ライフサイエンスコーパス: immune tissue

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

2 evelopment and its maintenance in peripheral immune tissue.

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

4 hages compared with lymphoid cells and whole immune tissues.

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

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

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

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

9 l alterations in the epigenetic landscape of immune tissues.

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

11 7H/B7RP-1 is expressed on B cells and in non-immune tissues after injection of lipopolysaccharide int

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 The immune tissue printing method also highlights the detail

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

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

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

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

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

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

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

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

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

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

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

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

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