ライフサイエンスコーパス: hemizygote

1 log is present than when it is absent (i.e., hemizygote).

2 could explain the occurrence of seizures in hemizygotes.

3 and causes delayed eyelid closure in Map3k1 hemizygotes.

4 uction are associated with mortality in male hemizygote Acta1 H40Y mice.

5 In G hemizygotes, ADHD symptoms are associated with increased

6 rebral hemorrhage was found in 4 patients (3 hemizygotes and 1 heterozygote).

7 ily testing led to the identification of 594 hemizygotes and 1,270 heterozygotes.

8 ar circulation was symptomatic in 67% of the hemizygotes and 60% of the heterozygotes.

9 than cone dysfunction, and the end stage in hemizygotes and heterozygotes is that of typical RP, wit

10 Hemizygotes and heterozygotes were evaluated clinically

11 erebrovascular manifestations of FD, in both hemizygotes and heterozygotes, are predominantly due to

12 ce form of Dab1 (p45) found that Dab1(p45/-) hemizygote, but not Dab1(p45/p45) and Dab1 heterozygote

13 knockout mutants compared with wild type and hemizygote controls, whereas the number of granule cells

14 erence, we demonstrated that homozygotes and hemizygotes could be differentiated unambiguously when m

15 dies of prometaphase and metaphase I in mtrm hemizygotes demonstrate that achiasmate chromosomes are

16 s develop as females whereas homozygotes and hemizygotes develop as diploid and haploid males, respec

17 wapl(AG) hemizygotes die as pharate adults and have an extra sex

18 escent zebrafish in which a homozygote and a hemizygote differ by only twofold.

19 Interestingly, Mekk1-Jnk1-Jnk2 triple hemizygotes display a partial eye-open phenotype at birt

20 If the two reciprocal hemizygotes display different phenotypes, then the two p

21 e have also generated mice that are compound hemizygotes for the transgenes SYN-LEPR-B and neuron-spe

22 of alcohol-related pancreatitis in men (male hemizygote frequency is 0.26, whereas female homozygote

23 Hemizygotes from the RP24 family have early onset of rod

24 ber of X-linked adrenoleukodystrophy (X-ALD) hemizygotes from the United States identified each year

25 ubcutaneous osmotic pumps for 6 days in male hemizygote G6PD mutant (G6PD(mut)) and wild-type (WT) C3

26 pain, hemiataxia, and ataxia of gait, in the hemizygote group; and memory loss, dizziness, ataxia, he

27 lly disappears at 4 to 6 weeks, whereas male hemizygotes have severe, generalized tremor that persist

28 The minimum frequency of hemizygotes identified in the United States is estimated

29 A hemizygote in the third decade of life had barely measur

30 The phenotype of these hemizygotes is characterized by no apparent neurological

31 In ry506 (null allele) homozygotes or hemizygotes, JH III or pyriproxifen (a JHM) had little e

32 In A hemizygotes of the expression single nucleotide polymorp

33 own), was insufficient to cause lethality in hemizygotes or mottling of the coat in heterozygotes, bu

34 For male hemizygotes (P = 0.07) compared to male noncarriers, the

35 ates is estimated to be 1:42,000 and that of hemizygotes plus heterozygotes 1:16,800.

36 capillary flow heterogeneity in asymptomatic hemizygotes predominantly in the white matter regions an

37 Transgenic A-line mice were obligate hemizygotes, since homozygous expression resulted in dev

38 nic interactions; approximately 4800 complex hemizygote strains were constructed between an actin-nul

39 '-mah/pl heterozygotes, but not from Pl'-mah hemizygotes, suggesting that fixation of the high-expres

40 HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicat

41 For the hemizygotes, the recurrence rate for cerebrovascular dis

42 , we assessed the susceptibility of Ikkalpha hemizygotes to chemical carcinogen-induced skin carcinog

43 Two hundred fifty of the newly identified hemizygotes were asymptomatic and represent the group in

44 Only 5% of male probands and 1.7% of X-ALD hemizygotes were found to have new mutations.

45 tern, as all the affected family members are hemizygotes, whereas healthy family members are either h

46 All X-ALD hemizygotes who had not previously received Lorenzo's oi

47 CHM hemizygotes with REP-1 mutations, spanning an age range

48 acid (C22:0), were measured in 1,097 males (hemizygotes) with X-ALD, 1,282 women heterozygous for th