ライフサイエンスコーパス: snap freeze

1 Cerebral cortex was snap frozen.

2 or intraperitoneal injection of cocaine and snap frozen.

3 r either transmission electron microscopy or snap frozen.

4 ter lobectomy, tumor and lung specimens were snap frozen.

5 muscles from both hindlimbs were removed and snap-frozen.

6 eft carotids and contralateral controls were snap-frozen.

7 Fresh snap-frozen (20 mum) cryosections dried at room temperat

8 % of gestation, newborn and adult sheep were snap frozen after four 6-mg dexamethasone or placebo inj

9 The arteries were snap-frozen after angioplasty, and MAPK activity was mea

10 thy human limbal tissue that was immediately snap-frozen after excision from patients undergoing cata

11 Also, sclera from human donor eyes was snap frozen and sectioned.

12 ntitative RT-PCR) in 3 cohorts, including 18 snap-frozen and 83 FFPE tissues.

13 equencing and small RNA profiling on matched snap-frozen and FFPE specimens exposed to different dela

14 a subset of RNAs was found to differ between snap-frozen and FFPE specimens in a consistent manner ac

15 ge trends in a single short amplicon between snap-frozen and FFPE tissues was only 36%.

16 1 day prior to birth) and foetal brains were snap-frozen and genome-wide gene expression data generat

17 Biopsy samples were snap-frozen and stored at -80 degrees C, mRNA was extrac

18 Eyes were enucleated at 20 weeks of age, snap frozen, and analyzed for hypoxic regions and tumor

19 Tissue was macrodissected, snap frozen, and stored at -80 degrees C.

20 Tumors were isolated, immediately snap-frozen, and sectioned, and then, the molecular dist

21 of the vastus lateralis muscle was taken and snap frozen at -80 degrees C.

22 cimens into the hydrogel matrix, followed by snap-freezing at -160 degrees C.

23 Whole brains were snap-frozen at necropsy and were subsequently sectioned

24 control and FSHD deltoid and biceps muscles, snap-frozen at resting length, were cryosectioned, indir

25 cose tolerance test, immediately followed by snap freezing before in situ analysis of metabolic pathw

26 Snap-frozen biopsies from epiglottis, supraglottis, glot

27 titative proteomics and phosphoproteomics on snap-frozen biopsies of hepatocellular carcinoma (HCC) a

28 Ninety-eight snap-frozen brain blocks from 13 SPMS cases together wit

29 ignificance of PI3K pathway activation using snap-frozen clinical specimens.

30 In this report, 10 cases of snap-frozen endemic BL tumors are characterized in terms

31 Snap-frozen FCDIIb specimens were tested for HPV DNA usi

32 and age-matched oxygen-treated animals were snap frozen for immunohistochemical analysis with antibo

33 ted LNs were divided into two parts: one was snap-frozen for OSNA and the other underwent rapidly fro

34 In comparison to snap-freezing, formalin fixation changed the relative pr

35 Tumor tissue was collected and snap-frozen from 35 sequential patients with histologica

36 DNA was extracted from snap-frozen gastric corpus tissues and 16S rRNA was sequ

37 mogeneous ex vivo tumor samples, sections of snap frozen human breast cancer murine xenografts were s

38 brain microvessel preparations isolated from snap-frozen human and mouse tissues by laser capture mic

39 Snap-frozen human prostate samples including 22 examples

40 t such spot acidification in ex vivo stained snap-frozen human squamous cell carcinoma tissue correla

41 RNA was isolated from snap-frozen IEN lesions for microarray analyses, followe

42 te (3.2%) tubes, centrifuged, and the plasma snap frozen in liquid N2 and stored at -80 degrees C.

43 kidneys (n = 4, each group) were harvested, snap frozen in liquid nitrogen, and analyzed for CaR mes

44 Tissues from mice were collected, snap frozen in liquid nitrogen, and stored at -80 degree

45 (n=10) or recirculating perfusion (n=8), and snap frozen in liquid nitrogen.

46 Snap-freezing in isopentane preserved tissue morphology

47 energetic state than does the commonly used snap-freezing in liquid nitrogen.

48 sh specimens of 62 periampullary tumors were snap-frozen in liquid nitrogen and adjacent tissue was f

49 Resected tumor was snap-frozen in liquid nitrogen and AGT activity analyzed

50 re separated from the globes and immediately snap-frozen in liquid nitrogen at -70 degrees C.

51 The left atrial appendage (LAA) was snap-frozen in situ after pacing (640 bpm) for 3 minutes

52 ammation-dependent way, and investigated 299 snap-frozen intestinal biopsies from inflamed and non-in

53 al hepatic gene expression was determined in snap-frozen liver biopsy specimens from 4 groups: (1) pa

54 cific CD8(+) T cells in peripheral blood and snap-frozen liver biopsy specimens of two chimpanzees (P

55 of protein targets in commercially available snap-frozen lung, liver, kidney, and spleen of European

56 similar studies, our data were obtained from snap-frozen needle HCC biopsies (n=52) matched with thei

57 patients underwent colectomy and harvest and snap-freezing of normal mucosa, adenoma, and carcinoma.

58 leus-plantaris muscle group was isolated and snap frozen, or underwent 30 min of electrically evoked

59 Eyes were enucleated, dissected, and snap-frozen, or they were fixed for histology.

60 more efficiently than long amplicons both in snap-frozen (P = 0.0006) and FFPE (P = 0.0152) tissues.

61 A, total RNA, and protein were isolated from snap-frozen pieces of duodenal biopsy samples from CVID

62 tumors, we sequenced RNA transcripts in five snap frozen retinoblastomas which invaded the optic nerv

63 njection, at which time brains were removed, snap frozen, sectioned and quantitatively analyzed for f

64 eated mice bearing HER2 + breast tumors were snap-frozen, sectioned, and imaged using autoradiography

65 rectus EOMs attached and TAs were dissected, snap frozen, serially sectioned, and stained for acetylc

66 oduced results similar to that obtained from snap-frozen specimens, although the protein quantity was

67 y acid profiles compared against immediately snap-frozen stool.

68 Fresh snap-frozen strips from the central and peripheral parts

69 Snap-frozen STS specimens from 65 patients were analyzed

70 reperfusion, LPO was determined by assay of snap frozen tissue for thiobarbituric acid (TBA) concent

71 ures of normal human OSE, EOC cell lines and snap frozen tissue from EOCs.

72 eeze-fracture electron microscopy of unfixed snap-frozen tissue samples confirmed this supramolecular

73 c analysis of 48 patients with GISTs who had snap-frozen tissue was performed.

74 Snap-frozen tissue was processed and analyzed by Sciex 6

75 E tissue and can generate similar results as snap-frozen tissue.

76 anomas, using early-passage cell strains and snap-frozen tissues (n = 18 and n = 24, respectively) co

77 with low protein synthesis rates, including snap-frozen tissues and immune cells from an individual'

78 RNA and DNA were extracted from a snap frozen tumor sample with a fraction of cancer cells