ライフサイエンスコーパス: long arm of chromosome

1 lies has provided evidence of linkage to the long arm of chromosome 1 (1q24-25).

2 localized to a 0.5-centiMorgan region on the long arm of chromosome 1 at q31.3.

3 performed high-density mapping of the entire long arm of chromosome 1 in 13 CDC tumor samples.

4 utations to a 2-cM overlapping region of the long arm of chromosome 1 of tomato, a region not previou

5 lications involving all or part of the whole long arm of chromosome 1 presumably occur as secondary a

6 Relative overexpression of genes on the long arm of chromosome 1 was shown in all tumours that s

7 like factor CTD6, which is located at on the long arm of chromosome 1, area 36.2-36.1 in the region o

8 nt to the pericentric heterochromatin on the long arm of chromosome 1.

9 n other regions of the genome, including the long arm of Chromosome 1.

10 arkers from 81.8-242.9 cM are located in the long arm of chromosome 1.

11 s 4 and 5, and paracentric inversions in the long arm of chromosomes 1 and 4; the latter is in a segm

12 b family (19 affected relatives) maps to the long arm of chromosome 10 (10q25; nonparametric linkage

13 The l2 locus was mapped to the long arm of chromosome 10 and positional cloning reveale

14 persyn genomic locus and localized it to the long arm of chromosome 10 in the q23.2-q23.3 region.

15 togenetic studies indicated that loss of the long arm of chromosome 10 is a frequent event in small c

16 The long arm of chromosome 10 is frequently affected by alle

17 sceptibility gene for type 2 diabetes to the long arm of chromosome 10, where we have previously iden

18 sor gene that resides at region 24-26 of the long arm of chromosome 10.

19 0 tumors had at least one allele loss on the long arm of chromosome 10.

20 an approximately 52 kb of the genome, on the long arm of chromosome 10.

21 rt arm of chromosome 2, and snm2 maps to the long arm of chromosome 10.

22 Deletions of the long arm of chromosome 11 (11q) have been noted in prima

23 Abnormalities of the long arm of chromosome 11 are also evident in a wide var

24 Mutations in the ATM gene located on the long arm of chromosome 11 at 11q22-23 cause ataxia-telan

25 ommon adult leukemia, carry deletions of the long arm of chromosome 11 at 11q22-23.

26 mmediately adjacent to the centromere on the long arm of chromosome 11 in band 11q11.

27 uggest the tumor suppressor gene maps to the long arm of chromosome 11 in the region of 11q13-qter.

28 er(11)t(X;11) chromosome lacking most of the long arm of chromosome 11 into A388.6TG.c2 does not affe

29 f a melanoma tumor suppressor gene(s) on the long arm of chromosome 11 through suppression of tumorig

30 kage, a 40-Mb YAC contig covering the distal long arm of chromosome 11 was assembled.

31 ies tend to cluster in the lower half of the long arm of chromosome 11, indicating the possible prese

32 equently by terminal deletion of part of the long arm of chromosome 11, with breakpoints in 11q23.3-1

33 Both patients had abnormalities of the long arm of chromosome 11.

34 have been mapped to two distinct loci on the long arm of chromosome 11.

35 t a melanoma tumor suppressor resides on the long arm of chromosome 11.

36 isorder caused by a terminal deletion of the long arm of chromosome 11.

37 in families linking to the EVR1 locus on the long arm of chromosome 11.

38 ave localized a tumor suppressor gene to the long arm of chromosome 11.

39 es, the human MYCN gene was localized to the long arm of chromosome 12 band 12q24 which is the corres

40 hiwi maps to the long arm of chromosome 12, band 12q24.33, a genomic regi

41 hSPRY2 maps to the long arm of chromosome 13 (13q31.1), where loss of heter

42 Loss of heterozygosity (LOH) involving the long arm of chromosome 13 has been reported to occur in

43 nt of a tumor suppressor gene located on the long arm of chromosome 13, between the retinoblastoma (R

44 of patients with hemizygous deletions of the long arm of chromosome 13, we have defined a discrete re

45 epresentation toward locations on the distal long arm of chromosome 13, with no localizations noted i

46 ing a panel of 11 probes spanning the entire long arm of chromosome 13.

47 specimens analysed had an allele loss on the long arm of chromosome 13.

48 a single copy gene located in band 22 of the long arm of chromosome 14 (14q22).

49 he malignant and atypical tumors were on the long arm of chromosome 14.

50 l pyoderma gangrenosum-acne-arthritis to the long arm of chromosome 15 (maximum two-point LOD score,

51 The causative gene maps to the long arm of chromosome 15 but has not yet been identifie

52 include the imprinted region on the proximal long arm of chromosome 15 underlie a complex neurobehavi

53 ck a paternally derived copy of the proximal long arm of chromosome 15, and eat uncontrollably; in An

54 ataract was mapped to a 6.5-Mb region of the long arm of chromosome 15, at 22.33-24.2 between CYP11A

55 tected significant linkage to markers on the long arm of chromosome 15, in a region encompassing RLBP

56 AC) clone containing HuAZ2 at band 22 of the long arm of chromosome 15.

57 c microsatellite markers spanning the entire long arm of chromosome 15.

58 identified a second PKC locus (EKD2) on the long arm of chromosome 16 in a large Indian family with

59 The long arm of chromosome 16 is frequently deleted in human

60 d together with a substantial portion of the long arm of chromosome 16.

61 total of 906 overgos were selected from the long arm of chromosome 16.

62 cogene are located in close proximity on the long arm of chromosome 17 (17q11-21).

63 tary neuralgic amyotrophy gene to the distal long arm of chromosome 17 (17q24-qter).

64 with polymorphic short tandem repeats on the long arm of chromosome 17 revealed maximal pairwise LOD

65 ross a minimal 50-Mb region of primarily the long arm of chromosome 17 showed LOH in 8 cases, whereas

66 , while a third tribrid had a portion of the long arm of chromosome 17 translocated to mouse as its o

67 study to 70 tumors with 17 markers from the long arm of chromosome 17.

68 tosomal retinitis pigmentosa, located on the long arm of chromosome 17.

69 gest that allelic loss of sequences from the long arm of chromosome 18 may be a useful prognostic ind

70 netically to have a terminal deletion of the long arm of chromosome 18.

71 nal STRs spanning approximately 11 cM on the long arm of chromosome 18.

72 oss of the short arm of chromosome 1 and the long arm of chromosome 19, or 1p19q codeletion; and (c)

73 ization of scsae and 8 linked markers on the long arm of chromosome 1D.

74 Forty-two of the Rf alleles mapped to the long arm of chromosome 2 (2L), and 5 of these were furth

75 and high-resolution deletion mapping of the long arm of chromosome 2 (2q) in invasive cervical carci

76 ocus designation PDE6D) was localized to the long arm of chromosome 2 (2q35-q36) by fluorescence in s

77 ta) has been characterized and mapped to the long arm of chromosome 2 (HSA2q35-q36) where a new autos

78 pped a gene for ADHED (EDA3) to the proximal long arm of chromosome 2 (q11-q13).

79 One of these is on the long arm of chromosome 2 and is linked with loci encodin

80 cus has recently been assigned to the distal long arm of chromosome 2 in two families.

81 One locus on the long arm of chromosome 2 is coincident with genes encodi

82 ng approximately 40 centiMorgans (cM) on the long arm of chromosome 2.

83 opy number of DNA sequences derived from the long arm of chromosome 20 (20q) has been commonly observ

84 The l3mbtl1 gene is located on the long arm of chromosome 20 (q12), within a region commonl

85 eloproliferative neoplasms (MPN) affects the long arm of chromosome 20 and has been predicted to harb

86 lin-resistant type 2 diabetes located on the long arm of chromosome 20 around marker D20S196.

87 gene (or genes) in the "MODY1 region" of the long arm of chromosome 20 contributes to the development

88 -1 family, was cloned during a search on the long arm of chromosome 20 for genes whose expression and

89 Deletions of the long arm of chromosome 20 have been reported in a wide r

90 An acquired deletion of the long arm of chromosome 20 is a recurrent abnormality in

91 Deletion of the long arm of chromosome 20 represents the most common chr

92 splastic syndromes in whom a deletion of the long arm of chromosome 20 was detectable by G-banding an

93 A deletion of the long arm of chromosome 20, del(20q), is a recurring abno

94 ic loss at 39 highly polymorphic loci on the long arm of chromosome 20.

95 linkage was found for a 10-cM region on the long arm of chromosome 20q13.1-q13.2 between markers D20

96 In contrast to the distal half of the long arm of chromosome 21, the proximal half of approxim

97 Genes on the long arm of chromosome 22 and near the neurofibromatosis

98 ualized as MLH1 foci, localize to the distal long arm of chromosome 22 in 75% of human spermatocytes

99 egregation patterns linked to an area on the long arm of chromosome 22, localizing the gene encoding

100 s involved loss of the whole, or part of the long arm, of chromosome 22.

101 this processed pseudogene to band 28 on the long arm of chromosome 3 by fluorescence in situ hybridi

102 sed to map the Def-1 gene to a region on the long arm of chromosome 3 that is genetically separable f

103 s frequently reveal additional copies of the long arm of chromosome 3.

104 3/p73L) and localized the gene to the distal long arm of chromosome 3.

105 as been placed on the tomato RFLP map on the long arm of chromosome 4 and does not demonstrate linkag

106 Deletions of the long arm of chromosome 4 detectable by cytogenetic analy

107 Loss of the long arm of chromosome 4 has been identified previously

108 P thus provides an additional marker for the long arm of chromosome 4 that should facilitate studies

109 The long arm of Chromosome 4 underwent a dramatic developmen

110 and mapped to the subtelomeric region of the long arm of chromosome 4(4H).

111 ne encoding human enamelin is located on the long arm of chromosome 4, in a region previously linked

112 nger domain containing genes, located on the long arm of chromosome 4, is expressed in a sharp peak d

113 ls contained an interstitial deletion in the long arm of chromosome 4, where the p16(INK4a) gene resi

114 sociated with a chromosomal inversion on the long arm of chromosome 4.

115 s encoded by a single gene at a locus on the long arm of chromosome 4.

116 by a reciprocal translocation involving the long arms of chromosomes 4 and 5, and paracentric invers

117 hort arm of chromosomes 7A and 7D and on the long arm of chromosome 4A.

118 ed to deletion bins in the distal 42% of the long arm of chromosome 4B (4BL) were ordered in silico b

119 A heterozygous deletions of the long arm of chromosome 5 [del(5q)], observed in 40% of p

120 A deletion of the long arm of chromosome 5 is a recurring abnormality in m

121 Complete loss or deletion of the long arm of chromosome 5 is frequent in myelodysplastic

122 The distal portion of the long arm of chromosome 5 is linked to hypertension and c

123 alysis in two families with 46,XY DSD to the long arm of chromosome 5 with a combined, multipoint par

124 of a whole chromosome 5 or a deletion of the long arm of chromosome 5, -5/del(5q), is a recurring abn

125 htly linked to the Msx2 homeobox gene on the long arm of chromosome 5, and that affected individuals

126 ring interstitial loss of all or part of the long arm of chromosome 5, del(5q), is a hallmark of myel

127 Partial deletion of the long arm of chromosome 5, del(5q), is the cytogenetic ha

128 e scan localized the disease interval to the long arm of chromosome 5, with a maximum two-point param

129 ients, while 4 had a deletion of part of the long arm of chromosome 5.

130 chTRF1 gene was localized on the long arm of chromosome 5.

131 ed by the expression of the Ph1 locus on the long arm of chromosome 5B.

132 map of one highly recombinant region on the long arm of chromosome 5B.

133 omosome 4F with barley chromosome 4H and the long arm of chromosome 5H.

134 Deletion of the long arm of chromosome 6 (6q) is one of the most common

135 After stringency washes, the entire long arm of chromosome 6 (6q) was microdissected.

136 , including duplications of a portion of the long arm of chromosome 6 and uniparental disomy, implica

137 ion, the human MCH-2R gene was mapped to the long arm of chromosome 6 at band 6q16.2-16.3, a region r

138 equent deletions of the distal region on the long arm of chromosome 6 have been reported in multiple

139 Though deletion of the long arm of chromosome 6 is one of the most common aberr

140 A genomewide scan identified a region on the long arm of chromosome 6 that is significantly associate

141 es (TBP AND PSMB1) are tightly linked on the long arm of chromosome 6, in a region syntenic with the

142 d nonrandom chromosomal abnormalities of the long arm of chromosome 6.

143 h lung cancer are frequently observed in the long arm of chromosome 6.

144 of patients with WM harbour deletions in the long arm of chromosome 6.

145 lit into two main locations on the short and long arms of chromosome 6.

146 Complete or partial deletions of the long arm of chromosome 7 (7q- and -7) are nonrandom abno

147 Deletions involving the long arm of chromosome 7 have not been described in RCCs

148 y pancreatitis (HP) to a small region of the long arm of chromosome 7 in a large four-generation kind

149 During the sequencing of the long arm of chromosome 7 in the Human Genome Project, a

150 sor in acute leukemias with deletions of the long arm of chromosome 7 or in other types of human mali

151 1 to 2 megabase deletion of a portion of the long arm of chromosome 7 that encompasses ELN.

152 from nine patients with abnormalities of the long arm of chromosome 7, and in each case one allele of

153 of heterozygosity for large portions of the long arm of chromosome 7, resulting in retention of only

154 ons (EROs), have demonstrated linkage on the long arm of chromosome 7.

155 the other quantitative trait locus is on the long arm of chromosome 7.

156 Gains in the long arm of chromosome 8 (8q) are believed to be associa

157 Allele loss from the long arm of chromosome 8 was also observed with 30.0% (6

158 5 loci on the short arm and one locus on the long arm of chromosome 8 were used for PCR-based LOH ana

159 mosomes due to an extra isochromosome of the long arm of chromosome 8, and the near-diploid karyotype

160 Slug maps to the long arm of chromosome 8, closely linked to D8S2090 betw

161 ydomonas reinhardtii, which we mapped to the long arm of chromosome 8, provides a good experimental s

162 ences contained within a "half-YAC" from the long arm of chromosome 8, that is, a YAC containing the

163 human alpha1B subunit gene, localized to the long arm of chromosome 9 (9q34) by fluorescence in situ

164 Allelic losses in the long arm of chromosome 9 are commonly encountered in man

165 Deletions of the long arm of chromosome 9 are the most common genetic alt

166 ported reassignment of marker BNL4053 to the long arm of chromosome 9.

167 reas 23-201 was located in the middle of the long arm of chromosome A2, suggesting the presence of se

168 homologous regions near the telomeres of the long arm of chromosome I and the short arm of chromosome

169 sod2 gene, located near the telomere on the long arm of chromosome I, encodes a Na+ (or Li+)/H+ anti

170 of the budding yeast genome, but not of the long arm of chromosome XII that contains the rDNA repeat

171 necessary to mediate the segregation of the long arm of chromosome XII.

172 The human GC-F gene was localized to the long arm of chromosome Xq22 by fluorescence in situ hybr

173 MCT-1 was localized to the long arm of chromosome Xq22-24 by flourescence in situ h