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monde    音标拼音: [m'ɑnd]
n. 时髦社会;上流社会;交际范围

时髦社会;上流社会;交际范围

Monde \Monde\ (m[^o]Nd), n. [F. See {Mundane}.]
The world; a globe as an ensign of royalty. [R.] --A.
Drummond.
[1913 Webster]

{Le beau monde} [F.], fashionable society. See {Beau monde}.


{Demi monde}. See {Demimonde}.
[1913 Webster]


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  • AAV-Sparcl1 promotes hair cell regeneration by increasing supporting . . .
    Chai and colleagues demonstrated that the secretory protein Sparcl1 plays a critical role in hair cell regeneration by acting as a reprogramming factor for supporting cells, revealing a connection between the extracellular matrix and inner ear hair cell regeneration, which promotes the development of gene therapy approaches for hearing restoration
  • SPARCL1 - Wikipedia
    SPARC-like protein 1 (SPARCL1 or SC1), also known as hevin (short for high endothelial venule protein), is a secreted protein with high structural similarity to SPARC [5] [6] Biology It interacts with the extracellular matrix to create intermediate states of cell adhesion [7]
  • Matricellular protein SPARCL1 regulates tumor microenvironment . . . - JCI
    At present, antiangiogenic therapy is the major stromal cell–directed therapy This approach is based on the concept that tumor growth requires angiogenesis Among other reasons, SPARCL1 is a member of the SPARC family of secreted matricellular proteins, together with SPARC osteonectin, SMOCs, testicans,
  • SPARCL1 Gene - GeneCards | SPRL1 Protein | SPRL1 Antibody
    SPARCL1 (SPARC Like 1) is a Protein Coding gene Diseases associated with SPARCL1 include Stromal Corneal Dystrophy and Amelogenesis Imperfecta, Type Ie Among its related pathways are Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) and Metabolism of proteins Gene Ontology (GO) annotations related to this gene include
  • SPARCL1 sparkles new insight into corneal dystrophies - Nature
    The variant and gene, SPARCL1, indeed is a possible cause for corneal dystrophies-genetic testing and therapy Cornea 2022;41:1337–44 2 Weiss JS, Rapuano CJ, Seitz B, Busin M, Kivela TT
  • Profile and clinical significance of SPARCL1 and its prognostic . . .
    verification can provide insights into the role of SPARCL1 in breast cancer pathogenesis and its potential as a biomarker for the disease However, further investigations are warranted to validate these findings and provide a more comprehensive understanding of the implications of SPARCL1 therapy in patients with breast cancer Introduction
  • Androgen-Regulated SPARCL1 in the Tumor Microenvironment Inhibits . . .
    Sparcl1 − − 129 SvEv mice (n = 18) who did not receive therapy prior to radical prostatectomy (NT) and cases (n = 46) who were treated with a luteinizing hormone-releasing hormone agonist (antiandrogen therapy) before sampling at RP was examined for SPARCL1 expression by IHC I,
  • SPARCL1 Gene: Function, Expression, and Role in Disease - Mapmygenome
    The SPARCL1 (SPARC like 1) is a protein-coding gene located on chromosome 4 SPARC-like protein 1 (SPARCL1 or SC1), also known as hevin (short for high endothelial venule protein), is a secreted protein with high structural similarity to SPARC It interacts with the extracellular matrix to create intermediate states of cell adhesion
  • AAV-Sparcl1 promotes hair cell regeneration by increasing supporting . . .
    RNA-seq analysis revealed that Sparcl1 overexpression stimulates supporting cell proliferation via follistatin (Fst) activation and extracellular matrix (ECM) remodeling Notably, both AAV-ie-Sparcl1 delivery and recombinant Sparcl1 protein administration effectively induced supporting cell differentiation into hair cells in vivo
  • Sparcl1 and Atherosclerosis | JIR - Dove Medical Press
    Sparcl1, also known as Hevin, SC1, and ECM2, belongs to the SPARC family, an extracellular matrix protein family involved in the regulation of cell adhesion, Everett BM, Thuren T, et al Antiinflammatory therapy with canakinumab for atherosclerotic disease N Engl J Med 2017;377:1119–1131 14 Ait-Oufella H, Salomon BL, Potteaux S, et al





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