Automated Author Profile

Vidal, Enric

0000-0002-4965-3286

Current S-Index

4.1

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.5

Average Dataset Index per dataset

Total Datasets

8

Total datasets for this author

Average FAIR Score

82.0%

Average FAIR Score per dataset

Total Citations

1

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Source Data Files from publication: A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of infectious prions, Nature Communications 2024

This Dataset contains all the Source Data corresponding to the results from the manuscript entitled "A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of infectious prions", accepted for publication in Nature Communications Journal. The dataset includes uncropped scans of all gels and blots used to generated the final figures and tables (including Supplementary figures and tables), as well as the raw data used to generate the plots shown in the manuscript.The dataset is organized by Figures and Tables, with the source data files containing all the information used in each figure or table included in a compressed (.zip) file. The figure and table numbering used in the manuscript is kept, with source data available for: Figures 1 & 2, Figure 3, Supplementary figure 1, Supplementary figure 2,  Supplementary figure 3, and Supplementary figure 4.Manuscript abstract:Prion diseases are a group of rapidly progressing neurodegenerative disorders caused by the misfolding of the endogenous prion protein (PrPC) into a pathogenic form (PrPSc). This process, despite being the central event underlying these disorders, remains largely unknown at a molecular level, precluding the prediction of new potential outbreaks or interspecies transmission incidents.In this work, we present a method to generate infectious bona fide recombinant prions de novo, allowing a comprehensive analysis of protein misfolding across a wide range of prion proteins from mammalian species. We studied more than 380 different prion proteins from mammals and classified them according to their spontaneous misfolding propensity and their conformational variability.This study aims to address fundamental questions in the prion research field such as defining infectivity determinants, interspecies transmission barriers or the structural influence of specific amino acids and provides invaluable information for future diagnosis and therapy applications.

Authors

  • Eraña, Hasier ;
  • Sampedro Torres Quevedo, Cristina ;
  • Charco, Jorge M. ;
  • Díaz Domínguez, Carlos M. ;
  • Peccati, Francesca ;
  • San-Juan-Ansoleaga, Maitena ;
  • Vidal, Enric ;
  • Gonçalves-Anjo, Nuno ;
  • Pérez-Castro, Miguel A. ;
  • González-Miranda, Ezequiel ;
  • Piñeiro, Patricia ;
  • Fernández-Veiga, Leire ;
  • Galarza-Ahumada, Josu ;
  • Fernández-Muñoz, Eva ;
  • Perez de Nanclares, Guiomar ;
  • Telling, Gelnn C. ;
  • Geijo, María V. ;
  • Jiménez-Osés, Gonzalo ;
  • CASTILLA, JOAQUÍN
1 Citation0 Mentions79% FAIR0.8 Dataset Index
10.5281/zenodo.105795182024

Source Data Files from publication: A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of infectious prions, Nature Communications 2024

This Dataset contains all the Source Data corresponding to the results from the manuscript entitled "A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of infectious prions", accepted for publication in Nature Communications Journal. The dataset includes uncropped scans of all gels and blots used to generated the final figures and tables (including Supplementary figures and tables), as well as the raw data used to generate the plots shown in the manuscript.The dataset is organized by Figures and Tables, with the source data files containing all the information used in each figure or table included in a compressed (.zip) file. The figure and table numbering used in the manuscript is kept, with source data available for: Figures 1 & 2, Figure 3, Supplementary figure 1, Supplementary figure 2,  Supplementary figure 3, and Supplementary figure 4.Manuscript abstract:Prion diseases are a group of rapidly progressing neurodegenerative disorders caused by the misfolding of the endogenous prion protein (PrPC) into a pathogenic form (PrPSc). This process, despite being the central event underlying these disorders, remains largely unknown at a molecular level, precluding the prediction of new potential outbreaks or interspecies transmission incidents.In this work, we present a method to generate infectious bona fide recombinant prions de novo, allowing a comprehensive analysis of protein misfolding across a wide range of prion proteins from mammalian species. We studied more than 380 different prion proteins from mammals and classified them according to their spontaneous misfolding propensity and their conformational variability.This study aims to address fundamental questions in the prion research field such as defining infectivity determinants, interspecies transmission barriers or the structural influence of specific amino acids and provides invaluable information for future diagnosis and therapy applications.

Authors

  • Eraña, Hasier ;
  • Sampedro Torres Quevedo, Cristina ;
  • Charco, Jorge M. ;
  • Díaz Domínguez, Carlos M. ;
  • Peccati, Francesca ;
  • San-Juan-Ansoleaga, Maitena ;
  • Vidal, Enric ;
  • Gonçalves-Anjo, Nuno ;
  • Pérez-Castro, Miguel A. ;
  • González-Miranda, Ezequiel ;
  • Piñeiro, Patricia ;
  • Fernández-Veiga, Leire ;
  • Galarza-Ahumada, Josu ;
  • Fernández-Muñoz, Eva ;
  • Perez de Nanclares, Guiomar ;
  • Telling, Gelnn C. ;
  • Geijo, María V. ;
  • Jiménez-Osés, Gonzalo ;
  • CASTILLA, JOAQUÍN
0 Citations0 Mentions69% FAIR0.4 Dataset Index
10.5281/zenodo.105795172024

Additional file 2 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 2 SESC-SDPV cases summary including information about age, breed, sex, organ, gross findings, meat inspector suspicion and final diagnosis. NA = Not Available; N/A = Not applicable; Piglet = 1.5 to 3 months; Fattening = 4 months to 1 year; Adult (sow) = Breeding female; Adult (boar) = Breeding male; F=Female; M = Male; (+) = positive; (−) = negative; DLBCL = Diffuse large B-cell Lymphoma, unspecified; DLBCL-CB=Diffuse large B-cell Lymphoma - Centroblastic subtype; B-SLL = B-cell Small lymphocytic lymphoma; PTCL = Peripheral T-cell Lymphomas, unspecified; Null cell = Non-T non B; B-LBL = B-lymphoblastic leukemia; UC=Unclassified.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.5 Dataset Index
10.6084/m9.figshare.143856272021

Additional file 3 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 3 SESC-SDPV Lymphoma cases and classification following the current classification of lymphoid neoplasms for domestic animals adopted by the WHO. NA = Not Available; N/A = Not applicable; Piglet = 1.5 to 3 months; Fattening = 4 months to 1 year; Adult (sow) = Breeding female; Adult (boar) = Breeding male; F=Female; M = Male; LN = Lymph node; DLBCL = Diffuse large B-cell Lymphoma, unspecified; DLBCL-CB=Diffuse large B-cell Lymphoma - Centroblastic subtype; B-SLL = B-cell Small lymphocytic lymphoma; PTCL = Peripheral T-cell Lymphomas, unspecified; Null cell = Non-T non B; B-LBL = B-lymphoblastic leukemia; UC=Unclassified.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.5 Dataset Index
10.6084/m9.figshare.14385630.v12021

Additional file 1 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 1 Summary of the systematic literature review of the domestic pig (Sus scrofa domesticus) neoplasms reported between 1956 and 2021. Miniature breeds not included. NA = Not Available; d = days; m = months; w = weeks; y = years; F=Female; M = Male.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.5 Dataset Index
10.6084/m9.figshare.143856242021

Additional file 3 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 3 SESC-SDPV Lymphoma cases and classification following the current classification of lymphoid neoplasms for domestic animals adopted by the WHO. NA = Not Available; N/A = Not applicable; Piglet = 1.5 to 3 months; Fattening = 4 months to 1 year; Adult (sow) = Breeding female; Adult (boar) = Breeding male; F=Female; M = Male; LN = Lymph node; DLBCL = Diffuse large B-cell Lymphoma, unspecified; DLBCL-CB=Diffuse large B-cell Lymphoma - Centroblastic subtype; B-SLL = B-cell Small lymphocytic lymphoma; PTCL = Peripheral T-cell Lymphomas, unspecified; Null cell = Non-T non B; B-LBL = B-lymphoblastic leukemia; UC=Unclassified.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.5 Dataset Index
10.6084/m9.figshare.143856302021

Additional file 2 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 2 SESC-SDPV cases summary including information about age, breed, sex, organ, gross findings, meat inspector suspicion and final diagnosis. NA = Not Available; N/A = Not applicable; Piglet = 1.5 to 3 months; Fattening = 4 months to 1 year; Adult (sow) = Breeding female; Adult (boar) = Breeding male; F=Female; M = Male; (+) = positive; (−) = negative; DLBCL = Diffuse large B-cell Lymphoma, unspecified; DLBCL-CB=Diffuse large B-cell Lymphoma - Centroblastic subtype; B-SLL = B-cell Small lymphocytic lymphoma; PTCL = Peripheral T-cell Lymphomas, unspecified; Null cell = Non-T non B; B-LBL = B-lymphoblastic leukemia; UC=Unclassified.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.4 Dataset Index
10.6084/m9.figshare.14385627.v12021

Additional file 1 of Neoplastic lesions in domestic pigs detected at slaughter: literature review and a 20-year review (1998–2018) of carcass inspection in Catalonia

Additional file 1 Summary of the systematic literature review of the domestic pig (Sus scrofa domesticus) neoplasms reported between 1956 and 2021. Miniature breeds not included. NA = Not Available; d = days; m = months; w = weeks; y = years; F=Female; M = Male.

Authors

  • Morey-Matamalas, Antonia ;
  • Vidal, Enric ;
  • Martínez, Jorge ;
  • Alomar, Jaume ;
  • Ramis, Antonio ;
  • Marco, Alberto ;
  • Domingo, Mariano ;
  • Segalés, Joaquim
0 Citations0 Mentions85% FAIR0.5 Dataset Index
10.6084/m9.figshare.14385624.v12021