ライフサイエンスコーパス: Haemophilus influenzae

1 enes, Staphylococcus aureus, and potentially Haemophilus influenzae).

2 hylococcus and Gram-negative bacteria and to Haemophilus influenzae.

3 t line of defense against the human pathogen Haemophilus influenzae.

4 ococcus pneumoniae, and 54% for non-typeable Haemophilus influenzae.

5 were previously misidentified as nontypeable Haemophilus influenzae.

6 ainst efflux-negative strains of E. coli and Haemophilus influenzae.

7 s successful in creating unmarked mutants in Haemophilus influenzae.

8 crobial peptides (sap operon) in nontypeable Haemophilus influenzae.

9 luding the phylogenetically related pathogen Haemophilus influenzae.

10 eria gonorrheae, Neisseria meningitidis, and Haemophilus influenzae.

11 dA from Yersinia enterocolitica and Hia from Haemophilus influenzae.

12 on between influenza virus and the bacterium Haemophilus influenzae.

13 Bordetella pertussis, Escherichia coli, and Haemophilus influenzae.

14 of both typeable and nontypeable strains of Haemophilus influenzae.

15 fastidious gram-negative pathogens including Haemophilus influenzae.

16 y bacterial pathogens, including nontypeable Haemophilus influenzae.

17 d is absent from the closely related species Haemophilus influenzae.

18 ccus pneumoniae, Neisseria meningitidis, and Haemophilus influenzae.

19 ng Streptococcus pneumoniae and non-typeable Haemophilus influenzae.

20 nd in some regions, for all pathogens except Haemophilus influenzae.

21 ssue, which included known pathogens such as Haemophilus influenzae.

22 representing a reduced relative abundance of Haemophilus influenzae (35.3% [5.5-91.6] vs 6.7% [0.8-74

23 Haemophilus influenzae, a gram-negative pathogen causing

24 Pathogenic bacteria such as Haemophilus influenzae, a major cause of lower respirato

25 ibrocytes) are able to recognize nontypeable Haemophilus influenzae, a major pathogen of middle ear i

26 Haemophilus influenzae also uses an enzyme, GlpQ, to hyd

27 colonization by Streptococcus pneumoniae and Haemophilus influenzae among children has been noted in

28 Neisseria meningitidis and ceftriaxone, and Haemophilus influenzae and ceftriaxone.

29 sensitivity and specificity for identifying Haemophilus influenzae and differentiating it from H. ha

30 activity has been achieved against wild-type Haemophilus influenzae and efflux-deficient mutants of E

31 Distinguishing nontypeable Haemophilus influenzae and Haemophilus haemolyticus isol

32 ator to the respiratory pathogen nontypeable Haemophilus influenzae and identify the Haemophilus surf

33 n represents the initial interaction between Haemophilus influenzae and its human host.

34 s pneumoniae and the Gram-negative pathogens Haemophilus influenzae and Moraxella catarrhalis .

35 nization with Gram-negative bacteria such as Haemophilus influenzae and Moraxella catarrhalis was fou

36 animal models of the Gram-negative pathogens Haemophilus influenzae and Neisseria meningitidis We hyp

37 reveal their striking genetic similarity to Haemophilus influenzae and other members of the Pasteure

38 in several gram-negative bacteria including Haemophilus influenzae and Pasteurella multocida.

39 or murine origin in response to nontypeable Haemophilus influenzae and Staphylococcus aureus.

40 vaccination with conjugate vaccines against Haemophilus influenzae and Streptococcus pneumoniae has

41 Haemophilus influenzae and Streptococcus pneumoniae were

42 piratory syncytial virus; RSV) and bacteria (Haemophilus influenzae and Streptococcus pneumoniae) in

43 ion of EVI1 itself is induced by nontypeable Haemophilus influenzae and TNF-alpha in an NF-kappaB-dep

44 In the Gram-negative bacteria Haemophilus influenzae and Vibrio cholerae, the master r

45 ccus aureus, 10 Streptococcus pneumoniae, 10 Haemophilus influenzae, and 5 Escherichia coli isolates

46 orins from Neisseriae, Shigella, Salmonella, Haemophilus influenzae, and Fusobacterium nucleatum, whi

47 Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis are th

48 antitative PCR for Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis were p

49 ovirus, bocavirus, Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis were s

50 c airway bacteria (Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis) were

51 ive conjugate vaccines against S pneumoniae, Haemophilus influenzae, and Neisseria meningitides to ch

52 as Escherichia coli, Neisseria meningitidis, Haemophilus influenzae, and Pasteurella multocida.

53 phocholine, phosphocholine-modified LPS from Haemophilus influenzae, and phosphocholine-modified prot

54 phylococci (CoNS), Streptococcus pneumoniae, Haemophilus influenzae, and Pseudomonas aeruginosa.

55 eumoniae, Staphylococcus aureus, Nontypeable Haemophilus influenzae, and Pseudomonas aeruginosa.

56 thogens: Pseudomonas aeruginosa, nontypeable Haemophilus influenzae, and Salmonella enterica serovar

57 atients, including Burkholderia cenocepacia, Haemophilus influenzae, and Staphylococcus aureus.

58 ptococcus pneumoniae, Moraxella catarrhalis, Haemophilus influenzae, and Staphylococcus aureus.

59 Neisseria meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae are

60 atory tract pathogens Moraxella catarrhalis, Haemophilus influenzae, and Streptococcus pneumoniae, bu

61 is caused mainly by Neisseria meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae, in

62 w that EVI1 negatively regulates nontypeable Haemophilus influenzae- and TNF-alpha-induced NF-kappaB-

63 Immunoglobulin (Ig)A proteases of Haemophilus influenzae are highly specific endopeptidase

64 ococcus aureus, Streptococcus pneumoniae and Haemophilus influenzae are the major causes of conjuncti

65 Here, using non-typeable Haemophilus influenzae as a model organism, we report th

66 eudomonas aeruginosa, Staphylococcus aureus, Haemophilus influenzae, Aspergillus species, Streptococc

67 5922 (0.008 to 0.03 mug/ml and 30 to 36 mm), Haemophilus influenzae ATCC 49247 (0.002 to 0.015 mug/ml

68 pneumoniae ATCC 49619 (disk and broth), and Haemophilus influenzae ATCC 49247 (disk and broth).

69 ureus ATCC 29213 (MIC range, 1 to 4 mug/ml), Haemophilus influenzae ATCC 49247 (MIC and disk diffusio

70 and ATCC 25923, Escherichia coli ATCC 25922, Haemophilus influenzae ATCC 49247, and Streptococcus pne

71 23, Streptococcus pneumoniae ATCC 49619, and Haemophilus influenzae ATCC 4927 strains were evaluated.

72 in Southern England immunized with DTaP5/IPV/Haemophilus influenzae b (Hib-TT) vaccine at 2-3-4 month

73 syncytial virus, parainfluenza viruses, and Haemophilus influenzae being the most common.

74 The Hia autotransporter of Haemophilus influenzae belongs to the trimeric autotrans

75 The Haemophilus influenzae beta-carbonic anhydrase (HICA) al

76 Haemophilus influenzae beta-carbonic anhydrase (HICA) is

77 with the emergence of the clonal variants of Haemophilus influenzae biogroup aegyptius causing Brazil

78 protection against PC-expressing nontypeable Haemophilus influenzae, but not PC-negative nontypeable

79 ccus pneumoniae, Neisseria meningitidis, and Haemophilus influenzae, but the mechanism by which they

80 We present the Arg160His mutation of Haemophilus influenzae carbonic anhydrase (HICA), which

81 ve a significantly lower risk of nontypeable Haemophilus influenzae carriage in particular (relative

82 Pneumococcus, meningococcus, and Haemophilus influenzae cause a similar spectrum of infec

83 ella kingae (HACEK) clinical isolates and 20 Haemophilus influenzae clinical isolates.

84 Non-typeable Haemophilus influenzae contains an N(6)-adenine DNA-meth

85 homodimeric periplasmic domain of TolR from Haemophilus influenzae, determined with conventional, NO

86 Using Haemophilus influenzae Eagan strains expressing well-cha

87 Haemophilus influenzae efficiently colonizes and persist

88 son of derivatives of a laboratory strain of Haemophilus influenzae expressing either surface-associa

89 , we turned our attention to bacteria, i.e., Haemophilus influenzae, expressing cell-surface adhesins

90 Unencapsulated Haemophilus influenzae frequently causes noninvasive upp

91 marker for differentiating nontypeable (NT) Haemophilus influenzae from Haemophilus haemolyticus in

92 terial burden and a significant outgrowth of Haemophilus influenzae from the existing microbiota of s

93 The e (P4) phosphatase from Haemophilus influenzae functions in a vestigial NAD(+) u

94 oach was applied to comprehensively identify Haemophilus influenzae genes required to delay bacterial

95 ed AIMIE to analyze the Escherichia coli and Haemophilus influenzae genomes in order to demonstrate t

96 A related human pathogen, Haemophilus influenzae, has been better studied, and man

97 Haemophilus influenzae (Hi) causes respiratory tract inf

98 Clearance of encapsulated Haemophilus influenzae (Hi) required both TLR and nucleo

99 y to inhibit catalytic activity of DapE from Haemophilus influenzae (HiDapE) and ArgE from Escherichi

100 he ferric uptake systems V. cholerae Fbp and Haemophilus influenzae Hit was expressed.

101 and its close sequence homologue HI0827 from Haemophilus influenzae (HiYciA).

102 The Haemophilus influenzae HMW1 adhesin is an N-linked glyco

103 The Haemophilus influenzae HMW1 adhesin is secreted via the

104 The Haemophilus influenzae HMW1 adhesin mediates adherence t

105 Secretion of the Haemophilus influenzae HMW1 adhesin occurs via the two-p

106 ch data across various human pathogens (e.g. Haemophilus influenzae, human immunodeficiency virus (HI

107 colonization by Streptococcus pneumoniae and Haemophilus influenzae in a Toll-like receptor (TLR)-dep

108 ficiency further affected internalization of Haemophilus influenzae in bronchial epithelial cells.

109 d for TolR is of the periplasmic domain from Haemophilus influenzae in which N- and C-terminal residu

110 % vs 23%-31% of AOM isolates), while that of Haemophilus influenzae increased (41%-43% vs 56%-57%) pr

111 In this study, we found that nontypeable Haemophilus influenzae induces the association of Itch w

112 he survival rate after a lethal non-typeable Haemophilus influenzae infection in wild-type mice, but

113 tudy persistent Streptococcus pneumoniae and Haemophilus influenzae infections, to show that structur

114 Novel mouse models of Chlamydia, Haemophilus influenzae, influenza, and respiratory syncy

115 Nontypable Haemophilus influenzae is a common cause of human diseas

116 Haemophilus influenzae is a gram-negative bacterium that

117 Haemophilus influenzae is a Gram-negative human pathogen

118 Haemophilus influenzae is a human-specific gram-negative

119 Nontypeable Haemophilus influenzae is a major cause of localized res

120 Haemophilus influenzae is a rare cause of soft tissue in

121 Haemophilus influenzae is a significant causative agent

122 Haemophilus influenzae is an obligate human pathogen tha

123 Non-typeable Haemophilus influenzae is an opportunistic pathogen of t

124 Haemophilus influenzae is both a human respiratory patho

125 lmonary inflammation induced by non-typeable Haemophilus influenzae is significantly attenuated in IR

126 a catarrhalis, Streptococcus pneumoniae, and Haemophilus influenzae, is associated with later develop

127 configurations were predicted in nontypeable Haemophilus influenzae isolates based on the presence of

128 e operon was significantly more prevalent in Haemophilus influenzae isolates causing otitis media and

129 -resolution X-ray structure determination of Haemophilus influenzae KDO8PP bound to KDO/VO3(-) and Ba

130 In contrast, Haemophilus influenzae KdtA (HiKdtA) transfers only one

131 d antimicrobial activity against a strain of Haemophilus influenzae lacking its major efflux pump.

132 tly from CSF specimens: Escherichia coli K1, Haemophilus influenzae, Listeria monocytogenes, Neisseri

133 we have shown that the C-terminal domain of Haemophilus influenzae LpoA (HiLpoA) has a highly conser

134 Here, we have purified E. coli and Haemophilus influenzae LpxB to near homogeneity on a 10-

135 , and detailed enzymatic characterization of Haemophilus influenzae LpxH (HiLpxH).

136 ccines with/without protein D of nontypeable Haemophilus influenzae, M. catarrhalis has become a high

137 ed as having meningococcal, pneumococcal, or Haemophilus influenzae meningitis in the period 1977-200

138 Haemophilus influenzae (MIC(50), </= 0.008 microg/mL; MI

139 were cultured for Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staph

140 piratory pathogens Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staph

141 irways with the pathogenic bacterial strains Haemophilus influenzae, Moraxella catarrhalis, and Strep

142 y associated with bacterial coinfection with Haemophilus influenzae, Moraxella catarrhalis, or Strept

143 We assessed this association for Haemophilus influenzae, Moraxella catarrhalis, Staphyloc

144 pathogens were detected frequently, notably Haemophilus influenzae (mostly nontypeable) together wit

145 ium, Bacillus subtilis, Helicobacter pylori, Haemophilus influenzae, Mycobacterium tuberculosis, Pseu

146 re Pseudomonas aeruginosa (n = 10 patients), Haemophilus influenzae (n = 12), Prevotella (n = 18), an

147 s simplex virus [n = 5], adenovirus [n = 5], Haemophilus influenzae [n = 5], and Streptococcus pneumo

148 lude Escherichia coli, Campylobacter jejuni, Haemophilus influenzae, Neisseria meningitidis, and Past

149 Infection with Haemophilus influenzae, Neisseria meningitidis, and Stre

150 cterial pathogens (Streptococcus pneumoniae, Haemophilus influenzae, Neisseria meningitidis, Mycoplas

151 It is closely related to nontypeable Haemophilus influenzae (NT H. influenzae).

152 ta-lactamase-producing strain of nontypeable Haemophilus influenzae (NTHi 86-028NP) and an isogenic m

153 The mucosal pathogen nontypeable Haemophilus influenzae (NTHi) adheres to the respiratory

154 Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investig

155 Biofilms formed by nontypeable Haemophilus influenzae (NTHI) are central to the chronic

156 Haemophilus haemolyticus and nontypeable Haemophilus influenzae (NTHi) are closely related upper

157 by Streptococcus pneumoniae and nontypeable Haemophilus influenzae (NTHi) are frequently implicated

158 Nontypeable Haemophilus influenzae (NTHI) are Gram-negative bacteria

159 istic human respiratory pathogen nontypeable Haemophilus influenzae (NTHI) are required for type IV p

160 Nontypeable Haemophilus influenzae (NTHI) bacteria are commensals in

161 typically recovered quantity of nontypeable Haemophilus influenzae (NTHi) bacteria in an ex vivo mid

162 ocator function is necessary for nontypeable Haemophilus influenzae (NTHI) behaviors that mediate dis

163 ram-negative commensal bacterium nontypeable Haemophilus influenzae (NTHI) can cause respiratory trac

164 Nontypeable Haemophilus influenzae (NTHi) causes pulmonary infection

165 Nontypeable Haemophilus influenzae (NTHi) exclusively infects humans

166 Nontypeable Haemophilus influenzae (NTHI) forms biofilms in the midd

167 Nontypeable Haemophilus influenzae (NTHi) frequently causes noninvas

168 Studies of nontypeable Haemophilus influenzae (NTHi) have demonstrated that a n

169 reptococcus pneumoniae (Spn) and nontypeable Haemophilus influenzae (NTHi) in stringently defined oti

170 xed Streptococcus pneumoniae and nontypeable Haemophilus influenzae (NTHi) infections (M-OM) and thos

171 Nontypeable Haemophilus influenzae (NTHi) initiates infection by col

172 Nontypeable Haemophilus influenzae (NTHi) is a bacterium that reside

173 Nontypeable Haemophilus influenzae (NTHI) is a commensal inhabitant

174 Nontypeable Haemophilus influenzae (NTHi) is a commensal microorgani

175 Nontypeable Haemophilus influenzae (NTHI) is a common commensal and

176 Nontypeable Haemophilus influenzae (NTHI) is a Gram-negative bacteri

177 Nontypeable Haemophilus influenzae (NTHi) is a Gram-negative, opport

178 Nontypeable Haemophilus influenzae (NTHI) is a leading cause of oppo

179 Nontypeable Haemophilus influenzae (NTHI) is a leading cause of otit

180 Nontypeable Haemophilus influenzae (NTHi) is a major bacterial patho

181 Non-typeable Haemophilus influenzae (NTHi) is a major cause of mucosa

182 Nontypeable Haemophilus influenzae (NTHI) is a respiratory commensal

183 Nontypeable Haemophilus influenzae (NTHI) is an extremely common air

184 Nontypeable Haemophilus influenzae (NTHi) is an important bacterial

185 Virulence of nontypeable Haemophilus influenzae (NTHi) is dependent on the decora

186 am-negative pathogenic bacterium nontypeable Haemophilus influenzae (NTHi) is surface exposed and a l

187 Nontypeable Haemophilus influenzae (NTHI) is the causative agent of

188 Nontypeable Haemophilus influenzae (NTHi) is the dominant bacterium

189 Nontypeable Haemophilus influenzae (NTHi) is the leading bacterial p

190 Twenty-one nontypeable Haemophilus influenzae (NTHi) isolates from the throats

191 vaccine against nonencapsulated isolates of Haemophilus influenzae (NTHi) lies in the genetic divers

192 ere we examine the impact of the nontypeable Haemophilus influenzae (NTHI) ModA2 phasevarion on patho

193 Nontypeable Haemophilus influenzae (NTHi) organisms are obligate par

194 Nontypeable Haemophilus influenzae (NTHi) persists in the airways in

195 Many publications state that nontypeable Haemophilus influenzae (NTHi) produces biofilms.

196 A subset of invasive nontypeable Haemophilus influenzae (NTHI) strains has evidence of IS

197 Nontypeable Haemophilus influenzae (NTHi) was selected as a model pa

198 ce lipooligosaccharides (LOS) of nontypeable Haemophilus influenzae (NTHi), a human-specific commensa

199 Nontypeable Haemophilus influenzae (NTHI), an opportunistic pathogen

200 Nontypeable Haemophilus influenzae (NTHI), an opportunistic pathogen

201 with bacterial opportunists like nontypeable Haemophilus influenzae (NTHi), and a wealth of evidence

202 were calculated for pneumococcal, nontypable Haemophilus influenzae (NTHi), Moraxella catarrhalis, St

203 of several adhesins expressed by nontypeable Haemophilus influenzae (NTHI), the outer membrane protei

204 l collapse of biofilms formed by nontypeable Haemophilus influenzae (NTHI), those directed against a

205 ctions with pathogens, including nontypeable Haemophilus influenzae (NTHI), yet the reasons for this

206 l impairment of phagocytosis for nontypeable Haemophilus influenzae (NTHI).

207 ce exposed to cigarette smoke or nontypeable Haemophilus influenzae (NTHi).

208 E) responses of ccl3(-/-)mice to nontypeable Haemophilus influenzae (NTHi).

209 after middle ear infection with nontypeable Haemophilus influenzae (NTHi).

210 8(-/-) mice were inoculated with nontypeable Haemophilus influenzae (NTHi).

211 by respiratory pathogens such as nontypeable Haemophilus influenzae (NTHi).

212 diseases are commonly caused by nontypeable Haemophilus influenzae (NTHi).

213 onization strategies employed by nontypeable Haemophilus influenzae (NTHi).

214 evelopment and colonization with nontypeable Haemophilus influenzae (NTHi).

215 asion by lung microbiota such as nontypeable Haemophilus influenzae (NTHi).

216 tly colonized with bacteria [eg, nontypeable Haemophilus influenzae (NTHi)] that cause pulmonary infl

217 In contrast, responses to Haemophilus influenzae occurred after either basolateral

218 crystal structure of a bacterial homologue (Haemophilus influenzae) of SLAC1 at 1.20 A resolution, a

219 or upon acute exposure to either nontypeable Haemophilus influenzae or ovalbumin.

220 onfidence interval [CI], 1.90 and 10.19) and Haemophilus influenzae (OR, 2.04; 95% CI, 1.38 and 3.02)

221 During model murine nasal colonization, Haemophilus influenzae outcompetes another member of the

222 (p = 0.001), NFkB activation by nontypeable Haemophilus influenzae (p = 0.001), TLR4 (p = 0.008) and

223 nces, most notably in potentially pathogenic Haemophilus influenzae (P = 2.7 x 10(-20)), from a preex

224 used to vaccinate children globally against Haemophilus influenzae, pneumococcus, and meningococcus.

225 ts of the 10-valent pneumococcal nontypeable Haemophilus influenzae protein D-conjugate vaccine (PHiD

226 Haemophilus influenzae protein F (PF) is an important vi

227 The arfA hairpins from Haemophilus influenzae, Proteus mirabilis, Vibrio fische

228 The crystal structure of HI0827 from Haemophilus influenzae Rd KW20, initially annotated "hyp

229 m phylogenetically distant Aquifex aeolicus, Haemophilus influenzae Rd, and Synechocystis sp. were fo

230 influenzae, but not PC-negative nontypeable Haemophilus influenzae, relative to wild-type mice.

231 lls) to the respiratory pathogen nontypeable Haemophilus influenzae resulted in a marked increase in

232 us, while challenge of Trim29(-/-) mice with Haemophilus influenzae resulted in lethal lung inflammat

233 morphism in humans evades TbpA variants from Haemophilus influenzae, revealing a functional basis for

234 tococcus pneumoniae, Neisseria meningitidis, Haemophilus influenzae, S suis) and O tsutsugamushi, Ric

235 The introduction of the Haemophilus influenzae serotype b (Hib) conjugate vaccin

236 tis in a healthy adult patient, secondary to Haemophilus influenzae serotype f infection, and we revi

237 rologous genetic background of a nonadherent Haemophilus influenzae strain, and quantitative assays r

238 d the ability to bind FN to a non-FN-binding Haemophilus influenzae strain.

239 Haemophilus influenzae strains are classified as typeabl

240 Haemophilus influenzae strains OM12, which expresses the

241 and 24 months of age were cultured to detect Haemophilus influenzae, Streptococcus pneumoniae, Moraxe

242 Chinchillas were infected with nontypeable Haemophilus influenzae, Streptococcus pneumoniae, or a c

243 usters characterized by enrichment of either Haemophilus influenzae, Streptococcus, Corynebacterium,

244 e show that glucocorticoids and non-typeable Haemophilus influenzae synergistically upregulate IRAK-M

245 abs positive for Streptococcus pneumoniae or Haemophilus influenzae than were males (OR 9.09; 95% CI

246 Signaling mechanisms used by Haemophilus influenzae to adapt to conditions it encount

247 Upon exposure of serum-sensitive Haemophilus influenzae to human serum, Ecb protected the

248 of a collection of compound fragments using Haemophilus influenzae TrmD identified inhibitory, fused

249 n the first detection of 2 cases of invasive Haemophilus influenzae type a (Hia) disease in Italy.

250 t diphtheria, tetanus, pertussis, polio, and Haemophilus influenzae type b (DTaP-IPV-Hib) administere

251 s-acellular pertussis-inactivated poliovirus-Haemophilus influenzae type b (DTaP-IPV-Hib) vaccine sin

252 A conjugate vaccine containing Haemophilus influenzae type b (Hib) and group C meningoc

253 treptococcus pneumoniae (S. pneumoniae), and Haemophilus influenzae type b (Hib) are three most commo

254 ed (DTaP), inactivated poliovirus (IPV), and Haemophilus influenzae type b (Hib) conjugate vaccine (D

255 e United States in the early 1990s, when the Haemophilus influenzae type b (Hib) conjugate vaccine fo

256 Haemophilus influenzae type b (Hib) conjugate vaccine, d

257 The widespread use of Haemophilus influenzae type b (Hib) conjugate vaccines h

258 The incidence of invasive Haemophilus influenzae type b (Hib) disease has signific

259 Haemophilus influenzae type b (Hib) is a leading cause o

260 ng hospital in Malawi during introduction of Haemophilus influenzae type b (Hib) vaccination and the

261 rst country in Africa to introduce conjugate Haemophilus influenzae type b (Hib) vaccine, which, as i

262 Streptococcus pneumoniae polysaccharide and Haemophilus influenzae type b (Hib) vaccines in ITP pati

263 Protection against Haemophilus influenzae type b (Hib), a rapidly invading

264 ribitol (PRP) polysaccharides extracted from Haemophilus influenzae type b (Hib), and the correspondi

265 duction of vaccines against pneumococcus and Haemophilus influenzae type b (the most important causes

266 become the predominant invasive pathogen as Haemophilus influenzae type b and pneumococcal vaccine u

267 ca, the widespread use of vaccines targeting Haemophilus influenzae type b and Streptococcus pneumoni

268 and of occult bacteremia since the advent of Haemophilus influenzae type b and Streptococcus pneumoni

269 -tetanus-acellular pertussis-inactived polio-Haemophilus influenzae type b combined vaccine (DTaP-IPV

270 C, W, Y polysaccharide vaccine (PsACWY); or Haemophilus influenzae type b conjugate vaccine (Hib-TT)

271 Literature on hepatitis B, rotavirus, Haemophilus influenzae type b conjugate, and pneumococca

272 clinical significance and characteristics of Haemophilus influenzae type b genogroup strains isolated

273 Five genetic islands (HiGI) found in Haemophilus influenzae type b strain Eagan were used as

274 a, tetanus, pertussis, measles, rubella, and Haemophilus influenzae type b vaccine antigens were comp

275 s-acellular pertussis-inactivated poliovirus/Haemophilus influenzae type b vaccine; age 6/10/ 14 week

276 that pediatric providers conserve available Haemophilus influenzae type B vaccines by delaying the a

277 Because of a notable recall of Haemophilus influenzae type B vaccines by Merck & Co Inc

278 r pertussis, inactivated polio, hepatitis B, Haemophilus influenzae type b vaccines); (2) 4CMenB at 2

279 ng countries in 2015, using pneumococcal and Haemophilus influenzae type b vaccines.

280 , and whole-cell pertussis; hepatitis B; and Haemophilus influenzae type b) and pneumococcal vaccine.

281 , tetanus, pertussis, hepatitis B virus, and Haemophilus influenzae type b), yellow fever, measles, a

282 ent vaccine (diphtheria, tetanus, pertussis, Haemophilus influenzae type b, and hepatitis B) at 6, 10

283 include pneumococcus, group B Streptococcus, Haemophilus influenzae type b, and meningococcus vaccine

284 against some types of bacterial meningitis (Haemophilus influenzae type b, Neisseria meningitidis gr

285 to characterise disease syndromes caused by Haemophilus influenzae type b, pneumococcus, rotavirus,

286 cine priming, before a booster of a combined Haemophilus influenzae type b-MenC conjugate vaccine and

287 from ALRI, after pneumococcal pneumonia and Haemophilus influenzae type b.

288 and, when applicable, use of vaccine against Haemophilus influenzae type b.

289 pathogens were Streptococcus pneumoniae and Haemophilus influenzae (type B and non-type B).

290 The bacterium Haemophilus influenzae typically colonizes the human upp

291 The obligate human pathogen Haemophilus influenzae utilizes a siderophore-independen

292 the sialic acid-specific SBP, SiaP, from the Haemophilus influenzae virulence-related SiaPQM TRAP tra

293 ctivity against an efflux-negative strain of Haemophilus influenzae was 4- to 8-fold higher, the comb

294 Haemophilus influenzae was present in more adenoids from

295 Working with the bacterium Haemophilus influenzae, we found that MolBC-A functions

296 caused by either Streptococcus pneumoniae or Haemophilus influenzae were compared for pathogen-specif

297 phtericum and Corynebacterium propinquum and Haemophilus influenzae were significantly more abundant

298 the sialic acid TRAP transporter SiaPQM from Haemophilus influenzae, where the membrane proteins are

299 een H. parainfluenzae and its close relative Haemophilus influenzae, which is also commonly carried w

300 on X-ray crystal structures of the DapE from Haemophilus influenzae with one and two zinc ions bound