ライフサイエンスコーパス: genetic cross

1 within the last 10,000 years after a single genetic cross.

2 ferential methylation between the parents of genetic crosses.

3 oduced this locus into the Col background by genetic crosses.

4 s within tumors generated from numerous fish genetic crosses.

5 s retained in all transformants through both genetic crosses.

6 inkage analysis using two sets of multilocus genetic crosses.

7 d establishing stable mutant strains through genetic crosses.

8 ination of an endonuclease in the progeny of genetic crosses.

9 egregate with a defect in phototropism after genetic crosses.

10 segregated with methylammonium resistance in genetic crosses.

11 produce hybrids that develop melanomas after genetic crossing.

12 ppeared spontaneously in 1986 during routine genetic crosses [1,2].

13 In genetic crosses, a heterozygous Shp-2 mutation dominantl

14 In genetic crosses, allelic variation at Mc1r explains 9.8%

15 ents for large and complex multigenerational genetic crosses among sexually reproducing diploid speci

16 Here we use genetic crosses and comparative genomics to identify spe

17 Using genetic crosses and genome-wide association mapping, we

18 imentally in complementation tests and other genetic crosses and it maps the mutated gene to a define

19 protocols for collecting pollen and outlines genetic crosses and phenotypic assays that are useful fo

20 olymorphic in the zebrafish strains used for genetic crosses and provide a means to compare genetic s

21 Genetic crosses and recombination tests revealed that al

22 Based on combination of genetic crosses and RNA-Seq data, we have designed a hig

23 Genetic crosses and segregation analyses revealed that a

24 s to acquire donor source and time-consuming genetic crossing and has already been used to identify a

25 R loci in a drug-selected line, progeny of a genetic cross, and 334 field isolates demonstrates broad

26 ng the offspring from a P. yoelii YM and N67 genetic cross, and identify a putative HECT E3 ubiquitin

27 , and ethical considerations regarding human genetic crosses are but some of the reasons to study air

28 Even with vegetative propagated crops, genetic crosses are conducted during varietal improvemen

29 ly, plastids and mitochondria, in a standard genetic cross, are transmitted to the seed progeny by th

30 psis allotetraploid lines were produced by a genetic cross between A. thaliana and A. arenosa autotet

31 Now, a genetic cross between AS-ART and the artemisinin-sensiti

32 Examination of 19 progeny from a genetic cross between HB3 and 3D7A revealed complex inhe

33 When females from an extensive genetic cross between R and susceptible A. gambiae (G3)

34 enes that influence VWF level, we analyzed a genetic cross between RIIIS/J and CASA/Rk, two strains o

35 ele of SHM1, shm1-2, and the F1 progeny of a genetic cross between shm1-1 and shm1-2 displayed the sa

36 high-level resistance in the 16 progeny of a genetic cross between sulfadoxine-sensitive (HB3) and su

37 Furthermore, a genetic cross between Tg-WT and transgenic mice with car

38 In this study, we have used a genetic cross between the strains HB3 and 3D7 to study i

39 s a highly significant lod score of 6.7 in a genetic cross between the susceptible strain, C57BL/6J,

40 erately virulent type II based on successful genetic cross between these lineages.

41 g germline influence on gene expression in a genetic cross between two divergent mouse species and in

42 Using genetic crosses between BALB/cJ and C3H/HeN mice, we wer

43 Genetic crosses between cavefish and surface fish reveal

44 opical population, confirmed by fully viable genetic crosses between continents, extensive intralocus

45 Genetic crosses between DDT resistant and susceptible Ac

46 Forward genetic analysis of genetic crosses between different lineages has been used

47 xperimental organisms are applicable only to genetic crosses between inbred lines.

48 s have dominated the statistical analysis of genetic crosses between inbred strains.

49 Here, we compare findings from two large genetic crosses between mouse strains C3H/HeJ and C57BL/

50 the parasite in the snail host, we performed genetic crosses between parasite-resistant and -suscepti

51 oneal fat Ucp1 mRNA expression in progeny of genetic crosses between the A/J and C57BL/6J parental st

52 Using genetic crosses between the carcinoma-resistant Copenhag

53 Genetic crosses between the two species reveal that the

54 ction in natural populations, we carried out genetic crosses between threespine stickleback fish with

55 Here we use genetic crosses between type II and III lines to show th

56 Here, using genetic crosses between type II and type III Toxoplasma

57 notype: retention of Chi hotspot activity in genetic crosses but loss of detectable nucleolytic degra

58 We have used genetic crosses, cell culture assays and Tsk-specific an

59 Genetic cross data suggest that DNA secondary structures

60 two common morphological trait syndromes in genetic crosses demonstrated that the phenotypes are cau

61 Genetic crosses established the gene order to be cobB pe

62 The findings of classical genetic crossing experiments, together with data from se

63 variation, we have searched a P. falciparum genetic cross for quantitative trait loci (QTL).

64 red fluorescent trypanosomes for visualizing genetic crosses has now identified this stage.

65 Quantitative trait locus (QTL) analysis of genetic crosses has proven to be a useful tool for ident

66 Use of these partial t haplotypes in genetic crosses has resulted in the general location of

67 Genome-wide scans of different genetic crosses have been used to map several disease-li

68 Genetic crosses have shown that apolipoprotein E and TGF

69 on fragment length polymorphism markers in a genetic cross (HB3xDd2).

70 genome either by cotransformation or through genetic crossing, hereby signifying an intein-mediated p

71 In interspecies genetic crosses, however, recipients with the mutSDelta8

72 rove the scalability and throughput of major genetic crosses in ends-out gene targeting.

73 Here we use genetic crosses in sticklebacks to investigate the paral

74 The results of genetic crosses indicate that suppression of TBP mutants

75 Genetic crosses indicated that 12 had lesions in a singl

76 for T. gondii genetic manipulation including genetic crosses, insertional mutagenesis, chemical mutag

77 When introduced by genetic crosses into plants carrying a silencing transge

78 elop statistical methods for QTL mapping for genetic crosses involving noninbred lines.

79 on that interacts epistatically with QTLs in genetic crosses is a unique and potentially powerful met

80 Analysis of two multilocus genetic crosses localized Pak1 and Pak3 to a position on

81 ucing the transposase gene through classical genetic crossing, making this system functional for targ

82 growth inhibition phenotype in the Dd2 x HB3 genetic cross mapped the clag3 genomic locus, consistent

83 resistance (CQR) in a Plasmodium falciparum genetic cross maps to a 36 kb segment of chromosome 7.

84 e of this compound's affinity in a Dd2 x HB3 genetic cross maps to a single parasite locus on chromos

85 ne cosegregates with the MATa mating type in genetic crosses, maps within the mating-type locus on a

86 A genetic cross-modal correlation was seen between the ven

87 Using a genetic cross of clonal lines derived from migratory and

88 To address this challenge, we established genetic cross of dioecious plant Rumex acetosa and gener

89 he present study indicates that performing a genetic cross of these strains and total genome scan sho

90 type plants was observed in the progeny of a genetic cross of these two transformants in which both i

91 claim, based solely upon extrapolation from genetic crosses of D. santomea and D. melanogaster, a mu

92 n be generated rapidly, as can data from the genetic crosses of gene-deficient mice on autoimmune-sus

93 Genetic crosses of laboratory mice have provided extensi

94 Immunohistochemistry and genetic crosses of P2rx4 tdTomato mice with cell-specifi

95 Genetic crosses of phenotypically distinct strains of th

96 Studies of genetic crosses of sensitive DBA/2 with resistant C57BL/

97 been developed, alongside the production of genetic crosses of wild relatives with commercial variet

98 Genetic crosses of yeast strains containing different md

99 into the met1 mutant background, either via genetic cross or DNA transfer.

100 Subsequent genetic crosses or phage transduction allow two neighbor

101 In two P. falciparum genetic crosses, particular pfcrt and pfmdr1 alleles fro

102 Using a combination of genetic crosses, phenotyping of a trait underlying ecolo

103 Genetic crosses produced NOD/LtSz mice doubly homozygous

104 e suffers high-frequency mutation in certain genetic crosses, resulting in buff-colored progeny.

105 CYP6P4, and genotyping of the progeny of the genetic crosses revealed a maximum penetrance value f(2)

106 Furthermore, genetic crosses segregating Cas9/sgRNA transgenes away f

107 Genetic crosses show that Crg1-1 and Crg1-2 segregate as

108 Genetic crosses show that development of these tumorigen

109 Genetic crosses show this factor to be under control of

110 Genetic crosses showed that SC2 was identical to S17 ide

111 Genetic crosses showed this recessive resistance to be g

112 Reciprocal genetic crossing suggested that CEK4 knockout causes emb

113 In 21 independent recombinant progeny of a genetic cross, susceptibility to this agent mapped in pe

114 functional module (protein complex), but the genetic cross talk between modules can differ substantia

115 This revealed a genetic cross-talk governing Golgi homeostasis, an addit

116 rearrangements, that unfolded in the wake of genetic crosses that brought together two broken chromos

117 Here we demonstrate via genetic crosses that the source of IgG2a is the mother,

118 In genetic crosses, the three lst mutant alleles fail to co

119 a perturbation of the biological system, and genetic crosses, through the processes of recombination

120 dlr knockout mouse model in an interspecific genetic cross to map atherosclerosis susceptibility loci

121 We originally used Ter in genetic crosses to identify loci that control tumorigene

122 ly, transgenic seeds were obtained only from genetic crosses using infiltrated plants as the pollen r

123 To detect variants at this and other loci, a genetic cross was carried out between two laboratory mou

124 idate the basis of this extreme virulence, a genetic cross was performed between a highly virulent ty

125 A genetic cross was used to construct such a map from 901

126 expression and glucose utilization, standard genetic crossing was performed to introduce a fast-twitc

127 Using standard genetic crosses, we confirmed that the mutation segregat

128 Combining these results with data from genetic crosses, we find that crossing-over is restricte

129 wide linkage mapping in marine-freshwater F2 genetic crosses, we find that the genetic basis of evolv

130 Through genetic crosses, we show that the rate of water loss in

131 Using a series of genetic crosses, we show that this spatial restriction o

132 By genetic crosses, we showed that IgE-mediated tumor prote

133 ation that all progeny clones in a Dd2 x HB3 genetic cross were the result of fertilization events be

134 hanisms that are responsible for resistance, genetic crosses were established between the Ndja strain

135 stern blot, bone marrow transplantation, and genetic crosses were performed for phenotypic characteri

136 sequencing data on parents and progeny from genetic crosses, which has enabled us to perform the fir

137 Similar results were obtained in a genetic cross with LDL receptor-deficient mice.

138 s caused by misregulation of CAPN3 activity, genetic crosses with CAPN3 overexpressing transgenic (C3

139 's full potential likely will be realised by genetic crosses with other models to interrogate the rol

140 Genetic crosses with the mdx mouse showed that neither t

141 /wox3 loss-of-function mutant and performing genetic crosses with the stf mutant.

142 phenotype of Scn2a(Q54) mice, we carried out genetic crosses with two mutant alleles of Kcnq2.