ライフサイエンスコーパス: Turner

1 Turner et al. measured sedimentation from Hurricanes Kat

2 Turner syndrome (TS) is a neurogenetic disorder characte

3 Turner syndrome (TS) is associated with a characteristic

4 Turner syndrome (TS) is associated with aortic coarctati

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

6 Turner syndrome is a genetic disorder that results from

7 Turner syndrome is a relatively common disorder of femal

8 Turner syndrome is caused by complete or partial loss of

9 Turner syndrome is characterized by short stature and is

10 Turner syndrome is the complex human phenotype associate

11 Turner syndrome is the most common established cause of

12 Turner syndrome, one of the most common cytogenetic abno

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

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

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

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

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

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

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

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

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

22 om spermatogenic failure to sex reversal and Turner syndrome.

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

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

25 in sex differentiation, spermatogenesis, and Turner syndrome.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 and subsequent gonadal degeneration found in Turner syndrome.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 disposing finding other than the presence of Turner syndrome.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 a phenotype significantly more abnormal than Turner syndrome.

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

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

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

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

99 syndromes of gonadal dysgenesis and Ullrich-Turner syndrome.

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

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

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

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

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

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

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

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

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

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

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

111 was significantly reduced in the group with Turner syndrome.

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

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

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

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

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

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

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

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

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

121 1, 2010, was performed of all patients with Turner syndrome.

122 (2.6%) of pilomatricomas among patients with Turner syndrome.

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

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

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

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

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

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

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

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

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

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

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

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

135 100-fold in young and middle-aged women with Turner syndrome.

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

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

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

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