ライフサイエンスコーパス: major tissue

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

23 tions may trigger hepatic regeneration after major tissue loss.

24 regeneration following combined ischemia and major tissue loss.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 AtCpNIFS is expressed in all major tissue types.

51 The cholesterol contents of major tissues were not altered.