ライフサイエンスコーパス: radiation hybrid map

1 me 8, between markers D8S256 and D8S284 on a radiation hybrid map.

2 from large-insert clones, linkage maps, and radiation hybrid maps.

3 ed on EST sequence comparisons combined with radiation hybrid maps.

4 localization and markers on the genetic and radiation hybrid maps.

5 lly as a YAC contig, incorporating data from radiation hybrid maps.

6 dded to the Illinois-Texas 5,000-rad RH (RH, radiation hybrid) map.

7 RD was localized to human chromosome 3q27 by radiation hybrid mapping.

8 tu hybridization and is linked to D10S603 by radiation hybrid mapping.

9 a was excluded from this disease interval by radiation hybrid mapping.

10 arrowest disease interval by STS content and radiation hybrid mapping.

11 the gene on chromosome 2q by high resolution radiation hybrid mapping.

12 on human chromosome 11q25, as determined by radiation hybrid mapping.

13 human chromosome 5q (near the centromere) by radiation hybrid mapping.

14 and between markers D15S209 and AFM321ZD5 by radiation hybrid mapping.

15 using fluorescent in situ hybridization and radiation hybrid mapping.

16 both fluorescence in situ hybridization and radiation hybrid mapping.

17 ificial chromosome (YAC) pool screening, and radiation hybrid mapping.

18 ce in situ hybridization, YAC screening, and radiation hybrid mapping.

19 23 regions, respectively, by cytogenetic and radiation hybrid mapping.

20 d integrated with the current genetic map by radiation hybrid mapping.

21 ed by fluorescence in situ hybridization and radiation hybrid mapping.

22 ous hit to WI-4874, which is at 78 cR on the radiation hybrid map, 3.36 cR, by radiation hybrid mappi

23 Based on the resulting radiation hybrid map and our mouse genetic and physical

24 The radiation hybrid map and YAC/BAC physical map enable pre

25 Using human radiation hybrid mapping and BAC contig construction, we

26 mapped this gene to human chromosome 4q22 by radiation hybrid mapping and by hybridization to two ove

27 This localization was confirmed by radiation hybrid mapping and coincides with that of HuR

28 locks, we analyzed 148 markers on CFA9 using radiation hybrid mapping and established a four-way comp

29 ene maps to chromosome 1q32 as determined by radiation hybrid mapping and FISH analysis.

30 ion of selected STSs and bacterial clones by radiation hybrid mapping and fluorescence in situ hybrid

31 Both radiation hybrid mapping and fluorescent in situ hybridi

32 length human enamelin cDNA and determined by radiation hybrid mapping and fluorescent in situ hybridi

33 somal localization of Optc was determined by radiation hybrid mapping and its genomic structure deter

34 mapping, restriction enzyme fingerprinting, radiation hybrid mapping and optical mapping.

35 ntiation Complex (EDC) at chromosome 1q21 by radiation hybrid mapping and STS content of genomic clon

36 By radiation hybrid mapping and the use of surrounding gene

37 By radiation hybrid mapping and the use of surrounding mark

38 hairless, was localized in this interval by radiation hybrid mapping, and a missense mutation was fo

39 Radiation hybrid mapping assigned the mda-7 gene to huma

40 Radiation hybrid mapping assigns this kallikrein-gene-ri

41 The LRP7 gene was also localized by radiation hybrid mapping between markers D11S24270 and D

42 approach that is analogous to linkage or to radiation hybrid mapping, but that circumvents many of t

43 the interval between D16S510 and D16S509 by radiation hybrid mapping, corresponding to chromosomal b

44 mapping data for the mouse with the incoming radiation hybrid map data.

45 Radiation hybrid mapping data indicate that the human lo

46 Radiation hybrid mapping data indicate that the porcine

47 Genetic linkage and radiation hybrid mapping data show that Fgd2 and the hum

48 Genetic linkage and radiation hybrid mapping data show that Fgd3 and the hum

49 Complete information, including radiation hybrid mapping data, is also maintained locall

50 To date, we have generated radiation-hybrid-mapping data for >14,000 novel ESTs ide

51 Radiation hybrid mapping demonstrated that sciellin is l

52 A high-resolution radiation hybrid map encompassing 9.5 Mb between the PLC

53 arge datasets of mouse full-length cDNAs and radiation-hybrid mapped ESTs, the continued development

54 In this study, by radiation hybrid mapping, FISH analysis, BAC clone seque

55 Using T31 mouse radiation hybrid mapping, Folbp3 was mapped to a region

56 A fine-structure radiation hybrid map for the region that extends from D8

57 cR on the radiation hybrid map, 3.36 cR, by radiation hybrid mapping, from WI-4874.

58 all LOD 3 chromosomal maps consisting of 775 radiation-hybrid-mapped genetic markers and ESTs.

59 The radiation hybrid map has 5% error in order and 34% error

60 This radiation hybrid map has the highest resolution of any p

61 Radiation hybrid mapping has become an established tool

62 g DNA loci that exploits many advantages of 'radiation hybrid' mapping in taxa for which such hybrids

63 order of the polymorphic markers within this radiation hybrid map is consistent with published geneti

64 Radiation hybrid mapping is an important technique for d

65 Radiation hybrid mapping is an important technique for d

66 Radiation hybrid mapping is an important technique for d

67 er of published landmark loci in genetic and radiation hybrid maps is in general agreement.

68 Radiation hybrid mapping localised disp1 to the same reg

69 rmed to originate from BAC 78138 at 19q13.3; radiation hybrid mapping localized EHD3 and EHD4 to 2p21

70 Radiation hybrid mapping localized hMARCO to chromosome

71 Radiation hybrid mapping localized human CLOCK to the lo

72 Radiation hybrid mapping localized human LMCD1 to the te

73 Radiation hybrid mapping localized the AXIN2 gene to hum

74 Radiation hybrid mapping localized the mouse gene to chr

75 Radiation hybrid mapping localized this gene to a region

76 Radiation hybrid mapping localized TR1 and TL2 to 8q24 a

77 The previously isolated and radiation hybrid-mapped markers Bda84F03, 1QTEL019, and

78 Previously isolated and radiation hybrid-mapped markers TEL17P37, TEL17P49, and

79 l artificial chromosome (BAC) clones for the radiation hybrid-mapped markers, end sequencing of the B

80 Radiation hybrid mapping, Northern blot analysis, in sit

81 A high-resolution radiation hybrid map of human chromosome 18 has been dev

82 Here we report a radiation hybrid map of mouse genes, a combined project

83 We have constructed a genetic and radiation hybrid map of the centromeric portion of mouse

84 port the construction of a 1.5-Mb-resolution radiation hybrid map of the domestic cat genome.

85 This STS-based radiation hybrid map of the human genome brings us one s

86 n improved version of the integrated linkage-radiation hybrid map of the rat containing 2058 microsat

87 sents, for the first time, a high-resolution radiation hybrid map of wheat chromosome 1D (D genome) i

88 Radiation hybrid mapping of MLP placed it between geneti

89 is supported by phylogenetic analysis and by radiation hybrid mapping of murine I-TAC (gene symbol Sc

90 Radiation hybrid mapping of Nope, Punc, and Neogenin pla

91 other two maps used for this effort were the radiation hybrid maps of chromosome 16 from Whitehead In

92 atic cell hybrid breakpoint physical map and radiation hybrid maps of human chromosome 16 to construc

93 romosome walking, to build both physical and radiation hybrid maps of the CFA12 13-21 region.

94 er localize the gene for NBS, we generated a radiation-hybrid map of markers at 8q21 and constructed

95 Of 36,678 STSs on the TNG radiation hybrid map, only 3604 (9.8%) were absent from

96 nalysis of molecular marker retention in our radiation hybrid mapping panel allowed the localization

97 Analysis of the GeneBridge 4 radiation hybrid mapping panel localized CACNB4 to posit

98 ailability of the zebrafish EST database and radiation hybrid mapping panels has dramatically expande

99 By somatic cell and radiation hybrid mapping panels, SNAIL was localized to

100 iety of human-rodent somatic cell hybrid and radiation hybrid mapping panels, the human SMCC gene was

101 Using human-hamster radiation hybrid mapping panels, we mapped DLG3 to Xq13.

102 CR analysis of somatic cell hybrid (SCH) and radiation hybrid mapping panels.

103 Using radiation-hybrid mapping panels, we mapped the DLG4 locu

104 Radiation hybrid mapping placed LIMAB1 in a 37-cR interv

105 Radiation hybrid mapping placed this STS with very high

106 Radiation hybrid mapping places the human tauCstF-64 gen

107 ion, RGD provides tools for gene prediction, radiation hybrid mapping, polymorphic marker selection a

108 A radiation hybrid mapping population was developed from a

109 The densest linkage map combined with a radiation hybrid map, reported by Steen et al., includes

110 Radiation hybrid mapping revealed that 33 of the 76 zebr

111 Both genes were found to be X-linked: radiation hybrid mapping revealed that the human H9 gene

112 Radiation hybrid mapping studies indicate that the human

113 Radiation hybrid mapping studies placed the rat RISC loc

114 the BAC contig with a map of loci ordered by radiation hybrid mapping suggested the most likely genom

115 ed on fluorescence in situ hybridization and radiation hybrid mapping, the human gene has been locali

116 By radiation hybrid mapping, the human gene was localized t

117 By radiation hybrid mapping, the human ortholog RAD51D was

118 By radiation hybrid mapping, the human TRIP6 gene was assig

119 Using radiation hybrid mapping, the MCT3 gene was mapped to ch

120 By radiation hybrid mapping, the RGS3 gene was assigned to

121 oups have developed whole-genome genetic and radiation hybrid maps, the depth of coverage for 15q11-q

122 13 by fluorescence in situ hybridization and radiation hybrid mapping; the cDNA for the human homolog

123 We have localized the receptor by radiation hybrid mapping to a region of about 500-kb pai

124 Human RASAL has been localized by radiation hybrid mapping to chromosome 12q23-24.

125 to metaphase chromosomes and by whole genome radiation hybrid mapping to chromosome 1p36.1 between DI

126 The human RAIDD/CRADD was mapped using radiation hybrid mapping to human chromosome 12, 2.9 cR

127 Rat Ush2a has been localized by radiation hybrid mapping to rat chromosome 13 between d1

128 The gene was mapped by high-resolution radiation-hybrid mapping to the interval between microsa

129 lop two new types of models for whole-genome radiation hybrid mapping using the general multipoint fr

130 describe lessons and pitfalls of developing radiation hybrid maps, using the example of mouse Chromo

131 ntegration of the BAC fingerprint map with a radiation-hybrid map via assembled expressed sequence ta

132 Using a radiation hybrid map, we have determined the correct mar

133 By radiation hybrid mapping, we localized CDC14A to chromos

134 By means of radiation hybrid mapping, we placed the human IRS-2 gene

135 Using radiation-hybrid mapping, we show that the DHCR7 gene is

136 stimulated peripheral blood lymphocytes and radiation hybrid mapping were used for localization of t

137 racterize these markers further, genetic and radiation hybrid maps were constructed.

138 Radiation hybrid mapping with Stanford G3 and TNG panels