Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Guillem Vila-Julià"'
Autor:
Neda Razzaghi, Pol Fernandez-Gonzalez, Aina Mas-Sanchez, Guillem Vila-Julià, Juan Jesus Perez, Pere Garriga
Publikováno v:
Molecules, Vol 26, Iss 10, p 3032 (2021)
Rhodopsin is the G protein-coupled receptor of rod photoreceptor cells that mediates vertebrate vision at low light intensities. Mutations in rhodopsin cause inherited retinal degenerative diseases such as retinitis pigmentosa. Several therapeutic st
Externí odkaz:
https://doaj.org/article/62ee022c99b547fea591167445101a0c
Publikováno v:
Journal of Chemical Information and Modeling.
Publikováno v:
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Dipòsit Digital de la UB
Universidad de Barcelona
Universitat Politècnica de Catalunya (UPC)
Dipòsit Digital de la UB
Universidad de Barcelona
Apoptosis is a key cell death pathway in mammalian cells. Understanding this process and its regulation has been a subject of study in the last three decades. Members of the Bcl-2 family of proteins are involved in the regulation of apoptosis through
Autor:
María Guadalupe Herrera-Hernández, Neda Razzaghi, Pol Fernandez-Gonzalez, Laia Bosch-Presegué, Guillem Vila-Julià, Juan Jesús Pérez, Pere Garriga
Publikováno v:
Cellular and Molecular Life Sciences
Mutations in the photoreceptor protein rhodopsin are known as one of the leading causes of retinal degeneration in humans. Two rhodopsin mutations, Y102H and I307N, obtained in chemically mutagenized mice, are currently the subject of increased inter
Autor:
Pere Garriga, Pol Fernandez-Gonzalez, Guillem Vila-Julià, Aina Mas-Sanchez, Neda Razzaghi, Juan J. Perez
Publikováno v:
Molecules
Volume 26
Issue 10
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Molecules, Vol 26, Iss 3032, p 3032 (2021)
Volume 26
Issue 10
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Molecules, Vol 26, Iss 3032, p 3032 (2021)
Rhodopsin is the G protein-coupled receptor of rod photoreceptor cells that mediates vertebrate vision at low light intensities. Mutations in rhodopsin cause inherited retinal degenerative diseases such as retinitis pigmentosa. Several therapeutic st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c9a519f69dc3d327a141f7d3cb28701
https://pubmed.ncbi.nlm.nih.gov/34069614/
https://pubmed.ncbi.nlm.nih.gov/34069614/