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Relevant bibliographies by topics / Hyaluronidase

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Academic literature on the topic 'Hyaluronidase'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Hyaluronidase"

1

Reitinger, Stephan, Gerhard Thomas Laschober, Christine Fehrer, Brigitte Greiderer, and Günter Lepperdinger. "Mouse testicular hyaluronidase-like proteins SPAM1 and HYAL5 but not HYALP1 degrade hyaluronan." Biochemical Journal 401, no. 1 (2006): 79–85. http://dx.doi.org/10.1042/bj20060598.

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Besides SPAM1 (sperm adhesion molecule 1; formerly named PH-20), further hyaluronidase-like proteins, HYAL5 (hyaluronoglucosaminidase 5) and HYALP1 (hyaluronoglucosaminidase pseudogene 1) are also expressed in murine testicular tissue. As they share a high degree of sequence similarity with known hyaluronidases, all three polypeptides could potentially exhibit hyaluronidase activity, a function that is beneficial for spermatozoa in order to penetrate the hyaluronan-rich cumulus, which surrounds the oocyte. Recently, it was reported that SPAM1-deficient mice are fertile and spermatozoa derived

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Hart, Mark E., Morgan J. Hart, and Anna J. Roop. "Genotypic and Phenotypic Assessment of Hyaluronidase among Type Strains of a Select Group of Staphylococcal Species." International Journal of Microbiology 2009 (2009): 1–8. http://dx.doi.org/10.1155/2009/614371.

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Hyaluronidases degrade hyaluronic acid, a major polysaccharide of the extracellular matrix of tissues, and are considered important for virulence in a number of Gram-positive and -negative bacteria. The purpose of the present study was to determine the prevalence of hyaluronidase among clinical strains ofStaphylococcus aureusand among otherStaphylococcusspecies. Spent media and chromosomal DNA were assessed for hyaluronidase activity and the absence or presence of a hyaluronidase gene (hysA) by Southern analysis, respectively. AllS. aureusstrains examined exhibited at least one hybridizing ban

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Maji, Debnath, Verónica Miguela, Andrew D. Cameron, et al. "Enhancing In Vivo Electroporation Efficiency through Hyaluronidase: Insights into Plasmid Distribution and Optimization Strategies." Pharmaceutics 16, no. 4 (2024): 547. http://dx.doi.org/10.3390/pharmaceutics16040547.

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Electroporation (EP) stands out as a promising non-viral plasmid delivery strategy, although achieving optimal transfection efficiency in vivo remains a challenge. A noteworthy advancement in the field of in vivo EP is the application of hyaluronidase, an enzyme with the capacity to degrade hyaluronic acid in the extracellular matrix, which thereby enhances DNA transfer efficiency by 2- to 3-fold. This paper focuses on elucidating the mechanism of hyaluronidase’s impact on transfection efficiency. We demonstrate that hyaluronidase promotes a more uniform distribution of plasmid DNA (pDNA) with

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Helm II, Standiford. "Hyaluronidase in Neuroplasty: A Review." November 2019 6, no. 22;6 (2019): E555—E560. http://dx.doi.org/10.36076/ppj/2019.22.e555.

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Background: Neuroplasty, also known as percutaneous adhesiolysis, is an effective treatment for persistent axial and radicular pain. Objectives: One issue of concern is whether hyaluronidase should be used when performing neuroplasty. The objective of this narrative review is to evaluate the current literature relating to hyaluronidase and its role in neuroplasty. Methods: The literature relating to hyaluronidase was examined via a search of PubMed and Google Scholar until April 2019, review of the citations of relevant literature, and the authors’ knowledge of the literature and activity in t

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Botzki, Alexander, Daniel J. Rigden, Stephan Braun, et al. "l-Ascorbic Acid 6-Hexadecanoate, a Potent Hyaluronidase Inhibitor." Journal of Biological Chemistry 279, no. 44 (2004): 45990–97. http://dx.doi.org/10.1074/jbc.m406146200.

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Hyaluronidases are enzymes that degrade hyaluronan, an important component of the extracellular matrix. The mammalian hyaluronidases are considered to be involved in many (patho)physiological processes like fertilization, tumor growth, and metastasis. Bacterial hyaluronidases, also termed hyaluronate lyases, contribute to the spreading of microorganisms in tissues. Such roles for hyaluronidases suggest that inhibitors could be useful pharmacological tools. Potent and selective inhibitors are not known to date, althoughl-ascorbic acid has been reported to be a weak inhibitor ofStreptococcus pne

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Bharathi, A. Christian, Pradeep Kumar Yadav, and B. Syed Ibrahim. "Sequence diversity and ligand-induced structural rearrangements of viper hyaluronidase." Molecular BioSystems 12, no. 4 (2016): 1128–38. http://dx.doi.org/10.1039/c5mb00786k.

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The study focuses on ligand-induced structural changes of viper hyaluronidase and also provides insight into structure-based drug design for eukaryotic hyaluronidases, which could be future drug targets in cancer treatment, and venom spreading.

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Schmaus, Anja, Sofia Spataro, Paul Sallmann, et al. "A Novel, Cell-Compatible Hyaluronidase Activity Assay Identifies Dextran Sulfates and Other Sulfated Polymeric Hydrocarbons as Potent Inhibitors for CEMIP." Cells 14, no. 2 (2025): 101. https://doi.org/10.3390/cells14020101.

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Hyaluronan (HA) levels are dynamically regulated homeostatically through biosynthesis and degradation. HA homeostasis is often perturbed under disease conditions. HA degradation products are thought to contribute to disease pathology. The hyaluronidase CEMIP requires the presence of living cells for its HA depolymerizing activity. CEMIP is overexpressed in a variety of pathological conditions, and the inhibition of its hyaluronidase activity therefore has therapeutic potential. To identify novel inhibitors of the CEMIP hyaluronidase activity, we established here a cell-compatible, medium-throu

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Yamamoto, Hayato, Yuki Tobisawa, Toshihiro Inubushi, Fumitoshi Irie, Chikara Ohyama, and Yu Yamaguchi. "A mammalian homolog of the zebrafish transmembrane protein 2 (TMEM2) is the long-sought-after cell-surface hyaluronidase." Journal of Biological Chemistry 292, no. 18 (2017): 7304–13. http://dx.doi.org/10.1074/jbc.m116.770149.

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Hyaluronan (HA) is an extremely large polysaccharide (glycosaminoglycan) involved in many cellular functions. HA catabolism is thought to involve the initial cleavage of extracellular high-molecular-weight (HMW) HA into intermediate-size HA by an extracellular or cell-surface hyaluronidase, internalization of intermediate-size HA, and complete degradation into monosaccharides in lysosomes. Despite considerable research, the identity of the hyaluronidase responsible for the initial HA cleavage in the extracellular space remains elusive. HYAL1 and HYAL2 have properties more consistent with lysos

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Dzgoev, S. G. "Modeling of rheumatoid arthritis is accompanied by a change in the cortico-papillary ratio of hyaluronidase activity of the kidneys." Nephrology (Saint-Petersburg) 27, no. 3 (2023): 86–91. http://dx.doi.org/10.36485/1561-6274-2023-27-3-86-91.

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Background. Rheumatoid arthritis is a disease that is accompanied by impaired kidney function in most patients, which attracts the attention of researchers to this problem. Both in the joints and in the kidneys, hyaluronic acid plays an important role, the degree of polymerization of which depends on the functioning of these organs. The degradation of hyaluronic acid by hyaluronidases may be a factor involved in the development of the inflammatory process in rheumatoid arthritis as well as in the realization of osmoregulatory functions of the body. In this regard, the purpose of this work was

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Steiner, Bret, Sandra Romero-Steiner, Donna Cruce, and Robert George. "Cloning and sequencing of the hyaluronate lyase gene fromPropionibacterium acnes." Canadian Journal of Microbiology 43, no. 4 (1997): 315–21. http://dx.doi.org/10.1139/m97-044.

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The hyaluronate lyase (hyaluronidase) gene from Propionibacterium acnes was cloned and sequenced. The gene was isolated on an EcoRI-generated 3-kb piece of DNA. Expression was less in Escherichia coli than in P. acnes; in E. coli, active enzyme was only cell associated and not secreted. The gene is 2256-bp long and codes for a protein of 82 kDa. Amino terminal sequencing of the protein of the partially purified gene indicated the presence of a 32-amino-acid leader sequence. The leader sequence showed a membrane-spanning domain and all of the features usually associated with the leader for a se

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Dissertations / Theses on the topic "Hyaluronidase"

1

Lace, D. "Studies on modified hyaluronidase." Thesis, Bucks New University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384600.

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Savitsky, M. J. "Studies on mammalian hyaluronidase enzymes." Thesis, Bucks New University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.382493.

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Lo, Bello M. "Studies on human placental hyaluronidase." Thesis, Cranfield University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385849.

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Joy, M. B. "Studies on the hyaluronidase of animal origin." Thesis, Bucks New University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376418.

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Ibberson, Carolyn Brook. "Hyaluronidase in Staphylococcus aureus physiology and pathogenesis." Diss., University of Iowa, 2015. https://ir.uiowa.edu/etd/5778.

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Staphylococcus aureus encodes for a secreted hyaluronidase, hysA. Hyaluronidases are bacterial enzymes that cleave hyaluronic acid (HA) at the β-1,4 glycosidic bond, yielding unsaturated disaccharides. Initially, little was known about the regulation of this enzyme as well as its roles in S. aureus physiology and pathogenesis. The goal of this dissertation was to determine the regulation of hysA, and to determine the biological and physiological roles of this enzyme. Studies presented in Chapter II focus on determining the regulation of hysA and role of hysA in S. aureus pathogenesis. By scree

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6

Muckenschnabel, Ingo. "Analytische Untersuchungen zum Einsatz von Hyaluronidase als Adjuvans in der Krebschemotherapie : quantitative Bestimmung und Pharmakokinetik von Hyaluronidase, Melphalan und Vinblastin /." [S.l.] : [s.n.], 1997. http://www.gbv.de/dms/bs/toc/245499245.pdf.

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Asteriou, Trias. "Cinétique de la réaction d'hydrolyse du hyaluronane catalysée par la hyaluronidase testiculaire bovine : Transposition à une hyaluronidase extraite de tumeurs cancéreuses humaines." Rouen, 2002. http://www.theses.fr/2002ROUES005.

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Le hyaluronane (HA) est un polysaccharide anionique linéaire constitué de motifs disaccharidiques (N-acétyl-D-glucosamine-b(1,3)-acide-D-glucuronique) liés en b(1,4). In vivo, son catabolisme est assuré par une famille d'enzymes, les hyaluronidases (HAase). Les HAase de type testiculaire hydrolysent les liens b(1,4). La réaction d'hydrolyse du HA catalysée par la HAase testiculaire et les paramètres qui la régulent n'ont été que peu étudiés. Par ailleurs, cette réaction semble impliquée dans le développement tumoral. Le présent manuscrit constitue une étude approfondie du mode de fonctionnemen

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8

Farrera, Sal Martí. "Enhanced hyaluronidase and tumor neoepitope expression by oncolytic adenoviruses." Doctoral thesis, Universitat de Barcelona, 2020. http://hdl.handle.net/10803/671748.

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The oncolytic viruses (OVs) preferentially infect tumor and selectively replicate in cancer cells without harming normal tissues. OVs have been tested in clinical trials as monotherapy or combined with chemotherapy, radiotherapy, and immunotherapy. Nonetheless, the intratumoral spreading and the immune response hamper the treatment efficacy. In this thesis, these two challenges have been addressed in three separate chapters. First, VCN-01, a hyaluronidase-expressing oncolytic adenovirus, was tested in a clinical trial in pancreatic cancer patients. We assessed the immune response triggered b

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Gatphayak, Kesinee. "Molecular characterization of the porcine hyaluronidase gene cluster on SSC13q21." Doctoral thesis, [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=970693656.

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Chowdhury, Biswajit. "Determining the role of murine hyaluronidase 2 in hyaluronan catabolism." The American Society for Biochemistry and Molecular Biology, 2013. http://hdl.handle.net/1993/31154.

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Hyaluronidase 2 (HYAL2) is a GPI-linked protein that is proposed to initiate the degradation of hyaluronan (HA), a major extracellular matrix component of many vertebrate tissues. Hyal2 knockout (KO) mice displayed craniofacial abnormalities and severe preweaning lethality. 54% of the surviving KOs developed a grossly dilated left or right atrium, requiring euthanasia, by 3 months of age. We hypothesize that the absence of HYAL2 leads to the accumulation of HA in organs/tissues where HA is normally abundant resulting in developmental defects and organs dysfunction. Molecular and histologic

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Books on the topic "Hyaluronidase"

1

Baumgartner, Gerhard, and Alfred Moritz, eds. Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3.

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2

David, Evered, and Whelan Julie, eds. The Biology of hyaluronan. Wiley, 1989.

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3

Hyde, Cheryl Elaine. The regulation of the Xenopus nodal related-1 gene, Xnr-1 and the isolation and characterisation of a novel Xenopus hyaluronidase, XEH1. typescript, 2000.

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4

D, Stern Robert M., ed. Hyaluronan in cancer biology. Academic Press, 2009.

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5

Baumgartner, Gerhard, A. Horaczek, and H. P. Kluza. Hyaluronidase. Springer Wien, 1988.

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6

Kennedy, J. F. Hyaluronan: Proceedings of an International Meeting, September 2000, North East Wales Institute, UK. Woodhead Publishing, 2002.

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7

Stern, Robert. Hyaluronan in Cancer Biology. Elsevier Science & Technology Books, 2009.

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8

Kramer, Christoph. Blutspiegeluntersuchungen bei Lokalanästhesie mit Hyaluronidase- und CO₂-Zusätzen. 1986.

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9

Baumgartner, Gerhard, G. Baumgartner, Alfred Moritz, A. Horaczek, and H. P. Kluza. Hyaluronidase: Anwendung in der Onkologie Übersicht über Experimentelle und Klinische Daten. Springer London, Limited, 2013.

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10

Durante, Gary Gerard. Hyaluronidase: Purification and inhibition by a gold complex and a steroid derivative. 1987.

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Book chapters on the topic "Hyaluronidase"

1

Baumgartner, Gerhard, and Alfred Moritz. "Einleitung." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_1.

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2

Baumgartner, Gerhard, and Alfred Moritz. "Klinische Anwendungen von Hyaluronidase." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_10.

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Baumgartner, Gerhard, and Alfred Moritz. "Nebenwirkungen." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_11.

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Baumgartner, Gerhard, and Alfred Moritz. "Wechselwirkungen — Vorsichtsmaßnahmen." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_12.

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Baumgartner, Gerhard, and Alfred Moritz. "Kompatibilität mit verschiedenen zytostatischen Substanzen." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_13.

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Baumgartner, Gerhard, and Alfred Moritz. "Schwangerschaft und Stillzeit." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_14.

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Baumgartner, Gerhard, and Alfred Moritz. "Interferenz mit Labortests." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_15.

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Baumgartner, Gerhard, and Alfred Moritz. "Anwendungshinweise und Dosierung." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_16.

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Baumgartner, Gerhard, and Alfred Moritz. "Chemisch-physikalische Eigenschaften." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_2.

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Baumgartner, Gerhard, and Alfred Moritz. "Pharmakodynamik." In Hyaluronidase. Springer Vienna, 1988. http://dx.doi.org/10.1007/978-3-7091-9017-3_3.

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Conference papers on the topic "Hyaluronidase"

1

Shvetsova, Alexandra, Alexey Churin, Maxim Korolev, Konstantin Ershov, Natalya Bondarenko, and Pavel Madonov. "Ultrastructural and General Toxic Parallels of Pegylated Hyaluronidase." In 2024 IEEE International Multi-Conference on Engineering, Computer and Information Sciences (SIBIRCON). IEEE, 2024. http://dx.doi.org/10.1109/sibircon63777.2024.10758512.

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Addotey, J., M. Lechtenberg, F. Petereit, I. Lengers, J. Jose, and A. Hensel. "Naturstoffe als Inhibitoren der humanen Hyaluronidase-1." In Phytotherapie 2017 „Von der Innovation zur Evidenz“. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1607153.

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Akbarov, U., A. Shikov, O. Pozharitskaya, D. Demchenko, and V. Makarov. "Anti-hyaluronidase activity of traditional Uzbekistan medicine Eryxin." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608596.

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Luo, Huajun, Junzhi Wang, Yuan Zhou, and Kun Zou. "Molecular Docking Study of Chlorogenic Acid as a Hyaluronidase Inhibitor." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5514947.

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Khaybrakhmanova, Elvira A., Stanislav V. Kozyrev, and Irina Yu Ponedel’kina. "In Vitro Biodegradability of Phosphorylated Hyaluronic Acid by Testicular Hyaluronidase." In ECSOC 2023. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16107.

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Li, Xiaoming, Ping Jiang, Rebecca Symons, et al. "Abstract 3796: Pegylated human recombinant hyaluronidase PH20 reduces solid tumor hypoxia." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3796.

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Mirzapoiazova, Tamara, Nurbek Mambetsariev, Bolot Mambetsariev, Frances E. Lennon, and Patrick A. Singleton. "Hyaluronidase-1 Is A Novel Regulator Of Human Pulmonary Endothelial Barrier Disruption." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a4174.

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Lengers, Isabelle, Zoya Orlando, Matthias Melzig, Armin Buschauer, Andreas Hensel, and Joachim Jose. "Inhibition of the cancer target human hyaluronidase Hyal‑1 by natural substances." In 1st International Electronic Conference on Medicinal Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a014.

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Dzgoev, S. G. "The effect of sodium ions on the activity of serum hyaluronidase type 1." In ТЕНДЕНЦИИ РАЗВИТИЯ НАУКИ И ОБРАЗОВАНИЯ. НИЦ «Л-Журнал», 2018. http://dx.doi.org/10.18411/lj-10-2018-153.

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Dubey, Ashok, Rajeev Singla, and Mohammed Ali. "Isolation of Novel Hyaluronidase Inhibitor from the Hard Shell of Coconut." In MOL2NET 2018, International Conference on Multidisciplinary Sciences, 4th edition. MDPI, 2018. http://dx.doi.org/10.3390/mol2net-04-05433.

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Reports on the topic "Hyaluronidase"

1

Zhang, Lurong. Membrane-Bound Hyaluronidase in Breast Cancer Progression. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada398227.

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Zhang, Lurong. Membrane-Bound Hyaluronidase in Breast Cancer Progression. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada390511.

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Lokeshwar, Vinata B. Hyaluronic Acid and Hyaluronidase in Prostate Cancer: Evaluation of Their Therapeutic and Prognostic Potential. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada434622.

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Lokeshwar, Vinata B. Hyaluronic Acid and Hyaluronidase in Prostate Cancer: Evaluation of Their Therapeutic and Prognostic Potential. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada422975.

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