ライフサイエンスコーパス: primary tissue

1 e in cell isolation from minimally processed primary tissue.

2 en analyzed in metastatic tissue rather than primary tissue.

3 al miR targeting data, particularly in human primary tissues.

4 rgets across a panel of human cell lines and primary tissues.

5 identify trans-eQTLs specific to one of four primary tissues.

6 secreted from essentially all cell types and primary tissues.

7 usefulness of LCLs as a surrogate model for primary tissues.

8 ncreased p38gamma and MMP9 expression in the primary tissues.

9 that affects gene expression levels in human primary tissues.

10 in other expression contexts, such as human primary tissues.

11 expression levels in one or more of the five primary tissues.

12 ed and primary neural cells, and eight other primary tissues.

13 ine AtT-20 corticotroph cells and in several primary tissues.

14 Motor neurons are the primary tissue affected in SMA.

15 In both primary tissue and cell culture models, overexpression o

16 tein, B5, that is broadly expressed in human primary tissue and cell lines.

17 eir basal fibres throughout mitosis, both in primary tissue and in older organoids.

18 differ from radial glial (RG) cells in both primary tissue and in stem cell-derived organoids.

19 rotein are selectively expressed in specific primary tissues and cancer cell lines, and HEPL maintain

20 downregulation of the SFRP gene family in MM primary tissues and cell lines as well as several other

21 visualize Hi-C data generated from 21 human primary tissues and cell lines.

22 Organoids are derived from primary tissues and have the capacity for long-term grow

23 gene is unmethylated in telomerase-negative primary tissues and nonimmortalized cultured cells, indi

24 n-Fas complexes in B-cell lymphoma cells and primary tissues, and the absence of such complexes in B-

25 cities, how closely they resemble the target primary tissues, and the potential safety issues associa

26 tic processes in HFD mice indicates that the primary tissues are another facet of the immune system d

27 The genotype effects in the primary tissues are consistently in the same direction a

28 mapping of protein environment directly from primary tissue as well as the identification of interact

29 e CNV mutation is accessing DNA derived from primary tissues as opposed to cell lines.

30 is challenging to surmount in neurons, where primary tissue availability is poor.

31 e analysis of the immune microenvironment in primary tissue biopsy samples can be used to stratify pa

32 oncogenic mir-17-92 cluster was detected in primary tissues but also in blood from patients.

33 ingle-cell (clonogenic) cell population from primary tissue can differentiate into functional derivat

34 Solid CRC tissues, either primary tissues collected from surgical specimens or xen

35 ectopic production of Myc or Ras proteins in primary tissue culture cells properly predict the activi

36 chromatid exchange at the frequency of 5% in primary tissue culture cells, whereas higher levels were

37 Primary tissue culture methods also are described, and t

38 spontaneously formed Mallory Denk bodies in primary tissue cultures.

39 In 51 human primary tissues derived from normal prostate, benign pro

40 Identifying the microbiome composition from primary tissues directly affords an opportunity to study

41 Three primary tissues, enamel (enameloid), dentin, and bone, a

42 e often advanced for evaluations using human primary tissue explants relevant to the in vivo mucosal

43 e mucosal layer of conducting airways is the primary tissue exposed to inhaled microorganisms, allerg

44 readily available libraries of cell lines or primary tissues expressing fluorescent proteins and does

45 Skeletal muscle is the primary tissue for glucose utilization, and insulin resi

46 t UV-DDB is also deficient in cell lines and primary tissues from rodents.

47 that allow the long-term expansion of adult primary tissues from small intestine, stomach, liver and

48 ammalian cell lines differ from those of the primary tissues from which they were derived, exhibiting

49 ne promoters are frequently methylated in MM primary tissue (>80%).

50 cation of cis-acting regulatory variation in primary tissues has the potential to elucidate the genet

51 sion levels across individuals in five human primary tissues (heart, kidney, liver, lung and testes).

52 tinoblastoma tumor suppressor protein, using primary tissues in vivo, ex vivo, and in vitro, as well

53 nt in the mitochondria of cultured cells and primary tissues, including the liver and heart.

54 RNA blot analysis of mouse and human primary tissues indicated that both CTLA4 and T-cell rec

55 Analysis of primary tissues indicated that the TMS1 gene is unmethyl

56 are characterized by different mechanisms of primary tissue injury that mostly affect lung.

57 has been hindered by limited availability of primary tissue, intraspecies variability associated with

58 rimary and secondary proteomes suggests that primary tissue is predictive of the metastatic phenotype

59 This study of glioblastoma cells and primary tissues is the first to implicate PDGF-C and -D

60 ted, the alpha subunits are secreted between primary tissue layers and become distributed in differen

61 and in early cell fate decisions leading to primary tissue layers during in vitro development of plu

62 ng, and differentiate into each of the three primary tissue layers.

63 pe A scavenger receptor-induced apoptosis in primary tissue macrophages and in macrophage apoptosis i

64 ptome sequencing on a discovery cohort of 18 primary tissue MCL samples and 2 cell lines.

65 In aspen stem primary tissues, PtCAD was immunolocalized exclusively t

66 Electron microscopic examination of primary tissues revealed intralesional accumulations of

67 We further analyzed DNA extracted from primary tissue samples and found the same pattern of CpN

68 rinting from allelic expression data in 1582 primary tissue samples from 178 individuals from the Gen

69 m14 and Mv(4;11) leukemia cells, but also in primary tissue samples from AML patients.

70 panel of breast cancer cell lines as well as primary tissue samples from breast cancer patients to in

71 sing murine Ba/F3 cells, human K562 cells or primary tissue samples from CML patients, whereas fmk tr

72 g mutations of the c-kit gene occur in GCTs, primary tissue samples of 33 testicular and ovarian tumo

73 Here, we studied primary tissue samples to characterise human epicardium

74 d data, cell lines perturbed pathways and in primary tissues samples including The Cancer Genome Atla

75 onditions and is applicable for detection in primary tissue sections.

76 achinery of the placenta thus represents the primary tissue site for regulating fetal Ca homeostasis.

77 Primary tissue specimens therefore appeared to be a bett

78 Using immunohistochemistry to analyze primary tissue specimens, we found that high SIRT1 expre

79 However, the primary tissue target remains unidentified.

80 from women ages 16 to 91 years, derived from primary tissues, to investigate the molecular changes th

81 bidopsis fruit comprises an ovary with three primary tissue types: the valves, the replum and the val

82 dependence on developmental stage or origin (primary tissue vs. stem cell), notable species-dependent

83 m molecular degradation experiments of human primary tissues, we introduce a method-quality surrogate

84 mbryogenesis and seed germination and is the primary tissue where gene imprinting occurs.

85 stromal cells in the microenvironment of the primary tissues wherein B-cell development occurs, ie, f

86 on onto adjacent proteins in fixed cells and primary tissues, which allows proteins in close proximit

87 of cell-specific gene expression patterns in primary tissues with a complex mixture of cell types.

88 hods for successful generation of short-term primary tissue xenografts from benign and tumor-derived