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1  formation are the most common serious human congenital defect.
2 nown as exencephaly/anencephaly, is a lethal congenital defect.
3  delivery, preterm delivery, macrosomia, and congenital defects.
4 llowing resection of a sarcoma or to address congenital defects.
5 o traditional open-heart surgery to mitigate congenital defects.
6 fetus of pregnant women, resulting in severe congenital defects.
7 fetus of pregnant women, resulting in severe congenital defects.
8 ) is a mosquito-borne flavivirus that causes congenital defects.
9 ut not other pathogenic flaviviruses, causes congenital defects.
10 a leading cause of frequent miscarriages and congenital defects.
11 s as a result of trauma, tumor resection, or congenital defects.
12 ation with increased risk of miscarriage and congenital defects.
13  gene haploinsufficiency causes a variety of congenital defects.
14  light on the developmental underpinnings of congenital defects.
15 ysis in developmental pathologies, including congenital defects.
16 occurs, can lead to abnormal development and congenital defects.
17 ure of which results in clinically important congenital defects.
18 sive surgery and in heart surgery to correct congenital defects.
19 nd limb development, and by a range of other congenital defects.
20 intended pregnancies and to minimize risk of congenital defects.
21 improved survivals for even the most complex congenital defects.
22 s the DAG-PKC cascade and is correlated with congenital defects.
23 fects and control infants (n = 3,029) had no congenital defects.
24  Zika virus uniquely causes microcephaly and congenital defects.
25 rly pregnancy and are one of the most common congenital defects.
26 cytopenia and bleeding, skin involvement, or congenital defects.
27  custom ocular prostheses due to eye loss or congenital defects.
28 n (3), aspiration (6), panbronchiolitis (1), congenital defect (1), ABPA (11), rheumatoid arthritis (
29  tetraplegia, 81% learning difficulties, 60% congenital defects, 41% neuropsychiatric problems and 28
30 one or multiple cranial sutures, is a common congenital defect affecting more than 1/2000 infants and
31  Cardiomelic or heart-hand syndromes include congenital defects affecting both the forelimb and heart
32 " linked to variants that drive multi-system congenital defects and are found in hnRNPs.
33 edgehog (Hh) signaling is implicated in both congenital defects and cancers arising from the gastroin
34           These AP-2-null mice have multiple congenital defects and die at birth.
35                                    Surges in congenital defects and Guillain-Barre syndrome alerted t
36 cy because ZIKV infection has been linked to congenital defects and Guillain-Barre syndrome.
37                                   Mid stage, congenital defects and neurological lesions in foetuses
38 can occur as a result of injury, disease, or congenital defects and treatment options are often limit
39 ses, matched to living controls by age, sex, congenital defect, and surgical repair.
40 sitivity to DNA damage, bone marrow failure, congenital defects, and cancer.
41 ling has been implicated in various cancers, congenital defects, and cardiovascular diseases.
42         Trauma, cancer, birth complications, congenital defects, and other surgical diseases potentia
43 linical features, including various cancers, congenital defects, and progeroid pathologies.
44 cessively inherited disease characterized by congenital defects, bone marrow failure and cancer susce
45  by interstrand cross-link hypersensitivity, congenital defects, bone marrow failure, and cancer pred
46  is an autosomal recessive disease marked by congenital defects, bone marrow failure, and cancer susc
47 a (FA) is a genetic disease characterized by congenital defects, bone marrow failure, and cancer susc
48  is an autosomal recessive disease marked by congenital defects, bone marrow failure, and high incide
49 ies account for about one-third of all human congenital defects, but our understanding of the genetic
50 ous potential for bone reconstructions after congenital defects, cancer resections, and trauma.
51     The patient groups with the most complex congenital defects carried the greatest risk of AF and c
52 ren with intellectual disability and various congenital defects (cases) to CNVs in 8,329 unaffected a
53        Neural tube defects (NTDs) are severe congenital defects caused by failed neural tube closure
54  signaling may contribute to pathogenesis of congenital defects caused by PKP2 deficiency.
55               Opitz G/BBB syndrome (OS) is a congenital defect characterized by hypertelorism and hyp
56 eningocele (MMC) is a devastating neurologic congenital defect characterized by primary failure of ne
57 ion in humans causes primary microcephaly, a congenital defect characterized by severe reductions in
58 logies, including developmental abnormality, congenital defect, chronic otitis media with cholesteato
59 re known to increase an individual's risk of congenital defects, DNMs have not been fully explored re
60                                     Although congenital defects impairing this peristalsis are a lead
61  by studying helper T cells from mice with a congenital defect in CD4 expression.
62      Clefting of the soft palate occurs as a congenital defect in humans and adversely affects the ph
63 ce of PLN HEVs in plt/plt mice, which have a congenital defect in T cell homing to PLNs.
64         Hyperinsulinism of infancy (HI) is a congenital defect in the regulated release of insulin fr
65 eatable form of male infertility caused by a congenital defect in the secretion or action of gonadotr
66 indings are relevant to our understanding of congenital defects in cardiac chamber morphogenesis.
67               Analyses of mouse strains with congenital defects in different aspects of secondary lym
68 ial for understanding respiratory disorders, congenital defects in human neonates, and how the disrup
69  that the susceptibility of this junction to congenital defects in humans, such as ureteral-pelvic ob
70 cial malformations, among the most prevalent congenital defects in humans.
71               Heart malformations are common congenital defects in humans.
72 r Bmp4 or Bmp7 lead to a similar spectrum of congenital defects in humans.
73 ility, the perturbation of which can lead to congenital defects in individuals with 22q11.2 deletion
74                                         Thus congenital defects in intrinsic immunity in brain-reside
75 d familial HLH or atypical manifestations of congenital defects in lymphocyte exocytosis.
76 ious disease among the immunocompromised and congenital defects in newborns, human cytomegalovirus (H
77 nd/or fetal spontaneous abortion, death, and congenital defects in pregnant women treated with any of
78  on novel molecular and cellular etiology of congenital defects in primitive choanae formation.
79 olt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.
80                                              Congenital defects in the Na/H exchanger regulatory fact
81 CAKUTHED syndrome, characterized by multiple congenital defects including congenital heart disease (C
82 ildhood cancers, and a complex assortment of congenital defects including skeletal abnormalities.
83 it from mother to fetus, potentially causing congenital defects, including microcephaly.
84 cism are increasingly associated with severe congenital defects, including those arising from failed
85 s offer promise for traumatic bone injuries, congenital defects, non-union fractures and other skelet
86    Patched expression is compatible with the congenital defects observed in the nevoid basal cell car
87  occurred in 31 (1.7%) versus 33 (1.8%), and congenital defects occurred in 18 (1.0%) versus 20 (1.1%
88                                    The first congenital defect of hypoxia-sensing homozygosity for VH
89                             Hypospadias is a congenital defect of the external genitalia that results
90 okitansky-Kuster-Hauser (MRKH) syndrome is a congenital defect of the Mullerian ducts characterized b
91  Vein of Galen malformations (VGMs) are rare congenital defects of cerebral vessels.
92 in vitamin deficiency states and in cases of congenital defects of one-carbon metabolism.
93                                 The exocrine congenital defects of Prox1(DeltaPanc) pancreata appeare
94 cipher mechanisms of pancreatic development, congenital defects of the pancreas, as well as genetic f
95 ected by craniofacial deformations caused by congenital defects or trauma.
96       Bone loss caused by trauma, neoplasia, congenital defects, or periodontal disease is a major ca
97 ed rate of 11.3 for the Metropolitan Atlanta Congenital Defects Program counties (p = 0.052), both of
98 cords obtained from the Metropolitan Atlanta Congenital Defects Program, which conducts active, popul
99 try modification of the Metropolitan Atlanta Congenital Defects Program.
100 emia (FA) is a rare disease characterized by congenital defects, progressive bone marrow failure and
101 e novel insights into the etiology of common congenital defects such as cleft palate.
102 rate eye and improper development results in congenital defects, such as microphthalmia or anophthalm
103 r (AV) electrical conduction can result from congenital defects, surgical interventions, and maternal
104     Bicuspid aortic valve (BAV) disease is a congenital defect that affects 0.5% to 1.2% of the popul
105 he pig abdominal system and show examples of congenital defects that can arise in CRISPR gene edited
106 TnT4 was significantly higher in hearts with congenital defects that caused congestive failure than i
107                         Traumatic wounds and congenital defects that require large-scale bone tissue
108 Thus, ES cells have the potential to reverse congenital defects through Id-dependent local and long-r
109                                              Congenital defects, trauma, and disease can compromise t
110  completed weeks of gestation without severe congenital defects were eligible for inclusion.
111                                     Multiple congenital defects were observed in the CNS of PDGF-C-nu
112 ypically mild in humans but can cause severe congenital defects when contracted during pregnancy.
113      Partial absence of the sacrum is a rare congenital defect which also occurs as an autosomal domi

 
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