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1 , race/ethnicity, age, household income, and birthplace.
2 ial/ethnic groups (n = 37,150) by gender and birthplace.
3 deration of race/ethnicity and SES, but also birthplace.
4 ng to age, sex, race, ethnic background, and birthplace.
5 onal deficiency based on their birthdate and birthplace.
6 en after controlling for shared parent-child birthplaces.
10 thnicity, family income, household size, and birthplace) and adiposity measured by dual-energy X-ray
11 subjects; those with Hispanic ethnicity, US birthplace, and higher level of household education; and
14 he rate of granule cell migration near their birthplace, but decreases the rate near their final dest
15 nglion formation depends on the interplay of birthplace, chemokine attraction, cell-cell interaction,
17 spring, as idiolect is predicted by parental birthplace, even after controlling for shared parent-chi
18 medial ganglionic eminence (MGE), the major birthplace for CINs, and on MGE-like cells differentiate
20 d odds ratio [aOR], 0.57 [95%CI, 0.46-0.60]).Birthplace in all continents was associated with lower o
22 a chain-like tangential migration from their birthplace in rhombomere (r) 4 to their final destinatio
24 overage, number of persons in the household, birthplace in the United States, and history of asthma,
25 overage, number of persons in the household, birthplace in the United States, ever history of asthma,
27 pulation Study (LOLIPOP) data, and find that birthplace is predicated to a median distance of 54 km f
33 island found new life in January 2012 as the birthplace of the first IFReC-SIgN Winter School on Adva
34 stellar environment very different from the birthplace of the Sun and other planet-hosting field sta
36 ariation were constructed and confirmed that birthplace outside the United States was associated with
37 diabetes or by other factors (e.g., maternal birthplace, prenatal care, reproductive history, age, so
38 adjusted for known confounders (gender, age, birthplace, race/ethnicity, poverty, education, history
40 , and nitrogen oxides were assigned based on birthplace residence and temporally adjusted using routi
41 : moves from high to low showed retention of birthplace risk only for those aged >15 years, whereas o
43 TE to the NFBC1966 data to estimate parental birthplace, testing with successively more PCs and findi
46 ng development, most neurons move from their birthplace to the appropriate layer, where they polarize
47 n the CNS are required to migrate from their birthplace to their final destination to develop into fu
48 eurons must travel long distances from their birthplace to their predetermined final location and, to
49 variables sex, education, and race/ethnicity/birthplace were independent predictors in at least 1 of
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