ライフサイエンスコーパス: segregation distortion

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

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

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

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

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

6 l RNA content, chromosomal rearrangement and segregation distortion.

7 hellia in their regulation of sex chromosome segregation distortion.

8 (46.5:53.5%), which does not support meiotic segregation distortion.

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

10 somatic and early embryonic instability and segregation distortion.

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

12 inkage group 3 which resulted in significant segregation distortions.

13 one family were demonstrated, with potential segregation distortions.

14 a previous generation as to parents showing segregation distortions.

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

16 Segregation distortion, a common feature of most populat

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

18 How segregation distortion among markers arises and its impa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

35 Segregation distortion has been reported to occur in a n

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

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

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

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

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

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

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

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

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

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

46 Segregation distortion involves three loci on the Bogota

47 Segregation distortion is a phenomenon that has been obs

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

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

50 Segregation distortion is detrimental to the power of de

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

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

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

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

55 A segregation distortion loci mapping strategy, based on a

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

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

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

59 Segregation distortion occurred in 49% of the mapped pro

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

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

62 Segregation distortion of markers can be considered to a

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

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

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

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

67 Based on segregation distortion, transmission studies, a microsco

68 Segregation distortion was detected for many markers, so

69 Segregation distortion was detected in a large region on

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

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

72 Segregation distortion was observed for 25% of the marke

73 Segregation distortion was significant in ahFAD2A in one

74 Severe segregation distortions were observed for both the ferti

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

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

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

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