Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tamara Postigo-Casado"'
Autor:
Carlos M. González-Casimiro, Patricia Cámara-Torres, Beatriz Merino, Sergio Diez-Hermano, Tamara Postigo-Casado, Malcolm A. Leissring, Irene Cózar-Castellano, Germán Perdomo
Publikováno v:
Cells, Vol 10, Iss 9, p 2446 (2021)
Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed Zn2+-metallopeptidase that regulates hepatic insulin sensitivity, albeit its regulation in response to the fasting-to-postprandial transition is poorly understood. In thi
Externí odkaz:
https://doaj.org/article/c6f270047e4e485495d8abea55f99a06
Autor:
Carlos M. González-Casimiro, Beatriz Merino, Elena Casanueva-Álvarez, Tamara Postigo-Casado, Patricia Cámara-Torres, Cristina M. Fernández-Díaz, Malcolm A. Leissring, Irene Cózar-Castellano, Germán Perdomo
Publikováno v:
Biomedicines, Vol 9, Iss 1, p 86 (2021)
Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed metalloprotease that degrades insulin and several other intermediate-size peptides. For many decades, IDE had been assumed to be involved primarily in hepatic insulin cle
Externí odkaz:
https://doaj.org/article/22708589f9ef4a9e8032286530c55b73
Autor:
Beatriz Merino, Elena Casanueva-Álvarez, Iván Quesada, Carlos M. González-Casimiro, Cristina M. Fernández-Díaz, Tamara Postigo-Casado, Malcolm A. Leissring, Klaus H. Kaestner, Germán Perdomo, Irene Cózar-Castellano
Publikováno v:
UVaDOC. Repositorio Documental de la Universidad de Valladolid
instname
Diabetologia, vol 65, iss 8
Digital.CSIC. Repositorio Institucional del CSIC
instname
Diabetologia, vol 65, iss 8
Digital.CSIC. Repositorio Institucional del CSIC
Producción Científica
Aims/hypothesis Type 2 diabetes is characterised by hyperglucagonaemia and perturbed function of pancreatic glucagon secreting alpha cells but the molecular mechanisms contributing to these phenotypes are poorly understoo
Aims/hypothesis Type 2 diabetes is characterised by hyperglucagonaemia and perturbed function of pancreatic glucagon secreting alpha cells but the molecular mechanisms contributing to these phenotypes are poorly understoo
Autor:
Malcolm A. Leissring, Beatriz Merino, Patricia Cámara-Torres, Tamara Postigo-Casado, Elena Casanueva-Álvarez, Cristina M. Fernández-Díaz, Irene Cózar-Castellano, Carlos M. González-Casimiro, Germán Perdomo
Publikováno v:
Biomedicines
Biomedicines, Vol 9, Iss 86, p 86 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biomedicines, Vol 9, Iss 86, p 86 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Producción Científica
Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed metalloprotease that degrades insulin and several other intermediate-size peptides. For many decades, IDE had been assumed to be involved pri
Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed metalloprotease that degrades insulin and several other intermediate-size peptides. For many decades, IDE had been assumed to be involved pri
Autor:
Germán Perdomo, Beatriz Merino, Cristina Parrado-Fernández, Carlos M. González-Casimiro, Irene Cózar-Castellano, Cristina M. Fernández-Díaz, Carmen D. Lobatón, Malcolm A. Leissring, Tamara Postigo-Casado
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Metabolism: clinical and experimental
instname
Metabolism: clinical and experimental
© 2020 The Authors.
The insulin-degrading enzyme (IDE) is a metalloendopeptidase with a high affinity for insulin. Human genetic polymorphisms in Ide have been linked to increased risk for T2DM. In mice, hepatic Ide ablation causes glucose into
The insulin-degrading enzyme (IDE) is a metalloendopeptidase with a high affinity for insulin. Human genetic polymorphisms in Ide have been linked to increased risk for T2DM. In mice, hepatic Ide ablation causes glucose into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56dc8a1f5dc6180b1d2d00e17d8b711c
http://hdl.handle.net/10261/226398
http://hdl.handle.net/10261/226398