ライフサイエンスコーパス: calcium pyrophosphate dihydrate

1 of the molecular and cellular mechanisms of calcium pyrophosphate dihydrate and apatite crystal form

2 the pathologic matrix mineralization seen in calcium pyrophosphate dihydrate and basic calcium phosph

3 the cellular responses to monosodium urate, calcium pyrophosphate dihydrate and basic calcium phosph

4 The pathologic matrix mineralization seen in calcium pyrophosphate dihydrate and basic calcium phosph

5 Calcium crystals, including calcium pyrophosphate dihydrate and basic calcium phosph

6 Calcium pyrophosphate dihydrate and basic calcium phosph

7 concerning clinical and etiologic aspects of calcium pyrophosphate dihydrate and basic calcium phosph

8 ystals of calcium oxalate, monosodium urate, calcium pyrophosphate dihydrate and cystine trigger casp

9 ved in the pathogenesis of monosodium urate, calcium pyrophosphate dihydrate and hydroxyapatite cryst

10 In addition to monosodium urate, calcium pyrophosphate dihydrate, and apatite crystals, a

11 Calcium pyrophosphate dihydrate (CPPD) and basic calcium

12 Calcium deposition diseases caused by calcium pyrophosphate dihydrate (CPPD) and basic calcium

13 Microcrystals of calcium pyrophosphate dihydrate (CPPD) and monosodium ur

14 Familial autosomal dominant calcium pyrophosphate dihydrate (CPPD) chondrocalcinosis

15 tion, and increased concentrations promoting calcium pyrophosphate dihydrate (CPPD) crystal depositio

16 Calcium pyrophosphate dihydrate (CPPD) crystal depositio

17 characterization of the role of NTPPHase in calcium pyrophosphate dihydrate (CPPD) crystal depositio

18 he pathologic mineralization that results in calcium pyrophosphate dihydrate (CPPD) crystal formation

19 In this study, following our earlier work on calcium pyrophosphate dihydrate (CPPD) crystal-induced m

20 Monosodium urate monohydrate (MSU) and calcium pyrophosphate dihydrate (CPPD) crystals cause ac

21 The formation of calcium pyrophosphate dihydrate (CPPD) crystals in artic

22 luding nanoscale silicon dioxide (NanoSiO2), calcium pyrophosphate dihydrate (CPPD) crystals, and mur

23 Articular calcium-containing crystals cause calcium pyrophosphate dihydrate (CPPD) deposition diseas

24 of fluid containing synthetic or native BCP, calcium pyrophosphate dihydrate (CPPD), or monosodium ur

25 ed spectroscopy revealed crystals resembling calcium pyrophosphate dihydrate (CPPD).

26 of ePPi while excess levels of ePPi leads to calcium pyrophosphate dihydrate crystal deposition (CPPD

27 load is a likely source of pyrophosphate in calcium pyrophosphate dihydrate crystal deposition disea

28 In familial calcium pyrophosphate dihydrate crystal deposition disea

29 hic arthropathy of the atlantoaxial joint in calcium pyrophosphate dihydrate crystal deposition disea

30 c pyrophosphate in cartilage matrix leads to calcium pyrophosphate dihydrate crystal deposits.

31 Current models of calcium pyrophosphate dihydrate crystal formation are le

32 view, the author discusses various models of calcium pyrophosphate dihydrate crystal formation from e

33 l for studying the major factors involved in calcium pyrophosphate dihydrate crystal formation.

34 Calcium pyrophosphate dihydrate crystals are common comp

35 Progress in understanding why and how calcium pyrophosphate dihydrate crystals form in articul

36 young animals might promote the formation of calcium pyrophosphate dihydrate crystals in aged cartila

37 Elimination of calcium pyrophosphate dihydrate crystals may occur extra

38 Tumoral deposition of calcium pyrophosphate dihydrate crystals may occur in si

39 The effect of calcium pyrophosphate dihydrate crystals on the progress

40 Addition of calcium pyrophosphate dihydrate crystals to a lapine men

41 osition of either basic calcium phosphate or calcium pyrophosphate dihydrate crystals, remains unclea

42 sphate (PPi) that promotes the deposition of calcium pyrophosphate dihydrate crystals.

43 A discussion of ANKH as the familial calcium pyrophosphate dihydrate deposition disease gene

44 radiographic techniques to the diagnosis of calcium pyrophosphate dihydrate deposition disease holds

45 nt as a definitive rheumatic disease such as calcium pyrophosphate dihydrate deposition disease or as

46 nts were identified that segregated with the calcium pyrophosphate dihydrate deposition disease pheno

47 t literature reminds us of the propensity of calcium pyrophosphate dihydrate deposition disease to mi

48 In genetic studies of familial calcium pyrophosphate dihydrate deposition disease, a re

49 as a potential positional candidate gene for calcium pyrophosphate dihydrate deposition disease, and

50 rs: craniometaphyseal dysplasia and familial calcium pyrophosphate dihydrate deposition disease.

51 evalence and significance of extra-articular calcium pyrophosphate dihydrate deposits, and demonstrat

52 play radiographically detectable crystals of calcium pyrophosphate dihydrate in their joint spaces.

53 lysis supports the role of ANKH mutations in calcium pyrophosphate dihydrate-induced arthritis.

54 ATD5 cells were basic calcium phosphate, not calcium pyrophosphate dihydrate, underlying the signific