ライフサイエンスコーパス: recessive gene

1 second gene modified the effect of the first recessive gene.

2 Each segregates as a single recessive gene.

3 is inherited as a fully penetrant autosomal recessive gene.

4 st dramatic (a 28-fold reduction) for a rare recessive gene.

5 d at least 1 in 5 pregnant women carries one recessive gene.

6 interactions involved additive, dominant, or recessive genes.

7 nate between mutations in known dominant and recessive genes.

8 AKUT may be caused partially by mutations in recessive genes.

9 ns of large homozygous effects and partially recessive gene action.

10 Through a forward genetic screen in mice for recessive genes affecting motor neurons, we identified t

11 ontribution to OA, with evidence for a major recessive gene and a multifactorial component, represent

12 Corn1 behaves as an autosomal recessive gene and is located on mouse chromosome 2, app

13 A mixed recessive model (i.e., major recessive gene and residual genetic effect) was the best

14 riction was likely due to the interaction of recessive genes at two nonlinked loci.

15 Lebanese population is ideal for uncovering recessive genes because of shared ancestry and a high ra

16 s cause a Lewy body disease spectrum whereas recessive genes cause a milder parkinsonism with variabl

17 , we provide evidence that a third autosomal recessive gene causes the degeneration in CCDKO mice and

18 lly promotes the preferential spread of rare recessive genes, compared with the expectations of tradi

19 An autosomal recessive gene conferred extremely high resistance to fo

20 uilibrium in the candidate region for xa5, a recessive gene conferring race-specific resistance to ba

21 enetic analyses indicated a single autosomal recessive gene controlled the dermatitis susceptibility

22 point mutation in murine nramp, an autosomal recessive gene controlling resistance to intracellular o

23 We have shown that recessive (gene deletion) or dominant (connexin45 overex

24 iants detected in only 6 different autosomal recessive genes explained 50% of the cases characterized

25 ummary, we present CHKA as a novel autosomal recessive gene for a neurodevelopmental disorder with ep

26 thor describes an asthma study of two common recessive genes for which 270 matched case-control pairs

27 n hypothesized that, in addition to X-linked recessive genes, Haldane's rule also reflects the faster

28 Two recessive genes have been identified that yield a nonhyp

29 TNNI3 is the first recessive gene identified for this condition, and we sug

30 leaf sectors due to the action of a nuclear recessive gene, IMMUTANS (IM).

31 ite sectoring due to the action of a nuclear recessive gene, IMMUTANS.

32 rosophila and for discerning the function of recessive genes in a heterozygous individual.

33 provides a rapid means of mapping autosomal recessive genes in consanguineous families by identifyin

34 encing model is advantageous for fixation of recessive genes in diploid organisms, especially with la

35 , compared with those altering phenotypes of recessive genes in normal diploid cells of about 10(-12)

36 e same genetic basis in each line - a single recessive gene located in a 1.1-Mb region on chromosome

37 owever, extensive simulations suggested that recessive genes may be detectable in aggregate.

38 These observations are reminiscent of other recessive gene mutations that produce an effective loss

39 d is often the causative factor in revealing recessive gene mutations that progress cells along the p

40 Recessive gene mutations underlie many developmental dis

41 ritance of a pair of alleles of an autosomal recessive gene on chromosome 13 is necessary and suffici

42 s with a single P/LP variant in an autosomal recessive gene or females with an X-linked recessive P/L

43 In contrast, mutations in several recessive genes (parkin, DJ-1, and PINK1) produce neuron

44 ted the resistance is controlled by a single recessive gene, recessive TuMV resistance 03 (retr03), a

45 ever, we have not yet fully resolved how the recessive genes relate to alpha-synuclein, or whether th

46 bks1-2), inherited in Mendelian fashion as a recessive gene residing on chromosome 11.

47 ymmetrical spastic cerebral palsy, to locate recessive genes responsible for this condition.

48 ce initial description in 1991, no causative recessive gene(s) have been described.

49 Whereas FAS(lpr) functions as a recessive gene, Sle1 exhibits a gene dosage effect.

50 ins, which differ only by a single autosomal recessive gene, the lpr mutation.

51 ROSA22 male mice are sterile due to a recessive gene-trap mutation that affects development of

52 etrovirus resistance is governed by a single recessive gene, virus infectivity controller 1 (vic1), m

53 given the confirmation that a high-frequency recessive gene was the best-fitting genetic model of fam

54 15:1 F2 segregation ratio suggested that two recessive genes were involved, and map-based cloning ide

55 this putative SLE gene in this region was a recessive gene with a population frequency of 5% and wit

56 el from the segregation analysis was a major recessive gene with a significant residual polygenic bac

57 which were determined to be the most common recessive genes with coding sequences not deliverable in