ライフサイエンスコーパス: knockout mutant

1 nsitive phenotype of the Arabidopsis mtp11-3 knockout mutant.

2 ein import-defective phenotypes of an hsp93V knockout mutant.

3 faced core gp120 probe and its cognate CD4bs knockout mutant.

4 revealed that this strain is not a true prrA knockout mutant.

5 al surface of the wild type but not the OppA knockout mutant.

6 plete absence of tassel branches in the bif2 knockout mutant.

7 in five times faster than into the fcbT1T2T3 knockout mutant.

8 ignaling might be affected in the Lpp double-knockout mutant.

9 n system were not affected in the lpp double-knockout mutant.

10 upernatant of cells infected with a cmvIL-10-knockout mutant.

11 s and T84 cells infected with the lpp double-knockout mutant.

12 e susceptible to infection by the lpp double-knockout mutant.

13 mitochondrial calcium uptake capacity in the knockout mutant.

14 opied an ACTIN DEPOLYMERIZING FACTOR4 (ADF4) knockout mutant.

15 Physcomitrella patens, we generated a pgrl1 knockout mutant.

16 and root epidermal protoplasts of the Atann1 knockout mutant.

17 oth responses are largely diminished in shyg knockout mutants.

18 were determined via SMRT sequencing of gene knockout mutants.

19 core proteins and their corresponding CD4bs knockout mutants.

20 pendent of target size, exclusively recovers knockout mutants.

21 y particle bombardment to engineer 1201 gene knockout mutants.

22 ploid-convertible heterozygous diploid yeast knockout mutants.

23 and XI-2/XI-B, using single and double gene-knockout mutants.

24 o molybdoenzymes in Arabidopsis thaliana PCD knockout mutants.

25 were studied by growth phenotype analysis of knockout mutants.

26 absence of LIP8 expression in the homozygous knockout mutants.

27 athogenicity island (PAI) mutants, or double knockout mutants.

28 ignal transduction pathway is present in the knockout mutants.

29 was slower than that of wild type and single knockout mutants.

30 he phenotype of Fz5/Fz8 compound conditional knockout mutants.

31 an explain some phenotypes observed in ife-4 knockout mutants.

32 nalyzed by using Tn5 transposon-mediated spu knockout mutants.

33 mizygous Bax +/- controls, and three Bax -/- knockout mutants.

34 hemizygous Bax +/- controls, and six Bax -/- knockout mutants.

35 p in resistance, we created double NspA/FHbp knockout mutants.

36 tor degeneration than that in the RPGR null (knockout) mutant.

37 Expression of VviCCC in an Arabidopsis ccc knockout mutant abolished the mutant's stunted growth ph

38 tein accumulation by systematically stacking knockout mutant alleles of all four members (alphaVPE, b

39 A mur3 knockout mutant also resists infection by H. parasitica

40 gregation and molecular analyses of the NPG1 knockout mutant and a cross with a male sterile mutant i

41 lso observed in a DeltapauA2DeltaphoU double knockout mutant and complemented by the wild-type phoU g

42 organisms in acid was absent in the alpha-CA knockout mutant and in the presence of acetazolamide, al

43 However, both the amyR knockout mutant and over-expression strains showed reduc

44 ng molecular and biological responses of the knockout mutant and overexpression lines of AtRAP upon b

45 Analysis of a thaxtomin dual module knockout mutant and single module knockout mutants revea

46 er of flagella was similar in the lpp double knockout mutant and the WT serovar Typhimurium.

47 Through a series of markerless gene knockout mutants and complementation tests, specific com

48 ological studies on Drosophila atm and mre11 knockout mutants and discovered a telomere defect that w

49 PLATZ1, PLATZ2, and AGL67 were confirmed by knockout mutants and overexpression in a desiccation-int

50 udy system, we employ reverse genetic tools (knockout mutants and RNA interference) to demonstrate th

51 ene and verified its identity by analysis of knockout mutants and transformation.

52 Using Oswrk47 knockout mutants and transgenic rice overexpressing OsWR

53 d transporter1 and ferric chelate reductase2 knockout mutants and was prioritized over immunity, as h

54 ies using gp120 core protein, single-residue knockout mutants, and chimeric viruses revealed that G37

55 n, we generated dcl2drb4 and dcl4drb4 double knockout mutants, and subjected them to infections with

56 ic screen for suppressors of chlorotic tic40 knockout mutant Arabidopsis thaliana plants.

57 ae and that several single and multiple gene-knockout mutants are computationally predicted to improv

58 cdkc;2 and cyct1;5 knockout mutants are highly resistant and cdkc;2 cyct1;5

59 Single fps1 and fps2 knockout mutants are phenotypically indistinguishable fr

60 larvae of B. mori infected with a BmNPV ptp knockout mutant (BmPTPD).

61 Analysis of pollen development in the knockout mutant by light microscopy showed normal pollen

62 ACC2 knockout mutants, by contrast, are hypersensitive.

63 emarkably, in some plant species, homozygous knockout mutants can be produced in a single generation.

64 oipA knockout mutants caused reduced inflammation and decreas

65 iae yeast strain, and Mn sensitivity of mtp8 knockout mutants characterized the protein as a vacuolar

66 Leaf senescence is delayed in the SAG113 knockout mutant compared with that in the wild type, sto

67 sed significantly by over 30% in the Bax -/- knockout mutants compared with wild type and hemizygote

68 ssing the two genes in trans in the two-gene knockout mutant complemented full virulence.

69 Expression of NPG1 in the knockout mutant complemented the mutant phenotype.

70 tenoid hydroxylase activities in vivo, T-DNA knockout mutants corresponding to beta-hydroxylases 1 an

71 Seed permeability assays of knockout mutants corresponding to signature genes reveal

72 in and an isogenic transcriptional regulator knockout mutant (covR) also were compared.

73 tored in the wild-type strain, as well as in knockout mutants defective in a variety of methylotrophy

74 accine strain measles virus (MV) or isogenic knockout mutants deficient for either V (V(ko)) or C (C(

75 -rbt1), its control (DAY286), homozygous rbt knockout mutants deficient in rbt1 (BCa7-4) or rbt4 (BCa

76 t mutant, DeltaaebG V. harveyi, and the NRPS knockout mutant, DeltaaebF V. harveyi, do not produce am

77 The FACL knockout mutant, DeltaaebG V. harveyi, and the NRPS knoc

78 The knockout mutant Deltamnx showed increased sensitivity to

79 The construction of nonpolar markerless phpP knockout mutants (DeltaphpP) in two pathogenic strains,

80 n from Taiwan, together with an isogenic PVL-knockout mutant (Deltapvl) and complemented PVL-positive

81 wild-type S. aureus cell but not the double knockout mutant DeltatarM/S, which lacks both alpha- and

82 ve cell-wall analytical assays of the double knockout mutant demonstrated reduced levels of pectin me

83 t construction and examination of single ccm knockout mutants demonstrated that membrane insertion an

84 Interestingly, the knockout mutant did not exhibit enhanced plant growth in

85 Hpse2 knockout mutants display a distended bladder (megacystis

86 mekk1 knockout mutants display a severe dwarf phenotype, const

87 e role of LjNPF8.6 on nodule functioning, as knockout mutants display N-fixation deficiency (25%) and

88 Interestingly, mri-knockout mutants display spontaneous PT and root-hair bu

89 Consistently with this observation, an npr3 knockout mutant displayed enhanced resistance to Pseudom

90 A Pseudomonas aeruginosa PPHD knockout mutant displays impaired growth in the presence

91 These knockout mutants document the importance of His biosynth

92 wer autophagosomes are generated in the NAP1 knockout mutant during starvation stress.

93 ALA10-knockout mutants exhibit reduced phospholipid uptake at

94 xpressing plants stayed green and the sgr2-1 knockout mutant exhibited early leaf yellowing under age

95 not observed in slice cultures from Munc13-1 knockout mutants exhibiting defective vesicle priming.

96 We further show that a pgp4 knockout mutant exhibits an in vitro phenotype similar t

97 The s3h knockout mutants fail to produce 2,3-DHBA sugar conjugat

98 that of wild-type A. hydrophila; the triple-knockout mutant failed to induce any detectable level of

99 A knockout mutant for Arabidopsis ADF4 has longer hypocoty

100 Physiological analysis of a transferred DNA knockout mutant for AtALMT1 as well as electrophysiologi

101 A knockout mutant for KNL2 shows a reduced level of cenH3

102 This indicates the possible usage of TTM2 knockout mutants for agricultural applications to genera

103 We isolated gene knockout mutants for all 13 class XI myosins present in

104 Knockout mutants for athb13 showed increased primary roo

105 Knockout mutants for BGLU45 or BGLU46 do not have a lign

106 les of peroxisomal LACS, we identified T-DNA knockout mutants for both genes.

107 gene switch status, as well as isogenic gene knockout mutants for cagE, oipA, babA2, hopZ, cagE/oipA,

108 Creation of knockout mutants for Cel48S (also known as CelS, S(S), a

109 o, we conducted a comparative study of T-DNA knockout mutants for each Tic gene, and for the most abu

110 Knockout mutants for putative BH4 synthetic enzyme genes

111 of Arabidopsis, including single and double knockout mutants for the high-affinity transporter, AtHA

112 d cytokinin degradation as well as different knockout mutants for the negative AUX/IAA regulators shy

113 lished a comprehensive study covering 269 TF knockout mutants for the yeast Saccharomyces cerevisiae.

114 of lignified tissues of various Arabidopsis knockout mutants (for AtCAD5, 6, and 9) at different sta

115 Unlike the wild type, an asr1734 knockout mutant formed 5% heterocysts after a nitrogen s

116 erichia coli, and each can rescue the double knockout mutant from osmotic downshock.

117 AOX1D expression is increased in aox1a knockout mutants from Arabidopsis (especially after rest

118 In nonimmune blood, fHBP knockout mutants from high-expressing stains do not surv

119 CML38-knockout mutants generated via T-DNA insertion were inse

120 nd glucan binding protein C (GbpC) in a tarC knockout mutant (GMS900), thereby supporting the notion

121 relA, csdA, and dac2 knockout mutants grew more slowly at low temperature, bu

122 Knockout mutants grew poorly, but attenuation of Zn(II)2

123 Moreover, multiple sac knockout mutants had an increased number of smaller stor

124 fzl knockout mutants have abnormalities in chloroplast and t

125 Remarkably, slp1 knockout mutants have reduced protein and activity level

126 The T-DNA knockout mutant hcf222-2 showed a more severe defect wit

127 icola ATCC 33520 flgE erythromycin-resistant knockout mutant HL210.

128 fer is specific to the donor strain; an lpqM knockout mutant in the recipient is still proficient in

129 Unlike the available set of homoplasmic knockout mutants in 25 plastid genes, the rbcL deletion

130 The system includes knockout mutants in all ABC and putative auxin transport

131 Analysis of alix knockout mutants in Arabidopsis showed that ALIX is esse

132 opy and that has not been reported with Mlh3 knockout mutants in Arabidopsis.

133 However, it has been shown that knockout mutants in fact reach the steady states with th

134 To address this, we generated knockout mutants in the moss Physcomitrella patens using

135 -Bar_gosGFP to produce activation-tagged and knockout mutants in the processing tomato cultivar M82.

136 lmonella enterica serovar Typhimurium double-knockout mutants in which either the lipoprotein A (lppA

137 y, we describe a method for rapidly creating knockout mutants in which we make use of yeast recombina

138 c program in Medicago truncatula TR25 (symrk knockout mutant) in the absence of rhizobia.

139 Analysis of knockout mutants indicated that GLR3.3 was a required co

140 Wall fractionation analysis of axy4 knockout mutants indicated that only a fraction containi

141 , the resulting nonfeasibility of creating a knockout mutant is a major limiting factor in studying i

142 However, an mfd knockout mutant is not hypersensitive to either aza-C-in

143 A triple cdkd knockout mutant is not viable, but a combination of null

144 igin of replication and the M. smegmatis glf knockout mutant is unable to grow at the higher temperat

145 wever, a striking characteristic of elt-2(0) knockout mutants is that while they die shortly after ha

146 rate that the backcrossing of wild mice with knockout mutant laboratory mice retrieves behavioural tr

147 An indh knockout mutant lacked complex I but had low levels of a

148 Knockout mutants lacking all EBs are viable and fertile

149 Targeted P. patens knockout mutants lacking either PpSMF1 or PpSCRM1 develo

150 and early seedling development, we utilized knockout mutants lacking one or more of these components

151 We show that a tpc1 knockout mutant lacks functional slow vacuolar channel a

152 A T-DNA knockout mutant (lacs9-1) was identified by reverse gene

153 Here, we report that rsp knockout mutants lead to global transcriptional and prot

154 A T-DNA knockout mutant, lecrka4.1-1, slightly enhanced ABA inhi

155 Chloroplasts isolated from the atHsp93-V knockout mutant line are still able to import a variety

156 cal, and pollen germination studies with the knockout mutant line indicate that NPG1 is not necessary

157 owth conditions, two independent Arabidopsis knockout mutant lines displayed significantly reduced le

158 Several Arabidopsis knockout mutant lines for genes involved in polyester bi

159 Lipidomic analysis of knockout mutant lines of these five genes showed a signi

160 rotein import into chloroplasts, we isolated knockout mutant lines that contain T-DNA disruptions in

161 m, we generated two cyp71a12 cyp71a13 double knockout mutant lines.

162 Generation of knockout mutant mice has currently been achieved by many

163 Sperm of the double knockout mutant mice show responses to stimulus by HCO3

164 types to those found in the respective Kcnq2 knockout mutant mice, suggesting that Kcnq2 haploinsuffi

165 By using conditional knockout mutant mice, we report that neuronal autophagy

166 Smad1/5(CKO) (cartilage-specific knockout) mutant mice are nearly identical to Smad1/5(CK

167 We find homozygous Mllt10 knockout mutants (Mllt10-KO) exhibit midline facial clef

168 Seed of a knockout mutant, nic2-1, had reduced nicotinamidase acti

169 By examining AHA2 localization in a knockout mutant of a receptor protein kinase, FERONIA, w

170 A null T-DNA knockout mutant of AtAGP19 was obtained and compared to

171 uppressor screen of a transfer DNA insertion knockout mutant of AtCNGC2 in order to identify downstre

172 A knockout mutant of AtGPAT9 demonstrates both male and fe

173 In this report, we generated a knockout mutant of crgA (DeltacrgA) in the serum-sensiti

174 Prior infection with an fpv014-knockout mutant of FWPV still blocked transfected poly(I

175 Creation of a gene 5a knockout mutant of MHV-A59 demonstrated that a major com

176 ar preparations of an isogenic lst insertion knockout mutant of N. gonorrhoeae F62 (strain ST01) expr

177 nti-VT2 antibodies, while a VT1 and VT2 gene knockout mutant of PM601 was unable to stimulate JNK act

178 M NaCl treatment in wild-type rice (WT); GR3 knockout mutant of rice (gr3); and the functional gr3-co

179 lonized more efficiently on the sgc protease knockout mutant of S. gordonii than on the parent biofil

180 uced by transfection of a nonreplicative NS1 knockout mutant of the MVC infectious clone, as well as

181 t findings of embryo death in the homozygous knockout mutant of the plastid LPAAT contrasts with earl

182 to the identification of a grazer-resistant knockout mutant of the wzm ABC O-antigen transporter gen

183 Generation of a knockout mutant of this regulatory gene in the nonfood b

184 We constructed a knockout mutant of VC1758 (int) with V. cholerae strain

185 In either of the knockout mutants of AHL3 and AHL4, encoding closely rela

186 next isolated and characterized insertional knockout mutants of all three isoforms confirming a comp

187 Knockout mutants of Arabidopsis, deficient in various ke

188 Knockout mutants of AT5G41040 show almost complete elimi

189 Knockout mutants of At5g63560 were severely reduced in t

190 Knockout mutants of bHLH142 exhibited retarded meiosis a

191 We constructed insertional knockout mutants of both the peb3 and cgpA genes, and su

192 Knockout mutants of CPRabA5e displayed delayed seed germ

193 sublethal levels in aerobically growing SOD knockout mutants of Escherichia coli.

194 , pollen fitness, and pollen tube growth for knockout mutants of five of the six myosin XI genes expr

195 Knockout mutants of genes for protease subunits are of l

196 Knockout mutants of GGT2 and GGT4 showed no phenotype.

197 e analyses of overexpressing hairy roots and knockout mutants of MtMYB5 and MtMYB14 indicate that MtM

198 Specific knockout mutants of pilABCD of strain D7S were construct

199 Knockout mutants of Plasmodium falciparum lacking pfpm1,

200 o indicated by frequently subdued effects of knockout mutants of regulators, their evolutionary losse

201 fter 24 h of focal cerebral ischemia in both knockout mutants of SOD1 (Sod1 -/+ and Sod1 -/-) and wil

202 In this study, we attempted to generate knockout mutants of the ortholog of yeast HOG1 MAP kinas

203 Previous work has established that the knockout mutants of these genes display heat-sensitive p

204 Knockout mutants of this transporter failed to grow on m

205 sition system to generate single- and double-knockout mutants of two tandemly duplicated cytochrome P

206 Knockout mutants of yajQ do not support the replication

207 ve heat shock response of mycobacterial sigE knockout mutants only in the presence of a functional my

208 cagA knockout mutants or CagA phosphorylation-defective mutan

209 In Arabidopsis, the oxoprolinase knockout mutants (oxp1-1 and oxp1-2) accumulate more 5-o

210 TF knockout mutant phenotypes are consistent with model pre

211 We further demonstrated that two knockout mutants (pilB and pilQ mutants) that are defici

212 AtTTM2 knockout mutant plants exhibit an enhanced hypersensitiv

213 In contrast, knockout mutant plants for atHsp93-III, the second Arabi

214 The size of AtHIPM knockout mutant plants of Arabidopsis was slightly large

215 overexpress BEE1 with bee1 bee2 bee3 triple-knockout mutant plants suggests that BEE1, BEE2, and BEE

216 fication and characterization of two atToc34 knockout mutants, plastid protein import 3-1 (ppi3-1) an

217 s (Arabidopsis thaliana) and phospholipase D knockout mutants pld zeta1, pld zeta2, and pld zeta1 pld

218 n FH domains 6 and 7 fused to Fc than double knockout mutants prepared from two sensitive meningococc

219 One knockout mutant produced fruiting bodies of abnormal sha

220 Knockout mutants produced more mycelium, particularly at

221 on is abrogated in double and quadruple pp2c knockout mutants, provoking, similarly to SnRK1 overexpr

222 in mice of 2,578 barcoded Plasmodium berghei knockout mutants, representing >50% of the genome, and c

223 SXD1 in a Synechocystis sp. PCC6803 slr1737 knockout mutant restored tocopherol synthesis, indicatin

224 Expression of CBP in the pme3 knockout mutant revealed that PME3 is required but not t

225 ariants produced by a M. tuberculosis Rv2181 knockout mutant revealed the presence of but a single Ma

226 ual module knockout mutant and single module knockout mutants revealed that 4-nitrotryptophan is an i

227 A novel, conditional FUS knockout mutant reveals that postnatal elimination of FU

228 nerated the recombinant rGLS virus and an NS knockout mutant, rGLSNSdelta virus, using reverse geneti

229 The knockout mutant sdg8 displays a reduced growth phenotype

230 lowed Arabidopsis wild type but not AtHSP101 knockout mutant seedlings to survive otherwise lethal te

231 s transposition in calli derived from dng701 knockout mutant seeds compared with that in wild-type ca

232 Rice cslf6 knockout mutants show a slight decrease in height and st

233 A mot1.3-1 knockout mutant showed impaired growth concomitant with

234 Interestingly, an sigH-knockout mutant showed increased sensitivity to a sustai

235 The znu knockout mutant showed marked impairment in its capacity

236 An oppA knockout mutant showed marked impairment in its capacity

237 In addition the NarK2 knockout mutant showed no defect in nitrite export.

238 susceptibility to H. schachtii, while a pme3 knockout mutant showed opposite phenotypes.

239 in different organs of wild-type and a ggt3 knockout mutant showed that GGT3 was a major contributor

240 Analysis of LDIP T-DNA knockdown and knockout mutants showed a decrease in LD abundance and a

241 lysaccharide preparations from RGP1 and RGP2 knockout mutants showed a significant reduction in total

242 Knockout mutants showed impaired stomatal closure in res

243 An fcbT1T2T3 knockout mutant shows a much slower growth rate on 4-chl

244 An atku80 knockout mutant shows hypersensitivity to the DNA-damagi

245 ation across experimental conditions for all knockout mutants simultaneously.

246 ota/1145/2007 (H3N2) (SIV 1145-WT), a PB1-F2 knockout mutant (SIV 1145-KO), and its N66S variant (SIV

247 The quadruple knockout mutants still contained about 10% of the wild-t

248 Plate-killing assays indicate that a PE-knockout mutant strain of Escherichia coli drastically o

249 n of the growth of the Escherichia coli uxaB knockout mutant strain on galacturonate.

250 The resulting putA knockout mutant strain was characterized by oxidative st

251 Third, using different knockout mutant strains for the PlcH operon, PlcH was fo

252 Arabidopsis hpat1/2/3 triple knockout mutants suffer from a strong male sterility def

253 RNA blots and analysis of enzyme activity in knockout mutants suggest that GGT1 is expressed most str

254 A triple-knockout mutant tga2-1 tga5-1 tga6-1 was shown previousl

255 We have now constructed an E knockout mutant that confirms that the highly defective

256 The acs1 knockout mutant that has a disruption in the plastidic a

257 and actin-interacting protein 1, as well as knockout mutants that lack Coronin and actin-interacting

258 In an fra1-5 knockout mutant, the expansion rate of the inflorescence

259 We used a fliL knockout mutant to gain further insight into the functio

260 Failure of an E. ictaluri urease knockout mutant to increase the ECV pH in the in vivo ra

261 ted the relative lethality of 11 known mouse knockout mutants to categorize essentiality.

262 The different phenotypes of Phox2 knockout mutants, together with their asynchronous onset

263 The increased sensitivity of atpollambda knockout mutants toward high salinity and MMC treatments

264 x-deficient cells, and so does the HCMV pp71 knockout mutant UL82(-/-) in normal cells.

265 ative analysis of seedling growth of snrk2.4 knockout mutants versus wild-type Arabidopsis suggests t

266 ally induced apoptosis indicated that the NS knockout mutant virus induces earlier and increased DNA

267 Compared to the wild-type virus, the ToV-PLP knockout mutant virus showed impaired growth and induced

268 tosis indicated that the NV-deficient and NV knockout mutant viruses induce apoptosis earlier in cell

269 ed earlier, amylovoran production in an amyR knockout mutant was about eight-fold higher than that in

270 t Dicarboxylate Transporter (tDT) in the tdt knockout mutant was associated previously with an impair

271 The lpp double-knockout mutant was avirulent in mice, and animals infec

272 The pgk3.2 knockout mutant was characterized by reduced growth but

273 d as a lipoprotein and purified, and an oppA knockout mutant was constructed.

274 The lpp double-knockout mutant was defective in invading and inducing c

275 To study its physiological role, a SynK-less knockout mutant was generated and characterized.

276 role of LytSR in biofilm development, a lytS knockout mutant was generated from a clinical S. aureus

277 In addition, the rgga knockout mutant was hypersensitive to ABA in root growth

278 t in reduced virulence; however, an mltE(EA) knockout mutant was reduced in virulence and growth in i

279 A series of knockout mutants was engineered, each mutant compromised

280 rimary roots in PLDzeta1 and PLDzeta2 double knockout mutants was slower than that of wild type and s

281 y comparative metabolomics of overexpression/knockout mutants, we identified a tryptophan-derived iro

282 ugh construction and analysis of a series of knockout mutants, we identified the genes necessary for

283 Moreover, while the ccm knockout mutants were completely incompetent for photosy

284 dadRAX knockout mutants were constructed and subjected to analy

285 Two constitutive double knockout mutants were generated (designated as dpe2-1xph

286 B'theta knockout mutants were impaired in peroxisomal beta-oxida

287 Strikingly, the pdx1 knockout mutants were impaired in root growth and early

288 MAM overproduction and knockout mutants were more and less mitogenic, respectiv

289 The knockout mutants were more efficiently ingested and kill

290 lated in As-treated Arabidopsis, and ggct2;1 knockout mutants were more tolerant to As and cadmium th

291 Corresponding knockout mutants were tested for the ability to mobilize

292 ssing the ppi3 mutants with ppi1, an atToc33 knockout mutant) were unsuccessful, indicating that the

293 In contrast, an isogenic fHbp knockout mutant, which grew well in broth, was rapidly k

294 wo independent pal1 pal2 pal3 pal4 quadruple knockout mutants, which are stunted and sterile.

295 h the investigation of independent complex I knockout mutants, which were found to have corresponding

296 t, and (iii) act and ast genes; and a triple-knockout mutant with truncation in all three genes, act,

297 the number of Purkinje and granule cells in knockout mutants with a deletion in the proapoptotic gen

298 pylori and isogenic oipA, hopZ, or cagE gene knockout mutants with gastric cancer cells.

299 e markedly opposite phenotypes to the double knockout mutant, with increased cell-wall methylesterifi

300 t created >5900 'molecularly barcoded' yeast knockout mutants (YKO mutants).