ライフサイエンスコーパス: Arabian

1 m the Levant (Natufians) than other mainland Arabians.

2 on events in the histories of: 1) Indian and Arabian ancestries, 2) Kalash ancestry, and 3) Native Am

3 s a mixture of ancestries closely related to Arabian ancestry and Nilo-Saharan or Omotic ancestry.

4 an and 1 Arabian-pony cross), and 2 foals (1 Arabian and 1 Arabian-pony cross) with severe combined i

5 ult Arabian horses, two 1-month-old foals (1 Arabian and 1 Arabian-pony cross), and 2 foals (1 Arabia

6 respect to nearby populations: Yemeni, other Arabian and Bedouin samples form a continuum towards the

7 s the land bridge formation between the Afro-Arabian and Eurasian landmasses.

8 Turkmen) and west/southwest breeds (Persian Arabian and Kurdish) into two phylogeographic clades ref

9 en studied in the context of Asian, Saharan, Arabian, and Australian storms, but there has been no re

10 , 102, and 113 for Turkmen, Caspian, Persian Arabian, and Kurdish breeds, respectively.

11 es suggestive of selective sweeps across the Arabian breed contain candidate genes for combating oxid

12 t no significant genomic contribution of the Arabian breed to the Thoroughbred racehorse, including Y

13 tember 2012 in samples obtained from a Saudi Arabian businessman who died from acute respiratory fail

14 abia, over an almost 2-year period and local Arabian camels over 2 months in the year after surveilla

15 yalipithecus) deep within the otherwise Afro-Arabian clade Parapithecoidea and indicates that transat

16 Saudi Arabian cohorts offer an opportunity to discover novel g

17 y characterised haplogroups, one observed in Arabian/Coldblooded and the other in Turkoman/Thoroughbr

18 Males in a Saudi Arabian community who were CSs or WPs had more MT and po

19 time, the sources of DNA became increasingly Arabian, consistent with evidence of growing interaction

20 the progressive aridification of the Saharo-Arabian desert and the fluctuations of savannah habitats

21 en monsoonal Asia to the east and the Saharo-Arabian desert belt to the west, making it a key thresho

22 Mediterranean Middle Paleolithic than to the Arabian Desert entity.

23 ests the episodic presence within the Saharo-Arabian Desert interior of water-dependent fauna (for ex

24 The Saharo-Arabian Desert is one of the largest biogeographical bar

25 idespread perennial shrub, Rhazya stricta in Arabian desert soils.

26 method characterizes the populations of the Arabian desert.

27 ed early modern humans to surpass the Saharo-Arabian deserts or if climatic changes triggered punctua

28 ith wetter climatic conditions in the Saharo-Arabian deserts.

29 In three Saudi Arabian families and one Egyptian family all affected by

30 Four patients from 3 Saudi Arabian families had delayed onset of immune deficiency

31 ne was performed with individuals from Saudi Arabian families with multiple, clinically confirmed, mo

32 e disease shows 50% penetrance in some Saudi Arabian families.

33 e facies in a number of consanguineous Saudi Arabian families.

34 ent in members of three consanguineous Saudi Arabian families.

35 d a positional candidate approach in a Saudi Arabian family affected with autosomal recessive SCAN1,

36 onsense mutation in the SPATA7 gene in Saudi Arabian family KKESH-060.

37 is c.1028C>T (p.Thr343Met), while in a Saudi Arabian family the variant is c.962G>A (p.Arg321Gln).

38 affected siblings in a consanguineous Saudi Arabian family we performed genome-wide linkage and mapp

39 quencing in a multiplex consanguineous Saudi Arabian family with a pallido-pyramidal syndrome, iron d

40 lelic inheritance in 7 Caucasian families, 1 Arabian family, and 1 Tunisian patient.

41 Immunocompetent Arabian foals and Arabian foals with severe combined imm

42 ly that the genetic SCID disease observed in Arabian foals is explained by a defect in V(D)J recombin

43 Immunocompetent Arabian foals and Arabian foals with severe combined immunodeficiency (SCI

44 ntaneous genetic immunodeficiencies in mice, Arabian foals, and recently in Jack Russell terriers hav

45 Comparisons with other Paleogene Afro-Arabian forms are generally inconclusive.

46 The Saudi Arabian G12 VP7 gene had a 99% nucleotide sequence ident

47 Coral communities in the Persian/Arabian Gulf (PAG) withstand unusually high salinity lev

48 ns in the world's warmest reefs, the Persian/Arabian Gulf (PAG), represent an ideal model system to u

49 dal of the highly urbanized southern Persian/Arabian Gulf (PAG).

50 atal Neonatal Outcomes Research Study in the Arabian Gulf (PEARL-Peristat Study) between April 2017 a

51 om reefs both inside and outside the Persian/Arabian Gulf across temperatures of 27.0 degrees C, 31.5

52 ine systems of the northeastern Arabia area (Arabian Gulf and Sea of Oman) and of these which ones ar

53 st, most extreme coral reefs in the southern Arabian Gulf and the nearby, but more environmentally be

54 measurements of high mixing ratios over the Arabian Gulf are adequately simulated, strong underpredi

55 We show that assemblages in the Arabian Gulf are half as diverse and less than 25% as ab

56 Reports from Arabian Gulf countries have demonstrated emergence of no

57 CC1153-MRSA were mainly observed in Arabian Gulf countries.

58 The Arabian Gulf nations are undergoing rapid economic devel

59 inium thermophilum, sp.nov. from the Persian/Arabian Gulf, a thermally tolerant coral symbiont.

60 At six monitoring sites (Persian/Arabian Gulf, Red Sea, northern and southern Galapagos,

61 New Caledonia, the northern Red Sea, and the Arabian Gulf, should become part of a judicious global s

62 emirates bordering the southern basin of the Arabian Gulf.

63 he world's hottest sea, the southern Persian/Arabian Gulf.

64 Polymorphism on the Y chromosome of Arabian hamadryas appears to be low compared to other pr

65 of polymorphism on the Y chromosome of Saudi-Arabian hamadryas baboons, Papio hamadryas hamadryas.

66 discussed, as well as characterization of an Arabian heavy vacuum gas oil in terms of the ring number

67 I genes were identified in cDNA clones from Arabian horse A2152, which presented both epitopes.

68 importantly, there was no evidence that the Arabian horse breed has clear subdivisions depending on

69 n understanding the evolution history of the Arabian horse breed.

70 Overall, our data support an origin of the Arabian horse in the Middle East, no evidence for reduce

71 aternal inheritance is an essential point in Arabian horse population genetics and strains classifica

72 The Arabian horse, one of the world's oldest breeds of any d

73 ed (OR = 1.9, 95% CI 1.2-2.8, P = 0.005) and Arabian horses (OR = 1.9, 95% CI 1.2-2.8, P = 0.005) wer

74 frequency of the defective DNA-PKcs genes in Arabian horses and in Jack Russell terriers.

75 s of oxidative status in 3 years old, racing Arabian horses during long term observation and the chan

76 Here we studied 378 Arabian horses from 12 countries using equine single nuc

77 of genetic variation and complex ancestry in Arabian horses from the Middle East region.

78 epends on maternal family lines using native Arabian horses from the Middle East.

79 sis of the maternal genetic diversity in the Arabian horses than using just the HVR1.

80 We sequenced the whole mtDNA D-loop of 251 Arabian horses to study the genetic diversity and phylog

81 this region identified one SNP found only in Arabian horses, located in exon 4 of TOE1 and approximat

82 xperimentally transmit EHCV to 4 young adult Arabian horses, two 1-month-old foals (1 Arabian and 1 A

83 ophy (CA) is a neurological disease found in Arabian horses.

84 e SCID allele in a series of 295 tumors from Arabian horses.

85 Patients admitted to ICUs in 14 Saudi Arabian hospitals.

86 n HHV-8 subgroups between American and Saudi Arabian iatrogenic KS patients.

87 biota between UC, CD and controls in a Saudi Arabian inflammatory bowel disease cohort.

88 how recurrent humid intervals in the central Arabian interior over the past 8 million years.

89 al at least five hominin expansions into the Arabian interior, coinciding with brief 'green' windows

90 Indeed, Arabian killifish edaradd crispants showed a potent redu

91 press the gene in another killifish species, Arabian killifish.

92 disease processes, HHV-8 derived from Saudi Arabian KS lesions were shown to have a distinct nucleot

93 nomadic pastoralism who speak a Modern South Arabian language.

94 ain phase of silicic volcanism from the Afro-Arabian large igneous province preserves some of the lar

95 nsisted of two major subclades: the Original Arabian lineage and the Turkoman horse lineage.

96 rcial green tea samples available in a Saudi Arabian local market.

97 ng 15-20 kya, when Levantines expanded while Arabians maintained smaller populations that derived anc

98 r gap exists in the Oligocene record of Afro-Arabian mammal evolution is now limited primarily to a p

99 Afro-Arabian mammalian communities underwent a marked transit

100 ions across a shelf-to-basin transect on the Arabian Margin (Neo-Tethyan Ocean).

101 The Arabian Margin record demonstrates the repeated expansio

102 The Qatari population, located at the Arabian migration crossroads of African and Eurasia, is

103 on in Jeddah that were reported to the Saudi Arabian Ministry of Health from January 1 through May 16

104 Saudi Arabian Ministry of Health, Wellcome Trust, European Com

105 llele frequencies between 1% and 5% in Saudi Arabians (n = 1,061), Vietnamese (n = 1,264), Thai (n =

106 oms the diverging plate dynamics between the Arabian, Nubian, and Somalian plates along the Red Sea,

107 from Africa to Spain during the long-lasting Arabian occupation that started in the seventh century,

108 In marked contrast to Afro-Arabian Oligocene primate faunas, this Asian fauna is do

109 pothesis that crown Strepsirrhini is of Afro-Arabian origin and that lemuriforms likely colonized Mad

110 support to the hypothesis of an ancient Afro-Arabian origin for crown Strepsirrhini and an Eocene div

111 human population samples is consistent with Arabian origin, a more eastern or Persian origin, and in

112 other species, such as African elephants and Arabian oryx, may alter their potential to experience RE

113 onstrable crown strepsirrhines from the Afro-Arabian Palaeogene--a galagid and a possible lorisid fro

114 or approximately 85% of the alleles in Saudi Arabian patients, the S379P, R441X, R474W, and F480L mut

115 U.S. (-0.39 +/- 0.10 mug m(-3) yr(-1)), the Arabian Peninsula (0.81 +/- 0.21 mug m(-3) yr(-1)), Sout

116 stics in hot-hyper arid regions, such as the Arabian Peninsula (AP).

117 The Arabian Peninsula accounts for approximately 6% of the w

118 identify wild dromedaries from the southeast Arabian Peninsula among the founders of the domestic dro

119 Qataris with Arabian Peninsula ancestry showed the lowest polygenic r

120 The virus is endemic in camels in the Arabian Peninsula and Africa and thus poses a consistent

121 Although native to the Arabian Peninsula and Africa, aloe vera is significantly

122 only ones from the early Late Miocene of the Arabian Peninsula and circumambient areas.

123 st, MERS is primarily a camel disease on the Arabian Peninsula and in Africa, with clinical disease i

124 dispersal to West Africa, and across to the Arabian Peninsula and Indian subcontinent, from source p

125 ation occurred in the eastern portion of the Arabian Peninsula and reveal substantial subsequent gene

126 the lack of data from certain regions, e.g., Arabian Peninsula and South Asia.

127 corridors from northeastern Africa into the Arabian Peninsula and the Levant and expanding further i

128 prominent glacial migration waves across the Arabian Peninsula and the Levant region around 106-94, 8

129 ontinuity among the populations of Iraq, the Arabian Peninsula and the Middle East.

130 Africa (SSA), with outbreaks reported in the Arabian Peninsula and throughout SSA.

131 ive distribution of the wild ancestor on the Arabian Peninsula and to the brief coexistence of early-

132 tire genomes of 104 unrelated natives of the Arabian Peninsula at high coverage, including 56 of indi

133 a zoonotic disease endemic in Africa and the Arabian Peninsula caused by the highly infectious Rift V

134 kable genetic homogeneity across most of the Arabian Peninsula coastline, with a genetic break toward

135 ans and livestock in sub-Saharan African and Arabian Peninsula countries.

136 a-the Eastern Mediterranean woodland and the Arabian Peninsula desert.

137 the presence of early cercopithecines on the Arabian Peninsula during the late Miocene reinforces the

138 ecoregions such as the Sahara desert and the Arabian Peninsula during various 30-year periods, pointi

139 ious world-wide biogeographical regions, the Arabian Peninsula exhibits the highest intra-population

140 The Arabian Peninsula experiences severe air pollution, the

141 Populations of the Arabian Peninsula have a complex genetic structure that

142 The Arabian Peninsula is a critical geographic landmass situ

143 The Arabian Peninsula is a key region for understanding homi

144 gical and paleoenvironmental research in the Arabian peninsula is transforming our understanding of a

145 circulates widely in dromedary camels in the Arabian Peninsula leading to zoonotic transmission.

146 carriers) and completely absent in those of Arabian Peninsula origin.

147 nd complex Structure profiles are seen among Arabian Peninsula populations underscoring the high gene

148 the potential to spread from Africa and the Arabian Peninsula to other regions.

149 nto Arabia by this time, suggesting that the Arabian Peninsula was a potential filter for cross-conti

150 The Arabian Peninsula was the initial site of the out-of-Afr

151 The virus is endemic to Africa and the Arabian Peninsula where outbreaks are characterized by a

152 A new coronavirus emerged in 2012 on the Arabian Peninsula with a clinical syndrome of acute resp

153 ds which ancestors colonized Africa from the Arabian peninsula) and tested to what extent historical

154 for emergence in new territories (e.g., the Arabian Peninsula).

155 inct ancestry groups: general Arab, Persian, Arabian Peninsula, Admixture Arab, African, and South As

156 nce of human and dromedary MERS-CoV from the Arabian peninsula, and genetically diverse dromedary vir

157 ving resided in or recently travelled to the Arabian peninsula, and is a global concern for public he

158 , zoonotic disease endemic to Africa and the Arabian Peninsula, and its spread outside of the endemic

159 d the Tibetan Plateau, Central Asia, and the Arabian Peninsula, and Western Siberia, respectively.

160 ations inhabiting the Levant rather than the Arabian Peninsula, but the principal route for the expan

161 espiratory illness with recent travel to the Arabian Peninsula, especially among healthcare workers.

162 st to all other genotyped populations of the Arabian Peninsula, genome-level analysis of the medieval

163 r An. stephensi across its full range (Asia, Arabian Peninsula, Horn of Africa) and a set of spatial

164 ated at the southeastern most portion of the Arabian Peninsula, in the tri-continental crossroads con

165 mmon with the rest of the populations in the Arabian Peninsula, it is unique in terms of its relative

166 number of families from three tribes of the Arabian Peninsula, Persia, and Oman, with indications of

167 nsively managed herds, ubiquitous across the Arabian Peninsula, present a major potential source of p

168 One high-frequency region-encompassing the Arabian Peninsula, southern Mesopotamia, and the souther

169 ile pastoralism in the desert regions of the Arabian Peninsula, the history of the Jews, and the spre

170 y Holocene ~ 9500 years ago somewhere in the Arabian Peninsula, the Levant, and southern Mesopotamia.

171 tial spreading of mice first to the southern Arabian Peninsula, thence eastward and northward into so

172 malaria vector native to South Asia and the Arabian Peninsula, was detected in Djibouti's seaport, f

173 rus widely distributed across Africa and the Arabian Peninsula, which causes devastating epidemics af

174 drocarbon measurements, performed around the Arabian Peninsula, with global model simulations that in

175 Medical Center or hCoV-EMC), emerged in the Arabian Peninsula.

176 largely explains the observed trend over the Arabian Peninsula.

177 ng in a wider geographical region beyond the Arabian peninsula.

178 as well as more recent migrations within the Arabian Peninsula.

179 ople and livestock throughout Africa and the Arabian Peninsula.

180 m the center of origin in East Africa to the Arabian Peninsula.

181 espiratory disease in humans, emerged in the Arabian Peninsula.

182 isease throughout Africa and portions of the Arabian Peninsula.

183 predicted across sub-Saharan Africa and the Arabian Peninsula.

184 of severe disease throughout Africa and the Arabian Peninsula.

185 s found mainly in sub-Saharan Africa and the Arabian Peninsula.

186 sease throughout Africa, Madagascar, and the Arabian Peninsula.

187 ease throughout Africa and more recently the Arabian peninsula.

188 izootics/epidemics throughout Africa and the Arabian peninsula.

189 th Asia, sub-Sahara, western Africa, and the Arabian peninsula.

190 independent consanguineous families from the Arabian Peninsula.

191 and public health problems in Africa and the Arabian Peninsula.

192 zoonotic diseases endemic to Africa and the Arabian Peninsula.

193 g camel-owning communities in Jordan and the Arabian Peninsula.

194 the Pleistocene and Holocene throughout the Arabian Peninsula.

195 rica, southern Africa, the Near East and the Arabian Peninsula.

196 st entry port of camels from Africa into the Arabian Peninsula.

197 is a lethal zoonotic pathogen endemic to the Arabian Peninsula.

198 vantine focus, and the third in the southern Arabian Peninsula.

199 -CoV) has repeatedly caused outbreaks in the Arabian Peninsula.

200 causing disease outbreaks in Africa and the Arabian Peninsula.

201 uman and livestock illness in Africa and the Arabian Peninsula.

202 hich they entered from what would become the Arabian Peninsula.

203 to be more diverse than those inhabiting the Arabian (Persian) Gulf and the Gulf of Oman.

204 rporting to explain Druze history that posit Arabian, Persian or mixed Near Eastern-Levantine roots.

205 In the Arabian/Persian Gulf, this situation has already occurre

206 an incipient suture zone that separates the Arabian plate from in situ Gulf of Oman oceanic crust an

207 me beneath the Turkish-Anatolian Plateau and Arabian Plate.

208 go, Ma) subtropical marine carbonates on the Arabian Plateau, Oman.

209 triple junction, between Nubian, Somali and Arabian plates, and for hosting environments at the very

210 the regional simple mantle flow beneath the Arabian Platform and eastern Turkey deflects as a circul

211 ich promoted the disintegration of the major Arabian polities.

212 an-pony cross), and 2 foals (1 Arabian and 1 Arabian-pony cross) with severe combined immunodeficienc

213 rses, two 1-month-old foals (1 Arabian and 1 Arabian-pony cross), and 2 foals (1 Arabian and 1 Arabia

214 Three additional young adult Arabian-pony crosses and 1 SCID foal were then inoculate

215 ade, and mainly female assimilation into the Arabian population as a result of miscegenation and manu

216 ficantly different between an African and an Arabian population, suggesting that loss of variation du

217 T2DM), and vitamin D deficiency in the Saudi Arabian population.

218 CYP1B1-associated PCG phenotype in the Saudi Arabian population.

219 ome (MetS) is rising alarmingly in the Saudi Arabian population.

220 diversity and phylogenetic relationships of Arabian populations and to examine the traditional strai

221 Asian and Afro-Arabian primate faunas responded differently to EOT clim

222 ed over the last 4 decades than to the Saudi Arabian prototype strain AV-1645 isolated in 1956.

223 The Great Escarpment of the Arabian Red Sea margin has several features that make it

224 ed along 13 degrees of latitude in the Saudi Arabian Red Sea, from shallow-water reefs to deep-sea ha

225 As a servant of the Saudi Arabian royal family, he appeared in the United States s

226 In addition, the large Saudi Arabian RVF outbreak in 2000 appears to have involved vi

227 All local Arabian samples contained strains of the virus that belo

228 at as is the case in C.B-17 SCID mice and in Arabian SCID foals, the defective factor in these SCID p

229 astern Tropical South Pacific (ETSP) and the Arabian Sea (AS).

230 clustering the cyclogenesis over the Eastern Arabian Sea (EAS) next to the Indian West coast in recen

231 sed delta(11)B record from the north-eastern Arabian Sea (NEAS) covering the mid-late Holocene (~ 8-1

232 The Arabian Sea accounts for a small fraction of Tropical Cy

233 ion of moist, westerly monsoon flow from the Arabian Sea across India, resulting in a smaller flux of

234 ent between the Middle East and the southern Arabian Sea and drives the changes of low-level jet (LLJ

235 na bulloides abundance in box cores from the Arabian Sea and found that monsoon wind strength increas

236 ta obtained from drill core samples from the Arabian Sea and neodymium isotope data.

237 e way to the development of upwelling in the Arabian Sea and possibly led to a strengthening of South

238 stern and southeastern coasts, adjoining the Arabian Sea and the Bay of Bengal, were assessed with el

239 Alongside prior Arabian Sea and tropical Atlantic rates, our results ind

240 ear, average sea surface temperatures in the Arabian Sea are warm enough to support the development o

241 ecord of seasonal warming and cooling in the Arabian Sea at a depth of 4000 m.

242 ing stratification of the upper layer of the Arabian Sea at a much faster rate than predicted by glob

243 African-descent Makranis, who reside on the Arabian Sea coast of Pakistan, as well that of four neig

244 es from three major mangrove sites along the Arabian Sea coast of Pakistan, Indus Delta, Sandspit and

245 substantial millennial-scale variability in Arabian Sea denitrification and productivity during the

246 In seven of eight experiments in the Arabian Sea denitrification is responsible for 87-99% of

247 s rapid, century-scale reorganization of the Arabian Sea ecosystem in response to climate excursions,

248 -pressure systems that traverse the northern Arabian Sea every winter and spring disrupt winter conve

249 fare of coastal populations dependent on the Arabian Sea for sustenance.

250 Over the past four decades, the Arabian Sea has also experienced a profound loss of inor

251 In the last decade, the northern Arabian Sea has witnessed a radical shift in the composi

252 oration, driving the convective formation of Arabian Sea High Salinity Water (ASHSW) during the winte

253 ution of denitrification to N(2) loss in the Arabian Sea indicates the global significance of denitri

254 trend of the Eurasian landmass is making the Arabian Sea more productive.

255 pproach in practice, nitrogen cycling in the Arabian Sea oxygen minimum zone (OMZ) was modeled to exa

256 In sediments underlying the Arabian Sea oxygen minimum zone (OMZ), we performed the

257 an increase in the intensity of pre-monsoon Arabian Sea tropical cyclones during the period 1979-201

258 Because most Arabian Sea tropical cyclones make landfall, our results

259 the Northeast Atlantic and tropical Western Arabian Sea with new data from the Northeast Pacific.

260 The warming of Arabian Sea's Subsurface Minima and the Indian Equatoria

261 ical and eastern tropical Pacific Ocean, the Arabian Sea, and the Bay of Bengal.

262 of the monsoon circulation over the northern Arabian Sea, as revealed by a compilation of proxy recor

263 d affect tropical cyclone intensity over the Arabian Sea, but so far no such linkage has been shown.

264 of the low-level monsoon westerlies over the Arabian Sea, driving surges of moisture supply, leading

265 In the northern Arabian Sea, high salinity levels are primarily sustaine

266 otable increase in extreme cyclones over the Arabian Sea, particularly in post-monsoon cyclones (Sept

267 wn independently of the Indus River into the Arabian Sea, perhaps along courses of now defunct rivers

268 ld in the Eastern Tropical South Pacific and Arabian Sea, respectively.

269 hich involves in-phase fluctuations over the Arabian Sea, the Bay of Bengal, and the South China Sea,

270 anammox dominates the N(2) loss term in the Arabian Sea, the largest and most intense OMZ in the wor

271 f data from the equatorial Pacific Ocean and Arabian Sea, we show that the relative direct and indire

272 cation dominates over anammox in the central Arabian Sea, which has important implications for the lo

273 eover, the trend in aerosol loading over the Arabian Sea, which is located downwind to Central India,

274 of Kachchh (Kutch), an infilled gulf of the Arabian Sea, which must have received input from the Sar

275 munities differentiated strongly moving from Arabian Sea-influenced high salinity (southerly; prasino

276 at define the monsoonal circulation over the Arabian Sea.

277 f the Eastern Tropical South Pacific and the Arabian Sea.

278 duction and up to half of that occurs in the Arabian Sea.

279 Pacific oceans in both hemispheres, and the Arabian Sea.

280 nds have been strengthening over the western Arabian Sea.

281 culate matter from the Pacific Ocean and the Arabian Sea.

282 ear chlorophyll-a variations in the northern Arabian Sea.

283 t loss and convective mixing in the northern Arabian Sea.

284 centrations of chlorophyll-a in the northern Arabian Sea.

285 ability of the low-level westerlies over the Arabian Sea.

286 retion complexes occupying almost the entire Arabian Shield and much of Egypt and parts of the small

287 While the American-Arabians showed relatively low diversity, the Syrian pop

288 tiated during this period, which we term the Arabian Standstill, include loci involved in the regulat

289 Arabian strains of the virus should be tested for change

290 red major gene deletions between African and Arabian strains of the virus.

291 ere performed based on two independent Saudi Arabian studies comprising 3950 MI patients and 2324 non

292 Arabians suffered a population bottleneck around the ari

293 aximize levels of heterozygosity and include Arabian, Thoroughbred, Welsh Cob, and Icelandic Horse br

294 ation structure, and the relationship of the Arabian to other horse breeds.

295 r recent interbreeding of Thoroughbreds with Arabians used for flat-racing competitions.

296 Data regarding the vitamin D status of Saudi Arabian women and its relation to breast cancer risk are

297 However, attracting Saudi Arabian women into the nursing profession has traditiona

298 Saudi Arabian women may be at greater risk of vitamin D defici

299 D [25(OH)D] and breast cancer risk in Saudi Arabian women.

300 ncentrations and breast cancer risk in Saudi Arabian women.