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1 altered innate immunity hypothesized to be a cause.
2 or were euthanized due to a possible cardiac cause.
3 ly known definitive genetic or environmental causes.
4 and limited data addressing risk factors for causes.
5 tility in sample-size distributions that can cause a nontrivial proportion of trials to assign more p
7 ly, the data show that FDD and FBD mutations cause a reduction of BRI2 levels and function at synapse
8 traumatic injury, corneal wound healing can cause a scarring response that stiffens the tissue and i
11 itability during the first 2 postnatal weeks caused a premature differentiation of oligodendrocytes s
13 coupling" scenario, the presence of effector causes a change in the DeltaH associated with substrate
14 failure, induced via myocardial infarction, causes a decrease of the cGMP levels generated by these
18 insect-transmitted orthobunyavirus that can cause abortions and congenital malformations in the offs
23 ace to solvent reduces protein stability and causes aggregation, even though the interface makes no d
25 ith molecular and physiological changes that cause alterations in lung function, diminished pulmonary
26 ial for cytokinesis and viability of disease-causing amastigotes but not for flagellar membrane traff
27 tanding of the harm to health from lifestyle causes among the general population is low, with a poor
30 plasmanylethanolamine desaturase deficiency causes an accumulation of plasmanyl species, a too littl
32 as more effective than TIV in preventing all-cause and P&I hospitalization from NHs during an A/H3N2
33 and shed light on the consistency, candidate causes, and potential functional corollaries of sex-bias
35 des pose a significant threat to agriculture causing annual yield losses worth more than 100 billion
40 A single episode of febrile UTI is often caused by a virulent Escherichia coli strain, whereas re
43 epair pathways of DNA interstrand crosslinks caused by an endogenous and alcohol-derived metabolite,
45 FXR seems to influence the degree of damage caused by atorvastatin depending on its interaction with
46 (MG) is a neuromuscular, autoimmune disease caused by autoantibodies that target postsynaptic protei
48 f Johanson-Blizzard syndrome (JBS), which is caused by bi-allelic variants in UBR1, notably by the pr
49 rome (BS) are disorders of DNA damage repair caused by biallelic disruption of the WRN or BLM DNA hel
52 ory enhancing effect (behavioral tagging) is caused by dopaminergic and noradrenergic neuromodulation
55 on of the N-module subunits due to attrition caused by its constant activity under physiological cond
57 s in GPHYSD1 patients with this mutation are caused by loss of O-fucosylation on TSR3 and impaired AD
58 cterized by premature cardiovascular disease caused by markedly elevated levels of low-density lipopr
59 uxin levels suggest these irregularities are caused by misregulation of ABCB19-mediated auxin distrib
60 X-linked (IPEX) syndrome is a lethal disease caused by mutations in a transcription factor critical f
62 ilial forms of Alzheimer's disease (FAD) are caused by mutations in the gene encoding amyloid precurs
63 neurodevelopmental disorder Rett syndrome is caused by mutations in the gene Mecp2 Misexpression of t
66 main (physical functioning, role limitations caused by physical health problems) remained statistical
72 (DILI) is a necro-inflammatory liver disease caused by several drugs commonly used in clinical practi
76 n opportunistic infection of the oral mucosa caused by the commensal fungus Candida albicans IL-17R s
77 ings were convened to address the challenges caused by the COVID-19 pandemic, review options for main
79 terized by a specific encephalopathy that is caused by toxic accumulation of lysine degradation inter
81 delayed onset compared to the onset of those caused by WT EBV, although the tumors occurred at a simi
82 ng and remodelling of the blood vasculature, causing cancer cell hypoxia and death in distant avascul
83 ete destruction of the bacterial chromosome, causing cell death prior to completion of phage replicat
84 n in expression patterns of regulatory genes causing changes in anisotropic cell expansion and divisi
85 n kinase (BCR-Abl) is a driver oncogene that causes chronic myeloid leukemia and a subset of acute ly
88 obstructive sleep apnea syndrome (OSAS), may cause compromise of respiratory gas exchange during slee
90 D(+)-binding site or the ARM-TIR interaction caused constitutive activation of SARM1 and thereby led
91 nd correction (where possible) of underlying causes, correction of nutritional deficiencies, and the
92 have CTDs, and inactivation of Crkl in mice causes CTDs, thus implicating this gene as a modifier.
93 ed with significantly increased risk for all-cause death (adjusted hazard ratio for moderate and seve
95 to date reveals that CHIKV-ECSA strains can cause death in individuals from both risk and non-risk g
96 ssess effects on cardiovascular death or all-cause death or to characterise effects in clinically imp
98 disrupt intermediary metabolic pathways and cause defective absorption and metabolism of dietary nut
99 KO in young mice, but not older adult mice, causes defects in muscle function, consistent with a pro
101 on when early ablation or overexpression can cause developmental defects or embryonic lethality.
102 uous chain of H-bonds that impart stability, causing difficulty in digestion for bottom-up measuremen
106 hes multivalent, synergistic H3-tail binding causing distinct cellular localization and enhanced H3K9
108 in cysteine string protein-alpha (CSPalpha) cause dominantly inherited adult-onset neuronal ceroid l
109 he underlying protein stability changes that cause dramatic cellular phenotypes observed at nonpermis
112 MHV infection in mice provides an efficient cause-effect experimental model to understand the mechan
113 roductive phenotypic variation, although the cause-effect relationships are difficult to discern, cal
114 found that treating these cells with laminin causes endogenous agrin to localize to the cell surface,
115 evolved with bat immune systems will likely cause enhanced virulence following emergence into second
118 Mutations of the ion pump alpha2-Na/K ATPase cause familial hemiplegic migraine, but the mechanisms b
119 cause of death worldwide and the number one cause for acquired long-term disability, resulting in a
120 9orf72 gene is the most common known genetic cause for amyotrophic lateral sclerosis (ALS) and fronto
126 in demonstrating that vaping of e-cigarettes causes health effects both similar to and disparate from
128 e mechanism through which verubecestat might cause hippocampal (and other brain region) volume loss b
129 associated with lower risk of mortality, all-cause hospital admission, and intubation, but no signifi
131 (PAMI) syndrome is a novel genetic disorder, causing hypercalprotectinemia and hyperzincemia with inf
134 Each year in the United States, influenza causes illness in 9.2 to 35.6 million individuals and is
137 c leukemia (ALL) are at risk for thrombosis, caused in part by the use of l-asparaginase (L-ASP).
138 om both cardiovascular and noncardiovascular causes in low-, middle-, and high-income countries.
139 secretion but impairs beta-cell function, 2) causes insulin resistance, and 3) reduces metabolic clea
142 (KSHV) is an oncogenic gammaherpesvirus that causes Kaposi's sarcoma and other lymphoproliferative di
144 t small changes in the activity of PTP1B can cause large shifts in the phosphorylation states of its
148 ions in the galactosidase beta 1 (GLB1) gene cause lysosomal beta-galactosidase (beta-Gal) deficiency
152 ePVAC develops signs of exudation over time, causing metamorphopsia and visual decline and therefore
153 e propose that mutations in centrosome genes cause microcephaly by delaying mitosis and pathologicall
157 demonstrated a significant reduction in all-cause mortality (ACM) risk with fluticasone furoate/umec
158 ls, PN was significantly associated with all-cause mortality (hazard ratio [HR], 1.49 [CI, 1.15 to 1.
159 atio [HR], 0.82 [95% CI, 0.72-0.92]) and all-cause mortality (HR, 0.83 [95% CI, 0.75-0.92]), whereas
160 ios for coronary heart disease, CVD, and all-cause mortality according to categories of BMI and CAC.
161 patients with T2MI had higher long-term all-cause mortality after adjustment for age and sex, driven
162 nship between handgun ownership and both all-cause mortality and suicide (by firearm and by other met
165 in/tazobactam for both endpoints: day 28 all-cause mortality was 15.9% with imipenem/cilastatin/releb
166 xgenotype interaction predicting time to all-cause mortality, adjusted for Meta-Analysis Global Group
168 ge) and sex and the composite outcome of all-cause mortality, LV assist device implantation, or heart
171 .84%) for the background population; and all-cause mortality: 10.88% (95% CI: 10.23% to 11.55%) for s
172 e interval: 0.68 to 0.88; p < 0.001) and all-cause-mortality (7.6% vs. 9.7%; adjusted hazard ratio: 0
173 in 886 index cases of PID found that disease-causing mutations in known genes that are implicated in
174 utation is one of the most prevalent disease-causing mutations, making it possible to obtain pre-symp
177 ort bi-allelic pathogenic HPDL variants as a cause of a progressive, pediatric-onset spastic movement
179 Respiratory syncytial virus (RSV) is a major cause of acute lower respiratory infection (ALRI) in you
181 e inhibitors that disable the most prevalent cause of antibiotic resistance in Gram-negative bacteria
183 syndrome (FXS), the most common monogenetic cause of ASD, has emerged as a powerful gateway for expl
184 er is the most common cancer, and the second cause of cancer-related deaths (after lung cancer) among
187 (aHR, 0.58; P = 0.001) and donor with anoxic cause of death (aHR, 0.51; P = 0.007) were associated wi
189 Tuberculosis (TB) is the leading infectious cause of death globally, and drug-resistant TB strains p
190 terial cardiovascular events are the leading cause of death in patients with JAK2V617F myeloprolifera
192 Cardiovascular disease (CVD) is the leading cause of death in women, who have a notable increase in
194 However, stroke remains the second leading cause of death worldwide and the number one cause for ac
201 ORTANCE Enteric viral infections are a major cause of gastroenteritis worldwide and have the potentia
203 ates of cardiomyopathies, which are a common cause of heart failure in young people, have increased d
204 zome as an ideal food material to manage the cause of hyperglycemia and resultant oxidative stress.
208 lmonary aspergillosis (IPA) is a significant cause of morbidity and mortality in lung transplant reci
210 Excessive alcohol use is the third leading cause of mortality in the United States, where alcohol u
211 Chronic ethanol consumption is a leading cause of mortality worldwide, with higher risks to devel
213 ealth problem worldwide and is the principal cause of parenterally transmitted non-A, non-B hepatitis
218 ssible to MNV infection, suggesting that the cause of resistance lies in the entry step of MNV infect
221 tions providing important insights about the cause of these diseases, which can help accelerate new p
222 rs that are likely to be contributing to the cause of this syndrome and consider how they might be mo
223 tees believes that myopia is a high-priority cause of visual impairment, warranting a timely evaluati
226 tera venom allergy ranks among the top three causes of anaphylaxis worldwide, and approximately one-q
230 In this review we discuss the potential causes of inflammaging, the cellular source of the infla
232 als vary in their vulnerability to different causes of mortality due to traits, life history stages,
237 Bordetella pertussis is among the leading causes of vaccine-preventable deaths and morbidity globa
239 Recent studies show hyperactivation of Nrf2 causes osteopenia in Keap1(-/-) mice, and Keap1(-/-) ost
240 airway narrowing disrupting ventilation, and causing oxyhemoglobin desaturation and poor sleep qualit
241 ple, we applied this approach to the malaria-causing parasite Plasmodium falciparum, an organism that
242 nd CHCHD10 (C10) were recently identified as causing Parkinson's disease and amyotrophic lateral scle
245 of observed cases to expected cases for all-cause pneumonia was 0.92 (95% CI 0.70-1.36) for children
248 r117HisfsTer10) in F3, the gene encoding TF, causing premature termination of TF (TFshort) in a woman
255 iced fah1-2 background mutation, which could cause salicylic acid- and EDS5-independent mutant phenot
261 undant Kindlin-2 and deleting its expression causes severe diabetes-like phenotypes without markedly
266 d abnormalities in its structure or function cause sick sinus syndrome, the most common reason for el
267 rvest use of glyphosate-based herbicides can cause significant differences in wheat protein chemistry
270 ,6-dichlorophenyl)ethenyl]-1H-pyrazole 2l 1) caused significant effects on the cell cycle in PC3 cell
271 to the CDKL5 promoter using three guide RNAs causes significant reactivation of the inactive allele i
272 tween the two strategies, the local strategy causes significantly fewer person-days of closure, even
275 eltaCa (i) variant in phloem companion cells caused strongly reduced rosette growth in the absence of
276 Energetic collisions with background gas can cause structural changes ranging from unfolding to subun
277 remodeling after myocardial infarction (MI) causes structural and functional changes in the heart le
278 he availability of food in each nest changed causing sub-colonies to change their inter-nest connecti
279 h quantitative RT-PCR, we found that feeding causes substantial and transient changes in gene express
280 irs suggests that either different pathogens cause the same gross lesions in different species or tha
285 end-stage renal disease, or death from renal causes), the individual components of this composite, an
287 d with Alzheimer's disease and is assumed to cause toxicity by its interaction with the neuron membra
288 ether, our data imply that Col6a2 deficiency causes trabecular bone loss by enhancing osteoclast diff
293 oxidase 2 (NOX2) generated oxidative injury causes upregulation of a constitutively active form of a
294 the use of agents like luciferin, which can cause variability due to changing bioavailability, it ca
295 We monitor F508del-CFTR, the most common CF-causing variant, and confirm rescue by low temperature,
297 erative diseases that share a common genetic cause, which is an expansion of CAG repeats in the codin
298 cause of the introduced fungal pathogen that causes white-nose syndrome (WNS), survival of the specie