“…RESULTS: Among 357 enrolled participants, the mean (SD) age was 39.3 (11.8) years; 195 participants (54.6%) were female, 40 (11.2%) were Hispanic, 243 (68.1%) were non-Hispanic White, and 74 (20.7%) were of other non-Hispanic races (including American Indian or Alaska Native, Asian or Pacific Islander, Black or African American, or multiracial). …”
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“…RESULTS: The mean (SD) age at enrollment of 519 children was 2.7 (0.1) years, 264 (50.9%) were girls, 196 (37.8%) lived in Spanish-speaking households, and 5 (0.9%) identified as Alaskan Native or American Indian, 17 (3.2%) as Asian American or Pacific Islander, 57 (10.8%) as Black, 199 (37.8%) as White, and 63 (12.0%) as other. …”
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“…RESULTS: Among 143 886 male veterans (median [IQR] age, 65 [60-71] years) with localized prostate cancer, 750 (0.5%) were American Indian or Alaska Native, 389 (0.3%) were Asian, 37 796 (26.3%) were Black or African American, 933 (0.6%) were Native Hawaiian or other Pacific Islander, 91 091 (63.3%) were White, and 12 927 (9.0%) were of unknown race; 7299 patients (5.1%) were Hispanic or Latino, 128 796 (89.5%) were not Hispanic or Latino, and 7791 (5.4%) were of unknown ethnicity. …”
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“…RESULTS: There were 52 944 unique, eligible patients with 1 or more visits in one of the 6 primary care practices during the entire study period (59% female; mean [SD] age, 48.9 [17.6] years; 178 [0.3%] American Indian/Alaska Native, 13 241 [25.0%] English-speaking Asian, 3588 [6.8%] English-speaking Black/African American, 4744 [9.0%] English-speaking Latino/Latina/Latinx, 760 [1.4%] Pacific Islander, 22 689 [42.9%] English-speaking White, 4857 [9.0%] English-speaking other [including individuals who indicated race and ethnicity as other and individuals for whom race and ethnicity data were missing or unknown], and 2887 [5.5%] with language barriers [non–English language preference]). …”
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“…RESULTS: The sample of 50 384 individuals comprised 82 (0.2%) American Indian or Alaska Native, 10 601 (21.0%) Asian, 2464 (4.9%) Black, 3291 (6.5%) Hispanic, 25 (0.1%) Native Hawaiian or Pacific Islander, 30 610 (60.8%) White, 2476 (4.9%) multiracial students, and 834 (1.7%) students of other races or ethnicities. …”
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“…Overall, 16 559 patients (23.5%) were Black, 36 184 (51.3%) were White, 14 133 (20.1%) were of other races (including 694 American Indian or Alaska Native [1.0%], 2216 Asian [3.0%], 372 Native Hawaiian or Pacific Islander [0.5%], and 10 850 other races [15.4%]), and 3597 (5.1%) were of unknown race. …”
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“…RESULTS: Among a total of 26 774 individuals (mean [SD] age, 32.9 [5.0] years; 11 196 Asian or Pacific Islander individuals [41.8%], 1083 Black individuals [4.0%], 7500 Hispanic individuals [28.0%], and 6049 White individuals [22.6%]), 4 glycemic control trajectories were identified: stably optimal (10 528 individuals [39.3%]), rapidly improving to optimal (9151 individuals [34.2%]), slowly improving to near-optimal (4161 individuals [15.5%]), and slowly improving to suboptimal (2934 individuals [11.0%]). …”
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“…Blastomycosis incidence was approximately six times as high among AI/AN persons (4.5) and approximately twice as high among non-Hispanic Asian and Native Hawaiian or other Pacific Islander persons (1.6) compared with White persons (0.7). …”
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“…RESULTS: Among 79,184 adults with diabetes, eGFR ≥60, and urine albumin/protein assessment (age 60.5 ±7.7y, 54.0% male), 40.3% were non-Hispanic White, 9.6% Black, 26.3% Asian/Pacific Islander (PI), and 21.0% Hispanic/Latinx race/ethnicity. 69.9% had hypertension. …”
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“…These were applied to all cytosine-guanine dinucleotide (CpG) sites, various genomic regions (genes, promoters, CpG Islands (CGIs)) and as a targeted analysis of imprinted genes and birth weight-associated CpG sites. …”
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“…Multivariate analysis demonstrated that adults (hazard ratio [HR] = 7.4), Asian or Pacific Islander (HR = 0.5), male (HR = 0.8), poorly differentiated histology (HR = 3.8), undifferentiated histology (HR = 4.5), regional spread (HR = 2.1), and distant spread (HR = 3.2) were associated with increased mortality (p < 0.05). …”
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“…With regard to race and ethnicity, 4295 participants (10.1%) identified as Asian or Pacific Islander, 5174 (12.1%) as Black, 14 289 (33.5%) as Hispanic, and 17 902 (41.9%) as White. …”
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“…Phylogenetic topology inferred from the BEAST and Network relationships reconstructed from the popART further showed the founding lineages from culturally/linguistically diverse populations, such as C2a/C2b was dominant in Mongolian people and O1a/O1b was dominant in island Li people. We also identified many lineages shared by more than two ethnolinguistically different populations with a high proportion, suggesting their extensive admixture and migration history. …”
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“…Overall, ASD prevalence was lower among non-Hispanic White children (24.3) and children of two or more races (22.9) than among non-Hispanic Black or African American (Black), Hispanic, and non-Hispanic Asian or Pacific Islander (A/PI) children (29.3, 31.6, and 33.4 respectively). …”
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“…Based on self-report, participants’ race was categorized as Asian or Pacific Islander (19 [14.1%]), White (62 [45.9%]), or other race (39 [28.9%]); race was missing or not reported for 15 participants (11.1%). …”
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“…The resemblance is made still more exact by the susceptibility of such dogs to acidosis and coma, as will be shown in later papers, and also by the similarity of the anatomic changes in the islands of Langerhans. These animals are therefore useful test objects for a therapeutic investigation. 2. …”
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“…In addition the following species were recorded for the first time from these provinces and territories: Yukon – Dendroctonus simplex LeConte, 1868; Phloetribus piceae Swaine, 1911 (both Curculionidae); Northwest Territories – Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Nunavut – Dendroctonus simplex LeConte, 1868 (Curculionidae); Alberta – Anthonomus tectus LeConte, 1876; Promecotarsus densus Casey, 1892; Dendroctonus ponderosae Hopkins, 1902; Hylastes macer LeConte, 1868; Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Saskatchewan – Phloeotribus liminaris (Harris, 1852); Rhyncolus knowltoni (Thatcher, 1940); Scolytus schevyrewi Semenov Tjan-Shansky, 1902 (all Curculionidae); Manitoba – Cosmobaris scolopacea Germar, 1819; Listronotus maculicollis (Kirby, 1837); Listronotus punctiger LeConte, 1876; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Tyloderma foveolatum (Say, 1832); (all Curculionidae); Ontario – Trichapion nigrum (Herbst, 1797); Nanophyes marmoratus marmoratus (Goeze, 1777) (both Brentidae); Asperosoma echinatum (Fall, 1917); Micracis suturalis LeConte, 1868; Orchestes alni (Linnaeus, 1758); Phloeosinus pini Swaine, 1915; Scolytus schevyrewi Semenov Tjan-Shansky, 1902; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Quebec – Trigonorhinus alternatus (Say, 1826); Trigonorhinus tomentosus tomentosus (Say, 1826) (both Anthribidae); Trichapion nigrum (Herbst, 1797); Trichapion porcatum (Boheman, 1839); Nanophyes marmoratus marmoratus (Goeze, 1777) (all Brentidae); Lissorhoptrus oryzophilus Kuschel, 1952 (Brachyceridae); Acalles carinatus LeConte, 1876; Ampeloglypter ampelopsis (Riley, 1869); Anthonomus rufipes LeConte, 1876; Anthonomus suturalis LeConte, 1824; Ceutorhynchus hamiltoni Dietz, 1896; Curculio pardalis (Chittenden, 1908); Cyrtepistomus castaneus (Roelofs, 1873); Larinus planus (Fabricius, 1792); Mecinus janthinus (Germar, 1821); Microhyus setiger LeConte, 1876; Microplontus campestris (Gyllenhal, 1837); Orchestes alni (Linnaeus, 1758); Otiorhynchus ligustici (Linnaeus, 1758); Rhinusa neta (Germar, 1821); Trichobaris trinotata (Say, 1832); Tychius liljebladi Blatchley, 1916; Xyleborinus attenuatus (Blandford, 1894); Xyleborus affinis Eichhoff, 1868 (all Curculionidae); Sphenophorus incongruus Chittenden, 1905 (Dryophthoridae); New Brunswick – Euparius paganus Gyllenhal, 1833; Allandrus populi Pierce, 1930; Gonotropis dorsalis (Thunberg, 1796); Euxenus punctatus LeConte, 1876 (all Anthribidae); Loborhynchapion cyanitinctum (Fall, 1927) (Brentidae); Pseudanthonomus seriesetosus Dietz, 1891; Curculio sulcatulus (Casey, 1897); Lignyodes bischoffi (Blatchley, 1916); Lignyodes horridulus (Casey, 1892); Dietzella zimmermanni (Gyllenhal, 1837); Parenthis vestitus Dietz, 1896; Pelenomus squamosus LeConte, 1876; Psomus armatus Dietz, 1891; Rhyncolus macrops Buchanan, 1946; Magdalis inconspicua Horn, 1873; Magdalis salicis Horn, 1873 (all Curculionidae); Nova Scotia – Dryocoetes autographus (Ratzeburg, 1837); Ips perroti Swaine, 1915; Xyleborinus attenuatus (Blandford, 1894) (all Curculionidae); Prince Edward Island – Dryocoetes caryi Hopkins, 1915 (Curculionidae); Newfoundland – Scolytus piceae (Swaine, 1910) (Curculionidae). …”
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“…In New Zealand, managers of the endangered Hihi (Notiomystis cincta) often rely on supplementary feeding to support reintroduced populations. On Kapiti island the reintroduced Hihi population has responded well to food supplementation, but the logistics of providing an increasing demand recently outstretched management capacity. …”
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“…The Mecyclothorax carabid beetle fauna of Haleakalā volcano, Maui Island, Hawai‘i is taxonomically revised, with 116 species precinctive to Haleakalā recognized, 74 newly described. …”
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“…The genus Pseudoameroseius gen. n., with type species Ameroseius michaelangeli Moraza, 2006 (from Canary Islands), is newly erected to further refine broad primary concept of Ameroseius as understood by some former authors (Karg, Bregetova). …”
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