Relevant bibliographies by topics / DPP-IV

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'DPP-IV'

Author: Grafiati
Published: 4 June 2021
Last updated: 22 June 2024

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Journal articles on the topic "DPP-IV"

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Hildebrandt, M., W. Reutter, and J. D. Gitlin. "Tissue-specific regulation of dipeptidyl peptidase IV expression during development." Biochemical Journal 277, no. 2 (1991): 331–34. http://dx.doi.org/10.1042/bj2770331.

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The patterns of dipeptidyl peptidase (DPP) IV activity and protein amount in different rat organs during development were compared. In order to elucidate the molecular basis for these patterns, total RNA was isolated from lung and kidney at different stages of development and analysed by Northern-blot hybridization using an oligonucleotide derived from the DPP IV cDNA sequence. This oligonucleotide hybridized to two distinct mRNAs of approx. 3.2 and 4.8 kb respectively. During kidney development, the pattern for DPP IV mRNA paralleled that of DPP IV activity and protein amount, suggesting that
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Stankovic, Milan, Predrag Vlahovic, Verica Avramovic, and Miroljub Todorovic. "Distribution of Dipeptidyl Peptidase IV in Patients with Chronic Tonsillitis." Clinical and Vaccine Immunology 15, no. 5 (2008): 794–98. http://dx.doi.org/10.1128/cvi.00054-07.

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ABSTRACT In the pathogeneses of recurrent tonsillitis (RT) and tonsillar hypertrophy (TH), different immunological mechanisms are involved. Dipeptidyl peptidase IV (DPP IV) and aminopeptidase N (APN) participate in the regulation of the immune response during inflammation. In this study, the localization of DPP IV and the enzymatic activities of DPP IV and APN in 32 patients, 13 with RT and 19 with TH, who underwent tonsillectomy were investigated. The localization of DPP IV in tonsils was studied using histochemical and immunohistochemical methods. The enzymatic activities of DPP IV and APN i
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Kim, Bo-Ram, Hyo Kim, Inhee Choi, Jin-Baek Kim, Chang Jin, and Ah-Reum Han. "DPP-IV Inhibitory Potentials of Flavonol Glycosides Isolated from the Seeds of Lens culinaris: In Vitro and Molecular Docking Analyses." Molecules 23, no. 8 (2018): 1998. http://dx.doi.org/10.3390/molecules23081998.

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Dipeptidyl peptidase IV (DPP-IV), a new target for the treatment of type 2 diabetes mellitus, degrades incretins such as glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide. DPP-IV inhibitors shorten the inactivation of GLP-1, permitting the incretin to stimulate insulin release, thereby combating hyperglycemia. In our ongoing search for new DPP-IV inhibitors from medicinal plants and foods, three flavonol glycosides (1–3) were isolated from the seeds of Lens culinaris Medikus (Fabaceae) and tested for their DPP-IV–inhibitory activity. We demonstrated for the first
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Darmoul, D., C. Rouyer-Fessard, A. Blais, et al. "Dipeptidyl peptidase IV expression in rat jejunal crypt-villus axis is controlled at mRNA level." American Journal of Physiology-Gastrointestinal and Liver Physiology 261, no. 5 (1991): G763—G769. http://dx.doi.org/10.1152/ajpgi.1991.261.5.g763.

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The expression of dipeptidyl peptidase IV (DPP IV), an intestinal brush-border hydrolase, has been studied in the rat jejunum crypt-villus axis. DPP IV enzyme activity is lower in crypt cells than in villus cells. Indirect immunofluorescence studies, using a polyclonal antibody raised against purified DPP IV, show a gradient of immunoreactivity from the crypts to the villi that was quantified using confocal laser scanning microscopy. Accordingly, Western blot analysis demonstrates that the steady-state amount of DPP IV is much lower in crypt cells than in villus cells. Northern blot analysis w
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Augustyns, K., G. Bala, G. Thonusa, et al. "The Unique Properties of Dipeptidyl-peptidase IV (DPP IV I CD26) and the Therapeutic Potential of DPP IV Inhibitors." Current Medicinal Chemistry 6, no. 4 (1999): 311–27. http://dx.doi.org/10.2174/0929867306666220208213543.

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Abstract: This review deals with the properties and functions of dipeptidyl peptidase IV (DPP IV, EC 3.4.14.5). This membrane anchored ecto-protease has been identified as the leukocyte antigen CD26. The following aspects of DPP IV/CD26 will be discussed: the structure of DPP IV and the new family of serine proteases to which it belongs, the substrate specificity, the distribu­tion in the human body, specific DPP IV inhibitors and the role of CD26 in the intestinal and renal handling of proline containing peptides, in cell adhesion, in peptide metabolism, in the immune system and in HIV infect
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El- Alameey, Inas R., Hanaa H. Ahmed, and Mones M. Abushady. "Dipeptidyl Peptidase IV: A Target for Improving Metabolic Syndrome Components in Obese Children and Adolescents." Biomedical and Pharmacology Journal 12, no. 04 (2019): 1701–13. http://dx.doi.org/10.13005/bpj/1799.

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Dipeptidyl peptidase-IV (DPP-IV) is a circulating glycoprotein that reduces uptake of insulin-stimulated glucose and is related to obesity and metabolic syndrome. However, the influence of exercise and nutritional plan on serum DPP-IV in children and adolescents with metabolic syndrome remains unclear. To judge serum activity of DPP-IV in obese children and adolescents with and without metabolic syndrome, and to assess the impact of exercise, and nutritional regimen on serum DPP-IV activity, metabolic syndrome components, and insulin resistance issue in children and adolescents with obesity. T
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&NA;. "DPP-IV inhibitors/sitagliptin." Reactions Weekly &NA;, no. 1371 (2011): 15–16. http://dx.doi.org/10.2165/00128415-201113710-00052.

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Cuchacovich, Miguel, Héctor Gatica, Paula Vial, Jorge Yovanovich, Salvatore V. Pizzo, and Mario Gonzalez-Gronow. "Streptokinase Promotes Development of Dipeptidyl Peptidase IV (CD26) Autoantibodies after Fibrinolytic Therapy in Myocardial Infarction Patients." Clinical and Vaccine Immunology 9, no. 6 (2002): 1253–59. http://dx.doi.org/10.1128/cdli.9.6.1253-1259.2002.

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ABSTRACT Dipeptidyl peptidase IV (DPP IV) (CD26) plays a critical role in the modulation and expression of autoimmune and inflammatory diseases. We recently reported that sera from patients with rheumatoid arthritis and systemic lupus erythematosus contained low levels of DPP IV and high titers of anti-DPP IV autoantibodies of the immunoglobulin A (IgA) and IgG classes and found a correlation between the low circulating levels of DPP IV and the high titers of anti-DPP IV autoantibodies of the IgA class. Since streptokinase (SK) is a potent immunogen and binds to DPP IV, we speculated that pati
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Piazza, G. A., H. M. Callanan, J. Mowery, and D. C. Hixson. "Evidence for a role of dipeptidyl peptidase IV in fibronectin-mediated interactions of hepatocytes with extracellular matrix." Biochemical Journal 262, no. 1 (1989): 327–34. http://dx.doi.org/10.1042/bj2620327.

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Dipeptidyl peptidase IV (DPP IV) is a cell surface glycoprotein which has been implicated in hepatocyte-extracellular matrix interactions [Hixson, DeLourdes, Ponce, Allison & Walborg (1984) Exp. Cell Res. 152, 402-414; Walborg, Tsuchida, Weeden, Thomas, Barrick, McEntire, Allison & Hixson (1985) Exp. Cell Res. 158, 509-518; Hanski, Huhle & Reutter (1985) Biol. Chem. Hoppe-Seyler 366, 1169-1176]. However, its proteolytic substrate(s) and/or binding protein(s) which mediate this influence have not been conclusively identified. Nitrocellulose binding assays using 125I-labelled DPP IV
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Gao, Jing, Han Gong та Xueying Mao. "Dipeptidyl Peptidase-IV Inhibitory Activity and Related Molecular Mechanism of Bovine α-Lactalbumin-Derived Peptides". Molecules 25, № 13 (2020): 3009. http://dx.doi.org/10.3390/molecules25133009.

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Identifying DPP-IV inhibitory peptides from dietary protein has attracted increased attention. In the present study, bovine α-lactalbumin hydrolysates were generated by alcalase for various hydrolysis times, and DPP-IV inhibitory activity of these hydrolysates was determined. The 4 h hydrolysates displayed the most potent DPP-IV inhibitory activity, with DPP-IV inhibition rate of 82.30 ± 1.39% at concentration of 1.0 mg/mL. DPP-IV inhibitory peptides were isolated from the 4 h-hydrolysates with gel filtration chromatography and reversed-phase high-performance liquid chromatography (RP-HPLC). U
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Dissertations / Theses on the topic "DPP-IV"

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Bermpohl, Felix. "Nachweis und Charakterisierung der Endopeptidase-Aktivität der Dipeptidylpeptidase-IV (DPP IV)." [S.l.] : [s.n.], 2002. http://www.diss.fu-berlin.de/2002/191/index.html.

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Aldewachi, Hasan. "Chromogenic detection of dipeptidyl peptidase IV (DPP-IV) activity using peptide-functionalized gold nanoparticles." Thesis, Sheffield Hallam University, 2017. http://shura.shu.ac.uk/18152/.

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Metal nanoparticles offer a useful platform for a wide range of biological applications especially for biosensing, bioimaging and drug delivery. This thesis presents a body of original research describing the synthesis, characterisation and development of a novel and convenient biosensing assay for detection of dipeptidyl peptidase IV (DPP-IV) enzyme activity using peptide functionalized gold nanoparticles. The distinctive optical and physical properties of gold nanoparticles (Au NP) were harnessed for the development of a colorimetric assay for rapid sensing of DPP-IV activities and screening
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Vivier, Isabelle. "Caractérisation biochimique d'une molécule d'activation des thymocytes murins (THAM) : l'équivalent murin de CD26, une dipeptidyl peptidase IV (DPP IV)." Aix-Marseille 2, 1991. http://www.theses.fr/1991AIX22019.

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Nous avons recemment identifie une molecule (tham) impliquee dans l'activation des thymocytes murins, independamment de la reconnaissance antigenique. Tham est une structure dimerique dont le niveau d'expression a la surface des cellules lymphoides est regule au cours des etapes de la maturation intrathymique. Une identite structurale a ete observee antre tham et une ectoenzyme, la dipeptidyl peptidase 4 de rat (dpp 4). Ceci nous a conduit a faire les observations suivantes: un anticorps specifique de tham deplete en activite dpp 4 des membranes solubilisees de thymome murin; tham purifiee par
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Bourgault, Steve. "Développement d'agonistes stables du récepteur PAC1 : étude des relations structure-activité du Pituitary Adenylate Cyclase-Activating Polypeptide." Rouen, 2009. http://www.theses.fr/2009ROUES027.

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Le PACAP a été isolé pour sa capacité à stimuler la formation d'AMPc dans les cellules antéhypophysaires. Le PACAP favorise la survie neuronale, effet régulé par le récepteur PAC1. Ce récepteur est considéré comme une cible thérapeutique. Il importe donc de développer de puissants agonistes du récepteur PAC1 affichant une stabilité métabolique accrue. Afin de conférer au PACAP une résistance face à la protéolyse, une librairie d'analogues comportant des modifications chimiques ciblant les principaux sites de clivages enzymatique a été développée. Afin d'acquérir des informations pouvant souten
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Aït-Slimane, Tounsia. "Caracterisation des signaux d'adressage apical de la dipeptidylpeptidase iv (dpp iv/cd 26) : implication du domaine transmembranaire et des processus de glycosylation." Paris 6, 2000. http://www.theses.fr/2000PA066006.

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La membrane plasmique des cellules epitheliales est divisee en deux domaines distincts : le domaine apical et le domaine basolateral. L'adressage des proteines vers ces deux domaines est un mecanisme fondamental qui permet d'etablir et de maintenir la polarite cellulaire. Deux types de signaux participent a l'adressage apical des proteines : (1) les glycanes et (2) l'interaction du domaine transmembranaire avec des microdomaines enrichis en glycosphingolipides et cholesterol (les rafts). Nous avons caracterise les signaux d'adressage apical de la dipeptidyl peptidase iv (dpp iv/cd26), une prot
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HAMAJIMA, NOBUYUKI, KENJI WAKAI, GUANG YIN, et al. "DPP4 Genetic Variants Influence Baseline Prostate-Specific Antigen Levels: The J-MICC Study." Nagoya University School of Medicine, 2013. http://hdl.handle.net/2237/17603.

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Bellé, Luziane Potrich. "AVALIAÇÃO DE BIOMARCADORES INFLAMATÓRIOS E DA ATIVIDADE DA ADENOSINA DEAMINASE E DIPEPTIDIL PEPTIDASE IV EM LINFÓCITOS DE PACIENTES COM DIABETES MELITO TIPO 2." Universidade Federal de Santa Maria, 2010. http://repositorio.ufsm.br/handle/1/8975.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Diabetes mellitus is a metabolic disease characterized by hyperglycemia due defective or deficient response to insulin secretion. Type 2 diabetes mellitus (Type 2 DM) is therefore associated with a general activation of the innate immune system, in which there is a chronic, cytokine-mediated state of low-grade inflammation. Dipeptidyl peptidase IV (DPP-IV) is a cell-surface protease that bind with Adenosine deaminase (ADA) and both enzymes act in the lymphocytes proliferation and citokyne production. Vitis vinifera is a plant that
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Roy, Emilie. "Synthèse d'activateurs PPARα et d'inhibiteurs de DPP-IV pour le traitement des troubles liés à un désordre métabolique". Poitiers, 2007. http://www.theses.fr/2007POIT2253.

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Les maladies cardiovasculaires représentent l'une des causes majeures de mortalité dans les sociétés occidentales. De nombreux facteurs de risque sont associés à ces maladies, parmi lesquelles les dyslipidémies, le diabète, la resistance à l'insuline et l'obésité. Un grand intérêt est porté à l'identification de nouveaux composés pour le traitement de ces désordres métaboliques. Une première partie de ce mémoire concerne la synthèse et l'évaluation de nouveaux agonistes des récepteurs PPARα (peroxisome proliferator-activated receptor), cible largement utilisé pour le traitement des dyslipidémi
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Ostertag, Rahel [Verfasser]. "Effekte des DPP-IV Inhibitors Sitagliptin auf die Ausdehnung und Stabilität arteriosklerotischer Läsionen in Apolipoprotein E defizienten Mäusen / Rahel Ostertag." Ulm : Universität Ulm. Medizinische Fakultät, 2012. http://d-nb.info/1022896334/34.

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Martins, Michelle Cristiane Melo Reis. "Estudos de HQSAR, acoplamento molecular e cálculos de propriedades eletrônicas de compostos com atividade biológica frente aos alvos DPP-IV e FAPa." reponame:Repositório Institucional da UFABC, 2018.

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Orientadora: Profa. Dra. Káthia Maria Honório<br>Dissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Ciência e Tecnologia/Química, Santo André, 2018.<br>Um dos alvos biologicos relacionado ao controle da glicemia e a enzima dipeptidil peptidase-IV (DPP-IV); ela esta associada com a estimulacao do pancreas na producao de insulina, sendo, portanto, um alvo de interesse da pesquisa e da industria farmaceutica para o tratamento do diabetes tipo 2. O diabetes e uma doenca cronica que se caracteriza por um aumento da glicemia causando uma serie de complicacoes fisiolog
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Books on the topic "DPP-IV"

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(Organization), DPP-FBSI. Jawaban DPP-FBSI terhadap pertanyaan-pertanyaan DPA dalam pertemuan konsultatip DPP-FBSI dengan Komisi IV/Kesra DPA, Jakarta, 30 September 1980. DPP-FBSI, 1989.

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Pusat, HKTI (Organization) Dewan Pimpinan. Pokok-pokok pikiran DPP HKTI menanggapi masalah-masalah pembangunan pertanian dan pedesaan: Disampaikan dalam rapat dengar pendapat umum antara Komisi IV DPR-RI dengan DPP HKTI, tanggal 7 Juni 1994. Dewan Pimpinan Pusat, Himpunan Kerukunan Tani Indonesia, 1994.

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Venkatesham, Allenki. Role of Dipeptidyl - Peptidase IV (Dpp-IV) in Type II Diabetes. Lulu Press, Inc., 2015.

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Book chapters on the topic "DPP-IV"

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Korom, Stephan, Ingrid De Meester, A. Belyaev, Georg Schmidbauer, and Konrad Schwemmle. "CD26/DPP IV in Experimental and Clinical Organ Transplantation." In Dipeptidyl Aminopeptidases in Health and Disease. Springer US, 2004. http://dx.doi.org/10.1007/0-306-47920-6_17.

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Elble, R. C., and B. U. Pauli. "Lu-ECAM-1 and DPP IV in Lung Metastasis." In Attempts to Understand Metastasis Formation I. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61107-0_8.

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Ojeda, María José, Adrià Cereto-Massagué, Cristina Valls, Gerard Pujadas, and Gerard Pujadas. "DPP-IV, An Important Target for Antidiabetic Functional Food Design." In Foodinformatics. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-10226-9_7.

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Van Damme, J., S. Struyf, A. Wuyts, et al. "The Role of CD26/DPP IV in Chemokine Processing." In Chemical Immunology and Allergy. KARGER, 1999. http://dx.doi.org/10.1159/000058725.

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Micouin, Anne, and Brigitte Bauvois. "Expression of Dipeptidylpeptidase IV (DPP IV/CD26) Activity on Human Myeloid and B Lineage Cells, and Cell Growth Suppression by the Inhibition of DPP IV Activity." In Advances in Experimental Medicine and Biology. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-9613-1_26.

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Bertone, Vittorio, Eleonora Tarantola, and Isabel Freitas. "Enzyme-Histochemistry Technique for Visualizing the Dipeptidyl-Peptidase IV (DPP-IV) Activity in the Liver Biliary Tree." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6788-9_3.

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Jung, Florian Johannes, Markus Cardell, Lin Yang, et al. "The Role of CD26/DPP IV in Preservation of Early Pulmonary Graft Function." In Advances in Experimental Medicine and Biology. Springer US, 2006. http://dx.doi.org/10.1007/0-387-32824-6_25.

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Korom, S., I. Meester, T. H. W. Stadlbauer, et al. "Auswirkung der spezifischen CD26/Dipeptidylpeptidase IV (DPP IV)-Inhibition auf die akute Transplantatabstoßung und die Immunantwort in Allotransplantatempfängern." In Chirurgisches Forum ’97 für experimentelle und klinische Forschung. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60717-2_39.

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Piron, J., and D. Tourwé. "Stereoselective Synthesis of Transition State Analog Inhibitors of DPP-IV Using 2-Substituted Thiazoles." In Peptides: The Wave of the Future. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_67.

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Blanco, Julià, Etienne Jacotot, Christian Callebaut, Bernard Krust, and Ara G. Hovanessian. "Further Characterization of DPP IV-β, a Novel Cell Surface Expressed Protein with Dipeptidyl Peptidase Activity." In Advances in Experimental Medicine and Biology. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-9613-1_25.

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Conference papers on the topic "DPP-IV"

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Singla, Rajeev K., Satish Kumar, and Arun Garg. "Docking Studies of Epigallocatechin Gallate as Natural DPP-IV Inhibitor." In MOL2NET 2019, International Conference on Multidisciplinary Sciences, 5th edition. MDPI, 2019. http://dx.doi.org/10.3390/mol2net-05-06241.

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Kurniawan, Isman, Attariq Muhammad Kasfilla, and Nurul Ikhsan. "QSAR Study on Predicting DPP-IV Inhibitors as Anti-Diabetic Agent by using Genetic Algorithm-Support Vector Machine." In 2022 10th International Conference on Information and Communication Technology (ICoICT). IEEE, 2022. http://dx.doi.org/10.1109/icoict55009.2022.9914824.

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Johari, Surabhi, Rajeev Sharmah, and Subrata Sinha. "Ligand binding studies for DPP IV a target protein responsible for Diabetes Mellitus Type 2: Structural based approach for drug designing." In 2011 2nd National Conference on Emerging Trends and Applications in Computer Science (NCETACS). IEEE, 2011. http://dx.doi.org/10.1109/ncetacs.2011.5751401.

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Ansari, Prawej, JM A. Hannan, Yasser H. A. Abdel-Wahab, and Peter R. Flatt. "Antidiabetic and insulinotropic properties of bark of Heritiera fomes: inhibits starch digestion, protein glycation, DPP-IV activity, and glucose absorption in gut." In GA – 69th Annual Meeting 2021, Virtual conference. Georg Thieme Verlag, 2021. http://dx.doi.org/10.1055/s-0041-1736789.

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Costa, Clara dos Santos Leal, Aline Portelinha Rodrigues Cunha, Eloá Costa Cândido Fontana, Guilherme Ribeiro Ramires de Jesus, and Marcos Augusto Bastos Dias. "Natimortalidade em mulheres com diagnóstico de LES e/ou SAF em um centro de referência do município do Rio de Janeiro: um estudo descritivo do período 2009 a 2018." In 47º Congresso da SGORJ e Trocando Ideias XXVI. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/jbg-2965-3711-2023133s1092.

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Objetivo: Lúpus eritematoso sistêmico (LES) e síndrome antifosfolipídio (SAF) são doenças autoimunes que afetam principalmente mulheres, com maior prevalência durante a idade reprodutiva. A literatura descreve um aumento na morbimortalidade materna e perinatal associada a essas condições. Método: Este estudo foi descritivo e analisou os casos de óbitos fetais (OF) em mulheres com diagnóstico de LES e/ou SAF em um centro de referência (CR) para atendimento de mulheres com morbidades graves no ciclo gravídico-puerperal no estado do Rio de Janeiro. Selecionaram-se os casos de gestações que result
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Baba, Waqas, and Sajid Maqsood. "Enhancing techno-functional and bioactive properties of whey proteins by conjugation with quercetin using combined treatment of redox pair and ultrasonication." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jtxr7155.

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Camel whey-quercetin conjugates were fabricated via free radicals using a combination of ultrasonication treatment and a redox-pair (ascorbic acid/H2O2). Conjugation of whey with quercetin was confirmed using UV-Vis. spectroscopy, FTIR and SDS-PAGE. UV-Visible spectroscopy showed a bathochromic shift and appearance of a hump around ≈350 nm (absent in whey sample) that can be attributed to binding of quercetin with whey protein. As indicated by FTIR, the association of whey with quercetin took place via covalent (appearance of new peak at 3399 cm-1) as well as noncovalent linkages (shift-ing of
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