關於「NOD like receptor 中文」標籤，搜尋引擎有相關的訊息討論：

The Nod-Like Receptor (NLR) Family: A Tale of Similarities and ...。

2008年4月30日 · Albrecht M, Takken FL (2006) Update on the domain architectures of NLRs and R proteins. Biochem Biophys Res Commun 339: 459–462. View Article ...。

Function of Nod-like Receptors in Microbial Recognition and Host ...。

NLRs are expressed in many cell types including immune cells and epithelial cells, although certain NLR family members are expressed primarily in phagocytes ...： tw | tw。

NOD-like receptor signaling beyond the inflammasome - NCBI。

Whereas the membrane-bound Toll-like receptors (TLRs) survey the extracellular milieu, members of the RIG-I-like receptors (RLRs) and NOD-like receptor (NLR) ...： 。

Polymorphisms in Toll-like receptor genes and risk of cancer - Nature。

2008年1月7日 · Hold GL, Rabkin CS, Chow WH, Smith MG, Gammon MD, Risch HA et al. (2007). A functional polymorphism of toll-like receptor 4 gene increases risk ...。

Functions of NOD-Like Receptors in Human Diseases - Frontiers。

2013年10月16日 · Genome-wide association studies (GWASs) have identified a number of risk alleles encompassing NLR genes in a host of diseases including ...： 。

Detection of Bacterial Membrane Vesicles by NOD-Like Receptors。

NLR activation is a key driver of inflammation in the host, and BMVs derived from both pathogenic and commensal bacteria have been shown to package PG and ...： 。

Nod-like receptors - 政府研究資訊系統GRB。

關鍵字：巨噬細胞；Tol -like receptor 訊息傳導；Zfand5. 敗血症仍是加護病房死因的前幾名，可是目前 ... Nod-Like Receptors (NLRs) 及NLR發炎體之結構及功能分析.。

NOD-Like Receptors: Versatile Cytosolic Sentinels。

Nucleotide binding oligomerization domain (NOD)-like receptors are cytoplasmic pattern-recognition receptors that together with RIG-I-like receptor ...。

Marine Organisms as Model Systems in Biology and Medicine。

... Rast JP (2012) Dynamic evolution of toll-like receptor multigene families ... Foret TW (2006) Non-parasitc symbioses between echinoderms and bacteria.。

Probiotics in Mental Health。

Toll-like receptor mRNA expression is selectively increased in the colonic mucosa of two animal models relevant to irritable bowel syndrome.