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1 hoprim for 24 h, the microbiota was strongly affected, with (1) up to 21-fold decrease in 16S rRNA ge
3 sexual relationships were the most adversely affected with 33%, 26%, and 23% of the women responding
5 ever, sub-Saharan Africa remains endemically affected with 5/7 serotypes currently known to be circul
11 t a 3-generation pedigree with 5 individuals affected with a dominantly inherited macrothrombocytopen
12 (2) located in nonfrigid zones has been salt-affected with a frequency of reoccurrence in at least th
15 luded a minimum of three available relatives affected with a psychotic illness and three available un
16 ac-Saint-Jean (SLSJ) region was particularly affected with a rate of 3.4 per 100000 person-years in 2
17 ls with de novo frameshift variants in NOVA2 affected with a severe neurodevelopmental disorder chara
18 n five children from four unrelated families affected with a similar pattern of severe intellectual d
19 a from thousands of samples from individuals affected with a wide range of diseases, but for whom the
20 s the rule-with relatives of insane patients affected with a wide variety of psychiatric, and sometim
24 er compounds not present in the extract were affected, with a different behaviour observed depending
25 gene specific; hTERT was most significantly affected, with a higher frequency of MAE in adult and ad
29 erived thymus/parathyroid primordia was also affected, with absent or hypoplastic primordia, delayed
33 cted high incidence of this DFSP in children affected with adenosine deaminase-deficient severe combi
35 togenesis in these mutants was progressively affected with age, resulting in decreased testis weight
36 continues to rise, the number of individuals affected with age-related cognitive decline and Alzheime
39 is of genomewide linkage studies of families affected with age-related maculopathy (ARM), we previous
41 osis and homeostasis but, unlike individuals affected with ALPS, also have defects in their activatio
47 e, we identified seven unrelated individuals affected with an apparent dominant ZSD in whom a heteroz
48 type and genetic information for individuals affected with an ASD and family members is crucial for t
49 s extent (40 and 33%, respectively) the most affected with an important descend in leucine release.
50 n this study, we investigated eight patients affected with an overlapping genodermatosis after recess
52 r molecular layer of dentate) were initially affected, with anterograde progression though the hippoc
53 adolescents are more likely than males to be affected with anxiety disorders, but less likely to have
55 ion of NF-kappaB responses, is most commonly affected, with approximately 30% of patients displaying
57 age 5 years, one third of all children were affected with at least one of the conditions of atopic d
58 with polyvascular disease (>=2 vascular beds affected with atherosclerosis), impaired renal function,
59 s performed on a family with identical twins affected with autism and severe, intractable seizures.
61 ions in whole genomes from 1,902 individuals affected with autism spectrum disorder (ASD) and their u
62 nome scan of 24 family members, including 14 affected with autoimmune disease, showed significant lin
63 candidate approach in a Saudi Arabian family affected with autosomal recessive SCAN1, we identified a
64 ions in several families of Pakistani origin affected with autosomal recessive woolly and sparse hair
65 Here we report two additional individuals affected with BBIS originating from the north of Europe
66 ng of a DNA sample from a 17-year-old female affected with BBS did not identify any mutation in the k
67 OX2R(-/-) and orexin(-/-) mice are similarly affected with behaviorally abnormal attacks of non-REM s
68 omain of K(V)7.2 have been found in children affected with benign familial neonatal seizures (R213W m
69 of 200 individuals from 41 families multiply affected with bipolar disorder (BD) to identify contribu
70 Approximately 1 in every 50 to 100 people is affected with bipolar disorder (BD), making this disease
71 Few neuroimaging studies compare individuals affected with bipolar disorder (BP), at high familial ri
72 d with schizophrenia and all of the families affected with bipolar disorder were multiply affected wi
73 can of 41 Ashkenazi pedigrees with a proband affected with bipolar I disorder (BPI) and at least one
74 disorder (BPI) and at least one other member affected with BPI or bipolar II disorder (BPII), we iden
78 In contrast, OX2R(-/-) mice are only mildly affected with cataplexy-like attacks of REM sleep, where
81 s in PMPCA in 17 patients from four families affected with cerebellar ataxia, including the large Leb
82 ugs--and atypical differences in individuals affected with certain clinical disorders (e.g., autism,
85 ed on 8 affected individuals from 3 families affected with chromosome 6-linked NCMD (MCDR1) and 2 ind
91 rozygous mutation in the SOX2 gene in a male affected with congenital bilateral anophthalmia, hypogon
92 ering of specific gene mutations in children affected with congenital central hypoventilation syndrom
93 T2) gene have been identified in individuals affected with congenital generalized lipodystrophy (CGL)
94 We describe a white family with two siblings affected with congenital hypotonia early-onset glaucoma,
95 uited more than 25 families in which members affected with corpus callosum hypoplasia (CCH) lacked sy
96 tive neutrophil phenotype, patients severely affected with COVID-19 are characterized by excessive pl
97 ed on the proband and first-degree relatives affected with CRC to reduce ascertainment bias and overe
100 e mutant alleles, also described in patients affected with CTLN1, interact to produce a range of phen
102 across the exome sequences of 48 individuals affected with DCM from 17 families to identify genetic c
103 N truncating variants carried by individuals affected with DCM in 7 of 17 DCM families (logarithm of
104 n contrast, myeloid development is adversely affected with decreased in vitro colony formation, decre
106 ine homozygous SH2B3 mutations in 2 siblings affected with developmental delay and autoimmunity, one
110 ich is severely disturbed in preterm infants affected with diffuse white matter injury, is incomplete
112 s ManNAc as a potential treatment for humans affected with disorders of glomerular hyposialylation.
113 ions at residues Glu724 and Asp725 were most affected with double mutations at these sites showing ap
117 ccus mutans in plaque-biofilms from children affected with early-childhood caries, a prevalent and co
118 enced the complete genomes of 72 individuals affected with early-onset familial Alzheimer's disease c
119 in two CAE-affected persons and two persons affected with EEG-recorded spike and/or sharp wave in a
120 We found that the surface expression is affected, with effects paralleling those seen with the b
121 nalysis of a large cohort of cases (n = 269) affected with either classic heterotaxy or looping CVM r
122 ferentiated between unaffected dogs and dogs affected with either mutation with a high degree of cert
123 poA-I 133+/-21 mg/dL) (P<0.0005) or subjects affected with either R1851Q (n=6) (HDL-C 36+/-8; ApoA-I
126 Our report highlights the fact that subjects affected with eye anomalies and harboring SOX2 mutations
127 e PPT primer, all mutants were significantly affected with F61Y and F61A being most severely impaired
129 ontrolled study of 41 subjects genotypically affected with familial adenomatous polyposis but phenoty
130 range, 8 to 25 years) who were genotypically affected with familial adenomatous polyposis but phenoty
132 ALB2 (also known as FANCN) in seven families affected with Fanconi anemia and cancer in early childho
134 encing on two families with multiple members affected with focal epilepsy and linkage analysis on one
136 , complementary results from mice and humans affected with GD1 not only pinpoint sphingosine as being
138 Interestingly, cerebellum was the area most affected, with greater myelination impairment and glia b
140 s now apparent that the majority of patients affected with HCM can achieve normal or near-normal life
142 cancer cells and linkage studies in families affected with hereditary prostate cancer (HPC) have impl
144 ound heterozygous mutations in four siblings affected with HHS, in the gene encoding the regulator of
151 from the perspective of cancers in patients affected with IEM and discuss how dysregulation of these
152 gas species on atmospheric particles may be affected, with important implications for climate predic
153 in kinase (MAPK) pathways were predominantly affected, with increased levels of phospho-p38 and phosp
154 amount of medium-range order seems slightly affected with increasing Ag concentration (0, 2, 5 at.%)
155 positive impact on individuals and families affected with inherited eye disease in a number of ways.
156 seropositivity rates compared between horses affected with insect bite hypersensitivity (IBH) and con
158 two-stage genomewide screen of 48 sib pairs affected with intracranial aneurysms (IAs) that revealed
160 regarding the molecular genetics of children affected with juvenile dermatomyositis and the impact th
162 d 17-HDHA were then tested in 62 individuals affected with knee osteoarthritis and 52 age matched con
164 fibres (<3 microm2) seem to be particularly affected, with large fibres remaining relatively preserv
165 y dispersed collection of families, multiply affected with late onset Alzheimer's disease, who were p
168 e mutation was found in three family members affected with late-onset atypical hemolytic uremic syndr
169 expressivity; while some patients are mildly affected with learning disabilities and subtle craniofac
171 by direct sequencing of DNA from 36 patients affected with Leber's congenital amaurosis (LCA), 62 wit
172 ring familial evaluation; 38 were clinically affected with left ventricular hypertrophy >/=13 mm.
179 g and management of patients at risk for and affected with Lynch syndrome as follows: Figure 1 provid
180 ogical offspring with 2 previous generations affected with major depression were at highest risk for
182 pedigree software, that 23 nuclear families affected with MCPHA are connected to a single ancestral
183 ly increased in the brains of human subjects affected with MDD and rats exposed to chronic social def
185 f the overall sample showed teeth/sites most affected with mean PD > 2.1 mm were molars (2,3,15,18,19
187 feasible alternative treatment for patients affected with mild/moderate CAEBV infection and that thi
190 The selenoprotein population was selectively affected with MMTV-Cre in breast and skin but not in the
192 y intervention in offspring of 2 generations affected with moderate to severely impairing MDD seems w
194 erventions in the offspring of 2 generations affected with moderately to severely impairing MDD seem
195 ied a large kindred with several individuals affected with molar oligodontia that was transmitted as
197 f cases, multiple chromosomes per tumor were affected, with most chromothriptic events on chromosomes
198 ctivating protein that is absent in a family affected with MRX, is required for dendritic spine morph
201 extent of surgical intervention in children affected with multiple endocrine neoplasia type 2 will l
202 dings, however, have indicated that patients affected with myofibrillar myopathy have a more distal t
203 drially encoded proteins were differentially affected, with near normal levels of cytochrome c oxidas
205 lies with two or more first-degree relatives affected with neuroblastoma to localize a hereditary neu
207 Clinically, the neurons in layer II are affected with neurofibrillary tangles, one of the two pa
208 howed that only the extent of inhibition was affected, with no change in agonist potency (EC(50) = 1
210 tations were detected in 4.4% of individuals affected with non-HPC as compared with 0.8% of unaffecte
211 ased sex ratio, whereas families of probands affected with non-sexually dimorphic autoimmune diseases
213 ons, p.Gly60Asp and p.Leu208Pro, in patients affected with nonsyndromic autosomal recessive intellect
215 ons can be found in the majority of families affected with one of the inherited syndromes, and, most
216 ilies studied, 1,507 had at least one member affected with one of three known forms of CAH, namely sa
218 skeletal fragility phenotype in individuals affected with osteoporosis-pseudoglioma is inadequate pr
219 We ascertained three different families affected with oto-dental syndrome, a rare but severe aut
220 5(+)FOXP3(+) T(reg) cells in 104 individuals affected with ovarian carcinoma, that human tumor T(reg)
221 s in which three or more family members were affected with pancreatic cancer, at least two of which w
222 ried out genetic analyses in 201 individuals affected with Parkinson disease and 221 age-matched unaf
224 Among never-smokers, fewer teeth/sites were affected with PD > 2.1 mm, whereas among smokers, number
225 Sequence analysis of 2p13 linked individuals affected with PD did not reveal any potentially pathogen
227 mous missense variant) in a pair of siblings affected with persistent lymphoedema caused by congenita
233 rtalized renal epithelial cells of a patient affected with progressive medullary cystic kidney diseas
237 n of CD57 on T cells in the skin of patients affected with psoriasis, comparing lesional and unaffect
240 to a consanguineous family with one subject affected with RCD and identified a homozygous nonsense m
244 ontumbling chemotaxis mutant was only weakly affected with regard to biofilm formation under nonflowi
245 We studied families with multiple members affected with renal cancer to delineate clinically disti
246 loss or of restoring the vision of patients affected with retinal degeneration through some type of
247 e has been shown to be up to 25% in subjects affected with rhinitis with persistence, comorbidity and
250 isorders among the offspring of parent pairs affected with schizophrenia (SCZ) and/or bipolar disorde
251 mortem expression analysis of 33 individuals affected with schizophrenia and 30 unaffected control su
253 implicated in psychotic illness in families affected with schizophrenia or psychotic bipolar disorde
254 family sample of 13 large families multiply affected with schizophrenia, 2 schizophrenia case-contro
255 ish individuals, including 4,877 individuals affected with schizophrenia, in ways informed by exome s
257 Plasma was infused into young horses (foals) affected with severe combined immunodeficiency (SCID), f
258 d that APOE-4 carriers are more likely to be affected with severe disease (P=.03), whereas a higher p
259 participants without skin lesions, patients affected with skin cancers had a significantly increased
260 ce quotient (approximately 50%) are commonly affected with specific neuropsychological problems, incl
262 hat female reproductive function may also be affected, with subsequent implications for fertility.
263 (OPRM1), among 382 European Americans (EAs) affected with substance dependence [alcohol dependence (
264 PBP4 DD-endopeptidase activity was also affected, with substitution of Asp155, Arg361, and Gln42
265 rofile and degree of inflammation of persons affected with such condition is an important step toward
266 ation assessing the insurability of families affected with Sudden Arrhythmia Death Syndromes (SADS) f
268 that it is likely that multiple pathways are affected with the administration of this drug that needs
269 ltered by TPE-OLD in myoblasts from patients affected with the age-associated genetic disease, facios
271 assified controls (i.e., individuals who are affected with the disease under study but who are classi
277 Increased IL-6 levels are found in tissues affected with these diseases, and KSHV exists in a laten
279 HPDL variants in each of the 17 individuals affected with this clinically heterogeneous autosomal-re
280 cacy of current treatments for those already affected with this disease has prompted the suggestion t
284 ltures of human fetal cells from pregnancies affected with trisomy 21 (t21) and trisomy 13 (t13).
285 fundus autofluorescence (FAF) images of eyes affected with tubercular SLC from the acute stage until
287 tinguishing between unaffected dogs and dogs affected with two different forms of inherited retinal d
288 unrelated patients (2 males and 13 females) affected with typical IH, 12 patients (9 males and 3 fem
289 We have identified 25 pedigrees that are affected with typical JOAG and that demonstrate autosoma
292 ic amplification (PMCA) in urine of patients affected with variant Creutzfeldt-Jakob disease (vCJD),
293 1.71-2.75; P<.001]) and number of body parts affected with vitiligo (P</=.009) but not laterality (P=
295 in IRF6 in 45 additional unrelated families affected with VWS and distinct mutations in 13 families
296 bors the causative mutation, all individuals affected with WARBM exhibit indistinguishable clinical p