ライフサイエンスコーパス: diploidy

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1 samples is challenging because of chromosome diploidy.

2 followed by massive gene loss that restored diploidy.

3 n is not followed by nuclear fusion and true diploidy.

4 l hypotheses on the functional importance of diploidy.

5 e-nucleotide polymorphisms while maintaining diploidy.

6 ex; disomies X, Y, or 21; or meiosis I or II diploidies.

7 inomas begin as tetraploid then descend into diploidy accompanied by genome-wide LOH.

8 ely 5-fold increases in sperm with disomies, diploidies and complex genotypes involving chromosome X,

9 Thus, diploidy and alternative splicing each increased toleran

10 an insect with social behavior and/or haplo-diploidy and are an indication of the unique nature of t

11 males in an age-structured population under diploidy and autosomal inheritance, the total reproducti

12 XY, disomy X, disomy Y, disomy 21, and sperm diploidy, and (b) examine the association between the fr

13 e, imprinted genes discard the advantages of diploidy, and for this reason the rationale for the evol

14 h as inbreeding depression, the evolution of diploidy, and levels of natural genetic variation.

15 positively correlated with low tumor grade, diploidy, and low S-phase fraction, all biological param

16 ercondensation, chromosome breakage, loss of diploidy, and premature sister chromatid separation.

17 crops due to its short seed-to-fruit cycle, diploidy, and sequenced genome.

18 Given that high-frequency MSI (MSI-H) and diploidy are correlated, we determined whether they are

19 ich the bacterium Bacillus subtilis enforces diploidy as it differentiates into a dormant spore.

20 S after adjustment for MYCN amplification or diploidy but had no significant effect on OS.

21 a model in which induction of SirA enforces diploidy by inhibiting replication initiation as B. subt

22 moting S phase and M phase, while preserving diploidy by suppressing endoreduplication.

23 ase in proliferating cells, while preserving diploidy by suppressing endoreduplication.

24 [DI] > 1) was clearly superior to those with diploidy (DI < or = 1): younger than 12 months, 83.7% +/

25 sperm with immature chromatin, aneuploidies/diploidies, FGFR2 mutations (Apert syndrome), or sex rat

26 es, and no general evolutionary advantage of diploidy has been demonstrated.

27 Cells deviating from diploidy have the ability to communicate with their micr

28 essary to promote proliferation and maintain diploidy in breast cancer cells.

29 It also demonstrates that the effects of diploidy in gene networks can have counter-intuitive con

30 to evolve: selection is more likely to favor diploidy in host species and haploidy in parasite specie

31 Diploidy is a fundamental genetic feature in mammals, in

32 By doubling the copy number of each gene, diploidy may increase the rate at which adaptive mutatio

33 nostic biologic findings included tumor-cell diploidy (n = 2) and unfavorable Shimada histopathology

34 or arbitrary modes of inheritance, including diploidy, polyploidy, sex linkage, cytoplasmic inheritan

35 As predicted, diploidy slowed adaptation by large populations but not

36 Little is known about the transition from diploidy to polyploidy but in some species, triploids ar

37 are predominantly diploid, the prominence of diploidy varies greatly among eukaryote life cycles, and

38 Diploidy was associated with better survival in MSI-H an

39 able (MSS)/low-frequency MSI (MSI-L) tumors, diploidy was associated with better survival.

40 lear genome was destroyed by irradiation and diploidy was restored by blocking the first embryonic cl

41 usion of two meiotic products to restore egg diploidy), whereas workers of other honeybee subspecies

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