ライフサイエンスコーパス: pseudoautosomal region

1 nce increases with genetic distance from the pseudoautosomal region.

2 ice because of a 4-Megabase expansion of the pseudoautosomal region.

3 n sex-determining gene DMRT1 and ends at the pseudoautosomal region.

4 x linked, not including those in recombining pseudoautosomal regions.

5 mosome lengths, flanked at either end by two pseudoautosomal regions.

6 G gene, which spans the boundary between the pseudoautosomal region 1 (PAR1) and the X-specific regio

7 x whole genome sequence (WGS), including the pseudoautosomal region 1 (PAR1).

8 avy chain gene IGH@ on 14q32 to CRLF2 in the pseudoautosomal region 1 of Xp22.3/Yp11.3, whereas 10 (3

9 SFR alpha chain, encoded in the X-chromosome pseudoautosomal region 1.

10 The 320-kb human pseudoautosomal region 2 (PAR2) at the tips of the long

11 pseudoautosomal region in distal Xq28 (PAR2; pseudoautosomal region 2), gave a combined maximum LOD s

12 , which is X-linked, human SPRY3 maps to the pseudoautosomal region 2; however, the human Y-linked al

13 We have also refined the pseudoautosomal region and boundary in the cat and show

14 The OA1 gene is located close to the pseudoautosomal region and predicts a novel protein whos

15 ersity among species in their composition of pseudoautosomal regions and degree of Z/W differentiatio

16 lation: SYBL1, a housekeeping gene in the Xq pseudoautosomal region, and GPC3, a tissue-specific gene

17 elative to autosomes, including those in the pseudoautosomal region, and the male-bias increases afte

18 V system) recovering the sex determining and pseudoautosomal regions, and then to the mating-type chr

19 ease/decrease in sharing when markers in the pseudoautosomal region are analyzed.

20 st that all CpG islands on Xq, including the pseudoautosomal region, are subject to X inactivation-in

21 Sequence exchange outside the pseudoautosomal regions could play a role in protecting

22 on the mammalian Y chromosome outside of the pseudoautosomal region do not recombine with those on th

23 human X-linked genes outside the X-Y pairing pseudoautosomal regions escape X-inactivation.

24 We examined the long arm XY pseudoautosomal region for linkage to asthma, serum IgE,

25 Pseudoautosomal regions have been described in a broad t

26 polymorphisms at the distal tip of the Xp/Yp pseudoautosomal region in 47,XYY males, their parents an

27 Marker DXYS154, which is located within the pseudoautosomal region in distal Xq28 (PAR2; pseudoautos

28 however, this gene spans the boundary of the pseudoautosomal region in mouse but not in humans.

29 the distal end of the bivalent acts as a neo-pseudoautosomal region in these males.

30 mice, there is synapsis between the X and Y pseudoautosomal regions; in XSxr(a)O mice, with a single

31 We find that, while PolII in the pseudoautosomal region occupies both chromosomes at simi

32 obligatory exchange occurs in PAR1, an Xp/Yp pseudoautosomal region of 2.6 Mb, which creates a male-s

33 It has been proposed that the pseudoautosomal region of mammals has evolved by sequent

34 One was a 1.6-Mb deletion in the pseudoautosomal region of one maternal X chromosome enco

35 e pairs were preferentially clustered in the pseudoautosomal region of the sex chromosomes and locate

36 ature homeobox-containing gene (SHOX) in the pseudoautosomal region of the sex chromosomes may cause

37 ce for close linkage to three markers in the pseudoautosomal region of the sex chromosomes.

38 red regions, analogous to the nonpairing and pseudoautosomal regions of animal sex chromosomes.

39 However, with this approach, data from the pseudoautosomal regions on the X chromosome pose special

40 Outside the pseudoautosomal regions on the X chromosome, we similarl

41 PCR assays potentially originating from the pseudoautosomal region or other areas of X-Y or autosome

42 nes located in the human and orangutan Xp/Yp pseudoautosomal region (p-PAR), where recombination is o

43 The S. latifolia pseudoautosomal region (PAR) includes several genes extr

44 The pseudoautosomal region (PAR) is a segment of shared homo

45 distal one-third of the long arm, where the pseudoautosomal region (PAR) is located terminally.

46 The pseudoautosomal region (PAR) of mammalian sex chromosome

47 The pseudoautosomal region (PAR) of mammalian sex chromosome

48 le for LWD, SHOX, localizes to the short-arm pseudoautosomal region (PAR) of the X and Y chromosomes.

49 that this molecular marker is located in the pseudoautosomal region (PAR) of the X and Y chromosomes.

50 id sulfatase (Sts) as this is located in the pseudoautosomal region (PAR) of the X-chromosome and con

51 The pseudoautosomal region (PAR) was strongly associated wit

52 Six of 783 non-pseudoautosomal region (PAR) X-chromosome genes (ATRX, C

53 over in a very small region of homology, the pseudoautosomal region (PAR).

54 ion (SDR) and proportionally elevated in the pseudoautosomal region (PAR).

55 mosomes, consistent with localization to the pseudoautosomal region (PAR).

56 cloned and mapped to Xp22.3, proximal to the pseudoautosomal region (PAR).

57 se characteristics are those residing in the pseudoautosomal regions (PAR) of the sex chromosomes.

58 GYG2 is outside the pseudoautosomal region PAR1 but still in a region of X-Y

59 lished linkage to the marker DXYS6814 in the pseudoautosomal region (PAR1) of the X and Y chromosomes

60 s hypothesis by studying the human short-arm pseudoautosomal region (PAR1), which recombines between

61 icated a critical region of <2 Mb within the pseudoautosomal region (PAR1).

62 s pairing and exchange occurs within the two pseudoautosomal regions (PARs) together comprising <5% o

63 at it is still ongoing in the recombining or pseudoautosomal, regions (PARs) of these chromosomes.

64 L1 gene (K=2.7%), located in the human Xq/Yq pseudoautosomal region (q-PAR), where recombination is k

65 t Moa1 is located much farther away from the pseudoautosomal region than its human homolog.

66 ls on the Y chromosome short arm outside the pseudoautosomal region that are homologous to Xq2l.3.

67 Outside the pseudoautosomal regions, the mammalian sex chromosomes a

68 ic map was 118.7 cM (female only) and of the pseudoautosomal region was 13.0 cM (male only).

69 stages from the mating-type locus toward the pseudoautosomal regions was not found, but evidence of s

70 In addition to the genes from the pseudoautosomal region, which have long been anticipated