ライフサイエンスコーパス: adult type

1 s differentiate from their neonatal to their adult types.

2 ion trajectories from piwi+ cells to diverse adult types.

3 a2+] solutions was similar in 10-day-old and adult type 1 cells.

4 lls are normal in patients with recent-onset adult type 1 diabetes, the ability of the Tregs in this

5 unterregulatory responses to hypoglycemia in adult type 1 diabetic patients.

6 A total of 13,467 adult-type 1 diabetics enrolled on the renal and renal-p

7 7,750 men and 4,736 women had a diagnosis of adult type 2 diabetes (30 years of age or older) obtaine

8 s associated with offspring birth weight and adult type 2 diabetes (T2D) risk loci show some overlap.

9 arker of body mass index, is associated with adult type 2 diabetes (T2D) risk.

10 d 22 circulating proteins causally linked to adult type 2 diabetes and 11 proteins with suggestive ev

11 ctive cross-sectional study was conducted on adult type 2 diabetes mellitus (T2DM) patients between J

12 ine the relation between prenatal famine and adult type 2 diabetes mellitus (T2DM).

13 Five hundred adult type 2 diabetes patients were recruited from three

14 fluences the association of birth weight and adult type 2 diabetes, using a cohort of 113,801 men and

15 (GDM), have been linked to increased risk of adult type 2 diabetes.

16 dent metabolomic GWAS and testing effects on adult type 2 diabetes.

17 In adult-type ACh receptors, the energy from the affinity c

18 itch from the fetal AChRgamma subunit to the adult-type AChRepsilon is required for synapse maturatio

19 rom the fetal (alpha, beta, gamma, delta) to adult-type (alpha, beta, delta, epsilon) AChRs is marked

20 tal type (alpha, beta, gamma, and delta) and adult-type (alpha, beta, epsilon, and delta) receptors w

21 ion to primitive (embryonic) and definitive (adult type) blood cells proceeds normally and without an

22 are familiar with the various pediatric- and adult-type brain tumors and their typical imaging morpho

23 e morphological and phenotypic features with adult types but have better prognosis.

24 This presentation closely resembles adult-type carnitine palmitoyltransferase II deficiency

25 sues of 2 distinct CD19(+) B-progenitors, an adult-type CD10+ve ProB-progenitor and a new CD10-ve Pre

26 er both phenotypic and molecular features of adult-type cells on neonatal megakaryocytes.

27 e already transformed from larval cells into adult-type cells, but the tail cells remain as larval ce

28 pediatric care, and both pediatric-type and adult-type CNS tumors occur at that age.

29 emerging biomarkers for refined allergy and adult-type diffuse glioma classification to inform futur

30 dated in 2 separate cohorts of patients with adult-type diffuse glioma from other institutions.

31 contributed to postoperative seizure risk in adult-type diffuse glioma patients, and that postoperati

32 the World Health Organization to define the adult-type diffuse glioma taxonomy (IDH mutation, 1p19q

33 y a minor role in the treatment landscape of adult-type diffuse glioma, and today are mainly limited

34 For the adult-type diffuse glioma, standard of care is a combina

35 IDH1 mutation status on a population of 275 adult-type diffuse gliomas (CNS WHO grade 4).

36 IDH-mutant adult-type diffuse gliomas are subdivided into grade 2,

37 Furthermore, the previous broad category of adult-type diffuse gliomas has been consolidated into 3

38 data show that postoperative seizure risk in adult-type diffuse gliomas varies in large part by molec

39 Seizures are a frequent complication of adult-type diffuse gliomas, and are often difficult to c

40 In adult-type diffuse gliomas, histologic classification ha

41 of many tumours and reorganizes gliomas into adult-type diffuse gliomas, paediatric-type diffuse low-

42 ng condition that is common in patients with adult-type diffuse gliomas, yet thromboprophylaxis is co

43 World Health Organization (WHO) grade 2 to 4 adult-type diffuse gliomas.

44 Loss of UHRF1 in the adult-type erythroid cell line HUDEP2 causes global deme

45 elopmental switch from embryonic to fetal to adult-type expression.

46 g the oncological role of surgery in diffuse adult-type gliomas as defined per WHO 2021 classificatio

47 s required for FOG-1-dependent activation of adult-type globin gene expression but is dispensable for

48 ete cytoreductive surgery(CRS) for recurrent adult type granulosa cell tumours of the ovary (GCT).

49 L2 transcription factor is pathognomonic for adult-type granulosa cell tumors (AGCT) and a diagnostic

50 Adult-type granulosa cell tumors (AGCT) are the most com

51 carrying a FOXL2 mutation characteristic of adult-type granulosa cell tumors shows that FOXL2 C134W

52 ansition from fetal-type scarless healing to adult-type healing with scar has been actively investiga

53 Definitive, adult-type hematopoiesis first appears in the fetal live

54 ols the development of endothelium producing adult-type hematopoiesis.

55 nsic proliferation and/or differentiation of adult-type hematopoietic lineages in the yolk sac and fe

56 The first definitive/adult-type hematopoietic stem cells (HSCs) in the mouse

57 R complex) that is restricted to definitive (adult-type) hematopoietic cells and that specifically bi

58 We found that in adult type HUDEP2 erythroid cells, the ATP-dependent chr

59 In contrast, a significant reduction of adult-type human and murine globin gene expression was f

60 Loss of ZNF410 in adult-type human erythroid cell culture systems and xeno

61 l regulation of T1alpha, a gene expressed by adult type I but not type II cells.

62 We studied 54 technically successful adult type I insulin-dependent diabetic recipients of ca

63 Although we used adult type I interferon receptor IFNAR knockout (Ifnar1(

64 on and could be categorized according to the adult type I, II, or III criteria.

65 anagement strategies for malignant tumors in adult-type (IDH-mutant gliomas) and pediatric-type gliom

66 t stimulator of LPCAT expression in cultured adult type II cells.

67 Three hundred twenty-eight eyes of 164 adult type II diabetic patients with varying levels of D

68 In the adult, type III collagen is a major component of the ext

69 maturation that is required to display full adult-type inflammation-induced leukocyte recruitment.(1

70 Adult-type intraembryonic hematopoiesis arises from spec

71 ngly, that this isoform is expressed only by adult-type Leydig cells in the mouse testis and that thi

72 Adult-type lympho-myeloid hematopoietic progenitors are

73 Some cell lines derived from adult-type lymphoid malignancies also show sensitivity t

74 Older patients tended to present with an adult-type MDS that is accommodated within the French-Am

75 cytic nevus, and conventional (also known as adult-type) melanoma.

76 ree energies) of these and other agonists in adult-type mouse AChRs having a mutation(s) at the trans

77 The energies associated with adult-type mouse neuromuscular nicotinic acetylcholine r

78 By contrast, epsilon-subunit (adult-type) mRNA was expressed at much higher levels in

79 Cs were significantly stronger than those of adult-type MSCs at each tested dose level.

80 MSCs proliferated significantly faster than adult-type MSCs.

81 also found in fetal-type MSCs compared with adult-type MSCs.

82 dissociation constants for acetylcholine in adult-type muscle mouse nicotinic receptors (AChRs) havi

83 We examined mouse adult-type muscle nAChR activation by physostigmine and

84 One hundred one patients had adult-type myelodysplastic syndrome (A-MDS), 60 had juve

85 rect nucleotide sequencing of H CDR3s showed adult-type N-nucleotide insertions and Ig gene utilizati

86 ctivation and inhibition of the mouse muscle adult-type nicotinic acetylcholine receptor by tetraethy

87 Adult-type nicotinic acetylcholine receptors (AChRs) med

88 tion induces endplate-specific expression of adult-type nicotinic acetylcholine receptors by selectiv

89 Efficient coinduction of embryonic and adult types of globin mRNA in bone marrow cell lines der

90 Adult type ovarian granulosa cell tumors (AGCT) are rare

91 pancreatoblastomas for alterations found in adult-type pancreatic ductal adenocarcinomas including m

92 strongly associated with the development of adult-type periodontitis.

93 in alveolar rhabdomyosarcoma (ARMS) and the adult-type pleomorphic rhabdomyosarcoma (PRMS) compared

94 and were linked to derivation from fetal- vs adult-type precursors in the thymus.

95 The most frequent adult-type primary CNS tumours are diffuse gliomas, but

96 L122R mutations and the other matching adult-type PRMS.

97 All agents inhibited activation of adult-type receptors by ACh, consistent with the idea th

98 f affinities is the same for both fetal- and adult-type receptors.

99 ls did not increase during the transition to adult-type repair in fetal skin, whereas LTBP-1 and fibr

100 ansitions from scarless fetal-type repair to adult-type repair with scar between day 16 (E16) and day

101 ansitions from scarless fetal-type repair to adult-type repair with scar between days 16 and 18 of ge

102 r to late gestation (E19) wounds manifesting adult-type repair with scar.

103 ic acetylcholine receptor synthesis, induces adult-type specific epsilon subunit gene expression via

104 t maturity and implant experience to undergo adult-type speech recognition tests, surgical series sho

105 rated that the generation of a fetal-type or adult-type Vgamma9Vdelta2 CDR3 repertoire is determined