ライフサイエンスコーパス: absolute requirement

1 NADH dehydrogenase I, although there was no absolute requirement.

2 ed activation but indicate that it is not an absolute requirement.

3 for all pairs, indicating that it is not an absolute requirement.

4 show that NMDA receptor activation is not an absolute requirement and that DDI can be evoked solely b

5 ll allele of germ cell-less to determine its absolute requirement during development.

6 rt/delta xprt mutant strain that exhibits an absolute requirement for 2'-deoxycoformycin, an inhibito

7 appa) genes in 3'E(kappa)(-/-) mice found no absolute requirement for 3'E(kappa) in kappa SHM.

8 ty and other DNA glycosylases do not have an absolute requirement for a cofactor.

9 e phosphatases, except that there was not an absolute requirement for a conserved acidic residue that

10 The enzyme has an absolute requirement for a divalent cation, an optimal p

11 It has an absolute requirement for a divalent metal cation and exh

12 The enzyme has an absolute requirement for a divalent metal ion and a mono

13 ral T and dA bases in a reaction that has an absolute requirement for a divalent metal ion, physiolog

14 resence or absence of FnrL, there remains an absolute requirement for a functional fnrL gene for phot

15 We demonstrate the absolute requirement for a functioning class II-restrict

16 Chemotaxis, however, had an absolute requirement for a G(i)-mediated pathway.

17 stead of a charged residue), but there is an absolute requirement for a Glu residue at position 6.

18 Ca(2+) release and therefore do not have an absolute requirement for a gradient in either inositol t

19 agnosis and treatment, such as the perceived absolute requirement for a ketogenic diet, the assumed l

20 time- and concentration-dependent, it had an absolute requirement for a peroxide substrate, and it wa

21 virus, that HPIV2 has a strong and seemingly absolute requirement for a polyhexameric genome.

22 Substrate analogue inhibitors display an absolute requirement for a positive charge at the positi

23 al translation elongation is striking in its absolute requirement for a third factor, the ATPase eEF3

24 However, the absolute requirement for Abeta42 for amyloid deposition

25 misfolding events occur that do not have an absolute requirement for abnormal Cys185-Cys187 disulfid

26 gen bonds between complementary bases are an absolute requirement for accurate DNA replication.

27 that tyrosine phosphorylation may not be an absolute requirement for actin recruitment.

28 roup in the flexible side chain of PTX is an absolute requirement for activity, but its precise role

29 ound only in algal APS reductases, is not an absolute requirement for activity.

30 The solubilised galactosyltransferase has an absolute requirement for added acceptor substrates.

31 cannot grow on 6-oxypurines and displays an absolute requirement for adenine or adenosine and 2'-deo

32 capable of complementation, demonstrating an absolute requirement for all cysteines in planta.

33 We demonstrate an absolute requirement for AML1 in functional HSCs.

34 of principle that TARP association is not an absolute requirement for AMPAR clustering at synapses, m

35 Thus, while aromatic residues are not an absolute requirement for amyloid formation by IAPP, they

36 ail (Vt) and residues 1-258 (D1), we find an absolute requirement for an interface involving the D4 d

37 ally, Ca(2+) waves mediated by NAADP have an absolute requirement for an NAADP gradient.

38 assay measuring loss of infectivity, is the absolute requirement for antibody-mediated protection in

39 These findings show that CD18 is not an absolute requirement for antilisterial innate immunity o

40 recently been demonstrated that there is no absolute requirement for any AMPAR subunit for the recep

41 ectable, suggesting such asymmetry is not an absolute requirement for any of the functions of the cor

42 asmic pentameric motifs of Glut1 revealed no absolute requirement for arginine side chains at any of

43 Our data establish that there is an absolute requirement for arginyl, as none of the [R46X]V

44 ibrary [XXX(pT)XXX] against FHA1 revealed an absolute requirement for Asp at the +3 position and a pr

45 mportance of histidine at position 1 and the absolute requirement for aspartic acid at position 9 for

46 The regression process exhibits an absolute requirement for ATP hydrolysis and is enhanced

47 Here we report an absolute requirement for BAFF in normal B cell developme

48 Together, these data suggest an absolute requirement for beta in MAPK-dependent modulati

49 t would not be obvious otherwise, such as an absolute requirement for beta4GalT1 during convergent ex

50 pha production, indicating that there was no absolute requirement for betaGR in this process.

51 An absolute requirement for Bim was documented, since Bim-d

52 servation that the C-13 side chain is not an absolute requirement for biological activity in a taxane

53 ative decarboxylation of d-malate and has an absolute requirement for both a divalent and monovalent

54 rate strong Ag-specific immunity that has an absolute requirement for both CD8(+) and CD4(+) T cells.

55 The beta2 subunit is an absolute requirement for both classes.

56 We were able to show an absolute requirement for both of the tyrosine residues f

57 trabismus are unable to signal, revealing an absolute requirement for both proteins in cell-cell comm

58 illin, we demonstrate for the first time the absolute requirement for c-Src in villin-induced regulat

59 urin specifically in thymocytes, we found an absolute requirement for calcineurin in positive selecti

60 MA-nSMase had an absolute requirement for cations such as Mg(2+) and Mn(2

61 ular protection after preconditioning has an absolute requirement for CD14-expressing myeloid cells a

62 umor protection is Ag independent; 2) had an absolute requirement for CD4(+) and NK1.1(+) cells; 3) C

63 Some reports indicate that there is an absolute requirement for CD4+ T cells in allogeneic reje

64 The absolute requirement for CD8+ T cells to initiate such a

65 fore, an intact brassinosteroid system is an absolute requirement for cell elongation.

66 Activation of the ERK signaling pathway, an absolute requirement for cell proliferation, results in

67 constituted in vitro at 23 degrees C with an absolute requirement for chaperonins GroEL/GroES and Mg-

68 These data support the absolute requirement for cholesterol synthesis in situ o

69 g membrane permeability but that there is an absolute requirement for cholesterol to mediate this eff

70 sister chromatid separation and revealed an absolute requirement for cohesin in hematopoietic stem c

71 ion is dependent on orientation and lacks an absolute requirement for common S region motifs.

72 icating that PCNA binding by Cdc17 is not an absolute requirement for completion of S-phase.

73 Dimerization was an absolute requirement for constitutive AR-V DNA binding a

74 Cu(I) cluster is unlikely to account for its absolute requirement for Cox11 function.

75 cPLA2) has been disrupted to demonstrate the absolute requirement for cPLA2 in both the immediate and

76 reveal that agonistic anti-CD40 mAbs have an absolute requirement for cross-linking by inhibitory Fcg

77 th activities are zinc-dependent and show an absolute requirement for cysteine residues 1123, 1125 an

78 The DeltametB(Hp) mutant had an absolute requirement for cysteine.

79 lectin wheat germ agglutinin, and showed an absolute requirement for cytoplasmic extract.

80 of DOCK8 via targeted deletion confirmed its absolute requirement for DC migration.

81 ggesting that NMDA receptor activation is an absolute requirement for dendrodendritic inhibition.

82 An absolute requirement for dioxygen as a cosubstrate and i

83 There was an absolute requirement for divalent cations (Ca(2+) > Mg(2

84 Rv2361c has an absolute requirement for divalent cations and an optimal

85 TPS did not show an absolute requirement for divalent cations, but activity

86 te (ThTP) to thiamine diphosphate and has an absolute requirement for divalent cations.

87 Phosphodiesterase activity of MJ0936 had an absolute requirement for divalent metal ions with Ni(2+)

88 25 +/- 14 microM) at 37 degrees C and has an absolute requirement for divalent metal.

89 The absolute requirement for dynamin-dependent endocytosis b

90 This inhibition of translocation displays an absolute requirement for EF-1alpha; however, the depende

91 r binding determinant, a 3' U tail is not an absolute requirement for efficient RBP16-RNA binding.

92 eIF4E S209 phosphorylation, indicating their absolute requirement for eIF4E S209 phosphorylation.

93 ition of ASIC currents by syntaxin 1A had an absolute requirement for either gamma- or delta-hENaC.

94 ical pathway for antigen processing, with an absolute requirement for endosomal/lysosomal acidificati

95 Tetrahydrobiopterin (BH4) is an absolute requirement for eNOS activity.

96 eficient allograft recipients, indicating an absolute requirement for expression of these genes in CD

97 K240M has an absolute requirement for FBP for catalysis.

98 Our results demonstrate an absolute requirement for G(i) in Shh-induced fibroblast

99 sential for antiviral activity but is not an absolute requirement for Gag binding, (ii) the trifluoro

100 We highlight an absolute requirement for Galphai signaling and actin cyt

101 embryos using reporter transgenes reveals an absolute requirement for Gata3 in controlling Fgf10 expr

102 suggests that nuclear localization is not an absolute requirement for gene silencing.

103 AT3 signaling in autoimmunity relates to its absolute requirement for generating T(H)17 T cell respon

104 hoenolpyruvate (PEP) from oxaloacetate is an absolute requirement for gluconeogenesis from mitochondr

105 Correlating with the absolute requirement for glutamine, T cell activation in

106 Fibrillar collagens have an absolute requirement for Gly as every 3rd residue, where

107 The absolute requirement for Gly at the N-terminus of substr

108 n of MITF by short hairpin RNA indicated its absolute requirement for Gpnmb induction.

109 Further, we demonstrate an absolute requirement for Hedgehog signaling in sclerotom

110 Further, we demonstrate an absolute requirement for Hedgehog signaling in sclerotom

111 ated NO production and call attention to the absolute requirement for heterotrimeric G-protein betaga

112 lay a necessary role in CAV, as shown by the absolute requirement for histoincompatibility between do

113 Although there is no evidence of an absolute requirement for Hox gene clustering in Drosophi

114 Gs), providing the first demonstration of an absolute requirement for HSPGs in integrin-mediated cell

115 These data suggest that there is an absolute requirement for Ift80 in hedgehog signalling, b

116 Here, we demonstrate an absolute requirement for IgE glycosylation in allergic r

117 bitory Fcgamma-receptor (FcgammaR) IIB is an absolute requirement for in vivo antitumor activity of a

118 dies, and released exosomes; 2) a common and absolute requirement for inflammasome assembly and activ

119 The polymerase exhibits an absolute requirement for initiation with a purine and a

120 lthough this extended base pairing is not an absolute requirement for initiation, it may convey added

121 These data demonstrate an absolute requirement for innate immunity in defense agai

122 These results demonstrate an absolute requirement for Insig proteins in the regulator

123 Moreover, we highlight the absolute requirement for intact alphaCaMKII expression a

124 tion, even though cellular mitosis is not an absolute requirement for integration.

125 rved hydrophobic patch on the AIPs and is an absolute requirement for interactions in self-activation

126 the possibility that genetic diversity is an absolute requirement for intraspecific chemical communic

127 Given the absolute requirement for iron by virtually all human pat

128 erae, the causative agent of cholera, has an absolute requirement for iron.

129 urther, since dipeptidyl peptidase IV has an absolute requirement for l-Pro, a more metabolically-sta

130 mice, suggesting that eosinophils are not an absolute requirement for larval killing or development o

131 mia development but does not appear to be an absolute requirement for leukemogenesis.

132 Seeds had an absolute requirement for light to complete dormancy rele

133 Ecto-AK presented an absolute requirement for magnesium and adenine-based nuc

134 The TRM5 enzyme does not have an absolute requirement for magnesium ions, whereas TrmD re

135 Mitochondrial ATP production is an absolute requirement for maintaining a low resting [Ca2+

136 glutamate from the extracellular space is an absolute requirement for maintaining information process

137 Thus, the absolute requirement for Mdm2 in organogenesis is unknow

138 However, the absolute requirement for Mdm2 throughout embryogenesis a

139 at expression from the melAB promoter has an absolute requirement for MelR binding to Site 2'.

140 he pore-forming mechanism of PFO exhibits an absolute requirement for membrane cholesterol, but the c

141 erol-dependent cytolysins (CDCs) exhibits an absolute requirement for membrane cholesterol.

142 The native enzyme showed an almost absolute requirement for Mg(2+) and was not very active

143 tile, we investigated for the first time the absolute requirement for motility in the mouse-tick life

144 Furthermore, the absolute requirement for myosin II in brain invasion und

145 hereas CD44s-fibrin(ogen) interaction has an absolute requirement for N-, but not O-, linked glycans.

146 se mEFs to prolonged hypoxia demonstrated an absolute requirement for N-terminal sites for HIF-1 alph

147 The proximal promoter (P1) had an absolute requirement for NAC; little or no transcription

148 Despite its absolute requirement for NAD, the regulation of Sir2 fun

149 In contrast to the absolute requirement for NHEJ to resolve DSBs associated

150 or the Fe(4)S(4) center and accounts for the absolute requirement for nickel.

151 lusively on cytoplasmic proteasomes, with an absolute requirement for nuclear export of p53 via the C

152 on cytoplasmic proteasomes and hence has an absolute requirement for nuclear export of p53 via the C

153 es of this somatic-germ cell interaction, an absolute requirement for oocyte maturation.

154 ressed whether oligomerisation of TatC is an absolute requirement for operation of the Tat pathway by

155 ically relevant chemotherapeutic agents, the absolute requirement for p53 in this induction, and thei

156 easier to open the channel, they were not an absolute requirement for pH gating in Kir1.1.

157 ) rhythms in the hippocampus, demonstrate an absolute requirement for phasic inhibitory synaptic tran

158 It was also observed that while SHP-1 has an absolute requirement for phosphorylation at both motifs

159 d like a bona fide Kir channel displaying an absolute requirement for PIP(2) and Mg(2+)-dependent inw

160 Thus, our data indicate that there is an absolute requirement for PKCdelta in PMA-induced C4-2 ap

161 n the maintenance of mesangial cells and its absolute requirement for prevention of glomerular diseas

162 The absolute requirement for primers in the initiation of DN

163 idues of the alignment domain is also not an absolute requirement for processive synthesis.

164 Overall, our data point to an absolute requirement for professional APCs and the expre

165 tment with caspase inhibitors, indicating an absolute requirement for programmed cell death and apopt

166 he presence of abundant antigen, CCR7 was an absolute requirement for protective immunity to T. gondi

167 adducts on the transcribed strand, where an absolute requirement for Rad6 and Rad18 was seen.

168 Interferon (IFN)-gamma is an absolute requirement for resistance against acute acquir

169 There is an absolute requirement for retinoids at the four- to five-

170 immunodeficiency virus type 1 (HIV-1) has an absolute requirement for ribosomal frameshifting during

171 Based on the absolute requirement for RNase P processing of all three

172 Here, we demonstrate that Pax7 is an absolute requirement for satellite cell function in adul

173 While PilO has an absolute requirement for Ser/Thr at this position, it is

174 Primary keratinocytes displayed an absolute requirement for serum to dissolve collagen.

175 oli-cell only phenotype, consistent with the absolute requirement for Sin3A in germ cells' developmen

176 The fusion showed absolute requirement for small Rab GTPases, and the stim

177 mplexes at lesions rather than to reflect an absolute requirement for Smc5/6 to complete HR.

178 wed that at least one of the reasons for the absolute requirement for spermidine for growth is the sp

179 methionine decarboxylase (Deltaspe2) have an absolute requirement for spermidine for growth.

180 directly depend on Erk activation but has an absolute requirement for Src/Erk-mediated TXA2 generatio

181 on about dietary lipid requirements, and the absolute requirement for sterol is of particular note.

182 ng, control of endogenous inflammation is an absolute requirement for success.

183 orming growth factor beta3 (Tgf-beta3) is an absolute requirement for successful palatal fusion, both

184 particularly because encapsulation is not an absolute requirement for successful re/folding.

185 The latter contrasts with the absolute requirement for Suppressor of Hairless and the

186 rbohydrate antigens because peptides have an absolute requirement for T cells.

187 These data demonstrate an absolute requirement for T-cell expression of CCR7 for t

188 and that, surprisingly, DC IL-12 was not an absolute requirement for Th1 development.

189 stimulating effects, apparently there is no absolute requirement for that molecule for the nuclear s

190 occurs in mammalian cells with regard to its absolute requirement for the action of Insigs, sensitivi

191 This dislocation exhibits an absolute requirement for the actions of Insigs and VCP/p

192 te for the first time, to our knowledge, the absolute requirement for the activity of MASP-1 protein

193 ggest that the expression of ClC-3 is not an absolute requirement for the activity of volume-sensitiv

194 ing mAb, we demonstrate that IFN-gamma is an absolute requirement for the antitumor effect of CD137 m

195 substitution on the nitrogen atom is not an absolute requirement for the antitumor effect of the ind

196 This is in contrast to the absolute requirement for the C-tail reported for BPV1 E1

197 es that some agonistic antibodies display an absolute requirement for the C-terminal tail for FADD bi

198 rowth substrate, indicating that there is an absolute requirement for the C1 oxidation/reduction path

199 Our data suggest that dimerization is not an absolute requirement for the catalytic activity of the E

200 In conclusion, the absolute requirement for the catalytic glutamate of APOB

201 tumor activities of these antibodies have an absolute requirement for the coengagement of an inhibito

202 d suppression mechanism in which there is an absolute requirement for the cognate antigen of both the

203 atory interactions involving CD28 are not an absolute requirement for the control of infection with M

204 Because Mg(2+) is an absolute requirement for the downstream activities of th

205 ortantly, AbetaP formation appeared to be an absolute requirement for the effects of hypoxia, since t

206 s aeruginosa exoenzyme S (ExoS) possessed an absolute requirement for the eukaryotic protein factor a

207 iable, indicating that this factor is not an absolute requirement for the formation of an active hepa

208 rganized secondary lymphoid tissue is not an absolute requirement for the generation of immune respon

209 We demonstrate an absolute requirement for the globular domain of the link

210 The absolute requirement for the histone deacetylase activit

211 There was an absolute requirement for the homeodomain, whereas deleti

212 ophobic reside at the -2-position but not an absolute requirement for the hydroxyl side chain of thre

213 l integrity of the 5BSL3 cruciform is not an absolute requirement for the kissing-loop interaction, s

214 We previously demonstrated an absolute requirement for the lipid chemoattractant leuko

215 ignal-regulated kinase (ERK) signaling is an absolute requirement for the maintenance of murine pluri

216 re and demonstrate that cancer cells have an absolute requirement for the membrane-anchored metallopr

217 In addition, we showed an absolute requirement for the MRX complex in signal joini

218 er, the location of MOR at lipid rafts is an absolute requirement for the observed adenylyl cyclase s

219 Tomato is a climacteric fruit, with an absolute requirement for the phytohormone ethylene to ri

220 lete independence of store depletion, and an absolute requirement for the pool of STIM1 that constitu

221 This was due to an absolute requirement for the position of this signal in

222 alters the amount of secretion but is not an absolute requirement for the processing and secretion of

223 Furthermore we show that PI-3-K is an absolute requirement for the proliferative response to R

224 Sequence-specific DNA places an absolute requirement for the proline repeat domain to dr

225 rather than at discrete origins and have an absolute requirement for the recombinase RadA, unlike st

226 tion of the enzyme-coenzyme complex shows an absolute requirement for the same monocations required i

227 Mutational analysis demonstrated an absolute requirement for the SP1/SP3 binding element in

228 ner nucleotide opposite the lesion is not an absolute requirement for the successful initiation of NE

229 gesting that, in these mice, there is not an absolute requirement for the T4SS to mediate persistence

230 Thus, H. pylori has an absolute requirement for the transition metal nickel, a

231 However, ctu is not an absolute requirement for the virulence of F. tularensis

232 age at the C-extein branch point, and (d) an absolute requirement for the WCT triplet Block F Cys.

233 c cleavage of factor B by factor D is not an absolute requirement for the zymogen to active enzyme co

234 To determine the absolute requirement for these cytokines in disease outc

235 vitro and in vivo indicate that part of the absolute requirement for these factors is derived from t

236 and Mxi-Spa functions are complicated by an absolute requirement for these virulence proteins in inv

237 ctivation in the duodenum, demonstrating the absolute requirement for this factor in vivo.

238 bunit of class I PI3-kinases demonstrated an absolute requirement for this form of the enzyme in GLUT

239 essels from P2X (-/-)(1) mice, confirming an absolute requirement for this receptor.

240 to wild-type (WT) cells, whereas DKO has an absolute requirement for thymidine.

241 he sympathetic nervous system, but it has an absolute requirement for thyroid hormone.

242 EMT has been postulated as an absolute requirement for tumor invasion and metastasis.

243 rsion of aldose and ketose sugars and has an absolute requirement for two divalent cations at its act

244 Finally, BbeI displays an absolute requirement for two sites in close physical pro

245 The absolute requirement for Vi capsule expression for infec

246 have shown that while the V2 loop is not an absolute requirement for viral entry, the absence of thi

247 )-induced thrombocytopenia, demonstrating an absolute requirement for VWF in this model (Stx has been

248 teraction of VP5 with pre-22a resulted in an absolute requirement for wild-type VP5 for growth of the

249 oposal that graded activity of Dpp is not an absolute requirement for wing growth.

250 we discovered an unexpectedly selective and absolute requirement for XBP1 in eosinophil differentiat

251 xes, was found to correlate with, and had an absolute requirement for, the induction and nuclear loca

252 lymerase holoenzyme (sigma54-holoenzyme) has absolute requirements for an activator protein and ATP h

253 nd disease progression is not universal, and absolute requirements for epitope spreading in progressi

254 H. pylori has surprisingly few absolute requirements for growth: 9 amino acids, sodium

255 c-Jun/AP-1 trans-activating activity are not absolute requirements for ras transformation or invasion

256 +) T cells and of the type I IFN system were absolute requirements for the antitumor effects to occur

257 Despite the absolute requirements for these factors in the developme

258 Because direct evidence for its absolute requirement in the viral life cycle is lacking,

259 ome segregation, which is exemplified by its absolute requirement in yeast for the anaphase segregati

260 structure-activity relationship we noted the absolute requirement of a long alkyl side chain, with an

261 the P(+1) cleavage site (Ser(518)) shows an absolute requirement of a Ser, Thr, or Cys residue for e

262 An absolute requirement of a two-residue spacing between th

263 t1 and Akt2 isoforms in this pathway, and an absolute requirement of Akt protein kinases for regulati

264 mportance of the WWD signature motif and the absolute requirement of all three histidines for the ass

265 hese results are unique in demonstrating the absolute requirement of alpha4 for sperm fertility.

266 Given the absolute requirement of auxiliary proteins in apoB mRNA

267 form of cell injury, but also demonstrate an absolute requirement of Bax for mitochondrial permeabili

268 The absolute requirement of c-Myc for cell cycle progression

269 pases are cleaved and activated by GzmB, the absolute requirement of caspase activation for GzmB-indu

270 t Arf6-GTP, such a circuit would fulfill the absolute requirement of cytohesins for activation by Arf

271 general not identified, consistent with the absolute requirement of cytosolic translation for develo

272 The absolute requirement of dephosphorylation in this proces

273 specific GRK5 gene deletion to determine the absolute requirement of endogenous GRK5 for cardiac hype

274 vitro and in vivo models, we demonstrated an absolute requirement of functional p53 in arsenic-mediat

275 n in PS1-deficient cells and demonstrate the absolute requirement of functional presenilins for Abeta

276 Analysis of GANAB-null cells showed an absolute requirement of GIIalpha for maturation and surf

277 Enzymatic analysis also shows an absolute requirement of magnesium or calcium ions in enz

278 optosis and growth arrest, demonstrating the absolute requirement of Mdm2 in embryogenesis.

279 7B2 as regards this enzyme appears to be the absolute requirement of PC2 for 7B2 in the generation of

280 In contrast to the absolute requirement of PI-3K and NF-kappaB/Rel for prol

281 d adenylate cyclase activation; there was an absolute requirement of PKA for PAF-induced Src phosphor

282 ucting translesion DNA synthesis despite the absolute requirement of RecA for SOS mutagenesis.

283 wild-type and mutant dvCcmE' demonstrate the absolute requirement of residue C127 for noncovalent hem

284 The absolute requirement of TFAM can be relaxed by condition

285 tract reinfection, IgA antibodies are not an absolute requirement of that protective response.

286 These results emphasize the absolute requirement of the binding of carbamoyl phospha

287 Last, the absolute requirement of the C1P/cPLA(2)alpha interaction

288 We show an absolute requirement of the HIF-alpha-c-Myc pathway for

289 The absolute requirement of the identified transcription ter

290 Finally, our findings demonstrate an absolute requirement of the KSR1 C1 domain in mediating

291 A-1 conformations by Fab, we demonstrate the absolute requirement of the open LFA-1 headpiece for adh

292 liminated apoB RNA editing, establishing the absolute requirement of these components of the core enz

293 The absolute requirement of this large structure for HIV tra

294 receptor delta null macrophages verifies the absolute requirement of this transcription factor in med

295 sts prepared from c-Abl null mice showed the absolute requirement of this tyrosine kinase in maturati

296 These results demonstrate the absolute requirement of VDR for 1,25(OH)(2)D(3)-induced

297 While confirming the absolute requirement of WC-1 for light responses, the da

298 To determine whether there is an absolute requirement of YidC for membrane protein insert

299 f allopurinol hypersensitivity, it is not an absolute requirement, suggesting that other factors also

300 fect on ToxR activity, although it is not an absolute requirement when ToxR is dimerized by a heterol