ライフサイエンスコーパス: segregation ratio

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1 lleles that cause sex-specific biases in the segregation ratio.

2 is reflected by the departure from Mendelian segregation ratio.

3 DNA fragment (electrophoretic band) from its segregation ratio.

4 xpression but do not show a simple Mendelian segregation ratio.

5 ait will deviate from the expected Mendelian segregation ratio.

6 rosses, multiple mechanisms act to influence segregation ratios.

7 some molecular markers often show distorted segregation ratios.

8 ii F2 population were surveyed for distorted segregation ratios.

9 In addition, the grand pooled segregation ratio, 127:243:54, deviates significantly fr

10 Unlinked modifiers that alter the segregation ratio are unable to invade such a population

11 that causes sex-specific modification of the segregation ratio at the primary locus.

12 Differences in segregation ratios between males indicate differences be

13 set of polymorphic alleles that show simplex segregation ratios can be used to locate QTLs.

14 a single clone, random spore analysis gave a segregation ratio close to 1:1 for DDP resistance and se

15 yos developed normally and exhibited a 1:2:1 segregation ratio for palmitate accumulation.

16 Segregation ratios for 11 of 14 loci are significantly h

17 Maximum likelihood tests based on distorted segregation ratios for single markers and for interval m

18 ssociated heterosis and distortion of marker segregation ratios, have been widely reported over the p

19 In subsequent generations, the segregation ratio in these families stabilized at approx

20 from massive distortions of zygotic, marker segregation ratios in F(2) families.

21 Segregation ratios in males were best explained by a mix

22 oportion of the markers exhibited unexpected segregation ratios in the light of their configurations

23 massive distortions of microsatellite-marker segregation ratios in two F(2) hybrid families, but we n

24 Markers with distorted segregation ratios occurred in blocks in both linkage ma

25 rn is apparently autosomally dominant with a segregation ratio of 40.1% for kindred members aged 50 y

26 Distorted segregation ratios of genetic markers are often observed

27 Distorted segregation ratios of markers on linkage group (LG) 5 we

28 al crossbreeding experiments, we compare the segregation ratios of microsatellite DNA markers at 6 hr

29 Segregation ratios of the progeny of BC3 plants, when cr

30 r picture was provided by examination of the segregation ratios of two marker genes among the F3 prog

31 For the first time, we track segregation ratios of vQTL-linked markers through the li

32 The segregation ratios of wild-type to mutant phenotypes in

33 Altered segregation ratios on near-isogenic host genotypes diffe

34 ansgenic plants (R1) established a phenotype segregation ratio showing a non-Mendelian inheritance pa

35 The 15:1 F2 segregation ratio suggested that two recessive genes wer

36 some viability loci that cause the observed segregation ratios to deviate from Mendelian expectation

37 us positions and effects were estimated from segregation ratios using a maximum-likelihood interval m

38 linkage map combining markers with different segregation ratios was assembled for this full-sib famil

39 Extreme distortion of marker segregation ratios was observed in populations in which

40 Region(s) with skewed segregation ratios were detected on chromosomes 1D, 3D,

41 Markers with distorted segregation ratios were unique to each population with b

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