Zobrazeno 1 - 10
of 42
pro vyhledávání: '"GAGs, glycosaminoglycans"'
Autor:
Paula Pleguezuelos-Beltrán, Patricia Gálvez-Martín, Daniel Nieto-García, Juan Antonio Marchal, Elena López-Ruiz
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
This research was funded by Fundacion Mutua Madrilena (FMM-AP17196-2019) , the Consejeria de Economia, Conocimiento, Empresas y Universidad de la Junta de Andalucia (ERDF funds, projects B-CTS-230-UGR18, PY18-2470, A-CTS-180-UGR20, SOMM17-6109, PYC20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a8dfaad3702b342e1ea9b8ae754f1da
https://doi.org/10.1016/j.bioactmat.2022.02.023
https://doi.org/10.1016/j.bioactmat.2022.02.023
Publikováno v:
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Vol 19, Iss, Pp 976-988 (2021)
Computational and Structural Biotechnology Journal, Vol 19, Iss, Pp 976-988 (2021)
Graphical abstract
Chemokines are crucial inflammatory mediators needed during an immune response to clear pathogens. However, their excessive release is the main cause of hyperinflammation. In the recent COVID-19 outbreak, chemokines may be the
Chemokines are crucial inflammatory mediators needed during an immune response to clear pathogens. However, their excessive release is the main cause of hyperinflammation. In the recent COVID-19 outbreak, chemokines may be the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a813633e01cb0494554b46fedd72c61
http://europepmc.org/articles/PMC7859556
http://europepmc.org/articles/PMC7859556
Autor:
Sofia Chiaraluce, Attilio Rovelli, Silvia Molinari, Rossella Parini, Serena Gasperini, Andrea Biondi, Alessandro Cattoni
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss, Pp 100787-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mucopolysaccharidosis I Hurler (MPS-IH) has been historically regarded as unsatisfactory. Nevertheless, the growth patterns recorded in transplanted pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::596666b5a246b3f0a65acc95c115670e
http://www.sciencedirect.com/science/article/pii/S2214426921000811
http://www.sciencedirect.com/science/article/pii/S2214426921000811
Autor:
Silvia Favilli, Elena Procopio, Maria Chiara Sanvito, Francesca Miselli, Maria Alice Donati, Katia Rossi, Giovanni Battista Calabri, Alice Brambilla, Francesco Torcetta, Luca Ragni
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss, Pp 100714-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Mucopolysaccharidosis are genetic disorders due to deficiency of lysosomal enzymes, resulting in abnormal glycosaminoglycans accumulation in several tissues. Heart involvement tends to be progressive and worsens with age. We describe the first case o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8dcb2341cf8db5b10c858cf0e7f862d
http://www.sciencedirect.com/science/article/pii/S2214426921000082
http://www.sciencedirect.com/science/article/pii/S2214426921000082
Autor:
Vincenza, Gragnaniello, Silvia, Carraro, Laura, Rubert, Daniela, Gueraldi, Chiara, Cazzorla, Pamela, Massa, Stefania, Zanconato, Alberto B, Burlina
Publikováno v:
Molecular Genetics and Metabolism Reports. 31:100878
Mucopolysaccharidosis type II (MPS II) is a multisystemic lysosomal storage disorder caused by deficiency of the iduronate 2-sulfatase enzyme. Currently, enzyme replacement therapy (ERT) with recombinant idursulfase is the main treatment available to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e066b2465be491cbaa9c2d84313fecd2
https://doi.org/10.1016/j.ymgmr.2022.100878
https://doi.org/10.1016/j.ymgmr.2022.100878
Publikováno v:
Molecular & Cellular Proteomics : MCP
This review covers recent developments in glycosaminoglycan (GAG) analysis via mass spectrometry (MS). GAGs participate in a variety of biological functions, including cellular communication, wound healing, and anticoagulation, and are important targ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a3f2eef0326a4dcbef46e6716a3866c
http://europepmc.org/articles/PMC8724624
http://europepmc.org/articles/PMC8724624
Autor:
Cospain, Auriane, Dubourg, Christèle, Gastineau, Swellen, Pichard, Samia, Gandemer, Virginie, Bonneau, Jacinthe, de Tayrac, Marie, Moreau, Caroline, Odent, Sylvie, Pasquier, Laurent, Damaj, Lena, Lavillaureix, Alinoë
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 24, Iss, Pp 100621-(2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Elsevier, 2020, 24, pp.100621. ⟨10.1016/j.ymgmr.2020.100621⟩
Molecular Genetics and Metabolism Reports, 2020, 24, pp.100621. ⟨10.1016/j.ymgmr.2020.100621⟩
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Elsevier, 2020, 24, pp.100621. ⟨10.1016/j.ymgmr.2020.100621⟩
Molecular Genetics and Metabolism Reports, 2020, 24, pp.100621. ⟨10.1016/j.ymgmr.2020.100621⟩
International audience; Chronic intestinal pseudoobstruction (CIPO) is a severe form of intestinal dysmotility, and patients often undergo iterative abdominal surgeries and require parenteral nutrition. Several genes are known to be responsible for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::efcb03bd66f6738c1b9440e52bf8361d
http://www.sciencedirect.com/science/article/pii/S2214426920300677
http://www.sciencedirect.com/science/article/pii/S2214426920300677
Autor:
Ari Helenius
Publikováno v:
Journal of Molecular Biology
Research over a period of more than half a century has provided a reasonably accurate picture of mechanisms involved in animal virus entry into their host cells. Successive steps in entry include binding to receptors, endocytosis, passage through one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba0f2c5f639faad126c3c8be30121b59
http://europepmc.org/articles/PMC7094621
http://europepmc.org/articles/PMC7094621
Autor:
Claudia Yazmín Cossío Mandujano, Hector Paul Quintero Montaño, Villarreal M Solano, Carmen Amor Avila-Rejon, Victor Hugo Espin
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss, Pp 100769-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Background: There is a paucity of real-world epidemiological data on patients with mucopolysaccharidoses (MPS) in Latin America. This real-world study assessed the disease burden, management patterns and multidisciplinary clinical approaches for MPS-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d269e26bb067258f4cfb1619cafd83
https://doi.org/10.1016/j.ymgmr.2021.100769
https://doi.org/10.1016/j.ymgmr.2021.100769
Autor:
Carmen Regla Vargas, Bruna Donida, Helen Tais da Rosa, Roberto Giugliani, Graziela S. Ribas, Jenifer Saffi, Marion Deon, Carlos Eduardo Diaz Jacques, Paula R. Manini, Desirèe Padilha Marchetti, Dinara Jaqueline Moura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 46-53 (2017)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Morquio A disease (Mucopolysaccharidosis type IVA, MPS IVA) is one of the 11 mucopolysaccharidoses (MPSs), a heterogeneous group of inherited lysosomal storage disorders (LSDs) caused by deficiency in enzymes need to degrade glycosaminoglycans (GAGs)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83981f248cbaa05dd8322a825abad972
https://doi.org/10.1016/j.ymgmr.2017.04.005
https://doi.org/10.1016/j.ymgmr.2017.04.005