ライフサイエンスコーパス: semidominant

1 onstrating that the mutant alleles are truly semidominant.

2 notypes, suggesting that these mutations are semidominant.

3 ing both B-boxes is deleted, are shown to be semidominant.

4 All alleles are semidominant.

5 s are dominant to wild type whereas sfaA1 is semidominant.

6 t the expression of mutations in GJB2 may be semidominant.

7 The semidominant allele has a charge change (E29K) in the ba

8 A semidominant allele of the gene that codes for CeTwist,

9 ku258 was isolated as a semidominant allele that suppresses the Multivulva pheno

10 , screens for dominant enhancer mutations of semidominant alleles of a given gene have proved far mor

11 ulate both when heterozygous; that is, it is semidominant and acts to stimulate DSBs in trans.

12 The mutant allele isolated, ZAP1-1up, is semidominant and caused high-level expression of ZRT1 an

13 terized mutation in this gene, Trp(P365), is semidominant and causes massive degeneration of photorec

14 ivalent mutation in yeast is hypomorphic and semidominant and enhanced the formation of gross chromos

15 The mutation is semidominant and is associated with small, irregularly s

16 The k10(C3H) allele is semidominant and is associated with the penetrance and e

17 The mutation was semidominant and resulted in pleiotropic phenotypes with

18 restingly, the aha4-1 mutation appears to be semidominant and was only partially complemented by the

19 he alr mutants showed that Al resistance was semidominant, and chromosome mapping of the mutants with

20 The hyperdeletion phenotype of dnaB107 was semidominant, and in dnaB107/dnaB+ heterozygotes recB wa

21 Additional dominant, semidominant, and recessive Sad-1 alleles have been gene

22 The lut2 mutations are semidominant, and their biochemical phenotype is consist

23 In this article, we show that Sos1 is a semidominant, antimorph mutation.

24 The tau mutation is a semidominant autosomal allele that dramatically shortens

25 phenotype and altered auxin responses of the semidominant axr3-1 mutant of Arabidopsis result from a

26 The semidominant bal allele maps to the RPP5 (recognition of

27 mutations that were originally identified in semidominant barley (Hordeum vulgare L.) mutants.

28 We discovered that inaC(P209) was semidominant, because inaC(P209) heterozygotes displayed

29 lls defective in mitotic exit, including the semidominant cdc5-ad mutation.

30 This plant carries a semidominant, conditional lethal mutation that confers c

31 The tps1-H223Y allele (glc6-1) that causes a semidominant decrease in glycogen accumulation exhibits

32 hat, in telomerase-positive cells, confers a semidominant decrease in telomere size and a recessive d

33 n, all three mutations are suppressed by the semidominant dilute-suppressor (dsu), providing genetic

34 than the wild-type parent enzyme; and (iii) semidominant drug resistance in spheroplast fusion strai

35 ATR homolog, and the use of it to document a semidominant effect on a larval mitotic checkpoint and m

36 tudies revealed that Kitl(Sl) mutations have semidominant effects; mild pigmentation defects and macr

37 ave identified two temperature-sensitive and semidominant embryonic-lethal Caenorhabditis elegans mut

38 The semidominant Extra cell layers1 (Xcl1) mutation in maize

39 rity of the nmd phenotype is attenuated in a semidominant fashion by a major genetic locus on chromos

40 J GUA initiation codon mutants and acts in a semidominant fashion.

41 end of chromosome 2 and appears to act in a semidominant fashion.

42 contribute to their multigenic control in a semidominant fashion.

43 cylic acid (SA) insensitivity, we isolated a semidominant gain-of-function mutation, designated ssi4,

44 sive, loss-of-function mutations and a novel semidominant, gain-of-function allele [hot1-4 (A499T)].

45 We isolated a semidominant, gain-of-function mutant, designated pdr9-1

46 ce bearing deletions presumably spanning the semidominant hammertoe locus (Hm) had no phenotype, sugg

47 These mutations are semidominant: heterozygotes have an intermediate phenoty

48 In addition, these mutations are semidominant; heterozygotes show a very mild phenotype w

49 Mutations within this locus are semidominant lethals of variable penetrance that result

50 The semidominant Liguleless3-O (Lg3-O) mutation disrupts lea

51 lesion incidence and macrocyst latency in a semidominant manner, and that suppression of lesion deve

52 By contrast, the semidominant MED5b mutation reduced epidermal fluorescen

53 This location is surprising since other semidominant mi mutations characterized to date have bee

54 otypic and molecular characterization of the semidominant Microphthalmia(brwnish) (Mi(b)) mutation.

55 Mom1 is a semidominant modifier of polyp size and multiplicity in

56 The semidominant mouse mutant dactylaplasia (Dac) disrupts t

57 The classical semidominant mouse mutant varitint-waddler (Va) exhibits

58 Here we show that the semidominant mouse mutation Nan ("neonatal anemia") carr

59 Belly spot and tail (Bst) is a semidominant mouse mutation that disrupts pigmentation,

60 Lurcher (Lc) is a spontaneous, semidominant mouse neurological mutation.

61 One semidominant MSH2 mutation was identified.

62 Small-eye (Sey) is a spontaneous, semidominant murine mutation that results from a point m

63 n the ethylene receptor ERS, whereas wei5, a semidominant mutant, was caused by a mutation in the EIN

64 A semidominant mutation at the GIBBERELLIN INSENSITIVE (GA

65 escue interactions during development with a semidominant mutation at the Vangl2 locus.

66 The autosomal semidominant mutation Bst (belly spot and tail) is often

67 Clock is a semidominant mutation identified from an N-ethyl-N-nitro

68 Hypodactyly (Hd) is a semidominant mutation in mice that maps in a genetic int

69 Danforth's short tail (Sd) is a semidominant mutation in mouse affecting the axial skele

70 BR-insensitive dwarf phenotype was due to a semidominant mutation in the BIN2 gene that mapped to th

71 e show that vascular defects are caused by a semidominant mutation in the procollagen type IV alpha 1

72 The semidominant mutation Liguleless3-O (Lg3-O) causes a bla

73 ze Barren inflorescence1 (Bif1), a classical semidominant mutation of maize.

74 lem7 is a semidominant mutation that maps to a novel locus on chro

75 Danforth's short-tail (Sd) mouse is a semidominant mutation that prevents completion of notoch

76 Lens opacity 12 (Lop12) is a semidominant mutation that results in an irregular nucle

77 ation TPE1-1 as a new allele of PDR1 and the semidominant mutation tpe2-1 as a new allele of PDR3.

78 The mouse Ulnaless locus is a semidominant mutation which displays defects in patterni

79 activity and sleep patterns, we identified a semidominant mutation, called earlybird, that shortens t

80 The Belly spot and tail (Bst) semidominant mutation, mapped to mouse Chromosome 16, le

81 ngs suggest that P325L is a gain-of-function semidominant mutation, which led to either hyper- or neo

82 rological mutant lurcher (Lc) results from a semidominant mutation.

83 n the mouse is inherited as an autosomal and semidominant mutation.

84 Semidominant mutations at the IXR1 and IXR2 loci of Arab

85 Previously described semidominant mutations in two other Arabidopsis IAA gene

86 Semidominant mutations shy2-1D, shy2-2, axr3-1, and axr2

87 s slightly sensitive to hydroxyurea and is a semidominant mutator for spontaneous base substitutions

88 the gamma- or delta-subunit of the ATPase is semidominant negative due to a decrease in the gene numb

89 encoding gamma or delta, suggesting that the semidominant negative effect is because of a gain of act

90 alleles generated in this study conferred a semidominant negative phenotype but only when Spo11p act

91 A semidominant Neurospora mutant, Sad-1, fails to perform

92 y determine whether a particular mutation is semidominant or dominant.

93 eletion size: (1) null hy4 alleles that were semidominant over wild type and contained small or moder

94 The semidominant pdr9-1 mutation affects an extremely highly

95 +) are haploid for Pax2 and have a variable, semidominant phenotype characterized by structural defec

96 n the fra5 (fragile fiber 5) mutant causes a semidominant phenotype in the reduction of fiber cell wa

97 The semidominant phenotype of this mutant can be recapitulat

98 idue near the outer mouth of the pore, has a semidominant phenotype, suggesting that the mutant seizu

99 deletion of the psbS gene, yet it exhibits a semidominant phenotype.

100 Loss of miRNA regulation in semidominant phv1 mutants misdirects lateral growth of l

101 We mapped rQTL1 to semidominant polymorphisms in HEI10, which encodes a con

102 The GA-insensitive, semidominant, semidwarf gai-1 mutant encodes a mutant pr

103 Arabidopsis thaliana semidominant shy2 (short hypocotyl) mutations cause leaf

104 The semidominant shy3-1 mutation changes an amino acid in KT

105 tic cell death in the stroma, resulting in a semidominant spleen regression.

106 ll allele e155 terminates after nine codons; semidominant su142sd eliminates the inhibitory and C-ter

107 s the inhibitory and C-terminal regions; and semidominant su195sd abbreviates the extreme C-terminus.

108 We identified bes1, a semidominant suppressor of bri1, which exhibits constitu

109 nt suppressor is in CBP1, while the other 10 semidominant suppressors define five distinct linkage gr

110 proline-233-Leu mutation were identified as semidominant suppressors of two different bri1 mutations

111 osophila sodium channel gene, para, causes a semidominant temperature-induced seizure phenotype.

112 of glycines in the Gly-X-Y domain and cause semidominant, temperature-sensitive lethality at the two

113 The cn+ gene functioned as a semidominant transgene and segregated in Mendelian ratio

114 irulent virus strains, and (iii) dominant or semidominant transmission of resistance in crosses with

115 The semidominant Va mutation results in an alanine-to-prolin

116 , whereas loss of Dact1 reciprocally rescued semidominant Vangl2 phenotypes.

117 f(Sl) allele (a 3-5-cM deletion) confirm the semidominant white forelock feature of the k10(C3H) alle

118 PX; MIM 303400) is inherited as a Mendelian, semidominant X-linked disorder and has been described in

119 oglossia (CPX; MIM 303400) is inherited as a semidominant X-linked disorder previously described in s

120 Patchy fur is a semidominant X-linked mutation in the mouse, resulting i