ライフサイエンスコーパス: disease caused by

1 used by PCV7 serotypes, 0.17 (0.07-0.42) for disease caused by 1, 5, and 7F serotypes, and 0.41 (0.25

2 ogy of schistosomiasis, a neglected tropical disease caused by a chronic infection with parasitic hel

3 Fatal familial insomnia is a rare disease caused by a D178N mutation in combination with m

4 ysis constitutes the first report of a human disease caused by a defect of the Gardos channel.

5 se) is a neurodegenerative lysosomal storage disease caused by a deficiency in palmitoyl protein thio

6 circuit are fundamentally altered in a brain disease caused by a known molecular defect and that fixi

7 keletal components play in the growth of and disease caused by a known pathogen, prompting future stu

8 lular and molecular basis for Hirschsprung's disease caused by a mutation in the gene PHOX2B.

9 ntington disease (HD) is a neurodegenerative disease caused by a mutation in the huntingtin (HTT) gen

10 a progressive, adult-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in t

11 n autosomal dominant fatal neurodegenerative disease caused by a polyglutamine expansion in the codin

12 sease (HD) is an inherited neurodegenerative disease caused by a polyglutamine expansion in the hunti

13 and severe human degenerative nervous system disease caused by a primary astroglial abnormality, to p

14 etanus is a life-threatening but preventable disease caused by a toxin produced by Clostridium tetani

15 neuronal ceroid lipofuscinosis (NCL, Batten disease) caused by a mutation in CLN5 In humans, mutatio

16 on's disease (HD) is a polyglutamine (polyQ) disease caused by aberrant expansion of the polyQ tract

17 e is an autosomal dominant neurodegenerative disease caused by abnormal polyglutamine expansion in hu

18 e 1 (DM1) and type 2 (DM2) are neuromuscular diseases, caused by accumulation of CUG and CCUG RNAs in

19 yndrome (APDS) is a primary immunodeficiency disease caused by activating mutations in either the leu

20 rms in vivo, with implications for the human diseases caused by ADAR mutations.

21 The burden of disease caused by aEPEC has recently increased in indust

22 TION: The incidence of invasive pneumococcal disease caused by all serotypes decreased due to a decli

23 ed transcriptomics based diagnosis tools for diseases caused by altered gene expression, or used for

24 ington's disease (HD) is a neurodegenerative disease caused by an abnormal expansion in the polygluta

25 is a dominantly inherited neurodegenerative disease caused by an expanded CAG repeat in HTT.

26 nic wasting disease is a fatal, neurological disease caused by an infectious prion protein, which aff

27 de repertoire and with resistance to Marek's disease caused by an oncogenic herpesvirus.

28 strophy (DMD) is a progressive neuromuscular disease, caused by an absence of dystrophin, inevitably

29 al importance within the context of neuronal diseases caused by an impaired glyoxalase system and ele

30 gical processes, including tumorigenesis and diseases caused by an overly aggressive immune response.

31 y in presentation and treatment responses of diseases caused by aneuploidy.

32 Diseases caused by antibiotic-resistant bacteria in hosp

33 zing antibodies can mitigate the severity of disease caused by arenaviruses, particularly species fou

34 role of the azole class in the management of diseases caused by Aspergillus.

35 While the mechanisms underlying disease caused by asymptomatic infections are unknown, i

36 n recognized so far as features of the liver disease caused by ATZ and are likely involved in metabol

37 d add new therapeutic entry points for liver disease caused by ATZ.

38 en disease, is a pediatric lysosomal storage disease caused by autosomal recessive mutations in CLN3,

39 thy (GAN) is a progressive neurodegenerative disease caused by autosomal recessive mutations in the G

40 scinosis (JNCL) is a fatal lysosomal storage disease caused by autosomal-recessive mutations in CLN3

41 r risk factor for melioidosis, an infectious disease caused by B. pseudomallei, is diabetes mellitus.

42 Clinical disease caused by B12 deficiency usually connotes severe

43 Human babesiosis is a tick-borne multisystem disease caused by Babesia species of the apicomplexan ph

44 the possibility for simultaneous therapy of diseases caused by bacterial infections.

45 NE myopathy is an autosomal recessive muscle disease caused by biallelic mutations in GNE, a gene enc

46 highlighted in a patient with mitochondrial disease caused by biallelic pathogenic variants in TOP3A

47 Schistosomiasis is a major parasitic disease caused by blood flukes of the genus Schistosoma.

48 It is a multisystem disease caused by Borrelia burgdorferi sensu lato genosp

49 e possible to develop therapies that control disease caused by both viruses.

50 iagnostics, and vaccine candidates to combat diseases caused by Bp and Bm.Melioidosis and glanders ar

51 on with antibiotic use, for the treatment of diseases caused by Burkholderia.

52 These diseases, caused by Burkholderia glumae, B. gladioli and

53 ) is an autosomal dominant neurodegenerative disease caused by CAG repeat expansion in the ATXN2 gene

54 healthy patients with other forms of severe disease caused by Candida, Trichophyton, Phialophora, an

55 therwise healthy patients with severe fungal diseases caused by Candida species, dermatophytes, or Ph

56 e responses of maize to grey leaf spot (GLS) disease caused by Cercospora zeina, a threat to maize pr

57 Cholera is a devastating diarrhoeal disease caused by certain strains of serogroup O1/O139 V

58 /PTX3 is a novel approach to prevent dry eye disease caused by cGVHD and allow us to test its safety

59 lepsy has traditionally been thought of as a disease caused by changes in neuronal properties exclusi

60 Since koalas frequently suffer from ocular diseases caused by Chlamydia infection, we also examined

61 Cushing's syndrome is a serious endocrine disease caused by chronic, autonomous, and excessive sec

62 scinosis (JNCL) is a fatal lysosomal storage disease caused by CLN3 mutations.

63 Development of anthracnose disease caused by Colletotrichum gloeosporioides Penz.

64 Illness and death from diseases caused by contaminated food are a constant thre

65 d progeria syndrome (HGPS) is a rare genetic disease caused by defective prelamin A processing, leadi

66 is a devastating inherited neurodegenerative disease caused by defects in the ABCD1 gene and affectin

67 overy adds to the emerging spectrum of human diseases caused by defects in the ubiquitin pathway and

68 nemia type 1 (HT1) is an autosomal recessive disease caused by deficiency in fumarylacetoacetate hydr

69 bry disease is an X-linked lysosomal storage disease caused by deficient activity of alpha-galactosid

70 vine footrot is a highly prevalent bacterial disease caused by Dichelobacter nodosus and characterise

71 Malaria is a life-threatening disease caused by different species of the protozoan par

72 platform for PoC serodiagnosis of infectious diseases caused by different types of microorganisms (pa

73 ing with Ellis-van Creveld syndrome (EvC), a disease caused by diminished Hh signaling.

74 rvival and iron deficiency; and mineral bone disease caused by disturbed vitamin D, calcium, and phos

75 g a gene editing approach as a treatment for diseases caused by DNA viruses.

76 99 % were aware that diabetes was a blinding disease caused by DR.11.5 % of the subjects were aware o

77 Invasive disease caused by drug-resistant strains, designated MRS

78 In this review, we discuss rare human diseases caused by dysregulated nucleic acid sensing, fo

79 rophy (DMD) is a severe, degenerative muscle disease caused by dystrophin mutations.

80 s of cystic echinococcosis or cystic hydatid disease caused by E. granulosus.

81 lthough there is no evidence for symptomatic disease caused by either Marburg or Ebola viruses in bat

82 acteristics, and management of patients with disease caused by Emmonsia sp., a novel dimorphic fungal

83 pt that this technology can be used to treat disease caused by epigenetic silencing of specific loci.

84 tivity is a potential therapeutic target for diseases caused by excessive PARP-1 activation.

85 Huntington's disease (HD) is a rare genetic disease caused by expanded polyglutamine repeats in the

86 7 (SCA7) is a debilitating neurodegenerative disease caused by expansion of a polyglutamine [poly(Q)]

87 Friedreich's Ataxia is a genetic disease caused by expansion of an intronic trinucleotide

88 's disease (HD) is a fatal neurodegenerative disease, caused by expansion of polyglutamine repeats in

89 Huntington's Disease, caused by expansion of the polyQ tract in exon

90 Millions of people die every year from diseases caused by exposure to outdoor air pollution.

91 omiasis is a debilitating neglected tropical disease, caused by flatworms of Schistosoma genus.

92 Dengue (DEN) is a mosquito-borne disease caused by four DENV serotypes (DENV-1, -2, -3, a

93 Allergic diseases caused by fungi are common.

94 Fusarium head blight (FHB) is a cereal disease caused by Fusarium graminearum, a fungus able to

95 Panama disease caused by Fusarium oxysporum f.sp. cubense infec

96 autosomal dominant combined immunodeficiency disease caused by gain-of-function mutation of the chemo

97 Long QT syndrome type 3 (LQT3) is a lethal disease caused by gain-of-function mutations in the SCN5

98 an 300 million people suffer from a range of diseases caused by gastropod-borne helminths, predominan

99 Diseases caused by gene haploinsufficiency in humans com

100 Kidney diseases caused by genetic or acquired dysregulation of

101 diagnosis and surveillance of infection and disease caused by H. haemolyticus and NT H. influenzae.

102 , potentially protecting against age-related disease caused by haploinsufficiency.

103 ere congenital neutropenia (SCN) 3 (Kostmann disease [caused by HAX1 mutations]).

104 tational knock-in at single alleles to model diseases caused by heterozygous mutations has not been r

105 Herein we describe a new disease caused by high-penetrance heterozygous germline

106 peutic approaches to prevent and treat human disease caused by highly pathogenic avian influenza viru

107 ataxia (FRDA) is a severe neurodegenerative disease caused by homozygous expansion of the guanine-ad

108 inal disease irrespective of HPV type (i.e., disease caused by HPV types included in the 9vHPV vaccin

109 high efficacy against incident infection and disease caused by HPV types that they specifically targe

110 treatment for the malignant or inflammatory diseases caused by HTLV-1.

111 Infection and disease caused by human cytomegalovirus (CMV) remain a s

112 , the pegiviruses, are thought to reduce the disease caused by human immunodeficiency virus (HIV) in

113 n diseases, including delayed progression of disease caused by human immunodeficiency virus type 1 (H

114 Psoriasis vulgaris is an inflammatory skin disease caused by hyperactivated T cells regulated by po

115 ge numbers of patients with end-stage kidney disease caused by IgA nephropathy are transplanted every

116 (LC) amyloidosis (AL) is a potentially fatal disease caused by immunoglobulin LC produced by clonal p

117 strophy (APECED), a T cell-driven autoimmune disease caused by impaired central tolerance, are suscep

118 -linked hypophosphatemia (XLH) is a skeletal disease caused by inactivating mutations in the PHEX gen

119 Anthrax is a life-threatening disease caused by infection with Bacillus anthracis, whi

120 Schistosomiasis is a debilitating tropical disease caused by infection with parasitic blood flukes.

121 Chagas disease, caused by infection with the protozoan parasite

122 for periodontitis as a chronic inflammatory disease caused by infectious agents in RA seems biologic

123 Tuberculosis (TB) is a significant human disease caused by inhalation of Mycobacterium tuberculos

124 reich's ataxia (FRDA) is a neurodegenerative disease caused by inherited deficiency of the mitochondr

125 Background Babesiosis, a tickborne zoonotic disease caused by intraerythrocytic protozoa of the genu

126 halitis is an acute zoonotic, mosquito-borne disease caused by Japanese encephalitis virus (JEV).

127 been vital for controlling the incidence of disease caused by JEV, particularly in rural areas of As

128 PEL) are two well-known inflammation related diseases caused by Kaposi's sarcoma-associated herpesvir

129 Leishmaniasis is a highly diverse group of diseases caused by kinetoplastid of the genus Leishmania

130 uide more-effective treatment of tegumentary disease caused by L. braziliensis.

131 Modelling human diseases caused by large genomic rearrangements has beco

132 on between a decrease of pericytes and liver disease caused by ligature-induced periodontitis in rats

133 igate the heterogeneity in manifestations of disease caused by Listeria monocytogenes and demonstrate

134 uscular atrophy (SMA) is a neurodegenerative disease caused by loss of motor neurons in patients with

135 Type 1 diabetes (T1D) is an autoimmune disease caused by loss of pancreatic beta cells via apop

136 pinal muscular atrophy (SMA) is a motoneuron disease caused by loss or mutation in Survival of Motor

137 Here, we report an autoinflammatory disease caused by loss-of-function mutations in OTULIN (

138 se model for Keutel syndrome, a rare genetic disease caused by loss-of-function mutations in the matr

139 al muscular atrophy (SMA) is a neuromuscular disease caused by low levels of SMN protein, primarily a

140 esent an overview of the diffuse cystic lung diseases caused by lymphoproliferative disorders, geneti

141 eds new light on the mechanism of the blight disease caused by M. oryzae.

142 s worldwide each year result from infectious diseases caused by microbial pathogens.

143 lly, new research, such as studies of severe diseases caused by miRNA malfunction, will benefit from

144 velopments, placing the greatest emphasis on diseases caused by mitochondrial DNA mutations.

145 monkeypox is an emerging zoonotic infectious disease caused by Monkeypox virus (MPXV).

146 athies are a group of phenotypically related diseases caused by monogenic mutations that primarily af

147 trials of patients with Charcot-Marie-Tooth disease caused by MPZ gene mutations.

148 lor FluoroSpot assay can be applied to other diseases caused by multiple pathogen serotypes in which

149 dermia and cardiomyopathy to the spectrum of disease caused by mutation in DSP, and identify a specif

150 e type 1b (GSD-1b) is an autosomal-recessive disease caused by mutation of glucose-6-phosphate transp

151 trypsin (AAT) deficiency (AATD) is a genetic disease, caused by mutation of the AAT gene.

152 is an autosomal recessive neurodegenerative disease caused by mutations in Frataxin (FXN).

153 as giant axonal neuropathy (GAN), a ravaging disease caused by mutations in GAN, encoding gigaxonin.

154 y considered to be a genetically homogeneous disease caused by mutations in PKHD1, has been associate

155 al muscular atrophy (SMA) is a neuromuscular disease caused by mutations in Survival Motor Neuron 1 (

156 dystrophy (APECED) is a monogenic autoimmune disease caused by mutations in the AIRE gene.

157 Gaucher's disease is a common genetic disease caused by mutations in the beta-glucocerebrosida

158 stic fibrosis (CF) is a major lethal genetic disease caused by mutations in the CF transmembrane cond

159 Cystic fibrosis is an autosomal recessive disease caused by mutations in the CFTR gene that lead t

160 rmolysis bullosa is a devastating blistering disease caused by mutations in the COL7A1 gene, which en

161 ataxia type 5 (SCA5) is a neurodegenerative disease caused by mutations in the cytoskeletal protein

162 ) is a severe and progressive muscle-wasting disease caused by mutations in the dystrophin gene.

163 DMD) is an incurable X-linked muscle-wasting disease caused by mutations in the dystrophin gene.

164 Giant axonal neuropathy (GAN) is a rare disease caused by mutations in the GAN gene, which encod

165 lar dystrophy (DMD) is an X-linked recessive disease caused by mutations in the gene encoding dystrop

166 phenocopying what has been reported for Dent disease caused by mutations in the gene encoding endosom

167 ephalomyopathy (MNGIE) is a fatal, recessive disease caused by mutations in the gene encoding thymidi

168 epidermolysis bullosa (RDEB) is an incurable disease caused by mutations in the gene encoding type VI

169 syndrome is a rare but devastating childhood disease caused by mutations in the IDS gene encoding idu

170 -C) is a progressive lysosomal lipid storage disease caused by mutations in the NPC1 and NPC2 genes.

171 of premature aging.HGPS is a premature aging disease caused by mutations in the nuclear protein lamin

172 a rare autosomal-dominant neurodegenerative disease caused by mutations in the TGM6 gene, which code

173 DYT1) is a dominantly inherited neurological disease caused by mutations in TOR1A, the gene encoding

174 F) is an IL-1beta-dependent autoinflammatory disease caused by mutations of Mediterranean fever (MEFV

175 Cystic fibrosis (CF) is a common genetic disease caused by mutations of the cystic fibrosis trans

176 Cystic fibrosis (CF) is a lethal genetic disease caused by mutations of the gene encoding the cys

177 taxia type 28 (SCA28) is a neurodegenerative disease caused by mutations of the mitochondrial proteas

178 ulation is particularly valuable in cases of disease caused by mutations that lead to disruption of n

179 uronal ceroid lipofuscinosis (JNCL or Batten disease) caused by mutations in the CLN3 gene is the mos

180 thies (NMs) are a group of congenital muscle diseases caused by mutations in at least 10 genes and as

181 asma factor H (FH) as exemplified by various diseases caused by mutations in its domains 19-20 (FH19-

182 tronuclear myopathies are early-onset muscle diseases caused by mutations in several genes including

183 sible therapeutic strategy for patients with diseases caused by mutations in the Mfn2 gene.

184 ncy and toxicity disorders Menkes and Wilson diseases caused by mutations in the p-type Cu-ATPase gen

185 stem to establish a mechanistic link between diseases caused by mutations in two distinct genes, hnRN

186 r adhesion, and informs our understanding of diseases caused by mutations in USH1C and ankyrin repeat

187 ify the molecular pathology of ALS and other diseases caused by mutations of Matrin3.

188 Bovine tuberculosis (TB) is a zoonotic disease caused by Mycobacterium bovis.

189 Leprosy is a chronic infectious disease caused by Mycobacterium leprae, which primarily

190 ts for tuberculosis (TB), a major infectious disease caused by Mycobacterium tuberculosis (Mtb), whic

191 accinees, although no cases of meningococcal disease caused by N. meningitidis B were reported among

192 s, we present an overview of the cystic lung diseases caused by neoplasms, infections, smoking-relate

193 By contrast, that of invasive pneumococcal disease caused by non-PCV13 serotypes increased, which s

194 The pooled IRR for invasive pneumococcal disease caused by non-PCV13 serotypes was 1.62 (1.09-2.4

195 valve, a phenotype that closely mimics human disease caused by NOTCH1 haploinsufficiency.

196 a genetic paradigm of cerebral small vessel disease caused by NOTCH3 mutations that stereotypically

197 therapeutic and preventative strategies for diseases caused by NTHI and many other human pathogens k

198 phy type 1 (DM1) is a dominant neuromuscular disease caused by nuclear-retained RNAs containing expan

199 specially in age-dependent neurodegenerative diseases caused by nucleotide repeat expansion, have hig

200 Leishmaniasis, a vector-borne disease caused by obligate intramacrophage protozoa, thr

201 gical response of the organism to infectious diseases caused by organisms such as bacteria, viruses,

202 system, indirectly affecting the severity of diseases caused by other pathogens.

203 es of natural antioxidants for prevention of diseases caused by oxidative stress.

204 Graves' hyperthyroidism, a common autoimmune disease caused by pathogenic autoantibodies to the thyro

205 Leishmaniasis comprises an array of diseases caused by pathogenic species of Leishmania, res

206 s important marker chemicals to detect plant diseases caused by pathogens.

207 caused by any serotype, 0.16 (0.07-0.40) for disease caused by PCV7 serotypes, 0.17 (0.07-0.42) for d

208 d help to design better treatments for human diseases caused by perturbations in fluid osmolarity.

209 Poliomyelitis is a highly infectious disease caused by poliovirus (PV).

210 ington's Disease (HD) is a neurodegenerative disease caused by poly-glutamine expansion in the Htt pr

211 al muscular dystrophy (OPMD) is a late onset disease caused by polyalanine expansion in the poly(A) b

212 trophy (SBMA) is a progressive neuromuscular disease caused by polyglutamine expansion in the androge

213 re fatal neurodegenerative and transmissible diseases caused by prions.

214 gests that the likelihood of having reported disease caused by PRN(-) compared with PRN(+) strains is

215 on diseases represent the archetype of brain diseases caused by protein misfolding, the most common s

216 on diseases represent the archetype of brain diseases caused by protein misfolding, with the most com

217 protect the global wheat crop from stem rust disease caused by Puccinia graminis f.

218 F) is characterized by early structural lung disease caused by pulmonary infections.

219 Poliomyelitis is a highly infectious disease caused by PV and is on the verge of eradication.

220 patients (>/=18 years) with invasive fungal disease caused by rare fungi, including mucormycosis, we

221 tifocal leukoencephalopathy (PML) is a fatal disease caused by reactivation of JC polyomavirus (JCPyV

222 A common feature of diseases caused by recessive RYR1 mutations is a decreas

223 al muscular atrophy (SMA) is a neuromuscular disease caused by reduced expression of survival of moto

224 However, diseases caused by resistant nonvaccine type (NVT) strai

225 Emerging and re-emerging infectious diseases caused by RNA viruses pose a critical public he

226 for an effective strategy to treat blinding diseases caused by RPE dysfunction.

227 target F can prevent viral entry and reduce disease caused by RSV.

228 e are large data gaps in the epidemiology of diseases caused by Salmonella enterica in West Africa.

229 , an important biocontrol agent against crop diseases caused by Sclerotinia sclerotiorum, was identif

230 ntion and treatment of some human autoimmune diseases caused by self-DNA.

231 Leishmaniases are diseases caused by several Leishmania species.

232 e 3 (SCA3), one of nine inherited, incurable diseases caused by similar mutations.

233 insights into the molecular mechanism of the disease caused by SNARE mutations.

234 y can be a promising method to treat genetic diseases caused by splicing errors, but the efficiency o

235 associated with human disease, the burden of disease caused by STEC strains that lacks LEE (LEE-negat

236 The burden of disease caused by Streptococcus agalactiae has increased

237 annually by preventing invasive pneumococcal disease caused by Streptococcus pneumoniae Some componen

238 Type 1 diabetes (T1D) is an autoimmune disease caused by T cell-mediated destruction of insulin

239 Botulism is a potentially fatal paralytic disease caused by the action of botulinum neurotoxin (Bo

240 ges in either group in invasive pneumococcal disease caused by the additional 11 serotypes covered by

241 Melioidosis, a severe human disease caused by the bacterium Burkholderia pseudomalle

242 Colorectal cancer (CRC) is a common complex disease caused by the combination of genetic variants an

243 Classic galactosemia is a potentially lethal disease caused by the dysfunction of galactose 1-phospha

244 is a dominantly inherited neurodegenerative disease caused by the expansion of a CAG repeat in the H

245 nic dystrophy Type 1 (DM1) is a rare genetic disease caused by the expansion of CTG trinucleotide rep

246 dystrophy type 2 is a genetic neuromuscular disease caused by the expression of expanded CCUG repeat

247 ntington's disease (HD), a neurodegenerative disease caused by the expression of mutant huntingtin pr

248 chocerciasis is a serious neglected tropical disease caused by the filarial nematode Onchocerca volvu

249 s) likely contributes to the pathogenesis of disease caused by the filoviruses Ebola virus and Marbur

250 pergillosis (IPA) is a life-threatening lung disease caused by the fungus Aspergillus fumigatus, and

251 Lethal disease caused by the fungus Cryptococcus neoformans is

252 In Europe, the emerging ash dieback disease caused by the fungus Hymenoscyphus fraxineus, co

253 alopathy (PML) is a lethal CNS demyelinating disease caused by the human neurotropic polyomavirus JC

254 nic hyperproliferative and inflammatory skin disease caused by the interplay of genetic and environme

255 kinson's disease (PD) is a neurodegenerative disease caused by the loss of dopaminergic neurons in th

256 lateral sclerosis (ALS), a neurodegenerative disease caused by the loss of motor neurons leading to p

257 fever, an acute and often chronic arthralgic disease caused by the mosquito-borne chikungunya virus (

258 sease (HD) is an inherited neurodegenerative disease caused by the mutant huntingtin gene (mHTT), whi

259 Buruli Ulcer is a devastating skin disease caused by the pathogen Mycobacterium ulcerans.

260 r the treatment of toxoplasmosis, which is a disease caused by the protozoan parasite Toxoplasma gond

261 ing mosquito-borne zoonotic infectious viral disease caused by the RVF virus (RVFV) (Bunyaviridae: Ph

262 chinson-Gilford progeria syndrome, a genetic disease caused by the synthesis of an internally truncat

263 ive up regulated resistant genes Coffee rust disease, caused by the fungus Hemileia vastatrix, is one

264 pe to treatment using the newly defined XMEN disease, caused by the genetic loss of the MAGT1 magnesi

265 Chagas disease, caused by the parasite Trypanosoma cruzi, is en

266 Chagas' disease, caused by the protozoan parasite Trypanosoma cr

267 Chagas disease, caused by the protozoan parasite Trypanosoma cr

268 Chagas disease, caused by the protozoan Trypanosoma cruzi, is e

269 , lupus nephritis and other autoinflammatory diseases caused by the decreased ability of ABIN1 or oth

270 hatic filariasis and loiasis are major human diseases caused by the insect-borne filarial nematodes B

271 information to discover the genetic basis of diseases caused by the mis-regulation of gene expression

272 uld explain the observed comorbidity between diseases caused by the same genetic alterations.

273 lth problems worldwide, and the incidence of diseases caused by the virus has increased dramatically.

274 have caused great reductions in pneumococcal disease caused by these serotypes.

275 he high mortality (>60%) associated with the disease caused by these viruses and the lack of protecti

276 ture drug development for a large variety of diseases caused by these agents.

277 e specific pathophysiological aspects of the diseases caused by these microorganisms.

278 emotherapies to assist in the eradication of diseases caused by these pathogens.

279 nail hosts define the geographical ranges of diseases caused by these worms.

280 nce: Infantile beriberi, a potentially fatal disease caused by thiamine deficiency, remains a public

281 proaches are necessary for the prevention of disease caused by this canine respiratory pathogen.

282 proaches are necessary for the prevention of disease caused by this important human respiratory patho

283 to develop more effective vaccines to combat disease caused by this important respiratory pathogen.

284 tly needed for the control and prevention of disease caused by this organism.

285 t improvement in the diagnosis of infectious diseases caused by this pathogen.

286 hodesian sleeping sickness, a fatal zoonotic disease caused by trypanosomes transmitted by tsetse fli

287 r Tan syndrome (UTS), to the growing list of diseases caused by tubulin variants.

288 sical osteogenesis imperfecta (OI) is a bone disease caused by type I collagen mutations and characte

289 tubulointerstitial kidney disease, the same disease caused by UMOD mutations.

290 nse and its potential participation in human diseases caused by unfolded protein response.IRE1alpha i

291 Inherited diseases caused by unstable repeated DNA sequences are r

292 cribe the genotype-phenotype correlations of diseases caused by variants in Fibroblast Growth Factor

293 erstanding of genetic disease in general and diseases caused by variation in FGFR1 specifically.

294 Cholera is an acute, watery diarrhoeal disease caused by Vibrio cholerae of the O1 or O139 sero

295 therapy for cholera, a severely dehydrating disease caused by Vibrio cholerae.

296 Management of rice false smut disease caused by Villosiclava virens is dependent on de

297 This is a contagious disease caused by viruses belonging to the family Orthom

298 sistant to most devastating bacterial blight diseases caused by Xanthomonas oryzae pv. oryzae (Xoo).

299 ic plague represents the most severe form of disease caused by Yersinia pestis due to its ease of tra

300 Diseases caused by zoonotic viruses (viruses transmittab