ライフサイエンスコーパス: immune tissue

1 d and compared to those of Envs derived from immune tissue.

2 evelopment and its maintenance in peripheral immune tissue.

3 ceramide and its mRNA is highly expressed in immune tissues.

4 rong repression of IGF-signalling in primary immune tissues.

5 hages compared with lymphoid cells and whole immune tissues.

6 lieve this reflects the absence of CYP1B1 in immune tissues.

7 and is abundantly expressed in brain and in immune tissues.

8 g and gain access to both local and systemic immune tissues.

9 se-1 mediated IL-1beta production in chicken immune tissues.

10 omes correlated with fluorescence, except in immune tissues.

11 heterologously expressed in D. melanogaster immune tissues.

12 l alterations in the epigenetic landscape of immune tissues.

13 7H/B7RP-1 is expressed on B cells and in non-immune tissues after injection of lipopolysaccharide int

14 This receptor is expressed in immune tissues, although its potential function in immun

15 associations specific to epigenomic marks in immune tissues and cell types, > 30 associations specifi

16 s both pro- and anti-inflammatory effects on immune tissues and cells.

17 istinctive splice variants were expressed in immune tissues and cells.

18 cytes, is limited in expression to primarily immune tissues and genetically maps to a region of susce

19 H(v)1 is expressed in immune tissues and manifests the characteristic properti

20 n (GILZ) is expressed in both epithelial and immune tissues and modulates a variety of cellular funct

21 ferentially spliced in the brain relative to immune tissues, and 6.6% of these showed major splicing

22 nocyte-built tissues than in macrophages and immune tissues, and DNA-driven response genes were not i

23 and IgD(+) plasma cells were detected in all immune tissues at a lower frequency than secretory IgM.

24 em (CNS)-associated lymph nodes and systemic immune tissues between genetic models and wildtype mice,

25 ew areas in the body where blood vessels and immune tissues can readily be observed from outside the

26 tential role in AD, and characterizing their immune-tissue/cell-specific expression, we leveraged pub

27 sinophils and mast cells (type 2) and to non-immune tissue cells, including the stroma and epithelium

28 hereas one major splice variant prominent in immune tissues completely lacks the carboxyl-terminal do

29 chromatin structure and enhancer regulation, immune-tissue crosstalk, bioelectric and metabolic cues

30 previous data for neuro-AIDS patients where immune tissue Envs mediated a range of macrophage infect

31 rs are intensely expressed in peripheral and immune tissues, expression in brain microglia has been a

32 ophila phagocytes in the activation of other immune tissues has not been clear, we show that inductio

33 tive B cells prior to their transit to other immune tissues; however, little is known of the genes th

34 Both EMR2 and CD97 are highly expressed in immune tissues; however, unlike CD97, which is ubiquitou

35 ng loop that contribute to b12 resistance in immune tissue in vivo.

36 ssue of some individuals, and (iv) Envs from immune tissue of the N/MC individuals were nearly all ti

37 d samples analyzed tested positive with both immune tissue printing and qPCR; whereas 95% were positi

38 The immune tissue printing method also highlights the detail

39 Both the immune capture PCR and immune tissue printing methods offer the advantages of l

40 IL-32 mRNA is highly expressed in immune tissue rather than other tissues.

41 ive of tropism in the coordination of host's immune tissue responses to infection by viral or bacteri

42 A higher proportion of immune tissue-specific enhancers are TE-rich compared to

43 They are highly expressed in immune tissues (spleen, lymph node and thymus) and are m

44 osine 1-phosphate (S1P) in blood, lymph, and immune tissues stimulates and regulates T cell migration

45 y, low levels of expression were detected in immune tissues such as spleen, thymus, and peripheral bl

46 iptome can help identify mechanisms by which immune tissues, such as the thymus, respond to heat stre

47 receptor is preferentially expressed in the immune tissues, suggesting a potential role in normal im

48 es in the candidate region were expressed in immune tissues, supporting their functional relevance in

49 The expression of bfl-1 in immune tissues supports the protective role of NF-kappaB

50 ally more effective in populating peripheral immune tissue than T(reg) cells with impaired IL-2 signa

51 eptide (VIP) is a neuroendocrine mediator in immune tissues that affects many T cell functions throug

52 aternal-fetal interface to systemic maternal immune tissues that might interact with circulating EVs.

53 matrix proteins in HIV-1 biology.IMPORTANCE Immune tissues within the gut are severely damaged by HI