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

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

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

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

6 7,750 men and 4,736 women had a diagnosis of adult type 2 diabetes (30 years of age or older) obtaine

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Adult-type intraembryonic hematopoiesis arises from spec

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

34 Adult-type lympho-myeloid hematopoietic progenitors are

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

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

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

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

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

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

41 MSCs proliferated significantly faster than adult-type MSCs.

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

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

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

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

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

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

48 Adult-type nicotinic acetylcholine receptors (AChRs) med

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

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

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

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

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

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

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

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

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

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

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

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

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