ライフサイエンスコーパス: Turner

1 Turner et al. measured sedimentation from Hurricanes Kat

2 Turner highlights survivorship bias in the study of neur

3 Turner of Yale University, who studies the evolutionary

4 Turner syndrome (TS) is a neurogenetic disorder characte

5 Turner syndrome (TS) is associated with a characteristic

6 Turner syndrome (TS) is associated with aortic coarctati

7 Turner syndrome (TS) results from whole or partial monos

8 Turner syndrome is a genetic disorder that results from

9 Turner syndrome is a relatively common disorder of femal

10 Turner syndrome is caused by complete or partial loss of

11 Turner syndrome is characterized by short stature and is

12 Turner syndrome is the complex human phenotype associate

13 Turner syndrome is the most common established cause of

14 Turner syndrome, one of the most common cytogenetic abno

15 Turner's syndrome is a sporadic disorder of human female

16 ormalities that include trisomies 18 and 21, Turner syndrome.

17 thoracic aortic disease (nsHTAD) (n = 378), Turner syndrome (TS) (n = 298), vascular Ehlers-Danlos s

18 We obtained an independent sample of 77 Turner syndrome females that we genotyped for 77 SNPs in

19 f this gene in the development of additional Turner stigmata.

20 Additionally, Turner Syndrome subjects, who are predisposed to chronic

21 Recent papers by Jackson et al. and Turner et al. have an important bearing on research in t

22 osed by Lu, Turner, and Mathews and Chen and Turner, respectively.

23 at, Wolf-Hirschhorn, Prader-Willi, Down, and Turner syndromes.

24 etic syndromes (for example, Klinefelter and Turner syndromes) and people with disorders of sexual de

25 sex hormones, and effects of Klinefelter and Turner syndromes.

26 ren with intrauterine growth retardation and Turner syndrome; however, serum insulin levels were elev

27 pulations, where they cause sex reversal and Turner syndrome and predispose individuals to infertilit

28 om spermatogenic failure to sex reversal and Turner syndrome.

29 resulting in infertility, sex reversal, and Turner syndrome.

30 ractal kinetic model proposed by Schnell and Turner, in which k(a) depends on time according to a Zip

31 in sex differentiation, spermatogenesis, and Turner syndrome.

32 he growth failure seen in the Leri-Weill and Turner syndromes, and in some familial cases of ISS.

33 f the Chelsea Technologies Group AQUAtracka, Turner Designs Cyclops, Satlantic SUNA and WET Labs, Inc

34 In an accompanying article, Turner et al. compare the joint effects of smoking and a

35 o X aneuploidy phenotypes in humans, such as Turner (X0) and Klinefelter (XXY) syndromes.

36 Sex chromosome aneuploidies, such as Turner syndrome (X0) and Klinefelter syndrome (XXY), are

37 th hormone deficiency and conditions such as Turner's syndrome, Prader-Willi syndrome, intrauterine g

38 In both Turner syndrome (TS) and Klinefelter syndrome (KS) copy

39 pothetical data similar to those reported by Turner et al.

40 Human monosomy-X (45,X) causes Turner syndrome (TS), altering craniofacial, skeletal, e

41 variation in the number of sex chromosomes: Turner syndrome, Klinefelter syndrome, XYY syndrome, and

42 In the combined Turner syndrome samples, the most strongly associated SN

43 ementation of RNA folding under the complete Turner 2004 model with coaxial stacking, out of several

44 Unlike the single grating Czerny-Turner configuration spectrometers, a super-high spectra

45 erapy in 78% of children with GH deficiency, Turner syndrome, or renal failure; of those recommended

46 Using a mouse model for Turner syndrome, we searched for locus-specific imprinti

47 Previous research found Turner syndrome women of normal verbal intelligence are

48 We derived iPSCs from Turner syndrome and control individuals and examined ger

49 and dicentric Xq isochromosomes (i(Xq)) from Turner syndrome probands, using FISH with cosmids and YA

50 demonstrate a variation of Cullen's and Grey Turner's sign, most often found in patients with hemorrh

51 cal findings of a modified Cullen's and Grey Turner's sign.

52 Charles Henry Turner was an African American scientist who, while ekin

53 The studyCrossingham I, Turner S, Ramakrishnan S, et al.

54 Aortic valve abnormalities in Turner syndrome occur with a spectrum of severity and ar

55 Variability in fear recognition accuracy in Turner syndrome suggested the existence of a quantitativ

56 FINDINGS: Recent work on social cognition in Turner syndrome has identified a range of difficulties d

57 -of-origin influences on social cognition in Turner syndrome might be due to the presence of imprinte

58 Thoracic aortic dilation in Turner syndrome must be evaluated in relation to body su

59 of the characteristics of aortic disease in Turner syndrome in comparison with Marfan-like syndromes

60 anomalies and risk for aortic dissection in Turner syndrome are strongly linked to a history of feta

61 Aortic dissection in Turner syndrome occurs in young individuals at smaller a

62 ce across both verbal and spatial domains in Turner syndrome, with greater impairment on tasks with W

63 and subsequent gonadal degeneration found in Turner syndrome.

64 nderstanding brain structure and function in Turner syndrome and identifies several critical research

65 rstanding of brain structure and function in Turner syndrome will generate new therapeutic approaches

66 studies have examined spatial WM function in Turner syndrome, none have directly compared the neural

67 s indicated altered emotional functioning in Turner's syndrome (TS) subjects (45,XO).

68 tion However, aortic dissection can occur in Turner syndrome without cardiac malformations or hyperte

69 ated to cause the short stature phenotype in Turner syndrome.

70 during visuospatial executive processing in Turner syndrome, suggesting a significant role for the X

71 le viability, and has unappreciated roles in Turner's syndrome and in phenotypic differences between

72 The abnormalities seen in Turner syndrome (monosomy X) presumably result from hapl

73 iopathic short stature in humans, as seen in Turner syndrome and Leri-Weill dyschondrosteosis, while

74 The boundary is also stable in Turner (45, X) females.

75 bly also contributes to the short stature in Turner individuals.

76 rted neonatal lymphedema, similar to that in Turner syndrome, associated with a t(Y;16)(q12;q24.3) tr

77 examine this framework in humans, including Turner syndrome (TS), where females are missing one X-ch

78 oluntarily participated in the International Turner Syndrome Aortic Dissection Registry.

79 In this issue, Turner et al.

80 ilis pyr operon previously proposed by R. J. Turner, Y. Lu, and R. L. Switzer.

81 found in human females with an XO karyotype (Turner syndrome).

82 ring aneuploid offspring (Down, Klinefelter, Turner, triple X, and XYY syndromes) or triploid embryos

83 For some, like Turner syndrome, recombinant human growth hormone has be

84 using the predictive models proposed by Lu, Turner, and Mathews and Chen and Turner, respectively.

85 ) mapping in 20 human females with monosomic Turner syndrome (TS) (mean age, 10.3 +/- 2.0 years) vers

86 henotype correlations, we mapped one or more Turner syndrome traits to a critical region in Xp11.2-p2

87 lly evaluated for the presence or absence of Turner syndrome features, and their deletions were mappe

88 to the X chromosome is the genetic basis of Turner syndrome in human females.

89 The Euler Characteristic Transform (ECT) of Turner et al. provides a way to statistically analyze no

90 We found an enrichment of Turner's syndrome among cases of depression compared wit

91 Principle features of Turner syndrome include short stature, ovarian failure,

92 arian failure are characteristic features of Turner's syndrome.

93 for trends in the contrast and intensity of Turner, Monet, and others' works, including after contro

94 l subjects should refine the localization of Turner syndrome loci and provide a rational basis for ex

95 cientific literature to inform management of Turner's syndrome.

96 ocytes from XO female mice, a mouse model of Turner Syndrome.

97 disposing finding other than the presence of Turner syndrome.

98 his is strongly supported by the presence of Turner-characteristic dysmorphic skeletal features in pa

99 date for involvement in the short stature of Turner syndrome.

100 It is suggested that the story of Turner can be used to increase interest in entomology, e

101 The study of Turner syndrome (TS) offers a unique window of opportuni

102 women with monosomy for the X chromosome, or Turner syndrome (TS).

103 rful faces in the condition of X-monosomy or Turner syndrome.

104 Parsonage-Turner syndrome (PTS), also known as neuralgic amyotroph

105 gic amyotrophy (NA), also known as Parsonage-Turner syndrome, is characterised by sudden pain attacks

106 2) 12 patients with HEV-associated Parsonage-Turner syndrome; and (3) 16 asymptomatic blood donors (c

107 logical manifestations, especially Parsonage-Turner syndrome.

108 These abnormalities include Parsonage-Turner syndrome and quadrilateral space syndrome, each o

109 gnosis of acute brachial neuritis (Parsonage-Turner syndrome) correlated with MR imaging results in a

110 e of the several known triggers of Parsonage-Turner syndrome (PTS).

111 t find any enriched pathway in the Parsonage-Turner syndrome group or in the controls.

112 o infectious diseases with a study from Paul Turner's group.

113 of genes implicated in gonadal sex reversal, Turner syndrome, graft rejection and spermatogenic failu

114 PURPOSE OF REVIEW: Turner syndrome, which results from the complete or part

115 Thurston GD, Burnett RT, Turner MC, Shi Y, Krewski D, Lall R, Ito K, Jerrett M, G

116 (disomy 21 sperm), Edward (disomy 18 sperm), Turner (nullisomy sex sperm), XYY (disomy Y sperm), trip

117 suospatial processing.SIGNIFICANCE STATEMENT Turner syndrome is caused by the absence of one of the t

118 target conditions have mainly been studied: Turner syndrome, coeliac disease, cystic fibrosis, growt

119 as Prader-Willi syndrome, Angelman syndrome, Turner's syndrome, bipolar depression and schizophrenia.

120 arche or premature menopause, Down syndrome, Turner syndrome, Williams syndrome, chronic fatigue synd

121 a phenotype significantly more abnormal than Turner syndrome.

122 ci responsible for various components of the Turner syndrome phenotype.

123 , all favorable pairings with respect to the Turner energy function are identified.

124 ate for gel formation is consistent with the Turner-Cates fusion mechanism, proposed originally to ex

125 c requirements of the X chromosome linked to Turner syndrome.

126 syndromes of gonadal dysgenesis and Ullrich-Turner syndrome.

127 Using Turner syndrome (XO) and Klinefelter (XXY) models, we fi

128 some--a near normal phenotype in mice versus Turner syndrome and multiple abnormalities in humans.

129 to impressionistic representations in J.M.W. Turner and Claude Monet's paintings in London and Paris

130 n altered the environmental context in which Turner and Monet painted, and our results indicate that

131 n addition, the question is raised as to why Turner did not receive an academic appointment, and simi

132 r (ASD) and Dravet, Fragile X, Prader-Willi, Turner, and Williams syndromes.

133 osage variation (X-monosomy) associated with Turner syndrome affects the functional neuroanatomy of t

134 X lead to growth retardation associated with Turner, Leri-Weill dyschondrosteosis, and Langer mesomel

135 sts recommended GH therapy for children with Turner syndrome, insurer policies covered GH therapy for

136 omen who were cytogenetically diagnosed with Turner syndrome in Great Britain between 1959 and 2002.

137 However, females with Turner syndrome (45,X) have even larger amygdalae than 4

138 DMD may also be observed in females with Turner syndrome (45,X), if the remaining X chromosome ca

139 Here we report a study of 80 females with Turner's syndrome and a single X chromosome, in 55 of wh

140 Previous work in girls with Turner syndrome (45,XO) has suggested that there are X-l

141 lthy controls and 40 prepubescent girls with Turner syndrome (TS), a condition caused by the absence

142 Specifically, girls with Turner syndrome have smaller early visual areas that pro

143 -dose estrogen on adult height in girls with Turner's syndrome.

144 was significantly reduced in the group with Turner syndrome.

145 isuospatial WM functions in individuals with Turner syndrome and normal controls.

146 significantly increased in individuals with Turner syndrome at all ages, highest during young adult

147 Individuals with Turner syndrome have a spectrum of anatomical, physiolog

148 of interventions to assist individuals with Turner syndrome in visual-spatial, mathematical, and soc

149 female volunteers and eight individuals with Turner syndrome performed a delayed-response WM task dur

150 Individuals with Turner syndrome who are >18 years of age with an ascendi

151 A patient with Turner syndrome died of a Stanford type A dissection at

152 valence of pilomatricoma among patients with Turner syndrome served as the catalyst for this multicen

153 In total, 311 patients with Turner syndrome were identified from these 3 institution

154 1, 2010, was performed of all patients with Turner syndrome.

155 (2.6%) of pilomatricomas among patients with Turner syndrome.

156 ment increases adult height in patients with Turner's syndrome.

157 s frequently observed in human patients with Turner, Leri-Weill and Langer syndromes.

158 rize aortic valve structure in subjects with Turner syndrome and to determine the prevalence of aorti

159 d by cardiovascular MRI in 208 subjects with Turner syndrome in an institutional review board-approve

160 he clinical characteristics among those with Turner syndrome and dissection have received little atte

161 One-third of women with Turner syndrome (45,X) have autism-like social and commu

162 increased among relatively young women with Turner syndrome (TS).

163 mapping of fear recognition in 93 women with Turner syndrome across the critical region was performed

164 Girls and women with Turner syndrome are at risk for aortic dissection and ru

165 Cancer risks in women with Turner syndrome have not been clearly established.

166 increased risk of gonadoblastoma, women with Turner syndrome seem to be at increased risk for meningi

167 neurysm, and rupture in girls and women with Turner syndrome.

168 100-fold in young and middle-aged women with Turner syndrome.

169 s of hormonal treatments given to women with Turner syndrome.

170 Girls and women with Turner's syndrome who come to medical attention older th

171 rs, and cffDNA from a fetus with monosomy X (Turner syndrome) had decreased hybridization signals on

172 ir role in the neurological phenotypes of XO Turner syndrome.

173 romosome aneuploidies (Klinefelter [47,XXY], Turner [45,X] and 47,XXX syndrome) revealed an intimate