ライフサイエンスコーパス: multiple allele

1 btype family, XVa, was identified containing multiple alleles.

2 from the case of two alleles to the case of multiple alleles.

3 sosomal storage disorder gene, and 21% carry multiple alleles.

4 ive trait loci were identified, and most had multiple alleles.

5 phenotypes that are the cumulative effect of multiple alleles.

6 a convenient method to study the function of multiple alleles.

7 ganisms where selection acts at a locus with multiple alleles.

8 ombinants and (v) the iterative targeting of multiple alleles.

9 ses to provide high-resolution evaluation of multiple alleles.

10 uivalency and selective forces acting on its multiple alleles.

11 or many pairs of loci, each locus often with multiple alleles.

12 een identified 14 different genes, many with multiple alleles.

13 the analyses extend immediately to loci with multiple alleles.

14 lly have only one X-chromosome pigment gene; multiple alleles allow different types of dichromatic co

15 represent phased or unphased genotypes with multiple alleles and achieved a speed of over 1000 times

16 evelopment and underscore the value of using multiple alleles and different experimental approaches t

17 accounts for segregation complexities due to multiple alleles and double reduction at autotetrasomic

18 e show how to extend the SDT to markers with multiple alleles and how to combine families with parent

19 s especially common when the sample includes multiple alleles and sparse data, thus rendering asympto

20 tion with quantitative traits, allowance for multiple alleles, and, in the case of dichotomous traits

21 For many HLA-associated diseases, multiple alleles-- and, in some cases, multiple loci--ha

22 al analysis of SerH genes indicates that the multiple alleles are neutral.

23 sion, in which oligonucleotide segments from multiple alleles are recombined into the expression site

24 us amino acid substitutions suggest that the multiple alleles are subject to purifying (negative) sel

25 selection that allows for the coexistence of multiple alleles at a locus with very small selective di

26 determination (sl-CSD), sex is determined by multiple alleles at a single locus.

27 This occurs because the presence of multiple alleles at each locus often precludes the measu

28 R analysis (MLVA) uses the combined power of multiple alleles at several marker loci.

29 erogeneous, with multiple causative loci and multiple alleles at some of the causative loci.

30 al and experimental approaches, we show that multiple alleles at the previously identified dormancy l

31 lay nonredundant roles in TG metabolism, and multiple alleles at these loci cumulatively contribute t

32 aster technique for sequential disruption of multiple alleles by integrative transformation using URA

33 between diallelic loci, but we also address multiple alleles, complex incompatibilities, and continu

34 pothesized that preferential transmission of multiple alleles does explain it.

35 because the same epitope can be presented by multiple alleles (epitope promiscuity).

36 not generated a comprehensive collection of multiple alleles for most mouse genes.

37 It is composed of multiple alleles for resistance and susceptibility that

38 reaction of intronic sequences demonstrated multiple alleles for rod arrestin.

39 ds to a correlation-based test for loci with multiple alleles: for a pair of loci with k and m allele

40 VNTR markers frequently identified multiple alleles (from two to nine), with Nei's diversit

41 penalties for multiple testing incurred with multiple alleles, greater heterozygosity results in grea

42 nly in a diallelic case, and an extension to multiple alleles has not been made.

43 ll death regulators, E74 and hid, as well as multiple alleles in CBP (nejire) and dTrf2.

44 and sequencing further shows the presence of multiple alleles in clec18a/b/c loci.

45 we successfully identified mutant genes with multiple alleles in near-saturation screens, including r

46 ntial for cell survival; 2) are expressed as multiple alleles in the normal population because of the

47 disease: one allele in the affected sibs and multiple alleles in unaffected sibs and parents.

48 member of family 31 glycosyl hydrolases, has multiple alleles, including a "null" allele and is poten

49 A complicated mating design involving multiple alleles mimics the actual breeding system.

50 y is well suited for the rapid generation of multiple alleles of a given locus, is hampered by its lo

51 This screen yielded multiple alleles of a previously uncharacterized gene, d

52 e inheritance of late Golgi elements yielded multiple alleles of CDC1.

53 We obtained multiple alleles of COX18, PNT1, and MSS2, as well as mu

54 The isolation and characterization of multiple alleles of encore revealed that they were all t

55 t is common for bacterial genomes to contain multiple alleles of flp-like genes, including the open r

56 suppressors of this phenotype, we identified multiple alleles of four genes in a G(o)/G(q) G-protein

57 As multiple alleles of genes are acquired through mutagenes

58 ations in several unknown loci, we recovered multiple alleles of groucho (gro) and Hairless (H).

59 Multiple alleles of Kif1C determine the susceptibility o

60 This data for the first time defines multiple alleles of KIR3DL in RM and shows an associatio

61 avioral screens in Drosophila, we identified multiple alleles of N-cadherin.

62 Multiple genes, multiple alleles of some genes, multiple mechanisms, and

63 ns to 23 complementation groups that include multiple alleles of Star and hedgehog as well as single

64 rom amplified L1 gene sequences suggest that multiple alleles of the L1 gene cocirculate in nature an

65 Multiple alleles of the P gene confer distinct patterns

66 Multiple alleles of the quaking (qk) gene have a variety

67 ws users to rapidly identify instances where multiple alleles of the same gene are present in the mut

68 recovered 30 dominant suppressors, including multiple alleles of the spectroplakin, short stop, a let

69 crosatellite loci was examined by sequencing multiple alleles of two compound microsatellites and sin

70 In addition, this screen identified multiple alleles of two newly identified genes, eor-1 an

71 We examined the interaction of multiple alleles of unc-1 and unc-8 with each other and

72 cautionary tale illustrating the need to use multiple alleles or complementation lines when attributi

73 and have none of the complications caused by multiple alleles or introns, which are occasionally foun

74 fication and tracking of cells that have had multiple alleles or loci modified by HR.

75 firmed (through molecular complementation or multiple alleles) or not confirmed.

76 s these methods significantly when there are multiple alleles per species.

77 ozygotes for variants at this locus from the multiple alleles present in Caucasian populations is unc

78 ed allelic or nonallelic combinations due to multiple alleles result in complex gene actions and inte

79 uency-dependent selection acting to maintain multiple alleles, suggesting that conflict may lead to s

80 Within any single population, however, multiple alleles tended to rise and fall synchronously d

81 In human populations, fractions for the multiple alleles that code for recessive deleterious syn

82 combination of oligonucleotide segments from multiple alleles to form unique hypervariable regions (H

83 Multiple alleles were isolated for the four complementat

84 At one of the two loci for which multiple alleles were sequenced, extensive homoplasy for

85 romosomes, and several chromosomes each have multiple alleles with divergent haplotypes.

86 ction of genetic variance in LDL-C is due to multiple alleles with modest effects that are present at