ライフサイエンスコーパス: C-telopeptide

1 act parathyroid hormone, and increased serum C telopeptide.

2 The C-telopeptide aldol dimers formed labile addition produc

3 mor burden of Neo cells, the serum levels of C-telopeptide and TRAP-5b never increase above the level

4 obic interactions involving the short alpha2 C-telopeptide are crucial determinants of its azimuthal

5 asures were type I collagen crosslinked beta C-telopeptide (betaCTX), and type 1 procollagen-N-propep

6 quantitative MRI and type I and II collagen C-telopeptide biomarkers.

7 ated peptides indicated that both the N- and C-telopeptides bound to a region between amino acid 776

8 ibril distribution and over-hydroxylation in C-telopeptide cross-linking lysine from a1(1) chain.

9 (PTH), bone alkaline phosphatase (BAP), and C-telopeptide (CTX) in youth infected with human immunod

10 These animals have high serum levels of the C-telopeptide derived from type I collagen as well as si

11 This difference between N- and C-telopeptide docked structures demonstrates how unique

12 links at molecular sites (mediated by N- and C-telopeptide domains) found in collagen II fibrils proc

13 , aldosterone, endothelin-1, troponin I, and C-telopeptide for type I collagen levels, suggesting mor

14 [procollagen III N-terminal peptide], CITP [C-telopeptide for type I collagen], IGFBP7 [insulin-like

15 h serum levels of the bone resorption marker C-telopeptide fragments of type I collagen (CTX), elevat

16 r-maximal reductions in mean levels of serum C-telopeptide from baseline were evident three days afte

17 d characteristics sex, serum type I collagen C-telopeptide, hip bone mineral density, urticaria pigme

18 d mouse skin, species that lack an alpha1(I) C-telopeptide histidine, revealed that HHL is a laborato

19 hormone (PTH), osteocalcin, type I collagen C-telopeptide, hormones, and metabolic factors.

20 lagen triple-helical segment followed by the C-telopeptides in their docked conformation, and then th

21 rone dosage decreased, the percent change in C-telopeptide increased.

22 th an increase in bone resorption, the serum C-telopeptide level was 25% higher in transgenic mice th

23 ls of bone resorption (serum type I collagen C-telopeptide), low hip bone mineral density, absence of

24 linked alpha1(I) chains as a result of their C-telopeptide lysines being more completely oxidized to

25 e alkaline phosphatase (b-ALP), and terminal C telopeptide of collagen Type I (CTX) were analyzed.

26 ed with the systemic marker of bone turnover C-telopeptide of type 1 collagen (r=0.6; P<0.001).

27 h continuing alendronate: 55.6% (P<.001) for C-telopeptide of type 1 collagen, 59.5% (P < .001) for s

28 Serum levels of C-telopeptide of type I collagen (CTx), a marker of bone

29 sient decrease in the bone resorption marker C-telopeptide of type I collagen (CTX-1) were observed.

30 propeptide of type I procollagen (PINP) and C-telopeptide of type I collagen (CTX-I) are markers of

31 groups had 70% higher levels of cross-linked C-telopeptide of type I collagen, a bone resorption mark

32 raphy and a significant decrease in systemic C-telopeptide of type I collagen, suggesting decreased o

33 Urinary C-telopeptide of type II collagen (CTX-II) levels were m

34 inoline, glycosylated Pyr (Glc-Gal-Pyr), and C-telopeptide of type II collagen (CTX-II) was assessed

35 for helical peptide of type II collagen and C-telopeptide of type II collagen, were observed after r

36 in the collagen triple helix or in the N- or C-telopeptides of collagen I.

37 ns of 2.5 mM, peptides with sequences in the C-telopeptides of the alpha1(I) and alpha2(I) chain inhi

38 ed at baseline, week 12, and week 28: B-SAP, c-telopeptide, procollagen type I intact N-terminal prop

39 C-telopeptide pyridinoline cross-links (ICTP), a host-de

40 cular fluid (GCF) analysis for the levels of C-telopeptide pyridinoline cross-links (ICTP), and genet

41 ecifically evaluate the relationship between C-telopeptide pyridinoline cross-links and periodontal d

42 species with a histidine in their alpha1(I) C-telopeptide sequence.

43 idinoline differed between N-telopeptide and C-telopeptide sites, and between the individual intercha

44 ins was cross-linked by pyridinolines at the C-telopeptide to helix site, [alpha1(I)C]2alpha1(I)helix

45 were identified, N-telopeptide to helix and C-telopeptide to helix.

46 Docking of the heterotrimeric C-telopeptide to its receptor showed that hydrophobic in

47 analysis of kinetics of binding of alpha1(I) C-telopeptide using an optical biosensor.

48 ncentrations of collagen type 1 cross-linked C-telopeptide was significantly decreased in the RCE gro