ライフサイエンスコーパス: fertile

1 n knock-out mice are surprisingly viable and fertile.

2 % of wild-type GlcCer levels were viable and fertile.

3 , but whereas males are sterile, females are fertile.

4 nlike their genetic source, these clones are fertile.

5 Canx null mice are growth retarded but fertile.

6 t NANOS2 allele and female knockout pigs are fertile.

7 n female sterility, whereas males were fully fertile.

8 TAF1b and mutant taf1b lines are viable and fertile.

9 o apparent phenotypic abnormalities and were fertile.

10 Mdr1a/b;Mrp2(-/-) mice, which are viable and fertile.

11 e crossing partners, whereas the hybrids are fertile.

12 Double nulls are viable and fertile.

13 n adult flies, both of which were viable and fertile.

14 -generation TIN2(+/DC) mice were healthy and fertile.

15 recombination, and female Brca1 mutants are fertile.

16 reach the flowering stage, but they are not fertile.

17 he nesprin-3-knockout mice and the mice were fertile.

18 develop normally and adults are healthy and fertile.

19 l brains and bodies, normal lifespan and are fertile.

20 ility, as Rbp9(+/-), su(Hw)(-/-) females are fertile.

21 3(+/Cre) mice were phenotypically normal and fertile.

22 zygous flies with each allele are viable and fertile.

23 null and hypomorphic animals were viable and fertile.

24 ales are infertile, whereas mutant males are fertile.

25 both male and female Lep(ob/ob) mice became fertile.

26 , attain normal weight and maturity, and are fertile.

27 ver from this initial germ cell loss and are fertile.

28 Flies null for fob are homozygous viable and fertile.

29 lopment, beyond which mutants are viable and fertile.

30 whereas those carrying missense changes were fertile.

31 we found that Pkm2(-/-) mice are viable and fertile.

32 gen1 plants, which develop normally and are fertile.

33 HAT-L4 knockout mice were viable and fertile.

34 l regulatory elements of the c-Kit gene, are fertile.

35 compared with wild-type females and are less fertile.

36 We propose that as animals enter fertile adulthood, EGF signalling switches the mechanism

37 ouble mutant mice are viable and mature into fertile adults with a full immune complement of myeloid

38 owever, result in the development of viable, fertile adults, with 100% of worms developing to adults

39 and Casp8 deficiency develop into viable and fertile adults, with the capacity to produce normal leve

40 dity with females being at lower risk during fertile age, but at higher risk otherwise.

41 In apparently healthy women of fertile age, prepregnancy obesity was associated with in

42 Costs are about 50% higher in fertile-age female patients.

43 dometrial biopsies collected from 17 healthy fertile-aged women from pre-receptive and receptive phas

44 ult mice were otherwise normal, healthy, and fertile, although slightly smaller, and homozygotes were

45 ng mice bred to homozygosity were viable and fertile, although Sprn(0/0) mice maintained in two genet

46 Furthermore, the fertile and CMS plastid genomes are conserved, differing

47 nge of ex vivo human HSC expansion remains a fertile and critically important area of investigation.

48 We observed that Muc4(ko) animals are fertile and develop normally, and adult mice exhibit no

49 Fgf22 null animals were viable, fertile and did not display any obvious abnormalities.

50 among three Arabidopsis LLG genes, are fully fertile and did not enhance reproductive defects in lre-

51 The cKO mice were fertile and did not show any detectable abnormalities in

52 ckout mutants lacking all EBs are viable and fertile and display normal pulling forces and spindle po

53 DeltaEx3/DeltaEx3) knockout mice are viable, fertile and do not display any overt phenotype.

54 nterestingly, these mice are both viable and fertile and do not exhibit any apparent gross abnormalit

55 Mmp1a(-/-) mice are viable and fertile and do not exhibit obvious abnormalities, which

56 These mutant mice are viable and fertile and do not show any spontaneous phenotype.

57 ea(-/-) mice, rg null mutants are viable and fertile and exhibit aberrant associative odor learning,

58 t were injected with the cultured FGSCs were fertile and generated multiple batches of normal offspri

59 ee independent pal1 pal2 double mutants were fertile and generated yellow seeds due to the lack of co

60 Heterozygous CD mice were viable, fertile and had a normal lifespan, while homozygotes wer

61 s lacking CP110 (CP110Delta) were viable and fertile and had no obvious defects in cell division, cen

62 The KO mice were fertile and had no visible anomalies.

63 he survivin gene in prostate epithelium were fertile and had normal prostate growth and development.

64 osophila lacking synaptogyrin are viable and fertile and have no overt deficits in motor function.

65 conditional deletion of Rab43 are viable and fertile and have normal development of cDCs but show a d

66 They are healthy and fertile and have normal longevity; however, they show ce

67 sion were also observed between embryos from fertile and infertile couples, which were largely equali

68 pressing this modified receptor not only are fertile and maintain a high level of insect defense, but

69 th maternally and zygotically are viable and fertile and no phenotype has so far been detected despit

70 These plants were fertile and produced viable seed.

71 ring DNA sequences at MAT locus of both self-fertile and self-sterile strains, found four mating type

72 Transplastomic plants were fertile and set viable seeds.

73 er with decreased nocturnal activity but are fertile and show no motor dysfunction.

74 alleles our deletion mutants are viable and fertile and show only mild defects in caudal vertebrae d

75 Comparisons of fertile and sterile hybrid males identified a set of gen

76 However Dmrt1 mutant females are fertile and the role of Dmrt1 in the ovary has not been

77 ice lack SOCE specifically in muscle but are fertile and thrive well into adulthood.

78 ut mice deficient in both Sho and PrP(C) are fertile and viable up to 690 d of age.

79 AM-null mice and found that they are viable, fertile, and apparently healthy.

80 oreover, because RIAM-null mice are healthy, fertile, and display no bleeding abnormalities, our resu

81 le PEX14 mRNA and PEX14 protein, was viable, fertile, and displayed residual peroxisome matrix protei

82 and Syt12 S97A-knockin mice were viable and fertile, and exhibited no measurable change in basal syn

83 The Cyp3a1/2 double KO rats were viable and fertile, and had no obvious physiological abnormities.

84 Mfap5(-/-) mice appear grossly normal, are fertile, and have no reduction in life span.

85 lacking MK alpha2beta1 develop normally, are fertile, and like their systemic alpha2beta1 knockout co

86 (LysM-Cre(+)MMP-14(fl/fl)) were healthy and fertile, and neither skin architecture nor differentiati

87 BP1-expressing adult mice are viable, fertile, and phenotypically indistinguishable from their

88 ttermates, do not develop skin blisters, are fertile, and survive >1.5 years.

89 Zan(-/-) males were fertile, and their spermatozoa readily fertilized mouse

90 only the mutant form of TTP were healthy and fertile, and their systemic inflammatory responses to LP

91 Homozygous Sepn1(-/-) mice are fertile, and their weight and lifespan are comparable to

92 Col1a1-cKO and Prx1-cKO mice were viable and fertile, and they did not manifest the epileptic seizure

93 s, both defects that result in sterility, to fertile animals with significantly reduced progeny numbe

94 pectroscopy, we show that Terra Preta soils (fertile anthropogenic dark earths in Amazonia that were

95 Transfer of the two genes to self-fertile Arabidopsis thaliana allowed the establishment o

96 of breathing remain elusive and represent a fertile area for future investigation.

97 the study of virus-microbiota interactions a fertile area for future investigation.

98 is for PCD in parasitic protozoa represent a fertile area for investigation and drug development.

99 survival and tolerance development remains a fertile area for investigation.

100 ngoing research in Leidenfrost droplets is a fertile area for scientists working on metallic nanodrop

101 uggest that antibody-mediated catalysis is a fertile area for study with broad applications in infect

102 ces and in connecting fragments has formed a fertile area of debate.

103 in induction and evasion of IFN represent a fertile area of research due to the significant large nu

104 in live bacterial cells represent a new and fertile area of research providing real-time, spatially

105 and largest scales will continue to provide fertile areas of investigation in its next century.

106 mp-1 only, develop normally, are healthy and fertile as adults, and efficiently generate mature plasm

107 It is fertile at room temperature but male sterile at modestly

108 gen or vitamin D deficiency, contribute to a fertile bone microenvironment that might promote bone me

109 sterile backcross males compared with their fertile brothers.

110 sed to identify 160 reliable and divergently fertile bulls for a dual strategy of targeted sequencing

111 show that CPEB heterozygous female mice are fertile but contain disorganized mammary epithelial cell

112 otide exchange factor binding are viable and fertile but exhibit abnormal development of the liver va

113 Adult brdp/+ mice are viable and fertile but exhibit behavioral phenotypes.

114 CLIC4(NULL) mice were viable and fertile but had smaller litters than did wild-type mice.

115 and Fadd(-/-)Mlkl(-/-) mice were viable and fertile but rapidly developed severe lymphadenopathy, sy

116 -/-) mice are viable, grow normally, and are fertile but show mild radiosensitivity.

117 mice deleted for Cyp2c genes were viable and fertile but showed certain phenotypic alterations in the

118 The RGS7(-/-) mouse is viable and fertile but smaller in body size.

119 Flies lacking Fic were viable and fertile, but blind.

120 Calr mcKO male mice were fertile, but fcKO female mice were sterile despite norma

121 se that survive to adulthood are healthy and fertile, but have alterations in the hypothalamus and ex

122 s, newly evolving hermaphrodites became self-fertile by co-opting either of the two redundant male pr

123 Basic knowledge, in close and fertile contact with medical and public health needs, pr

124 ressing PLCzeta in 71 males (22-54 years; 44 fertile controls and 27 infertile patients), along with

125 compared to menstrual stage matched healthy fertile controls in hopes of better understanding their

126 L-33 compared to the endometrium of healthy, fertile controls.

127 RM), recurrent implantation failure (RIF) or fertile controls.

128 t the plant-based subsistence in the eastern Fertile Crescent (southeast Turkey, Iran, and Iraq) focu

129 about 10,000 years before the present in the Fertile Crescent and became a founder crop of Neolithic

130 Neolithic pastoral agriculturalists from the Fertile Crescent and Northern Africa, as well as more re

131 49 common wheat landraces collected from the Fertile Crescent and surrounding areas carried the mutat

132 farming communities emerged in parts of the Fertile Crescent during the tenth millennium and early n

133 ian uprising that began in 2011, the greater Fertile Crescent experienced the most severe drought in

134 In the eastern Fertile Crescent exploitation of legumes, fruits, nuts,

135 ed pea in the Mediterranean Basin and in the Fertile Crescent in relation to the past and current cli

136 As early farming spread from the Fertile Crescent in the Near East around 10,000 years be

137 cereals in expansion of agriculture from the Fertile Crescent into diverse environments across the Me

138 ition to sedentary agrarian societies in the Fertile Crescent more than 10,000 years ago.

139 the chronology of dairying beginning in the 'Fertile Crescent' of the Near East and its spread across

140 omes from the Zagros region of Iran (eastern Fertile Crescent), where some of the earliest evidence f

141 locations in the Southern Levant part of the Fertile Crescent, an area with a high proportion of the

142 e range of ecogeographical conditions in the Fertile Crescent, has valuable "left behind" adaptive di

143 rvest traits of species originating from the Fertile Crescent, including those for which there is arc

144 modern fields in the geographic area of the Fertile Crescent, spanning the Aceramic Neolithic [10,00

145 During the origin of agriculture in the Fertile Crescent, the broad spectrum of wild plant speci

146 c people and agricultural colonists from the Fertile Crescent.

147 among the founder crops domesticated in the Fertile Crescent.

148 ewhat isolated from other populations of the Fertile Crescent.

149 Neolithic, when farming expanded west of the Fertile Crescent.

150 Heterozygous fII(WT/WE) mice were viable and fertile despite a shift toward an antithrombotic phenoty

151 Converting these sterile haploids into fertile diploids (termed "doubled haploids," DHs) produc

152 Although fertile, DKO animals were produced in less-than-predicte

153 Microglial research has entered a fertile, dynamic phase characterized by novel technologi

154 show that conditions for an immunologically fertile environment are met when TGF-beta blockade and v

155 ms in the world, it has become an especially fertile environment for developing and testing approache

156 Drosophila that produce sterile F1 males but fertile F1 females, a pattern consistent with Haldane's

157 inked genes in the testes of sterile but not fertile F1 males.

158 alleles shared by an XY sterile daughter and fertile father.

159 African cichlid fish, Astatotilapia burtoni, fertile females select a mate and perform a stereotyped

160 Although the mutant is generally healthy and fertile, females exhibit reduced lifespan and diminished

161 NOD background was essential for creating a fertile field for the development of liver-specific auto

162 One appealing concept in this fertile field is related to the design of gated material

163 abacum could be recognized by restoration of fertile flower anatomy.

164 s thaliana is essential for the formation of fertile flowers and has roles in the control of several

165 t play important roles in the development of fertile flowers and in defense against pathogens and her

166 styles and greater stigmatic exsertion than fertile flowers.

167 a salt flux system that has proven extremely fertile for growth of new materials: the potassium polys

168 st miR-122 targets, providing an environment fertile for the long-term oncogenic potential of HCV.

169 ults of stability analysis of the metastable fertile forest state.

170 rounds the sex-determining locus of the self-fertile fungus Neurospora tetrasperma.

171 nt activation of STAT5, thereby conferring a fertile genetic ground for tumorigenesis.

172 Quantum magnets have occupied the fertile ground between many-body theory and low-temperat

173 acility for isolation and expansion provides fertile ground for continued analysis to define factors

174 physiology and cognition, LIP has served as fertile ground for developing quantitative models that l

175 to the host response to infection, providing fertile ground for development of antiviral therapeutics

176 afforded by the target HER2 has proven to be fertile ground for drug development, but it has also cre

177 range of biological activities, promising a fertile ground for exploring novel natural products.

178 proposed that each of these questions offers fertile ground for future research on a diversity of pla

179 t supportive evidence, in hopes of providing fertile ground for future studies.

180 lex societies, and the Andes have provided a fertile ground for investigating this process.

181 ing low-energy carrier dynamics that offer a fertile ground for novel physics discovery.

182 How can we provide fertile ground for students to simultaneously explore a

183 we show that collaborative settings provide fertile ground for the emergence of corruption.

184 Planarians thus present a fertile ground for the identification of factors regulat

185 basic morphology and function, representing fertile ground for unraveling fundamental aspects of gli

186 ly on pi electrons from carbon atoms offer a fertile ground in the search for exotic states of matter

187 to execute learned tics and also provides a fertile ground of motor hyperactivity for tic learning.

188 We show that acoustic waves provide a fertile ground to apply the anomalous physics of Floquet

189 rfacial coupling and Zeeman energy provide a fertile ground to study phase transition between differe

190 nfancy, continued explorations promise to be fertile grounds for discoveries that will undoubtedly fu

191 Single-crystal BPs are shown to offer fertile grounds for the study of directed crystal nuclea

192 t to Klotho null mice, Ksp-KL(-/-) mice were fertile, had a normal gross phenotype, and did not have

193 Fut2(-/-) mice were viable and fertile, had lower body weight than wild-type (wt) litte

194 simply comply with 'the inability of a fully fertile hermaphrodite plant to produce zygotes when self

195 rhabditis nematode species have evolved self-fertile hermaphrodites from the obligately outcrossing f

196 Self-fertile hermaphrodites have evolved independently severa

197 s of VcMID produced functional eggs, or self-fertile hermaphrodites.

198 (i.e., have male and female sexes), but self-fertile hermaphroditic species are not uncommon, and par

199 l control, in the repeated evolution of self-fertile hermaphroditism in Caenorhabditis nematodes.

200 are recombination events that result in self-fertile homostyle flowers with anthers and stigma at the

201 ed by studying allele-specific expression in fertile hybrid males using mRNA-sequencing of whole test

202 orhabditis species pair capable of producing fertile hybrid progeny, the gonochoristic Caenorhabditis

203 mutant mice (Rip3(K51A/K51A)) are viable and fertile, in stark contrast to the perinatal lethality of

204 growth which should lead to heavier and more fertile individuals in the autumn.

205 etween mouse and human embryos, embryos from fertile/infertile couples, and following growth factor s

206 ertile interspecific hybrids matched MEGs in fertile intraspecific hybrids.

207 ve selection if the resulting traits benefit fertile kin, and that worker traits provide the primary

208 Agriculture and farming on the fertile land along the periodically flooded plains have

209 ived from large ascospores produce both self-fertile (large-spores) and self-sterile (small-spores) o

210 Six-rowed spikes show fertile lateral spikelets and produce increased grain yi

211 based on a fragment of a fertile leaf preserved in Burmese amber that represents

212 ENP-A nucleosome assembly through the entire fertile lifespan of the female (>1 year).

213 ppresses the immune system and establishes a fertile local and distant environment to support neoplas

214 econstruction of maize anther development in fertile, mac1 (excess germ cells), and msca1 (no germ ce

215 g, we sequenced the plastid genomes of three fertile maize lines (B37, B73, and A188) and the B37 cms

216 ty in about one-half of the males, and among fertile males the number of offspring is in the normal r

217 ckage of reproductive tract in infertile and fertile males, respectively.

218 We consider the likelihood that fertile men are undercounted and conclude that the mate-

219 vels when compared to the seminal fluid from fertile men.

220 men were significantly lower than those from fertile men.

221 Progeny analysis of the male-fertile (MF) plants (2n = 35) suggested that this gene,

222 Fertile mice were cloned from several neurons, establish

223 rise to embryonic stem (ES) cells and live, fertile mice.

224 ire the development of genomic resources for fertile mint species.

225 d to the next generation, resulting in fully fertile mosquito strains that produce >95% male offsprin

226 particular a quartet pedigree composed of a fertile mule showed a mosaic of sequences and number of

227 When we used fertile N. sylvestris as mothers, we obtained eight fert

228 ng two-photon microscopy (2PM) has created a fertile new avenue for noninvasive investigation of brai

229 m injection to produce chromosomally normal, fertile offspring.

230 s where new research approaches will provide fertile opportunities to advance this field.

231 on of sex-driven molecular pathways offers a fertile opportunity to increase the number of organs ava

232 sexpressed between sterile hybrids and their fertile parental taxa.

233 measure the degree of correspondence between fertile parts of opposite sex on complementary (inter-co

234 This homozygous-fertile phenotype uncouples MSUD from sexual development

235 Whole, fertile plants of Silene stenophylla Ledeb. (Caryophylla

236 ed to select recombination events from which fertile plants were regenerated.

237 are dominated by the offspring of a few self-fertile plants.

238 rting explants, with most producing healthy, fertile plants.

239 pollination of BnCysP1 male-sterile (female-fertile) plants with BnCysP1Si pollen resulted in normal

240 N. sylvestris as mothers, we obtained eight fertile plastid transmission lines, which did not transm

241 3D DSs have been a fertile playground in discovering novel quantum particle

242 . MeuCre40 and ACTB-Cre) produced viable and fertile PP5-deficient mice.

243 tet2(m/m) zebrafish are viable and fertile, providing an ideal model to dissect altered pat

244 The directed aldol reaction has served as a fertile proving ground for new concepts and new methods

245 mportance of boron in the formation of fully fertile reproductive organs.

246 ach of many highly developed tools from this fertile research area.

247 related ones to develop new advances in this fertile research area.

248 m and subsequent magmatism incorporated less fertile restite compositions only, producing mafic intru

249 its distinctiveness and diversity (deserts, fertile river basins, foothills and plains) had no stron

250 t from these sills exposed untapped volatile-fertile sediments to contact metamorphism, likely libera

251 and role of mating type genes during a self-fertile sexual cycle remain largely unknown.

252 f the plant tissues to regenerate a complete fertile shoot system after inductive cues, the mechanism

253 Sep15 KO mice were viable and fertile, showed normal brain morphology, and did not act

254 plants to produce more seeds per flower than fertile siblings after supplemental pollination.

255 localized soft modes correlate strongly with fertile sites for shear transformations: geometrically u

256 mple, become aerosolised in association with fertile soil dust particles.

257 -deficient tumor microenvironment provides a fertile soil for breast cancer tumor growth.

258 of distant organs, rendering those organs as fertile soil for subsequent metastatic cancer cell colon

259 Fertile soil was placed within the containers, which wer

260 ablation of Sox9 in Sertoli cells of adult, fertile Sox8(-/-) mice, testis-to-ovary genetic reprogra

261 urrent dogma assumes that in animals, intact fertile sperm within a single ejaculate are equivalent a

262 lection on phenotypic variation among intact fertile sperm within an ejaculate affects offspring fitn

263 itical level of Atp6v0a2 is required for the fertile spermatozoa and its decreased level in spermatoz

264 eading to a larger number of tillers bearing fertile spikes, and increases in seed number and size.

265 A self-fertile strain containing either SXI2a-URA5 or NEO-URA5

266 ng the deleted region were found in the self-fertile strain, but only one copy of this 146-bp motif (

267 MAT1-1-5, MAT1-2-1 and MAT1-2-4) in the self-fertile strain.

268 unidirectional mating type switching - self-fertile strains derived from large ascospores produce bo

269 ction into pre-blastoderm embryos, 20-40% of fertile survivors produced kmo alleles that failed to co

270 inbred lines, routinely recovering healthy, fertile T0 plants.

271 e airway and/or gut microbiome may represent fertile targets for prevention or management of allergic

272 adioactive heat-producing elements) and more fertile than depleted mantle reservoirs-may strongly aff

273 Although these mice are fertile, their sperm displayed a reduced ability to fert

274 Although AEG-1KO mice were viable and fertile, they were significantly leaner with prominently

275 posium, leading to the production of normal, fertile transgenic plants.

276 Bex2-deficient mice were viable and fertile under laboratory growth conditions showing no ob

277 ufficient to render these Sxl-mutant females fertile, we refer to this pathway as the tra-insufficien

278 hondrial gene flanking sequences from normal fertile wheat (Triticum aestivum) with those of Aegilops

279 Intriguingly, these plants were only fertile when expression was driven by the ubiquitin10 pr

280 ion: worms with reduced nhr-114 activity are fertile when fed E. coli K-12 strains but are sterile on

281 neration homozygous coq-3(ok506) mutants are fertile when fed the standard lab diet of Q-replete OP50

282 t atg12 plants are phenotypically normal and fertile when grown under nutrient-rich conditions.

283 The MAT1-2 isolates of A. pseudofelis were fertile when paired with the MAT1-1 isolate of A. felis

284 The MAT1-2 isolate of A. parafelis was fertile when paired with the MAT1-1 isolates of A. fumig

285 notation, barely detectable transcription in fertile wild-type wheat plants, and accumulated destruct

286 tners collected specimens during the woman's fertile window for each cycle.

287 Muc4(-/-) mice were viable, fertile with no apparent defects.

288 te development, as 10 members are viable and fertile with no obvious developmental defects.

289 Interestingly, these animals were fertile with normal spermatogenesis.

290 Homozygous mutants are viable and fertile with only minor morphological defects, including

291 iridinutans, and A. wyomingensis but was not fertile with the MAT1-1 isolate of A. lentulus.

292 However, adult Mrp4(-/-) mice are fertile, with a normal circulating testosterone concentr

293 These transgenic mice are viable and fertile, with an immune system resembling that of wild-t

294 Nevertheless, animals of both sexes were fertile, with females having smaller ovaries and reduced

295 K3 double-deficient mice that are viable and fertile without an overt phenotype and that survived pro

296 velop normally in barrier conditions and are fertile without overt epithelial defects, indicating tha

297 All potential fertile women aged 15 to 44 years registered within Clin

298 After a period of abstinence in proven-fertile women, duplicate sets of biopsies were taken fro

299 Eggs from fertile WT mice were activated when loaded in vitro with

300 Ds-tra-2 (ts2) mutants developed as normal fertile XX and XY adults at permissive temperatures belo