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1 on events in the histories of: 1) Indian and Arabian ancestries, 2) Kalash ancestry, and 3) Native Am
2 s a mixture of ancestries closely related to Arabian ancestry and Nilo-Saharan or Omotic ancestry.
3 an and 1 Arabian-pony cross), and 2 foals (1 Arabian and 1 Arabian-pony cross) with severe combined i
4 ult Arabian horses, two 1-month-old foals (1 Arabian and 1 Arabian-pony cross), and 2 foals (1 Arabia
5 en studied in the context of Asian, Saharan, Arabian, and Australian storms, but there has been no re
6 tember 2012 in samples obtained from a Saudi Arabian businessman who died from acute respiratory fail
11 ne was performed with individuals from Saudi Arabian families with multiple, clinically confirmed, mo
15 d a positional candidate approach in a Saudi Arabian family affected with autosomal recessive SCAN1,
17 affected siblings in a consanguineous Saudi Arabian family we performed genome-wide linkage and mapp
18 quencing in a multiplex consanguineous Saudi Arabian family with a pallido-pyramidal syndrome, iron d
21 ly that the genetic SCID disease observed in Arabian foals is explained by a defect in V(D)J recombin
23 ntaneous genetic immunodeficiencies in mice, Arabian foals, and recently in Jack Russell terriers hav
30 New Caledonia, the northern Red Sea, and the Arabian Gulf, should become part of a judicious global s
33 of polymorphism on the Y chromosome of Saudi-Arabian hamadryas baboons, Papio hamadryas hamadryas.
35 importantly, there was no evidence that the Arabian horse breed has clear subdivisions depending on
37 aternal inheritance is an essential point in Arabian horse population genetics and strains classifica
41 We sequenced the whole mtDNA D-loop of 251 Arabian horses to study the genetic diversity and phylog
42 this region identified one SNP found only in Arabian horses, located in exon 4 of TOE1 and approximat
43 xperimentally transmit EHCV to 4 young adult Arabian horses, two 1-month-old foals (1 Arabian and 1 A
48 disease processes, HHV-8 derived from Saudi Arabian KS lesions were shown to have a distinct nucleot
51 r gap exists in the Oligocene record of Afro-Arabian mammal evolution is now limited primarily to a p
56 on in Jeddah that were reported to the Saudi Arabian Ministry of Health from January 1 through May 16
58 from Africa to Spain during the long-lasting Arabian occupation that started in the seventh century,
60 pothesis that crown Strepsirrhini is of Afro-Arabian origin and that lemuriforms likely colonized Mad
61 support to the hypothesis of an ancient Afro-Arabian origin for crown Strepsirrhini and an Eocene div
62 human population samples is consistent with Arabian origin, a more eastern or Persian origin, and in
63 onstrable crown strepsirrhines from the Afro-Arabian Palaeogene--a galagid and a possible lorisid fro
64 or approximately 85% of the alleles in Saudi Arabian patients, the S379P, R441X, R474W, and F480L mut
65 U.S. (-0.39 +/- 0.10 mug m(-3) yr(-1)), the Arabian Peninsula (0.81 +/- 0.21 mug m(-3) yr(-1)), Sout
66 identify wild dromedaries from the southeast Arabian Peninsula among the founders of the domestic dro
68 dispersal to West Africa, and across to the Arabian Peninsula and Indian subcontinent, from source p
69 ation occurred in the eastern portion of the Arabian Peninsula and reveal substantial subsequent gene
70 corridors from northeastern Africa into the Arabian Peninsula and the Levant and expanding further i
71 prominent glacial migration waves across the Arabian Peninsula and the Levant region around 106-94, 8
72 ive distribution of the wild ancestor on the Arabian Peninsula and to the brief coexistence of early-
73 tire genomes of 104 unrelated natives of the Arabian Peninsula at high coverage, including 56 of indi
74 a zoonotic disease endemic in Africa and the Arabian Peninsula caused by the highly infectious Rift V
75 kable genetic homogeneity across most of the Arabian Peninsula coastline, with a genetic break toward
77 the presence of early cercopithecines on the Arabian Peninsula during the late Miocene reinforces the
78 ecoregions such as the Sahara desert and the Arabian Peninsula during various 30-year periods, pointi
79 ious world-wide biogeographical regions, the Arabian Peninsula exhibits the highest intra-population
83 nd complex Structure profiles are seen among Arabian Peninsula populations underscoring the high gene
85 nto Arabia by this time, suggesting that the Arabian Peninsula was a potential filter for cross-conti
87 A new coronavirus emerged in 2012 on the Arabian Peninsula with a clinical syndrome of acute resp
88 ds which ancestors colonized Africa from the Arabian peninsula) and tested to what extent historical
90 nce of human and dromedary MERS-CoV from the Arabian peninsula, and genetically diverse dromedary vir
91 ving resided in or recently travelled to the Arabian peninsula, and is a global concern for public he
92 ations inhabiting the Levant rather than the Arabian Peninsula, but the principal route for the expan
93 espiratory illness with recent travel to the Arabian Peninsula, especially among healthcare workers.
94 ated at the southeastern most portion of the Arabian Peninsula, in the tri-continental crossroads con
95 mmon with the rest of the populations in the Arabian Peninsula, it is unique in terms of its relative
96 number of families from three tribes of the Arabian Peninsula, Persia, and Oman, with indications of
97 tial spreading of mice first to the southern Arabian Peninsula, thence eastward and northward into so
116 rporting to explain Druze history that posit Arabian, Persian or mixed Near Eastern-Levantine roots.
118 an-pony cross), and 2 foals (1 Arabian and 1 Arabian-pony cross) with severe combined immunodeficienc
119 rses, two 1-month-old foals (1 Arabian and 1 Arabian-pony cross), and 2 foals (1 Arabian and 1 Arabia
121 ade, and mainly female assimilation into the Arabian population as a result of miscegenation and manu
122 ficantly different between an African and an Arabian population, suggesting that loss of variation du
126 diversity and phylogenetic relationships of Arabian populations and to examine the traditional strai
131 at as is the case in C.B-17 SCID mice and in Arabian SCID foals, the defective factor in these SCID p
133 ion of moist, westerly monsoon flow from the Arabian Sea across India, resulting in a smaller flux of
134 na bulloides abundance in box cores from the Arabian Sea and found that monsoon wind strength increas
136 ear, average sea surface temperatures in the Arabian Sea are warm enough to support the development o
137 African-descent Makranis, who reside on the Arabian Sea coast of Pakistan, as well that of four neig
138 substantial millennial-scale variability in Arabian Sea denitrification and productivity during the
140 s rapid, century-scale reorganization of the Arabian Sea ecosystem in response to climate excursions,
142 ution of denitrification to N(2) loss in the Arabian Sea indicates the global significance of denitri
144 pproach in practice, nitrogen cycling in the Arabian Sea oxygen minimum zone (OMZ) was modeled to exa
146 an increase in the intensity of pre-monsoon Arabian Sea tropical cyclones during the period 1979-201
148 the Northeast Atlantic and tropical Western Arabian Sea with new data from the Northeast Pacific.
150 d affect tropical cyclone intensity over the Arabian Sea, but so far no such linkage has been shown.
151 of the low-level monsoon westerlies over the Arabian Sea, driving surges of moisture supply, leading
152 wn independently of the Indus River into the Arabian Sea, perhaps along courses of now defunct rivers
154 hich involves in-phase fluctuations over the Arabian Sea, the Bay of Bengal, and the South China Sea,
155 anammox dominates the N(2) loss term in the Arabian Sea, the largest and most intense OMZ in the wor
156 f data from the equatorial Pacific Ocean and Arabian Sea, we show that the relative direct and indire
157 cation dominates over anammox in the central Arabian Sea, which has important implications for the lo
158 of Kachchh (Kutch), an infilled gulf of the Arabian Sea, which must have received input from the Sar
167 aximize levels of heterozygosity and include Arabian, Thoroughbred, Welsh Cob, and Icelandic Horse br
168 Data regarding the vitamin D status of Saudi Arabian women and its relation to breast cancer risk are
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