ライフサイエンスコーパス: insertion sequence

1 high levels as a result of a third mutation (insertion sequence).

2 when there are fewer than five copies of the insertion sequence.

3 with olefins via a C-H activation, migratory insertion sequence.

4 ix domain, and a transmembrane and cytosolic insertion sequence.

5 or ammonia catabolism, iron acquisition, and insertion sequences.

6 polymorphisms, and a unique distribution of insertion sequences.

7 racketed by the homologous ISV-A1 and ISV-A2 insertion sequences.

8 S1601 contains portions of three independent insertion sequences.

9 tive composite transposon bracketed by IS600 insertion sequences.

10 deletion via recombination between flanking insertion sequences.

11 harbors at least 12 copies of five distinct insertion sequences.

12 ation of the composite transposon's flanking insertion sequences.

13 ral mechanism for the formation of miniature insertion sequences.

14 n of all genomic rearrangements that involve insertion sequences.

15 ene, an intein (Cbu.DnaB) within dnaB and 29 insertion sequences.

16 re recognized: 13 capsule synthesis genes, 4 insertion sequences, 1 truncated biosynthesis gene, and

17 h several genomic rearrangements mediated by insertion sequences, 12 cryptic prophages, 372 pseudogen

18 time PCR assay with three targets, including insertion sequence 481 (IS481), IS1001, and an IS1001-li

19 in the United States, most laboratories use insertion sequence 481 (IS481), which is not specific fo

20 ary 1, 2001, and December 31, 2003, that had insertion sequence 6110 (IS6110) restriction fragment le

21 Insertion sequences, a phage genome, and/or loci from di

22 tative virulence genes, genomic islands, and insertion sequences across a collection of 33 strains is

23 While insertion sequence analysis using IS1634 clearly indicat

24 After removing rRNA, vector, bacterial insertion sequence and chimeric cDNA contaminants, small

25 ogenic bacterial plasmid "mobilome" includes insertion sequence and other transposable elements that

26 on is unusually G-C rich, and it has unusual insertion sequences and a minimal dependence on the EBS2

27 ing, sap typing, and the presence/absence of insertion sequences and a type I restriction modificatio

28 The genome is unusually rich in insertion sequences and displays anomalies in GC base-co

29 ither singly or in large multiple arrays, to insertion sequences and gene duplications of one kilobas

30 ools such as Optimized Annotation System for Insertion Sequences and IScan currently identify IS elem

31 plicated by the presence of repeat elements, insertion sequences and other similar factors that contr

32 strain chi7122 include complete and partial insertion sequences and phage-related DNA sequences, som

33 Divergent features included already reported insertion sequences and ragB, as well as additional hypo

34 n is a complex recombination event involving insertion sequences and repeat sequences.

35 omosome of each recipient, where it acquired insertion sequences and underwent deletions and rearrang

36 Several intact and partial insertion sequences and/or transposons were also found i

37 ransposon mutant library that is amenable to insertion sequencing and introduced this mutant pool int

38 olerae survival, and by combining transposon-insertion sequencing and transcriptomic data sets, we al

39 es-specific hypothetical genes, transposons, insertion sequences, and integrases and were located adj

40 wo strains exhibit differences in prophages, insertion sequences, and island structures.

41 d contains an unusual t-RNA island, numerous insertion sequences, and large repeated elements, includ

42 nactivated via frameshifts, point mutations, insertion sequences, and putative deletions.

43 ae are spread by plasmid-mediated integrons, insertion sequences, and transposons, some of which are

44 ke other obligate intracellular bacteria, 32 insertion sequences are found dispersed in the chromosom

45 Phages, phage-like elements, and insertion sequences are the major sources of variation b

46 mino acids of the peptide, also known as the insertion sequence, are found to be essential in reducin

47 While present in many bacterial insertion sequences as well as in the eukaryotic family

48 Selenocysteine insertion sequence-associating factors, adenosine, and A

49 TA proteins possess a hydrophobic membrane insertion sequence at their C-terminus such that it can

50 competes with endogenous GPX1 selenocysteine insertion sequence binding activity in COS-1 cytosol ext

51 region of selenoprotein mRNAs as well as Sec insertion sequence binding protein 2, Sec-tRNA(Sec), and

52 by a multiprotein complex that includes Sec insertion sequence-binding protein 2 (SECISBP2; also kno

53 ein B as the first eukaryotic selenocysteine insertion sequence-binding protein opens the way to the

54 rs to play a central role in the exchange of insertion sequences, but not the exchange of high-identi

55 ns of C. reinhardtii have short extension or insertion sequences, but overall the large subunit prote

56 Recombination between insertion sequence copies can cause genetic deletion, in

57 present a resource and analysis of 2,363 new insertion sequences corresponding to 720 genomic loci.

58 We have refined analysis of transposon-insertion sequencing data by normalizing for the effect

59 iated information inherent in all transposon-insertion sequencing data sets.

60 The presence of an insertion sequence defines the major phylogenetic pre-se

61 ruption in the A genome include retroelement insertions, sequence deletions, and mutations causing in

62 uence similarities to known genes, including insertion sequences, determinants of regulatory proteins

63 g a size greater than 30 kb, the presence of insertion sequences, distinct segmentation of K-12 and J

64 present was found at the junction of bvg and insertion sequence DNA.

65 /T rich (80%) and is an efficient target for insertion sequences during stationary phase.

66 eatures of the cDNA include a selenocysteine insertion sequence element approximately 4.8 kb 3' to th

67 on of mooV by the joining of the ends of the insertion sequence element at the circle junction.

68 Discrepancies between the insertion sequence element distribution patterns, the di

69 A common insertion sequence element in Escherichia coli, IS5, has

70 g protein that recognizes the selenocysteine insertion sequence element in human cellular glutathione

71 g from stop to Sec involves a cis-acting Sec insertion sequence element in the 3' untranslated region

72 ) and its insertion was dependent on the Sec insertion sequence element in the 3'UTR of TR1 mRNA.

73 rs713041 is located near the selenocysteine insertion sequence element in the GPX4 3' untranslated r

74 hia coli K-12 strain MG1655 contained an IS1 insertion sequence element in the regulatory region of t

75 The insertion sequence element is located on the plasmid bet

76 lis: (i) the transposition of the endogenous insertion sequence element IS1126 and (ii) the modulatio

77 determined that the endogenous P. gingivalis insertion sequence element IS1126 is capable of transpos

78 The insertion sequence element IS1358, found in both O1 and

79 A 155-159 bp insertion sequence element known as the Correia element,

80 depends on the nature of the selenocysteine insertion sequence element located in the 3' UTR of sele

81 the presence of a functional selenocysteine insertion sequence element that is highly active but onl

82 gly, however, we also observed that a 1.8-kb insertion sequence element was positioned between ccmB a

83 expressed when the Drosophila selenocysteine insertion sequence element was used, whereas the corresp

84 mRNA stem-loop structure, the selenocysteine insertion sequence element.

85 cal to that in O157:H7 is bounded by the IS1 insertion sequence element.

86 egion of the cDNA contains a canonical Secys insertion sequence element.

87 and >204 nucleotides from the selenocysteine insertion sequence element.

88 We describe the use of two insertion sequence elements (ISFtu1 and ISFtu2) in Franc

89 A total of 80 copies of three different insertion sequence elements are interspersed throughout

90 parent strain using all known P. gingivalis insertion sequence elements as probes suggested that no

91 idence that homologous recombination between insertion sequence elements can be a primary determinant

92 A-binding protein B binds the selenocysteine insertion sequence elements from the GPX1 and type I iod

93 Among these are 85 predicted insertion sequence elements in eight different families.

94 The insertion sequence elements in the composite transposon-

95 conversion and several other loci containing insertion sequence elements or phage-related gene insert

96 gingivalis was a concerted up-regulation of insertion sequence elements related to IS1 transposases.

97 se genes, conjugative functions and multiple insertion sequence elements suggests that the PAI, or se

98 The genome contains numerous insertion sequence elements that have mediated extensive

99 Here, we performed RFLP analyses using Insertion Sequence elements to resolve the phylogenetic

100 em-loop structures resembling selenocysteine insertion sequence elements were identified in the 3'-un

101 Although many phage and insertion sequence elements were missing from the core c

102 frame is homologous to a family of putative insertion sequence elements, although our evidence shows

103 vel program that searches for selenocysteine insertion sequence elements, followed by selenoprotein g

104 lication and maintenance regions, with seven insertion sequence elements, located mostly at the bound

105 PXO99A contains numerous copies of diverse insertion sequence elements, members of which are associ

106 accounted for by the presence or absence of insertion sequence elements.

107 vealed the presence of one or two classes of insertion sequence elements.

108 n to those previously known in dnaX and nine insertion sequence elements.

109 Three "insertion" sequence elements present in POLQ are not fou

110 ariable deletion events between the flanking insertion-sequence elements, all resulting in eliminatio

111 including phage-derived genes, plasmids, and insertion-sequence elements, highlighting its dynamic na

112 o high-throughput DNA sequencing (transposon-insertion sequencing) enables simultaneous and genome-wi

113 analysis of BiXyn10A demonstrated that such insertion sequences encode a new family of carbohydrate-

114 enovirus type 5 E3/19K endoplasmic reticulum insertion sequence (ES).

115 g decay through loss of functional genes and insertion sequence expansion, often indicative of adapta

116 ar homologous recombination occurred between insertion sequences following an initial transposition e

117 Chimeric insertion sequence footprints were observed at the delet

118 cise, reading frame-restoring excision of an insertion sequence from the coding region of expR, a gen

119 action of biological meaning from transposon-insertion sequencing genomic data.

120 These insertion sequences have subsequently allowed the amplif

121 bile genetic elements such as transposons or insertion sequences, i.e. they possess direct repeats at

122 vPCR of insertion sequences identified these same mutations and

123 The locus is replaced by an insertion sequence in B. pertussis, explaining the lack

124 single event, the transposition of an IS6110 insertion sequence in one of the strains, accounted for

125 designated ISPpu12, had the structure of an insertion sequence in that it was bordered by 24-bp near

126 A UGA codon and a selenocysteine insertion sequence in the 3'-untranslated region are the

127 in mRNA requires a nucleotide selenocysteine insertion sequence in the 3'-untranslated region.

128 s, resulting in an overall high abundance of insertion sequences in the genomes.

129 ility of internal deletion variants of other insertion sequences in these isolates suggests that this

130 om multiple inversions of genome segments at insertion sequences, in a manner consistent with present

131 the sea urchin Tsp family and Drosophila SGM insertion sequences; in addition, they possess regions o

132 Recent studies revealed that a hydrophobic insertion sequence (INS) in these LAADs also interacts w

133 Insertion sequencing (INSeq) is a method for determining

134 ersed repetitive elements (SINEs), and of an insertion sequence (InsIpCHSD) found in the neighborhood

135 onal events involved the transposition of an insertion sequence into a narrow window of a single gene

136 Molecular fingerprinting with the IS6110 insertion sequence is useful for tracking transmission o

137 Transposon insertion sequencing is a high-throughput technique for

138 addition to homologs of two other H. pylori insertion sequence (IS) element genes, orfA, which encod

139 quence studied is derived from a Roseiflexus insertion sequence (IS) element where the resulting tran

140 Streptomyces scabies 84.34 identified a new insertion sequence (IS) element, IS1629, with homology t

141 up (SFG) R. peacockii, we identified a novel insertion sequence (IS) element, ISRpe1, disrupting the

142 C-1, showed that it undergoes high-frequency insertion sequence (IS) element-mediated insertions and

143 ted ORFs are interspersed among three intact insertion sequence (IS) elements (IS100 and two new IS e

144 regions of Tn5385 are linked by a series of insertion sequence (IS) elements (IS256, IS257, and IS12

145 ed many of the lines for mutations involving insertion sequence (IS) elements and identified two gene

146 her elements such as transposons, integrons, insertion sequence (IS) elements and the 'new' ISCR (IS

147 The insertion sequence (IS) elements are the smallest but mo

148 We found that insertion sequence (IS) elements are unusually abundant

149 Prokaryotic insertion sequence (IS) elements behave like parasites i

150 ly syntenous, recombination between abundant insertion sequence (IS) elements has resulted in genome

151 he 16 kb region in P. furiosus is flanked by insertion sequence (IS) elements with inverted and direc

152 espite its small size, the genome harbors 73 insertion sequence (IS) elements, almost all of which ar

153 ltiple members of two classes of Francisella insertion sequence (IS) elements, ISFtu1 and ISFtu2, and

154 e plasmid harbors a 16-kb region, flanked by insertion sequence (IS) elements, that encodes the restr

155 , we present genetic maps of recently active Insertion Sequence (IS) elements, the simplest form of M

156 ents involve mobile genetic elements such as insertion sequence (IS) elements.

157 nes, a possible new replicon, and two intact insertion sequence (IS) elements.

158 each approximately 20 kb region separated by insertion sequence (IS) elements.

159 y to the transposition of direct repeats and insertion sequence (IS) elements.

160 of these were related to known and putative insertion sequence (IS) elements; no known bacterial pla

161 An insertion sequence (IS) excision enhancer (IEE) was disc

162 Here, we describe the first insertion sequence (IS) identified from R. salmoninarum.

163 1998, for which the W family was defined by insertion sequence (IS) IS6110 DNA fingerprinting, polym

164 A new insertion sequence (IS) of Mycoplasma fermentans is desc

165 a highly diagnostic set of markers based on insertion sequence (IS) site polymorphism and genomic re

166 IS605, an insertion sequence (IS) that is unusual in containing ho

167 G1655, resulting from a dramatic increase in insertion sequence (IS) transposition, especially IS150.

168 ent of a previously identified M. fermentans insertion sequence (IS)-like element.

169 ssibility, we have studied the occurrence of insertion sequence (IS)-like elements in P. gingivalis W

170 ycobacterium tuberculosis isolates underwent insertion sequence (IS)6110 restriction-fragment-length

171 Complete and fragmented insertion sequences (IS) make up 24% of the total DNA an

172 Nearly 40% of the prophages harbored insertion sequences (IS) previously described in H. pylo

173 a harbor simple transposable elements termed insertion sequences (IS).

174 P4 prophage-like integrase gene and numerous insertion sequences (IS).

175 ent length polymorphism (RFLP) analysis with insertion sequences IS100 and IS285 as probes.

176 An additional molecular marker, insertion sequence IS1301, was found to be present in 10

177 he isolates resulted from the presence of an insertion sequence, IS1301, in the intergenic region (IG

178 the ser2 gene cluster are flanked by a novel insertion sequence (IS1601) oriented as direct repeats.

179 three of these isolates, a newly discovered insertion sequence, IS1630 (of the IS30 class), was loca

180 PCR assays targeting insertion sequence IS481 (IS), pertussis toxin ptxA prom

181 The insertion sequence IS481 and its isoform IS1002 have bee

182 se-developed PCR test targeting the repeated insertion sequence IS481 for the detection of Bordetella

183 The insertion sequence IS481 is also present in Bordetella h

184 This assay (LC-PCR-IS) targets the insertion sequences IS481 and IS1001 of B. pertussis and

185 o those of a nested-PCR method targeting the insertion sequences IS481 and IS1001.

186 terium tuberculosis was performed, using the insertion sequence IS6110 and the plasmid pTBN12.

187 The mycobacterial insertion sequence IS6110 has been exploited extensively

188 insertion of the Mycobacterium tuberculosis insertion sequence IS6110.

189 The Mycobacterium tuberculosis-specific insertion sequence IS6110/986 has been widely used as a

190 The genome of M. tuberculosis carries insertion sequences (IS6110) that are relatively stable

191 The mobile insertion sequence, IS6110, is an important marker in tr

192 The insertion sequence IS903 encodes a 307 amino acid residu

193 The bacterial insertion sequence IS903 has the unusual ability to tran

194 Like many transposons the bacterial insertion sequence IS903 was thought to insert randomly.

195 additional copy of the previously identified insertion sequence ISMi1 was cloned.

196 A 3,372-bp insertion sequence, ISPpu12, has been identified on the

197 tial mobile units (PMUs), which contain tra5 insertion sequences (ISs) and genes for specialized sigm

198 Analyses of complete genomes indicate that insertion sequences (ISs) are abundant and widespread in

199 Insertion sequences (ISs) are simple transposable elemen

200 Insertion sequences (ISs) are transposable elements pres

201 COM1 also has 45 full or partial insertion sequences (ISs) compared to 35 in the referenc

202 Bacterial insertion sequences (ISs) from the IS200/IS605 family en

203 nd B. holmesii was developed using multicopy insertion sequences (ISs) in combination with the pertus

204 Like the three other insertion sequences (ISs) known in this gastric pathogen

205 ular forms are also known for some bacterial insertion sequences (ISs).

206 hat are part of transposable elements called insertion sequences (ISs).

207 A-2-3B'a(2-13) each host several families of insertion sequences (ISSoc families) at various copy num

208 The Synechocystis sp. PCC6803 insertion sequence ISY100 (ISTcSa) belongs to the Tc1/ma

209 Tandem amplification occurs via the flanking insertion sequences, leading to increased toxin producti

210 The insertion sequence led to an increase in the transcript

211 anatomical images, transgenic constructs and insertions, sequence-level gene models and molecular cla

212 owever, this prtP gene was interrupted by an insertion sequence-like element which we designated IS19

213 IS195, a 1,068-bp insertion sequence-like element, contained 11-bp inverte

214 ites that occurred within the selenocysteine insertion sequence-like structures.

215 This region also contains IS492, an insertion sequence located numerous times throughout a r

216 Extensive insertion sequence-mediated genome rearrangements and re

217 r bacterial NusG proteins contain a variable insertion sequence of approximately 70 residues in the c

218 performed DNA fingerprinting with the IS6110 insertion sequence of the organisms isolated from patien

219 this hypothesis, a mutation in the membrane insertion sequence of the v-SNARE synaptobrevin/vesicle-

220 sition cycle, has recently been proposed for insertion sequences of the IS3 family.

221 cur through homologous recombination between insertion sequences on both sides of a duplicated region

222 i are bracketed by or are in the vicinity of insertion sequences or long clusters of tandem repeats (

223 me is unusual in that there are virtually no insertion sequences or phage-associated sequences and ve

224 oxin, mycolactone, as well as by hundreds of insertion sequences, particularly IS2404.

225 IS1381, an insertion sequence previously described in Streptococcus

226 e sequence in the rDNA, with the most common insertion sequences promoting faster processing.

227 dons with the help of a putative pyrrolysine insertion sequence (PYLIS) element.

228 lation, but loss of a downstream pyrrolysine insertion sequence (PYLIS) significantly increased the U

229 a dynamic 2,571,010-bp genome containing 91 insertion sequences representing 12 families and organiz

230 archy of selenoprotein synthesis are the Sec insertion sequence RNA-binding proteins, SBP2 and nucleo

231 taining N-terminal extensions (S2 and S5) or insertion sequence (S3).

232 cess are the mRNA binding protein of the Sec insertion sequence, SBP2, and the specialized elongation

233 a 3 untranslated region (UTR) selenocysteine insertion sequence (SECIS) and the SECIS-binding protein

234 ing event is specified by the selenocysteine insertion sequence (SECIS) element and requires the sele

235 It is thought that the SelenoCysteine Insertion Sequence (SECIS) element and UGA codon are suf

236 c in mammalian selenoproteins requires a Sec insertion sequence (SECIS) element in the 3' untranslate

237 codon as selenocysteine (Sec) requires a Sec insertion sequence (SECIS) element in the 3' untranslate

238 re a set of highly specific factors: the Sec insertion sequence (SECIS) element in the 3' untranslate

239 rporation into selenoproteins requires a Sec Insertion Sequence (SECIS) element in the 3' untranslate

240 A selenocysteine insertion sequence (SECIS) element in the 3'-untranslate

241 ec-dedicated elongation factor SelB to a Sec insertion sequence (SECIS) element in the selenoprotein-

242 ated at UGA codons in mRNAs possessing a Sec insertion sequence (SECIS) element in their 3'-untransla

243 egion of this gene contains a selenocysteine insertion sequence (SECIS) element that deviates at one

244 two copies of tRNA-Sec and a selenocysteine insertion sequence (SECIS) element which were lost in pl

245 aryotes, incorporation of Sec requires a Sec insertion sequence (SECIS) element, a stem-loop structur

246 of UGA as Sec depends on the selenocysteine insertion sequence (SECIS) element, a stem-loop structur

247 a common stem-loop structure, selenocysteine insertion sequence (SECIS) element, that is necessary fo

248 The Sec insertion sequence (SECIS) element, which is the stem-lo

249 ependent on the presence of a selenocysteine insertion sequence (SECIS) element, which recruits the s

250 stream of a stem-loop structure known as Sec insertion sequence (SECIS) element.

251 ns as selenocysteine is specified by the Sec insertion sequence (SECIS) element.

252 acting mRNA structure, called selenocysteine insertion sequence (SECIS) element.

253 ons requires a cis-acting RNA structure, Sec insertion sequence (SECIS) element.

254 odon UGA with the help of the selenocysteine insertion sequence (SECIS) element.

255 the presence of a cis-acting selenocysteine insertion sequence (SECIS) element.

256 ranslated region (UTR), referred to as a Sec insertion sequence (SECIS) element.

257 ppresses UGA codons that are upstream of Sec insertion sequence (SECIS) elements bound by SECIS-bindi

258 However, the selenocysteine insertion sequence (SECIS) elements required for the dec

259 ly structured 3' UTR contains selenocysteine insertion sequence (SECIS) elements that are required fo

260 selenoprotein genes contained selenocysteine insertion sequence (SECIS) elements that were similar, b

261 y identified several genes with multiple Sec insertion sequence (SECIS) elements, one of which was a

262 for evolutionarily conserved selenocysteine insertion sequence (SECIS) elements, which are RNA struc

263 to UGA codons is directed by selenocysteine insertion sequence (SECIS) elements.

264 gency of the Escherichia coli selenocysteine insertion sequence (SECIS) requirements, libraries of SE

265 sertion requires a cis-acting selenocysteine insertion sequence (SECIS) usually located in the 3'UTR

266 untranslated region, termed a selenocysteine insertion sequence (SECIS), and SECIS-binding protein 2

267 ires the TGA opal codon and a downstream Sec insertion sequence (SECIS), which can be partially rando

268 ecific mRNA sequence known as selenocysteine insertion sequence (SECIS).

269 tructure and stability of the selenocysteine insertion sequences (SECIS) of human glutathione peroxid

270 g genomic deletions of 3' UTR selenocysteine-insertion-sequences (SECIS1 and SECIS2).

271 e subspecies and is bracketed by remnants of insertion sequences, suggesting a multistep process in t

272 Here, a transposon insertion sequencing technology called INSeq was used to

273 loci differ from wlbpe in that they lack the insertion sequence that defines the right-hand terminus

274 repeat (NR) and 3' NR] of the gene and in an insertion sequence that precedes the 3' NR region.

275 kynyliodonium salt/alkylidenecarbene/1,5 C-H insertion sequence that sets the pivotal quaternary cent

276 Downstream from the termination codon is an insertion sequence that was homologous to the ISVs1 elem

277 We discover 525 new insertion sequences that are not present in the human re

278 pproximately 5% of the genome is composed of insertion sequences that may contribute to genome rearra

279 ntify the chromosomal position of repetitive insertion sequences that typically flank horizontally ac

280 xpression levels of endogenous and exogenous insertion sequences that were 2 orders of magnitude high

281 uctural features, pathognomonic of a regular insertion sequence, this element was designated IS1414.

282 Transposon insertion sequencing (Tn-Seq) is a microbial systems-lev

283 Transposon insertion sequencing (Tn-seq) is an emerging technology

284 We applied high-throughput insertion sequencing to identify which bacterial genes a

285 We used transposon-insertion sequencing to screen for genes that contribute

286 racterized by means of a Transposon Directed Insertion Sequencing (TraDIS) approach.

287 previously developed the Transposon Directed Insertion Sequencing (TraDIS) protocol for this purpose,

288 n IR resistance by using transposon-directed insertion sequencing (TraDIS).

289 e analysis revealed the presence of multiple insertion sequences upstream and downstream of the aerob

290 ion studies of Acinetobacter baylyi ADP1, an insertion sequence was evident in approximately 2% of th

291 The phylogenetic utility of the IS1167 insertion sequence was examined with restriction fragmen

292 genomic DNA and, except for one deletion, an insertion sequence was found at the break point.

293 steria monocytogenes, although the consensus insertion sequence was the same.

294 a-D-glucosidase gene, with a novel PA14-like insertion sequence, was identified two genes downstream

295 Most insertion sequences were derived from homologous positio

296 Forty-eight unique insertion sequences were detected in the first animal an

297 ed OASIS, or Optimized Annotation System for Insertion Sequences, which automatically annotates ISs w

298 All isolates carried the IS1167 insertion sequence, with an average of 9.5 copies.

299 in is distinctive in its large complement of insertion sequences, with several genomic rearrangements

300 ces, a Y chromosome-specific sequence, or an insertion sequence within the glutathione S-transferase