ライフサイエンスコーパス: deletion mutation

1 confirmed by construction of an independent deletion mutation.

2 Finally, we generated an ftsH deletion mutation.

3 red the Op phenotype in strains with the wzb deletion mutation.

4 t with a dominant negative mechanism for the deletion mutation.

5 redominantly a -2 frameshift GC dinucleotide deletion mutation.

6 cted in the context of a glycoprotein L (gL) deletion mutation.

7 or a GAA expansion and a FXN point/insertion/deletion mutation.

8 r frequency of single base substitution than deletion mutations.

9 ional factor contributing to the bias toward deletion mutations.

10 pecies transgene rescue and more recently on deletion mutations.

11 ression of homology-mediated duplication and deletion mutations.

12 latter sequences mimic the bulged SMI for -2 deletion mutations.

13 e generation of more mutations, particularly deletion mutations.

14 ccumulated homology-mediated duplication and deletion mutations.

15 ression of homology-mediated duplication and deletion mutations.

16 , including some with nonsense and insertion/deletion mutations.

17 ermined the locations, rates, and extents of deletion mutations.

18 and used it to screen a series of point and deletion mutations.

19 eshift mutations, as well as splice-site and deletion mutations.

20 rrangement and end joining without insertion/deletion mutations.

21 We discovered 1 patient with an intronic deletion mutation, 4 patients with point mutations withi

22 ons of single fibers demonstrated that these deletion mutations accumulate to detrimental levels (>90

23 ogenase subunits NifD and NifK, and 2OG or a deletion mutation affecting the T-loop of NifI(2) preven

24 CLL/small lymphocytic lymphoma harboring ATM deletions/mutations; all but 1 patient had a decrease in

25 ming this interpretation, a constructed vanS deletion mutation also resulted in constitutive expressi

26 on proteolytic susceptibility and C-terminal deletion mutations also confirms the proposed structure.

27 These deletion mutations also rescue the MMS sensitivity of es

28 were identified by measuring the effects of deletion mutations, amino acid substitution mutations, a

29 Deletion/mutation analyses indicated that each of the th

30 Deletion mutation analysis demonstrated the importance i

31 Deletion mutation analysis identified the LSF-responsive

32 Using deletion mutation analysis in combination with biochemic

33 Deletion mutation analysis revealed a putative polarizat

34 Deletion/mutation analysis of reporter constructs was us

35 Further deletion/mutation analysis revealed that multiple transc

36 riptional activation by UVB in HFK, promoter deletion/mutation analysis was performed.

37 An aprA deletion mutation and a mutation in gene for a putative

38 Deletion mutation and gene knockdown assays revealed tha

39 Using a series of deletion mutations and chimeric receptors of p75(NTR) an

40 We carried out a series of deletion mutations and chimeric swaps within the leucine

41 ntaneously arising and MMS-induced insertion/deletion mutations and large rearrangements were also mo

42 We also detected three short deletion mutations and no insertions, giving a deletion

43 ation have a unique association with exon 19 deletion mutations and show distinct clinicopathologic f

44 We further analyzed the deletion mutations and the Rai1(-/+) allele in a pure C5

45 Exon 19 deletion mutations and the single-point substitution mut

46 he plasticity of gD to tolerate insertion or deletion mutations and to construct an oncolytic HSV-1 t

47 Deletions, mutations and promoter DNA hypermethylation c

48 ucleotide substitutions, small insertion and deletion mutations, and large genomic duplications and d

49 ion, remains chromatin-associated, generates deletion mutations, and maintains cell growth.

50 C, was examined by Ala scanning mutagenesis, deletion mutations, and mutant cycle analyses.

51 82 intraspecific substitution and insertion/deletion mutations, and provided evidence for correction

52 REB) protein in Caco2-BBE cells, whereas our deletion, mutation, and CDX2 overexpression analyses dem

53 riety of mechanisms including amplification, deletion, mutation, and epigenetic silencing.

54 Alterations--such as deletion, mutation, and proteolytic cleavage events--to

55 By promoter deletion, mutation, and transient transfection analyses,

56 genesis is a multistep process that involves deletions, mutations, and changes in expression of genes

57 ng the alterations newly identified, genomic deletions, mutations, and rearrangements recurrently tar

58 Novel deletion mutations are detected at c.739-742delAAAG in L

59 ter vinelandii and some other bacteria, glnD deletion mutations are not lethal in R. rubrum.

60 ate is surprisingly high, and that insertion-deletion mutations are unexpectedly common.

61 om NDMM patients identified presence of TP53 deletions/mutations as a necessary requirement for high-

62 This hydrogen bond network, along with a deletion mutation at alpha53, may lead to HLA-DM insensi

63 Less common point and in-frame deletion mutations at codons 591 to 603 remain incomplet

64 The high prevalence of deletion mutations at Pitx1 may be influenced by inheren

65 Patients with KIT exon 11 deletion mutations benefit most from the longer duration

66 The erb1Delta161-200 and erb1Delta201-245 deletion mutations block a later step than depletion of

67 olymerase lambda, which frequently generates deletion mutations, bound to such intermediates.

68 Most deletion mutations, but not alanine substitutions, of in

69 (Delta170)-F1 vector, bearing an attenuating deletion mutation (C(Delta170)) in the P/C gene and expr

70 e mutations (E399K, G709E and T754M) and one deletion mutation (c.99-100delTC)] absent in ethnically

71 enetic array analysis with a clathrin CLC-NT deletion mutation (clc1-Delta19-76).

72 r of smaller-sized bands (representing mtDNA deletions/mutations) compared with normal corneas.

73 Ms), structurally heterogeneous missense and deletion mutations concentrate at the ECD for unclear re

74 Experiments with deletion/mutation constructs have revealed the importanc

75 Analyses with deletion/mutation constructs reveal that protein domains

76 r shows that the naturally occurring robl(Z) deletion mutation contains the majority of the IC bindin

77 In-frame deletion mutation (Del-L955) in NaV1.7 sodium channel fr

78 ies show that a naturally occurring in-frame deletion mutation (Del-L955) of NaV1.7 channel, identifi

79 KIT exon 11 deletion mutations, deletions that involved codons 557 a

80 xotrophic Salmonella vaccine strain with the deletion mutation Delta(wza-wcaM)8 developed higher vagi

81 es of a Bacillus subtilis strain with a gerD deletion mutation (Delta gerD) responded much slower tha

82 E111A, R116V/K118A, and R160V/H162A, and two deletion mutations, Delta(61-78) and Delta(121-142), on

83 s was attenuated by the inclusion of a codon deletion mutation (Delta1313) and a missense mutation (I

84 the primary loop, W180G and Y185G, plus the deletion mutation Delta491RSRR494 and point mutation 491

85 A partial AP deletion mutation (DeltaAP) also confers a Tra(+) Pil(-)

86 Recently, an in-frame deletion mutation (DeltaE81) in a conserved region from

87 c disease cystic fibrosis (CF) often carry a deletion mutation DeltaF508 on the gene encoding the CF

88 phatase assays utilizing a virus with a UL97 deletion mutation (DeltaUL97 virus) indicated that Cdh1

89 The deletion mutation described resulted in a frameshift, pr

90 PCR products confirmed that this was a 2-bp deletion mutation, designated c.442delAG, leading to a p

91 Multiple quadruple Ser-to-Ala and deletion mutations did not disrupt the phosphorylation o

92 ion of C57Bl/6 mice heterozygous for a Gata4 deletion mutation died within 1 day of birth.

93 NA ternary complex was inhibited unless a 5' deletion mutation disrupted the second stem-loop structu

94 Likewise, deletion mutations disrupting the apoE-NS5A interaction

95 wn as CDX-110), a vaccine targeting the EGFR deletion mutation EGFRvIII, consists of an EGFRvIII-spec

96 Accordingly, the leu2Delta deletion mutation exacerbated Aco1p inactivation in cell

97 , our data provide an example of an in-frame deletion mutation exerting a 'polar' effect on nearby ge

98 A Myo1B deletion mutation exhibited normal larval gut physiology

99 t domains in the Ctr9 sequence, and based on deletion mutation experiments, we demonstrated the role

100 Deletion/mutation experiments have revealed the importan

101 A deletion mutation for type IX collagen is associated wit

102 s (hiPSCs), we efficiently create pathogenic deletion mutations for demonstrable disease models with

103 The deletions/mutations found in DLBCLs are largely monoalle

104 ment did not increase mitochondrial point or deletion mutation frequencies, despite evidence both com

105 ients with KIT exon 11 deletion or insertion-deletion mutation had better RFS when allocated to the 3

106 Seven missense mutations and one in-frame deletion mutation have been reported in the coagulation

107 Although mitochondrial DNA (mtDNA)-deletion mutations have been shown to accumulate with ag

108 Similarly, in the subset with KIT exon 11 deletion mutations, higher-than-the-median mitotic count

109 to generate Hsp70-deficient virions with gag deletion mutations, Hsp70 transdominant mutants, or RNA

110 HV mutational status, 11q deletion, and TP53 deletion/mutation identified CYP2B6*6 and TP53 mutation/

111 ng, the modified nucleotide is reported as a deletion mutation, identifying its location.

112 of the PITX3 gene revealed a heterozygous G deletion mutation in 25 of the 42 family members.

113 We report a novel, homozygous, deletion mutation in a child of Nicaraguan descent in ex

114 Here, we describe a 15-base pair deletion mutation in a regulatory element of GPR56 that

115 vl indicates these phenotypes result from a deletion mutation in an uncharacterized orphan G protein

116 -catenin or the prominent cancer-related S45 deletion mutation in beta-catenin present in human colon

117 in HCC827 and H4006 cells which have an EGFR deletion mutation in exon 19.

118 l pcd(Sid) mice and linked this deficit to a deletion mutation in exon 7 of Nna1.

119 tica strain RBX9, which contains an in-frame deletion mutation in fhaB, encoding filamentous haemaggl

120 A deletion mutation in GRR1, encoding a component of the S

121 reated Apc(Min) mice that carried a targeted deletion mutation in Kcnq1.

122 Furthermore, we found that common deletion mutation in mtDNA was more prevalent in distal

123 identified increased levels of mtDNA common deletion mutation in postmortem sural nerves of patients

124 equences for a recurrent autosomal-recessive deletion mutation in revealing the genetic basis of SPG2

125 m mice lacking RGS11 (RGS11(-/-)), or with a deletion mutation in RGS7 (RGS7(Delta/Delta)), or both,

126 We constructed an in-frame deletion mutation in rpoN (VP2670) in V. parahaemolyticu

127 Another line had an 11-bp deletion mutation in the cls gene.

128 A 4-bp deletion mutation in the Distal-Less 3 (DLX3) gene is et

129 Mice with a null deletion mutation in the gamma interferon (IFN-gamma) re

130 of alanine, while a mutant with an in-frame deletion mutation in the gene for alanine racemase lost

131 nts, Six3 protein with a naturally occurring deletion mutation in the helix 3 of the homeodomain does

132 r heterotopia, caused by an unusual in-frame deletion mutation in the meckelin C-terminus at the regi

133 A deletion mutation in the pgn_1932 gene had a significant

134 OSBP deletion mutation in the PH (DeltaPH) domain failed to l

135 We constructed an in-frame deletion mutation in the sagA gene and found that this m

136 (SHIV-Cs), we identified a 3-asparagine (3N) deletion mutation in the V2 loop stem of gp120 as the ma

137 (CEL maturity onset diabetes of youth with a deletion mutation in the VNTR (MODY)).

138 Wild-type spores carrying an insertion-deletion mutation in this cistron germinated normally; t

139 al aging human subjects and identified mtDNA-deletion mutations in all abnormal fibers.

140 ng keratin K6c, showed heterozygous in-frame deletion mutations in all three kindreds.

141 27 genes, including nonsense, missense, and deletion mutations in Bcl11b, Hist1h2ac, Npy2r, Notch3,

142 ecutive days, and quantified mtDNA point and deletion mutations in bone marrow and liver using our ne

143 heterozygous missense or in-frame insertion/deletion mutations in C1R (15 families) or C1S (2 famili

144 recently been used to generate insertion and deletion mutations in Caenorhabditis elegans, but not to

145 Yeast strains with deletion mutations in candidate SET domain-containing ge

146 y account for the 4.1-fold increase in mtDNA deletion mutations in DCM (P<0.05 versus nonfailing hear

147 n pathogenesis, we constructed disruption or deletion mutations in each of eight AT-encoding genes an

148 cancer tumours that have EGFR mutations have deletion mutations in exon 19 or the Leu858Arg point mut

149 e most common single-nucleotide substitution/deletion mutations in favorable histology Wilms tumors (

150 Furthermore, deletion mutations in genes encoding membrane nitrate re

151 bacterium Bacillus subtilis by constructing deletion mutations in genes predicted to be involved in

152 tients with nonsense, frameshift, splice, or deletion mutations in gp91(phox).

153 In this study, we constructed deletion mutations in gspD and gspE, T2SS genes encoding

154 We measured levels of common deletion mutations in mtDNA and expression levels of mit

155 rains, including C57BL/6J, carry nonsense or deletion mutations in Mx1 and thus a nonfunctional allel

156 In addition, we characterized deletion mutations in nonessential genes of unknown func

157 TR2 and TR3 showed deletion mutations in one (wzb) or multiple genes, respe

158 s who had deleterious truncating, splice, or deletion mutations in PALB2.

159 We constructed and characterized in-frame deletion mutations in several FrzS domains to determine

160 glaucoma revealed clustering of missense and deletion mutations in the 5-phosphatase domain and the R

161 S. flexneri strains containing deletion mutations in the entire suf operon (UR011) or t

162 Mutants with in-frame deletion mutations in the genes for alanine dehydrogenas

163 y missense, nonsense, frameshift, splice, or deletion mutations in the genes for p22(phox), p40(phox)

164 on of the successful attenuating capacity of deletion mutations in the guaBA operon in S. flexneri 2a

165 It is caused by deletion mutations in the last exon of the carboxyl este

166 eport the presence of acquired insertion and deletion mutations in the NF-E2 gene in MPN patients.

167 also has an elevated level of insertion and deletion mutations in the peri-telomeric genes, which is

168 bind HIV-1 gp120, we constructed a series of deletion mutations in the repeat regions of both recepto

169 st neutron (FN) radiation was used to induce deletion mutations in the soybean (Glycine max) genome.

170 We constructed deletion mutations in the usher genes for six of the add

171 g additional examples of previously reported deletion mutations in this region.

172 and six previously reported missense and two deletion mutations in TMEM154.

173 Complementation of the deletion mutations in trans restored drug resistance.

174 DNA sequencing revealed deletion mutations in TTDN1 ranging in size from a singl

175 We examined mtDNA-deletion mutations in vastus lateralis (VL) muscle of hu

176 We introduced nonpolar, defined deletion mutations in waaG (rfaG), waaI (rfaI), rfaH, wa

177 ions (IGH@-CRLF2, P2RY8-CRLF2, CRLF2 F232C), deletion/mutation in genes frequently associated with hi

178 genes were cloned, and chromosomal insertion-deletion mutations inactivating them were obtained to de

179 ases the CaM/Fas binding, and the C-terminal deletion mutation increases the CaM/Fas binding.

180 periodicity and linearity, reveal that while deletion mutations indicate a notable disruption in frac

181 proliferation assays with N- and C- terminal deletion mutations indicated that the central portion of

182 n of new origins is not suppressed by a greA deletion mutation, indicating an active role of DksA rat

183 he pathway (i.e. leu1Delta or leu2Delta gene deletion mutations) induced post-transcriptional up-regu

184 Introduction of the deletion mutation into wild-type gonococci resulted in l

185 n, specifically, a non-temperature-sensitive deletion mutation involving 6 nucleotides in the overlap

186 ith the copresence of complex karyotypes and deletions/mutations involving TP53 demonstrated a partic

187 RNA harboring a complete 3' noncoding region deletion mutation is infectious (not merely quasi-infect

188 In chronic lymphocytic leukemia (CLL), TP53 deletion/mutation is strongly associated with an adverse

189 explored their genetic interactions with 18 deletion mutations known to cause chromosome instability

190 Accordingly, the IEM deletion mutation L955 (DeltaL955) fails to produce resu

191 hat seven nontruncating missense or in-frame deletion mutations (L986F, delF1289, R1648C, F1661S, G16

192 Four discrete insertion/deletion mutations leading to frame shifts and premature

193 of the 5' flanking region by progressive 5' deletion mutations localized transcription repression el

194 breast tumors, there are specific insertion/deletion mutations located close to R-loop-mediated BRCA

195 f these mutations involve either missense or deletion mutations located in a region of the proSP-C mo

196 The insertion-deletion mutations may play an important role in Ycf1 ge

197 sed frequency of chromosomal translocations, deletions, mutations, micronuclei, and decreased plating

198 utations at pre-binding sites, insertion and deletion mutations, microsatellite expansions, or tandem

199 nctional effect of overexpression of a 21-bp deletion mutation (mt) of CYTB.

200 Protein 6 with C-terminal deletion mutations no longer interfered with nuclear imp

201 concomitantly reduces the occurrence of "-1 deletion" mutations observed opposite the lesion at lowe

202 identified and characterized a novel exon 27 deletion mutation occurring within the EGFR carboxyl-ter

203 ozygous missense or small in-frame insertion/deletion mutations occurring within one of the helix bou

204 ed to infantile RCM resulting from a de novo deletion mutation of glutamic acid 96.

205 lls containing intact wild-type genomes or a deletion mutation of the COX2 gene gave rise to populati

206 genomic editing, we discovered that a small deletion mutation of the Mel1a melatonin receptor (mtnr1

207 otide 'TAG' sequences incorporated into each deletion mutation of the yeast knockout collection, allo

208 tinct from previously described insertion or deletion mutations of a few nucleotides(5).

209 In-frame deletion mutations of all of the ctp genes, with the exc

210 Finally, heritable deletion mutations of at least 50 kbp can be readily ind

211 these genes in pathogenesis, large in-frame deletion mutations of bcaA and bcaB were constructed in

212 ation has negative genetic interactions with deletion mutations of both capping protein subunits and

213 that 18.3% of relapse cases had sequence or deletion mutations of CREBBP, which encodes the transcri

214 We generated isogenic MCF10A cell lines with deletion mutations of genes encoding cohesin subunits SM

215 viruses and was sensitive to specific glycan deletion mutations of HIV-1 glycoproteins, indicating th

216 ivo function, we generated and characterized deletion mutations of Id2 and of Id4.

217 Deletion mutations of irr and rirA, alone and in combina

218 Point and deletion mutations of Noxa confirmed that both the BH3 d

219 Deletion mutations of PTB in this system allowed us to i

220 Deletion mutations of retromer subunits cause ALM and PL

221 Precise null deletion mutations of the mshA gene were generated by sp

222 ial myosin-II heavy-chain gene (myo2-E1) and deletion mutations of the other myosin heavy-chain genes

223 The rate of insertion and deletion mutations of the replicase of Cucumber mosaic v

224 The duplication and deletion mutations of the S-SCAM/MAGI-2 gene are associa

225 Through deletion mutations of the TriMV 5' untranslated region (

226 iver and tumour tissue revealed insertion or deletion mutations of the tumour suppressor genes, inclu

227 We constructed deletion mutations of these genes in the F. tularensis l

228 Analogous single-gene deletion mutations of these genes showed significantly s

229 Mutants with in-frame deletion mutations of two of the genes identified from t

230 purified, and assayed a series of N-terminal deletion mutations of VP30 for RNA binding.

231 With one exception, deletion/mutation of a single terminal nucleotide in one

232 tightly linked to deletion of DDX3Y and that deletions/mutations of USP9Y can be transmitted from one

233 on immunogenicity and the efficacy of a sopB deletion mutation on two Salmonella enterica serovar Typ

234 f the cadherin point mutation W2A and domain deletion mutations on C-cadherin binding signatures.

235 t genes, permitting an extensive analysis of deletion mutations on protein function.

236 t is underexpressed in many cancers owing to deletions, mutations or gene silencing.

237 efit was also observed in patients with TP53 deletion, mutation, or both and in patients with unmutat

238 functions in a virus-specific mode, and its deletion, mutation, or replacement by the same subdomain

239 We find an absence of PTEN deletions, mutations, or protein mislocalization in PEL.

240 in mouse embryos, including indel (insertion/deletion) mutations, point mutations, large deletions, a

241 y identified 2 patients with novel insertion/deletion mutations predicted to result in mRNA nonsense-

242 PTEN genomic alterations (deletion, mutation), promoter methylation, and protein d

243 and X2392S (rs150529054) and a large exon 3 deletion mutation, Q2053del224.

244 letion mutations and no insertions, giving a deletion mutation rate of 1.2 x 10(-9) (95% confidence i

245 Deletion mutation rates were different for the two hosts

246 satory functions for the 3' noncoding region deletion mutation replication defect.

247 ice with a mutation that resembles the large deletion mutation reported in patients.

248 ration (STGD3), with a five base-pair (5 bp) deletion mutation resulting in the loss of 51 carboxy-te

249 reaction driven by dithiothreitol, the 43-51 deletion mutation retained 85% and C43A/C51A 112% of the

250 ype that results from the p.epsilonDeltaF266 deletion mutation revealed by the coinheritance of the l

251 Serial deletion mutations revealed a Dex-responsive 7-base pair

252 Embryonic stem cells with the SHP-2 deletion mutation showed markedly decreased sensitivity

253 ptional activity mediated by the PR NTD, and deletion mutations showed that a region (amino acids 327

254 A pspA deletion mutation significantly attenuates the virulence

255 nstable conformation, whereas the C-terminal deletion mutation stabilized the Fas conformation, and b

256 Deletion/mutation studies further show that a 26-bp prom

257 ere further grouped as deletion or insertion-deletion mutations, substitution mutations, insertion or

258 te the properties of this subdomain, a small deletion mutation (targeting aspartic acid 346 and glyci

259 fication had significantly more EGFR exon 19 deletion mutations than adenocarcinomas with disomy, and

260 However, an alternative comD deletion mutation that caused an increase in comE transc

261 We have generated a deletion mutation that eliminates 10 of the 12 viral miR

262 Site-specific deletion mutations that resulted in either aflagellate,

263 SCH9 overexpression or PPH22 deletion, mutations that activate target of rapamycin (T

264 After identifying an insertion-deletion mutation, the remaining 92 families were screen

265 utations were identified, including two 2-bp-deletion mutations, the first non-nonsense mutations ide

266 Here we took advantage of this deletion mutation to understand the role of the S6 helix

267 vivo was investigated by combining in-frame deletion mutations to generate all possible double, trip

268 e sites could allow single base insertion or deletion mutations to occur, and stringent DNA groove mo

269 Previous studies had utilized insertion and deletion mutations to show that portions of the MLD are

270 al sequences present in the in vitro-derived deletion mutation transcripts.

271 n induces an especially high frequency of -2 deletion mutations; vulnerability to these mutations is

272 The in-frame deletion mutation was found to be inherited from the mot

273 An sll1951 deletion mutation was introduced into Synechocystis and

274 er number of microsatellite expansion versus deletion mutations was observed, and expansion rates of

275 By deletion mutations, we identified the Nt regions importa

276 One MLH1 and one MSH2 deletion mutation were found in MSI-stable/low cases, in

277 ological role of LdTyrRS in Leishmania, gene deletion mutations were attempted via targeted gene repl

278 ysiological role of ASNA in Leishmania, gene deletion mutations were attempted via targeted gene repl

279 Deletion mutations were clonal within a fiber and concom

280 Deletion mutations were constructed in six genes of the

281 addition, compound heterozygous missense and deletion mutations were found in three additional unrela

282 Insertion-deletion mutations were generated in motB and fliI, whic

283 Repetitive-element-mediated deletion mutations were highly conserved within the spec

284 Here, a series of SLK19 in-frame deletion mutations were used to test whether Slk19p has

285 ound in high CRLF2 expressors, whereas IKZF1 deletions/mutations were distributed across the full coh

286 ght independent alleles, with frameshift and deletion mutations) were created in C3H and C57BL/6J bac

287 ingle nucleotide polymorphisms and insertion/deletion mutations when our Weiss (n = 4) and Nigg (n =

288 ique to a given line, except for a single-nt deletion mutation which occurred independently in two li

289 nd that RNF8 suppresses EJ without insertion/deletion mutations, which is a hallmark of C-NHEJ.

290 tection confirmed specific genomic insertion/deletion mutations with 99.5% penetrance in sorted cells

291 Each gene has a coding sequence insertion/deletion mutation within the SC species that produces a

292 We recovered a 15 bp deletion mutation within this enhancer that identified a

293 Using minigenes carrying deletion mutations within intron 11, we demonstrated tha

294 t contained frameshift, point, insertion, or deletion mutations within rdxA, possibly revealing genet

295 f HDAC6, stop/gain insertion in MORF4L1, and deletion mutations within SWI/SNF complex component SMAR

296 Recently, the V170D and the G54-P57 deletion mutations within the CAP1/Prss8 gene, identifie

297 Several deletion mutations within the pstSCAB-phoU operon were t

298 We report that deletion mutations within the S4-S5 linker (amino acids

299 made a collection of truncation and in-frame deletion mutations within the VP1/2 gene (UL36) and exam

300 Only five deletion mutations yielded lethal phenotypes, and these