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標(biāo)題: Titlebook: Dipeptidyl Aminopeptidases; Basic Science and Cl Uwe Lendeckel,Dirk Reinhold,Ute Bank Conference proceedings 2006 The Editor(s) (if applica [打印本頁(yè)]

作者: 密度 時(shí)間: 2025-3-21 16:42
書(shū)目名稱Dipeptidyl Aminopeptidases影響因子(影響力)

書(shū)目名稱Dipeptidyl Aminopeptidases影響因子(影響力)學(xué)科排名

書(shū)目名稱Dipeptidyl Aminopeptidases網(wǎng)絡(luò)公開(kāi)度

書(shū)目名稱Dipeptidyl Aminopeptidases網(wǎng)絡(luò)公開(kāi)度學(xué)科排名

書(shū)目名稱Dipeptidyl Aminopeptidases被引頻次

書(shū)目名稱Dipeptidyl Aminopeptidases被引頻次學(xué)科排名

書(shū)目名稱Dipeptidyl Aminopeptidases年度引用

書(shū)目名稱Dipeptidyl Aminopeptidases年度引用學(xué)科排名

書(shū)目名稱Dipeptidyl Aminopeptidases讀者反饋

書(shū)目名稱Dipeptidyl Aminopeptidases讀者反饋學(xué)科排名

作者: 裝飾 時(shí)間: 2025-3-21 21:51

作者: euphoria 時(shí)間: 2025-3-22 03:25

作者: 懦夫 時(shí)間: 2025-3-22 06:16

作者: 廣告 時(shí)間: 2025-3-22 09:57
Dipeptidyl Peptidase 8 Has Post-Proline Dipeptidyl Aminopeptidase and Prolyl Endopeptidase Activitiewere inhibited by the irreversible DPIV inhibitor ValboroPro. These data indicate that DP8 is a multifunctional enzyme and that therapeutics based on DPIV inhibition should be counter-screened against DP8.

作者: ARCH 時(shí)間: 2025-3-22 15:32

作者: ARCH 時(shí)間: 2025-3-22 17:29

作者: 符合國(guó)情 時(shí)間: 2025-3-22 23:03
Species of Aphytis of the World HN digestion. Consequently, PEP-inhibition might be a new target for apoptosis prevention..This study further uncovered a so far unknown enzymatic specificity for a post-cysteine cleavage of the mammalian exopeptidases DP2, DP4, DP8 and DP9 and the endopeptidase PEP.

作者: 侵略者 時(shí)間: 2025-3-23 01:34
Ekaterina Isaeva,Olga Baiburovar with DPIV to make a model based on two enzymatically active proteins. Simulated docking of substrates and inhibitors into the model may uncover subtle differences between the structures. This may aid in determining the reason for DP8’s multiple enzyme functionality and aid in the improvement of DPIV inhibitor specificity.

作者: shrill 時(shí)間: 2025-3-23 06:13
Michael F. Allen,Brent D. Mishlerific inhibition of DPIV and AAPs via small molecular compounds provides a new approach for the pharmacological treatment of autoimmune and inflammatory diseases that simultaneously interferes with two major axis of T cell function.

作者: Dissonance 時(shí)間: 2025-3-23 13:31

作者: 沒(méi)有希望 時(shí)間: 2025-3-23 15:09

作者: 我沒(méi)有命令 時(shí)間: 2025-3-23 20:40

作者: Generosity 時(shí)間: 2025-3-23 23:06
Species of Aphytis of the Worldwere inhibited by the irreversible DPIV inhibitor ValboroPro. These data indicate that DP8 is a multifunctional enzyme and that therapeutics based on DPIV inhibition should be counter-screened against DP8.

作者: Canopy 時(shí)間: 2025-3-24 06:25
Conference proceedings 2006 options have become imminent. The sections of the book will focus on various topics including DP IV and related enzymes in: expression and function, metabolic disorders, immune mechanisms and immune disorders, neuronal diseases and cancer, and related drug development. .

作者: impaction 時(shí)間: 2025-3-24 06:33
Ekaterina Isaeva,Olga Baiburovacant structural conservation in the catalytic triad between DPIV, PEP and ACPH. Further analysis is required to determine whether any differences in the substrate pockets or substrate access tunnel(s) may contribute to DP8’s ability to act as a dipeptidyl peptidase, endopeptidase and acylaminoacyl p

作者: Verify 時(shí)間: 2025-3-24 11:34

作者: connoisseur 時(shí)間: 2025-3-24 17:37
Species Diversity of Animals in Japane expression levels, DP8 and DP9 overexpression in transfected cells was quantified by expressing green fluorescent protein fusion proteins. We found that, like DPIV and FAP, cells overexpressing DP8 and DP9 exhibit behavioral changes in the presence of ECM components. We demonstrated that these eff

作者: 相一致 時(shí)間: 2025-3-24 20:20

作者: 排名真古怪 時(shí)間: 2025-3-25 01:09

作者: BILIO 時(shí)間: 2025-3-25 06:41

作者: 無(wú)瑕疵 時(shí)間: 2025-3-25 08:24

作者: amyloid 時(shí)間: 2025-3-25 14:04

作者: 扔掉掐死你 時(shí)間: 2025-3-25 17:22

作者: 多骨 時(shí)間: 2025-3-25 23:26

作者: 本能 時(shí)間: 2025-3-26 03:04
http://image.papertrans.cn/e/image/280552.jpg

作者: Immobilize 時(shí)間: 2025-3-26 05:09

作者: Aggrandize 時(shí)間: 2025-3-26 10:25
Geographic Variation in Primates of the relative contributions of GIP and GLP-1 to the glucose lowering activity of DP IV inhibition have been made, however, experimental data is required for conclusive resolution of this point. Only specifically designed studies can answer this question using selective antagonists of either the G

作者: Seizure 時(shí)間: 2025-3-26 16:22

作者: 擁護(hù) 時(shí)間: 2025-3-26 17:16
Phosphorus-Containing Inhibitors of Proteolytic Enzymes

作者: 慷慨不好 時(shí)間: 2025-3-27 00:29
Biochemical Properties of Recombinant Prolyl Dipeptidases DPP-IV and DPP8

作者: 警告 時(shí)間: 2025-3-27 01:36

作者: 非秘密 時(shí)間: 2025-3-27 07:42
In Vivo Effects of a Potent, Selective Dppii Inhibitor

作者: 膠狀 時(shí)間: 2025-3-27 11:14
Expression of Dipeptidyl Peptidase IV-Like Enzymes in Human Peripheral Blood Mononuclear Cells

作者: bonnet 時(shí)間: 2025-3-27 16:18
Distribution of Dipeptidyl Peptidase Iv-Like Activity Enzymes in Canine and Porcine Tissue Sections

作者: 小溪 時(shí)間: 2025-3-27 21:00

作者: 外星人 時(shí)間: 2025-3-28 00:54

作者: 幼兒 時(shí)間: 2025-3-28 05:09
Structure and Function in Dipeptidyl Peptidase IV and Related Proteinsrts are confounded by the ubiquitous expression of DPIV, inhibitor selectivity questions and the variety of identified substrates. DPIV is not essential, but is such a useful enzyme that all animal species express it. The enzyme activity’s ancient and primary function is probably nutritional, provid

作者: 瑣事 時(shí)間: 2025-3-28 07:28

作者: Thyroxine 時(shí)間: 2025-3-28 14:01
Dipeptidyl Peptidase 8 Has Post-Proline Dipeptidyl Aminopeptidase and Prolyl Endopeptidase Activitieifically has both prolyl dipeptidyl aminopeptidase and PEP activities. DPIV inhibitors varied in their selectivity against DP8 but all DP8 activities were inhibited by the irreversible DPIV inhibitor ValboroPro. These data indicate that DP8 is a multifunctional enzyme and that therapeutics based on

作者: Offstage 時(shí)間: 2025-3-28 15:46
Prolyl Endopeptidase Cleaves the Apoptosis Rescue Peptide Humanin and Exhibits an Unknown Post-Cystestrated in cell extract resulting in the inactivation of this potentially apoptosis-related factor. These findings lead to the hypothesis of a PEP-mediated control of HN homeostasis maintaining neuronal cell survival. This implicates a novel use of PEP inhibitors potentially preventing intracellular

作者: 平躺 時(shí)間: 2025-3-28 20:40