ライフサイエンスコーパス: Y-chromosome gene

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 Although it is often said that Y-Chromosome genes are lowly expressed outside the testi

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

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

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

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

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

13 Although many studies have focused on Y chromosome gene copy number and variants in fertility,

14 Moreover, we investigate the Y-chromosome genes, DAZ1/DAZ2/DAZ3/DAZ4, of which struct

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

16 Many Y chromosome genes expand in multi-copy families and som

17 enes on PH development, we knocked down each Y-chromosome gene expressed in the lung by means of intr

18 Here, we analyzed quantitative profiles of Y-Chromosome gene expression across 36 human tissues fro

19 Little is known about how human Y-Chromosome gene expression directly contributes to dif

20 testis, we report many instances of elevated Y-Chromosome gene expression in a nonreproductive tissue

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

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

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

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

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

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

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

28 cular and transcriptomic analyses identified Y-chromosome gene histone demethylase KDM5D as a transcr

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

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

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

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

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

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

35 Methods: To test the effect of Y-chromosome genes on PH development, we knocked down ea

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

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

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

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

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

41 The Y chromosome gene Sry encodes a transcription factor req

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

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

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

45 We previously showed that the Y-chromosome gene, SRY, directly regulates adult brain f

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

47 X chromosome inactivation or the presence of Y chromosome genes that are absent from XX cells.

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

49 surements and Main Results: Knockdown of the Y-chromosome gene Uty resulted in more severe PH measure

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

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

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

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