ライフサイエンスコーパス: Y-chromosome gene

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1 ncy which leads to an up-regulation of X and Y chromosome genes.

2 has been gained from the sequencing of four Y chromosome genes.

3 Data were analyzed for both detection of the Y chromosome gene and the ratio of the yield of the Y ch

4 istence of functional redundancy between the Y chromosome genes and their homologs encoded on other c

5 anscriptional activities observed from these Y-chromosome genes and 375 additional noncoding RNAs, ch

6 in sexual differentiation and reproduction, Y chromosome genes are rarely described because they res

7 Mutations in Deleted in Azoospermia (DAZ), a Y chromosome gene, are an important cause of human male

8 in sequences or shows a resemblance to known Y chromosome genes, but both show homology to known auto

9 mily contains at least three members: DAZ, a Y-chromosome gene cluster that arose 30-40 million years

10 there has been no perceptible degradation of Y chromosome gene content or activity.

11 in 22 Diptera species, revealing patterns of Y-chromosome gene-content evolution.

12 regulation of this TE family and its use for Y chromosome gene discovery is discussed.

13 The RBMY (RNA-binding motif, Y chromosome) gene family encodes a germ-cell-specific n

14 In particular, Y chromosome gene flow appears to be asymmetric, i.e., f

15 Therefore, Y chromosome gene flow between members of the gambiae co

16 ochondrial DNA gene flow, but high levels of Y chromosome gene flow.

17 e estimates suggested low levels of European Y-chromosome gene flow into Ashkenazi and Roman Jewish c

18 The functional study of Y chromosome genes has been hindered by a lack of mouse

19 cent findings of low sequence variability of Y chromosome genes has led to suggestions that the most

20 uito relative, suggesting rapid evolution of Y chromosome genes in this highly dynamic genus of malar

21 minor histocompatibility antigens encoded by Y-chromosome genes may contribute to a graft-versus-leuk

22 is found in the protein product of DFFRY, a Y chromosome gene not previously identified as the sourc

23 ition might explain the rapid decline in the Y chromosome gene number in chimpanzee.

24 Here, we show that Guy1, a unique Y chromosome gene of a major urban malaria mosquito Anop

25 coding exons and splice sites for 16 gorilla Y chromosome genes of the X-degenerate region.

26 Nepal, it accounts for 50.6% of the Tibetan Y-chromosome gene pool.

27 The resulting males with no Y chromosome genes produced haploid male gametes and sir

28 osome rearrangements over evolutionary time, Y chromosome gene repertoires differ between eutherian l

29 Eif2s3y may be the only Y chromosome gene required to drive mouse spermatogenesi

30 data set of DNA sequence variation at three Y chromosome genes (SMCY, DBY, and DFFRY) in a worldwide

31 The Y chromosome gene Sry encodes a transcription factor req

32 y the presence of a transgene containing the Y chromosome gene Sry This sex-reversal provided clear e

33 etal gonad by the presence or absence of the Y chromosome gene Sry, which controls whether bipotentia

34 against weak alleles of the sex-determining Y-chromosome gene Sry.

35 triggered by the transient expression of the Y-chromosome gene, Sry, which initiates a cascade of gen

36 lopment, even though male (XY) cells express Y-chromosome genes that are not present in female (XX) c

37 identified a ubiquitously transcribed mouse Y chromosome gene, Uty , which encodes a tetratricopepti

38 The dosage of X and Y chromosome genes varies systematically in males and fe

39 as from female XY mice selectively expressed Y chromosome genes, whereas genes known to escape X inac

40 Here we describe a novel mouse Y chromosome gene which we call Uty (ubiquitously transc

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