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1 iated disease; 14 [37%] of 38 with community-acquired disease).
2 patients (five with congenital and five with acquired disease).
3 ion SEPs (two with congenital and three with acquired disease).
4 pendent phosphorylation in human genetic and acquired disease.
5  patterns, including patients with community-acquired disease.
6 atients, including 4 patients with community-acquired disease.
7 ngly recognized as a model for inherited and acquired disease.
8 after myocardial infarction (MI), a model of acquired disease.
9  than those individuals with non-transfusion-acquired disease.
10 n their function underlie both inherited and acquired disease.
11 ic diseases, tumors, vascular anomalies, and acquired diseases.
12 rapies and research models for inherited and acquired diseases.
13  the genome and may manifest as inherited or acquired diseases.
14 inical trials to treat genetic disorders and acquired diseases.
15 n the clinical treatment of many genetic and acquired diseases.
16  target for gene therapies for inherited and acquired diseases.
17 n the management of several gene defects and acquired diseases.
18  therapeutic strategy for many inherited and acquired diseases.
19 is vector for the treatment of inherited and acquired diseases.
20 gical calcium signaling, both in genetic and acquired diseases.
21 the relevance of these findings in naturally acquired disease, a composite influenza A signature buil
22  channel that is important in hereditary and acquired diseases affecting urine-concentrating ability.
23  allow us to address the epigenetic state of acquired disease and whether original states, regenerati
24 lly treating a large array of hereditary and acquired diseases, and stands as the paradigm for stem c
25                   A variety of heritable and acquired diseases are linked to mitochondrial dysfunctio
26 imple sequence polymorphisms but no apparent acquired disease-associated mutations.
27 atients, of whom 96% likely had nosocomially acquired disease at 11 hospitals.
28 t of a growing, clinically relevant hospital-acquired disease, C. difficile infection.
29 tellation that develops secondary to various acquired diseases, especially intrathoracic neoplasm.
30 field of gene therapy for both inherited and acquired diseases, especially with regard to respiratory
31          An increasing number of genetic and acquired diseases has been associated with intracellular
32 at, when defective, can cause congenital and acquired disease in Homo sapiens.
33 ificantly associated with invasive community-acquired disease in humans.
34 nitially knew little about the diseases, but acquired disease information and increased knowledge of
35 s for phenotypic expression of heritable and acquired diseases involving abnormality in the ABCC6 gen
36                           Constitutional and acquired disease is poorly delineated, as lesions in som
37  finding in patients with both inherited and acquired diseases of heart muscle.
38 ent neurological disability in inherited and acquired diseases of myelin.
39                                Heritable and acquired diseases of podocytes can result in focal and s
40                               Congenital and acquired diseases of the biliary tree, or cholangiopathi
41                               Congenital and acquired diseases of the heart valves and great arteries
42 ly curative treatment for both inherited and acquired diseases of the hematopoietic compartment; howe
43 ay be differentially affected in genetic and acquired diseases of the human brain.
44 athies, a group of genetic developmental and acquired diseases of the liver.
45 tive differences in gene-for-gene, basal and acquired disease resistance and other aspects of plant i
46                                Such chronic, acquired diseases result when normal physiologic control
47 loped countries in the setting of genetic or acquired disease states.
48  is directly linked with both congenital and acquired disease states.
49 ients with congenital disease and those with acquired disease, suggesting that factors additional to
50 BM) of the kidney is impaired in genetic and acquired diseases that affect type IV collagen.
51               Most patients had nosocomially acquired disease, were infected with HIV, and unless pro
52  most important causative agents of hospital-acquired diseases worldwide.

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