ライフサイエンスコーパス: major tissue

1 had superior predictions of DE to tumors and major tissues.

2 d the mGRN+ into multiple modules across six major tissues.

3 y, such TTFL-based clocks are present in all major tissues across the organism, and the SCN is their

4 own of Mct6 (Slc16a5) gene expression in all major tissues analyzed when normalized to Mct6(+/+) mice

5 SM/PCA analysis suggested edge effects along major tissue and cerebrospinal fluid boundaries, indicat

6 We find that all major tissues and developmental stages are represented i

7 n the measurement of fluoro-DOPA activity in major tissues and in the bladder contents in humans afte

8 gical analysis did not reveal any defects in major tissues and organs, including the primary and seco

9 d muscles, which have been identified as the major tissues and/or cells that display high and variabl

10 widely distributed but concentrated in some major tissues, and rapidly excreted first through urine

11 show that it corrects IKBKAP splicing in all major tissues assayed, including the brain.

12 sent in the Brassicaceae representatives are major tissue asymmetries in cell wall structural compone

13 e Raman data acquired unveils the changes of major tissue biochemicals (e.g., triolein, elastin, kera

14 rum of known 3-hydroxyproline sites from all major tissue collagen types.

15 lubility protein-enriched fractions (LSF) of major tissues collected from mice of 6, 15, 24, and 30 m

16 In principle, the proportion of each major tissue component can be estimated from the profili

17 , we resolved the contributions of these two major tissue components toward impeding diffusive transp

18 egression models for in silico prediction of major tissue components.

19 The study highlights the potential for harm (major tissue damage and bone fractures) when commonly fo

20 The liver and the spleen were major tissue distribution sites.

21 spectra of NAD(P)H and collagen, two of the major tissue fluorophores.

22 l glucose metabolism renders the intestine a major tissue for glucose disposal, contributing to the i

23 Although skeletal muscle is the major tissue for insulin-mediated glucose disposal, litt

24 tu hybridization, the thymus appears to be a major tissue for retroviral expression in both larval an

25 We now show that T cells of the major tissue gamma/delta T cell subset recognize nonpoly

26 x project, containing 16 704 samples from 30 major tissues in six age groups ranging from 20 to 79 ye

27 y overexpressed in SSc dermal fibroblasts, a major tissue involved in disease pathogenesis.

28 more abundantly than that for CaT2 in three major tissues involved in transcellular calcium transpor

29 clinical safety, biodistribution across all major tissues, knee histopathology, and analgesic effica

30 regenerative capacity of fatty livers after major tissue loss is unknown.

31 is the only solid organ that can respond to major tissue loss or damage by regeneration to restore l

32 the regenerative capacity of the liver after major tissue loss remain unclear.

33 tions may trigger hepatic regeneration after major tissue loss.

34 regeneration following combined ischemia and major tissue loss.

35 Hepatic Kupffer cells (KC), the major tissue macrophage population, produce the septic r

36 ning cells in this tissue and possibly other major tissues, namely, epidermis and tracheal matrix.IMP

37 Additionally, radiation absorbed doses for major tissues of human were calculated based on the mous

38 apid release and purification of nuclei from major tissues of post-embryonic animals by fluorescence-

39 coelomic sacs of the larvae, from which the major tissues of the adult rudiment are derived.

40 rheumatoid arthritis, frequently target one major tissue/organ despite the systemic nature of the im

41 e abrupt developmental transitions involving major tissue remodeling, but the links with metabolic ch

42 s work, based on a carefully selected set of major tissues representing diverse stages of maize devel

43 n the proximal colon, which we found to be a major tissue reservoir of MNV persistence, suggesting th

44 together, inflammatory M4-macrophages form a major tissue reservoir of replication-competent HIV-1, w

45 Skeletal muscle is the major tissue responsible for insulin-stimulated glucose

46 Because skeletal muscle is the major tissue responsible for insulin-stimulated glucose

47 and intercellular communication that directs major tissue restructuring and the shift out of a dorman

48 on-islet neuroendocrine origin, and no other major tissue source of the mRNA was found.

49 hat cholesterol 24-hydroxylase constitutes a major tissue-specific pathway for cholesterol turnover i

50 We focused our analysis on three major tissue subgroups: frontal cortex (available from 4

51 Vdelta1 T cells, the major tissue subset, are unaffected by phosphoantigen ag

52 a simple conserved body plan based on three major tissue systems: the epidermal (L1), sub-epidermal

53 ernal RNA, early blastula, the time at which major tissue territories are specified, early and late g

54 signals play a crucial role in establishing major tissue territories in early embryos.

55 of various cells, and skeletal muscle is the major tissue that expresses MG53.

56 oughout gestation and in postnatal stages in major tissues that are known or predicted to be derived

57 mized rat skeletal muscle and liver, the two major tissues that degrade branched-chain amino acid was

58 es revealed that white and brown adipose are major tissues that express CTRP11, and its expression is

59 ian grinding dentitions are composed of four major tissues that wear differentially, creating coarse

60 tegrated with expression profiles across all major tissues to provide spatial classification of all p

61 amino acids 350 to 430 of VP1 function as a major tissue tropism determinant.

62 Xenopus tadpoles can fully regenerate all major tissue types following tail amputation.

63 the underlying substrate, is one of the four major tissue types in adult organisms.

64 Application to mouse embryos revealed major tissue types in early organogenesis as well as fin

65 of silver birch (Betula pendula) into eight major tissue types, and characterized these by a combine

66 dicates that AtCUTA mRNA is expressed in all major tissue types.

67 AtCpNIFS is expressed in all major tissue types.

68 d from more than 30,000 patients covering 31 major tissue types.

69 H&E-stained WSIs (>77 TB of data) across 20 major tissue types.

70 r-specific PCB body burden was quantified in major tissues using GC-MS/MS.

71 The cholesterol contents of major tissues were not altered.

72 nsive pharmacokinetics measurement of mAb in major tissues with a LC-MS-based method, where interesti