ライフサイエンスコーパス: segregation distortion

1 ve strongly biased transmission (i.e. strong segregation distortion).

2 rmful side-effects of the mechanisms causing segregation distortion.

3 well as wild-type pollen, leading to severe segregation distortion.

4 ic case of incipient speciation is caused by segregation distortion.

5 six markers showed no significant (P < 0.05) segregation distortion.

6 in regions in which there are high levels of segregation distortion.

7 essors, resulting in suppressed or "cryptic" segregation distortion.

8 hellia in their regulation of sex chromosome segregation distortion.

9 (46.5:53.5%), which does not support meiotic segregation distortion.

10 o analyze the effect of sex and cytoplasm on segregation distortion.

11 somatic and early embryonic instability and segregation distortion.

12 egation data, we find no evidence of meiotic segregation distortion.

13 l RNA content, chromosomal rearrangement and segregation distortion.

14 of QTLs were unlinked to reduced fitness or segregation distortion.

15 inkage group 3 which resulted in significant segregation distortions.

16 one family were demonstrated, with potential segregation distortions.

17 a previous generation as to parents showing segregation distortions.

18 rs, 101 were not used because of significant segregation distortion, 29 were unlinked, and 59 were el

19 Segregation distortion, a common feature of most populat

20 ed them to form an F2 population, quantified segregation distortion along the genome, measured 22 phe

21 Nearly 45% of the loci exhibited significant segregation distortion (alpha = 0.05).

22 How segregation distortion among markers arises and its impa

23 We genetically analyze this normally cryptic segregation distortion and show that it involves several

24 I develop a theory of segregation distortion and show that the presence of onl

25 pollen is defective in vivo, as evidenced by segregation distortion, and also has low rates of germin

26 The progenies showed poor seed set and segregation distortion, and we were unable to recover ho

27 The genetic bases of hybrid sterility and segregation distortion are at least partially--but not c

28 SPERMSEG program also showed no support for segregation distortion at the gamete level in this patie

29 This suggests that any greater amount of segregation distortion at the myotonic dystrophy locus m

30 tecture underlying hybrid male sterility and segregation distortion between the Bogota and USA subspe

31 uare test was used to determine if a meiotic segregation distortion bias existed.

32 s were genotyped at 23 loci, and significant segregation distortion (biased against C. briggsae) was

33 Here, we evaluate the role of piRNAs in segregation distortion by testing the effects of mutatio

34 mework maps were informative with respect to segregation distortion, chromosome fusion, rearrangement

35 tribution was sufficiently uniform, although segregation distortion could induce translocated marker

36 The high degree of segregation distortion detected in this intraspecific ma

37 These results prove that segregation distortion does not depend on any unique pro

38 There is no evidence of segregation distortion during male meiosis.

39 Two genomic regions showed strong segregation distortion favoring A. sagittata alleles in

40 s in plant breeding applications, to analyze segregation distortion for S and Z genes, as well as lin

41 Segregation distortion has been reported to occur in a n

42 Three regions of segregation distortion identified on chromosome 5D were

43 y declines with apomixis, and increases with segregation distortion if this occurs equally and indepe

44 sue-imposed dormancy gene contributes to the segregation distortion in a mapping population developed

45 ding populations via the detection of marker segregation distortion in either a single population or

46 t not sufficient for both male sterility and segregation distortion in F(1) hybrids between these sub

47 e, Overdrive, causes both male sterility and segregation distortion in F1 hybrids between the Bogota

48 ratio distortion is caused by sex chromosome segregation distortion in hybrid males.

49 e age has been found to affect the degree of segregation distortion in some Drosophila, we tested fli

50 Likelihood-based analysis of segregation distortion in the single sperm data using th

51 The pattern of segregation distortion, in favor of homozygotes on chrom

52 Segregation distortion involves three loci on the Bogota

53 Segregation distortion is a phenomenon that has been obs

54 Indeed the severity of segregation distortion is correlated with the severity o

55 A similar level of segregation distortion is detected in both maps.

56 Segregation distortion is detrimental to the power of de

57 We further show that segregation distortion is normally masked within the Bog

58 lysis shows that the genetic basis of hybrid segregation distortion is similar to that of hybrid male

59 e. construction of linkage groups in case of segregation distortion; (iv) data imputation on VCF file

60 n of markers can be considered to arise from segregation distortion loci (SDL).

61 A segregation distortion loci mapping strategy, based on a

62 an fitness at a polymorphic equilibrium with segregation distortion may be higher than mean fitness a

63 ponse to population size, allelic dominance, segregation distortion, missing data and random typing e

64 llelic inheritance, the null allele, allelic segregation distortion, mixed bivalent and quadrivalent

65 Segregation distortion occurred in 49% of the mapped pro

66 When segregation distortion of a locus is a random event, the

67 ent a maximum-likelihood model for examining segregation distortion of CTG-repeat alleles in normal f

68 Segregation distortion of markers can be considered to a

69 The observations that two segregation distortion regions overlap with maize flower

70 xpression modifiers, polyploidy, aneuploidy, segregation distortion, suppressed recombination, etc.,

71 mission is breached by allowing sex-specific segregation distortion, symmetry of expression is breach

72 genetic screen based on reduced seed set and segregation distortion to identify mutations affecting m

73 Based on segregation distortion, transmission studies, a microsco

74 Segregation distortion was detected for many markers, so

75 Segregation distortion was detected in a large region on

76 A specific chromosome associated with segregation distortion was detected in the female (GG) g

77 ost markers exhibited Mendelian inheritance, segregation distortion was observed for 25 predominantly

78 Segregation distortion was observed for 25% of the marke

79 Segregation distortion was significant in ahFAD2A in one

80 Severe segregation distortions were observed for both the ferti

81 we show that even wild-type RanGAP can cause segregation distortion when it is overexpressed in the m

82 t little two-locus linkage disequilibrium or segregation distortion, which indicated a limited role f

83 l models developed make it possible to study segregation distortion with high resolution by using spe

84 are shared genetic patterns of non-Mendelian segregation distortion within and among Mimulus species.