virus but also extends our understanding of microsatellite polymorphism in two important ways.

32 BD by linkage analysis of highly informative microsatellite polymorphisms in 43 families with multipl

33 hat are distinguished by point mutations and microsatellite polymorphisms in and near the CQR transpo

34 y to the p-1562 and (CA) dinucleotide repeat microsatellite polymorphisms in the promoter region of t

35 n tested shared a variant allele at 2 nearby microsatellite polymorphisms, indicating a common ancest

36 28 unrelated Europeans were used to estimate microsatellite polymorphism (number of alleles, heterozy

37 siblings, by using both ACE D/I and a nearby microsatellite polymorphism of the human growth hormone

38 Therefore, we evaluated LD between 21 common microsatellite polymorphisms on chromosome 18q21 in 2 ge

39 cell carcinoma (TCC) of the bladder using 30 microsatellite polymorphisms on chromosome 8.

40 describe here the identification of 11 novel microsatellite polymorphisms on human chromosome 19.

41 d short allele (<11 repeats) pentanucleotide microsatellite polymorphisms, respectively.

42 e association of severity measures with TNFa microsatellite polymorphisms stratified by SE status, an

43 In addition, we isolated a novel microsatellite polymorphism that maps 400 kb telomeric t

44 Alleles of the IL-10 (-)1064 promoter region microsatellite polymorphism that possess greater numbers

45 ariable number of tandem repeats (VNTRs), or microsatellite polymorphisms, this SNP-based method prov

46 kage analyses were performed with the use of microsatellite polymorphisms to determine a locus for th

47 h whole genome amplification and analysis of microsatellite polymorphisms to determine the frequency

48 Biallelic demethylation of the HUMARA microsatellite polymorphism was also found in one intram

49 Typing of TNF microsatellite polymorphisms was carried out by molecula

50 The association of disease with TNF microsatellite polymorphisms was investigated using chi-

51 DNA was isolated, and microsatellite polymorphisms were exploited to quantify

52 Fourteen microsatellite polymorphisms were selected based on thei

53 These microsatellite polymorphisms will be valuable in further

54 s no association of either the TNFd or IL-10 microsatellite polymorphisms with mortality (P =.43 and.

55 enotyped for an interferon-gamma (IFN-gamma) microsatellite polymorphism, within intron 1, for which