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1 an in muscles that are affected later or are nonaffected; and (2) in adult muscle biopsies, FAT1 expr
2 in and normal callused regions compared with nonaffected areas, and (2) TD101-treated PC skin reveale
3 onsenting family member (six affected, seven nonaffected) by amplifying, sequencing, and analyzing ex
4 r in the affected spinal cord but not in the nonaffected cerebellum in transgenic mutant SOD1 mice.
5  of allele frequencies between 625 Caucasian nonaffected controls and 1,117 Caucasian individuals wit
6 ongo red score more than or equal to 3+, and nonaffected controls.
7 silateral corticospinal projections from the nonaffected cortex, thereby compounding the impairment.
8 inant polycystic liver disease (ADPLD) using nonaffected family members as controls.
9  of bone marrow progenitors and reticulin in nonaffected family members of patients with familial PAH
10 , estimated according to numbers of affected/nonaffected family members, provide new insight into fam
11 nalysis was carried out in 12 affected and 3 nonaffected family members.
12 1620C (F540F) was found in some affected and nonaffected family members.
13 eased pulmonary vasculature, but findings in nonaffected family suggest myeloid abnormalities may be
14 man embryonic stem cells (hESCs) compared to nonaffected hESCs showed that fork direction through the
15 h have the SNP variant C, but present in the nonaffected hESCs, which have a T variant.
16 lication origin and the T variant similar to nonaffected hESCs.
17 quently in affected than in indeterminate or nonaffected individuals.
18                                              Nonaffected limbs of patients with unilateral I-FDVT (37
19 ven hematopoietic cell (HC) transplants from nonaffected littermates.
20 ced CT failed to differentiate affected from nonaffected lymph nodes.
21 ematological mutations, and the diagnosis of nonaffected male progeny in cases of X-linked haematolog
22 all testes, and stature shorter than that of nonaffected males.
23                       Affected (n = 233) and nonaffected (n = 152) family members were genotyped for
24 induces gray matter changes primarily within nonaffected neocortical regions of the cerebellar-cortic
25 ediate area and ventral horn, whereas 50% of nonaffected neurons were located in the dorsal horn.
26 lop dementia more often than expected in the nonaffected population, the overlap between these two co
27  pregnancy but not in the current pregnancy [nonaffected pregnancy (NAP); n = 98] and unaffected cont
28 lipoprotein cholesterol levels compared with nonaffected relatives (n=91).
29  dB and mean mesopic 17.2 dB) as compared to nonaffected retinal areas (18.2 dB and 18.4 dB) (P < .00
30 areas with RDR and 76.4 mum (P < .0001) over nonaffected retinal areas.
31  and enucleated eyes from 2 individuals with nonaffected retinas.
32 lysis was also preferentially transmitted to nonaffected siblings (P = 0.0008, Pc = 0.02).
33 cohort of age- and sex-matched T1D patients, nonaffected siblings, and unrelated control children, we
34 reased transmission of associated alleles to nonaffected siblings.
35 ntrol subjects (P<.05) for both affected and nonaffected sides of the brain.
36 sue morphology, consistent with reversion to nonaffected skin compared with vehicle-treated skin.
37                          Here we showed that nonaffected skin of psoriasis patients displayed lower e
38 ted mother, four affected daughters, and one nonaffected son.
39 on during working memory processing than her nonaffected twin.

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