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1 mutations in sarcomere protein genes as the cause of disease.
2 tation-induced loss of stability is a common cause of disease.
3 ed to the establishment of autoimmunity as a cause of disease.
4 r, a prime candidate gene, was excluded as a cause of disease.
5 ction of sophisticated exotoxins is the main cause of disease.
6 limination of classical biotype strains as a cause of disease.
7 h as multiple sclerosis may be a clue to the cause of disease.
8 21ins2) is the predominant but not exclusive cause of disease.
9 iquitous in the environment and an important cause of disease.
10 iral immune response within the brain is the cause of disease.
11 occus, serotype V (GBS-V), was an infrequent cause of disease.
12 T) were helpful in suggesting the underlying cause of disease.
13 atory mechanism regardless of the initiating cause of disease.
14 Chronic inflammation is a major cause of disease.
15 treatments address the symptoms, but not the cause of disease.
16 e therapies are designed to address the root cause of disease.
17 Genetic testing may elucidate an underlying cause of disease.
18 to disease, and relationship of organism to cause of disease.
19 es encoding the sarcomere is the predominant cause of disease.
20 ars due to its potential to address the root cause of disease.
21 of familiality is consistent with a genetic cause of disease.
22 rapid elucidation of the underlying genetic cause of disease.
23 ndent on the ability to identify the genetic cause of disease.
24 quitoes are an increasingly important global cause of disease.
25 gation is increasingly being recognized as a cause of disease.
26 Smoking is a common addiction and a leading cause of disease.
27 Mycobacterium mucogenicum was the leading cause of disease.
28 (tubulin beta-4; Arg2Gly) gene as the likely cause of disease.
29 action between the genetic and environmental causes of disease.
30 smaller subfibrillar oligomers are the prime causes of disease.
31 igins, susceptibility to illness and genetic causes of disease.
32 aware of inherited genetic abnormalities as causes of disease.
33 nt susceptibility to two vaccine-preventable causes of disease.
34 ditions by targeting the fundamental genetic causes of disease.
35 research to further our understanding of the causes of disease.
36 rom normality include diagnostic markers and causes of disease.
37 rect link between filament formation and the causes of disease.
38 ve analysis of genomic variants as potential causes of disease.
39 rated with the goal of identifying molecular causes of disease.
40 laboratory evaluations to exclude secondary causes of disease.
41 studies are important tools for identifying causes of disease.
42 cerned with determining the distribution and causes of disease.
43 edicines require understanding the molecular causes of disease.
44 worry, and depression are significant direct causes of disease.
45 sed to predict new functions in proteins and causes of disease.
47 ulation of Notch signaling is the underlying cause of diseases affecting the skeletal tissue, includi
50 r bacterium Rhodococcus equi is an important cause of disease and death in immunocompromised hosts, e
51 uman cytomegalovirus (HCMV) is a significant cause of disease and death in immunocompromised patients
52 s a ubiquitous herpesvirus and a significant cause of disease and death in the immunocompromised and
55 Seasonal influenza infection remains a major cause of disease and death, underscoring the need for im
58 trials to establish the similarities in the cause of disease and in treatment response between child
60 f mitochondrial DNA (mtDNA) are an important cause of disease and play a role in the ageing process.
64 lts because of uncertain similarities in the cause of disease and the treatment course between the 2
65 orical trial data suggests similarity in the cause of disease and the treatment response between neon
66 y demonstrated that ANCAs are a transferable cause of disease and this is supported by studies of the
68 will permit us to investigate the underlying cause of diseases and help us to develop therapeutics.
69 rting to take into account the polymicrobial cause of diseases and the repercussions of treatment and
70 Better understanding of the mechanisms and causes of disease and an increasingly extensive and robu
71 ssociated bacterial pneumonia (VABP), common causes of disease and death in hospitalized patients.
74 ility-adjusted life-years (DALYs) due to 359 causes of disease and injury burden from 2022 to 2050 fo
75 nts about health losses associated with many causes of disease and injury were elicited from the gene
76 ised approach is not tackling the underlying causes of disease and is not addressing inequalities in
77 this genome are now recognized as important causes of disease and may take the form of point mutatio
79 within 24 h of inclusion for main treatable causes of disease and second-line testing was done there
81 r and sensitive biomarkers both to track the causes of disease and to develop and evolve therapies du
82 g whole chromosomes, have been identified as causes of diseases and developmental abnormalities and a
83 rigorous and unbiased conclusions about the causes of diseases and their population-wide impact will
84 ate diagnosis, recognition of the modifiable causes of disease, assessment of symptoms and complicati
85 D1 may generate new insights into underlying causes of diseases associated with infertility or develo
86 Major depressive disorder (MDD) is a leading cause of disease-associated disability, with much of the
87 r age at diagnosis, sex, race and ethnicity, cause of disease, Barcelona Clinic Liver Cancer (BCLC) s
88 or injecting drug use (IDU) is a substantial cause of disease burden and a contributor to blood-borne
89 st cancer remains the leading cancer-related cause of disease burden for women, affecting one in 20 g
93 pwards of two billion people and are a major cause of disease burden in children and pregnant women.
96 arette smoking remains the leading avoidable cause of disease burden worldwide, and observational stu
99 late matter pollution (PM2.5) is one leading cause of disease burden, but no study has quantified the
103 aimed to quantify differences in the leading causes of disease burden between females and males acros
104 tes for females and males for the 20 leading causes of disease burden for individuals older than 10 y
105 ilable resources effectively to reduce major causes of disease burden globally and to decrease health
109 e therapeutics rarely address the underlying cause of disease but rather focus on managing or modifyi
110 ead in mammalian genomes and is an important cause of disease, but just how abundant and important st
111 chanisms integrate genetic and environmental causes of disease, but comprehensive genome-wide analyse
112 mples but could be distinguished as possible causes of disease by parsing for outlier organisms.
113 e proven to be helpful for finding genotypic causes of diseases, classifying disease subtypes, and id
114 r of lung fibrosis and remains a significant cause of disease despite strict regulations to limit exp
115 ined the human genome (G) mainly to discover causes of disease, despite evidence that G explains rela
118 bacco use remains the number-one preventable cause of disease, disability, and death in the United St
121 (immune-mediated pathology) is a ubiquitous cause of disease during infection, but how will parasite
122 kely that B. miyamotoi is an underrecognized cause of disease, especially in sites where Lyme disease
123 types that were disproportionately common as causes of disease, even taking into account their relati
126 sing mutations and may represent a molecular cause of disease for a number of inherited and somatic m
127 has been progress in defining the underlying cause of disease for some patients of muscular dystrophy
128 ts of this class are likely underreported as causes of disease for several reasons: Most clinical DNA
130 B meningococcus (MenB) remains an important cause of disease globally, and additional vaccines again
131 pectancy and health outcomes for preventable causes of disease have continued to lag in many populati
133 whether distinct genes represent independent causes of disease (heterogeneity) or whether they intera
134 mising tool for investigating the underlying causes of disease; however, this potential currently rem
135 data to understand underlying environmental causes of disease, identify biomarkers of exposure and r
139 ale germ cell-associated kinase (MAK) as the cause of disease in an isolated individual with RP.
140 la catarrhalis continues to be a significant cause of disease in both children and adults, the steps
141 m, trypanosomes, and Leishmania, are a major cause of disease in both humans and other animals, highl
145 s, they are now increasingly recognized as a cause of disease in dogs in temperate climates and urban
146 =0.0001) CFH variants were identified as the cause of disease in each family: CFH c.1243del, p.(Ala41
147 infections in children as well as a serious cause of disease in elderly and immunosuppressed populat
148 netic and genomic approaches to identify the cause of disease in extensive pedigrees comprising over
149 ogen Pneumocystis jirovecii is a significant cause of disease in HIV-infected patients and others wit
155 s organism has recently been recognized as a cause of disease in immunocompromised patients, presenti
157 is to efficiently determine the presence and cause of disease in order to provide the most appropriat
161 ions due to Cryptococcus neoformans, a major cause of disease in persons with AIDS and other disorder
162 lude Mycobacterium tuberculosis complex as a cause of disease in smear-positive respiratory specimens
164 genes were performed to identify the genetic cause of disease in the family with the Carney complex a
167 human pathogen continues to be a significant cause of disease in this broad spectrum of patients beca
172 actin-filament crosslinking protein, as the cause of disease in three families with an autosomal dom
173 ed primarily by Aedes mosquitos and is major cause of disease in tropical and subtropical regions.
174 we investigated the genetic and mechanistic cause of disease in two independent consanguineous famil
175 Although they are recognized as a leading cause of disease in young children, the cellular factors
178 individuals can be summed to understand the causes of disease in populations, academic epidemiology
179 fection with a microbe, considered to be the cause of disease, in cells, tissues, or organisms seen a
180 c trials, focus on addressing the underlying cause of disease, insufficient production of full-length
181 tations; however, the translation of genetic causes of disease into pathobiological understanding rem
183 in at least 5% of patients in whom a genetic cause of disease is identified, highlighting the fact th
185 candidate gene approach to identifying novel causes of disease is concept-limiting and in the new era
186 lop new approaches that directly address the cause of disease, leading to disease remission and ultim
187 cal information-demographic characteristics, cause of disease, liver-related blood tests, tumour char
188 le of multiple component, often interacting, causes of disease may be impossible with research tools
189 ility that both presynaptic and postsynaptic causes of disease might also exist in related disorders,
193 data indicate that subsequent to the genetic cause of disease, neuropathology is driven by pathogenic
195 ions in POLG are the most common single-gene cause of diseases of mitochondria and have been mapped o
196 tory microbiota of pigs that is also a major cause of disease on pig farms and an important zoonotic
197 ther directly address the underlying genetic cause of disease or induce fetal hemoglobin production b
198 scale, can generate valuable information on causes of disease outbreaks, reproductive losses and can
200 ernative approaches searched for preexisting causes of disease, particularly human genetic and immuno
201 stion might provide crucial insight into the cause of disease pathology at its earliest stages of dev
203 pse suggesting that progressive LOH may be a cause of disease progression and/or drug resistance.
205 ditional chromosomal abnormalities are major causes of disease progression in chronic lymphocytic leu
215 orders directed at correcting the underlying cause of disease represents the most significant recent
217 n study (GWAS) with MEVs pinpoints potential causes of disease risk, including a LINE-1 insertion ass
219 ry response induced by SARS-CoV-2 is a major cause of disease severity and death in infected patients
221 lammation triggered by SARS-CoV-2 is a major cause of disease severity, with activated macrophages im
222 altered RNA regulation by TDP-43 as a major cause of disease, specific changes within MNs that trigg
223 pe emm59 GAS, heretofore an exceedingly rare cause of disease, spread west to east across Canada over
226 tis, the same genotype was implicated as the cause of disease, suggesting persistence of the organism
227 mily cytokines is recognized as an important cause of disease susceptibility, it is unclear whether a
229 is considered both a defense mechanism and a cause of disease that leads to inflammation and psycholo
230 expression has been perceived as a potential cause of disease, there is mounting evidence that some E
231 Dystrophin deficiency is the underlying cause of disease; therefore, mutation-specific therapies
232 , insurance types, hospital characteristics, cause of disease, time to therapy, length of stay (LOS),
233 a second mutation, should not be taken as a cause of disease unless corroborated by family data and
234 le animal facility, designed to identify the causes of disease variability in the widely used dextran
236 ntific curiosity, but also to understand the causes of disease well enough to predict risks, make ear
237 tinues to evolve as it seeks to pinpoint new causes of disease with the hope of advancing personalize