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Tatiana Soldà

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Biological Procedures Online|July 1, 2009
Analyzing folding and degradation of metabolically labelled polypeptides by conventional and diagonal sodium dodecyl sulfate-polyacrylamide gel electrophoresisTatiana Soldà, Silvia Olivari, Maurizio Molinari
Molecular Biology of the Cell|February 20, 2015
A novel UGGT1 and p97-dependent checkpoint for native ectodomains with ionizable intramembrane residueJessica Merulla, Tatiana Soldà, Maurizio Molinari
Traffic (Copenhagen, Denmark)|March 26, 2013
Specificity and regulation of the endoplasmic reticulum-associated degradation machineryJessica Merulla, Elisa Fasana, Tatiana Soldà, et al.
Biochemical and Biophysical Research Communications|June 23, 2018
The reductase TMX1 contributes to ERAD by preferentially acting on membrane-associated folding-defective polypeptidesConcetta Guerra, Giorgia Brambilla Pisoni, Tatiana Soldà, et al.
The Journal of Biological Chemistry|January 13, 2006
Consequences of ERp57 deletion on oxidative folding of obligate and facultative clients of the calnexin cycleTatiana Soldà, Natalio Garbi, Günter J Hämmerling, et al.
Molecular Cell|July 24, 2007
Substrate-specific requirements for UGT1-dependent release from calnexinTatiana Soldà, Carmela Galli, Randal J Kaufman, et al.
Plos One|February 8, 2011
Malectin participates in a backup glycoprotein quality control pathway in the mammalian ERCarmela Galli, Riccardo Bernasconi, Tatiana Soldà, et al.
Life Science Alliance|September 30, 2024
TMX5/TXNDC15, a natural trapping mutant of the PDI family is a client of the proteostatic factor ERp44Tatiana Soldà, Carmela Galli, Concetta Guerra, et al.
The EMBO Journal|June 21, 2021
N-glycan processing selects ERAD-resistant misfolded proteins for ER-to-lysosome-associated degradationIlaria Fregno, Elisa Fasana, Tatiana Soldà, et al.
EMBO Reports|May 21, 2024
ER-to-lysosome-associated degradation acts as failsafe mechanism upon ERAD dysfunctionElisa Fasana, Ilaria Fregno, Carmela Galli, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Biological Procedures Online|July 1, 2009
Analyzing folding and degradation of metabolically labelled polypeptides by conventional and diagonal sodium dodecyl sulfate-polyacrylamide gel electrophoresisTatiana Soldà, Silvia Olivari, Maurizio Molinari
Molecular Biology of the Cell|February 20, 2015
A novel UGGT1 and p97-dependent checkpoint for native ectodomains with ionizable intramembrane residueJessica Merulla, Tatiana Soldà, Maurizio Molinari
Traffic (Copenhagen, Denmark)|March 26, 2013
Specificity and regulation of the endoplasmic reticulum-associated degradation machineryJessica Merulla, Elisa Fasana, Tatiana Soldà, et al.
Biochemical and Biophysical Research Communications|June 23, 2018
The reductase TMX1 contributes to ERAD by preferentially acting on membrane-associated folding-defective polypeptidesConcetta Guerra, Giorgia Brambilla Pisoni, Tatiana Soldà, et al.
The Journal of Biological Chemistry|January 13, 2006
Consequences of ERp57 deletion on oxidative folding of obligate and facultative clients of the calnexin cycleTatiana Soldà, Natalio Garbi, Günter J Hämmerling, et al.
Molecular Cell|July 24, 2007
Substrate-specific requirements for UGT1-dependent release from calnexinTatiana Soldà, Carmela Galli, Randal J Kaufman, et al.
Plos One|February 8, 2011
Malectin participates in a backup glycoprotein quality control pathway in the mammalian ERCarmela Galli, Riccardo Bernasconi, Tatiana Soldà, et al.
Life Science Alliance|September 30, 2024
TMX5/TXNDC15, a natural trapping mutant of the PDI family is a client of the proteostatic factor ERp44Tatiana Soldà, Carmela Galli, Concetta Guerra, et al.
The EMBO Journal|June 21, 2021
N-glycan processing selects ERAD-resistant misfolded proteins for ER-to-lysosome-associated degradationIlaria Fregno, Elisa Fasana, Tatiana Soldà, et al.
EMBO Reports|May 21, 2024
ER-to-lysosome-associated degradation acts as failsafe mechanism upon ERAD dysfunctionElisa Fasana, Ilaria Fregno, Carmela Galli, et al.
Pageof 2