Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 23 entries
Sorted by: Best Match Show Resources per page
The dual nature of mismatch repair as antimutator and mutator: for better or for worse.

Frontiers in genetics

Bak ST, Sakellariou D, Pena-Diaz J.
PMID: 25191341
Front Genet. 2014 Aug 21;5:287. doi: 10.3389/fgene.2014.00287. eCollection 2014.

DNA is constantly under attack by a number of both exogenous and endogenous agents that challenge its integrity. Among the mechanisms that have evolved to counteract this deleterious action, mismatch repair (MMR) has specialized in removing DNA biosynthetic errors...

Cite
Bak ST, Sakellariou D, Pena-Diaz J. The dual nature of mismatch repair as antimutator and mutator: for better or for worse. Front Genet. 2014;5:287doi: 10.3389/fgene.2014.00287.
Bak, S. T., Sakellariou, D., & Pena-Diaz, J. (2014). The dual nature of mismatch repair as antimutator and mutator: for better or for worse. Frontiers in genetics, 5287. https://doi.org/10.3389/fgene.2014.00287
Bak, Sara Thornby, et al. "The dual nature of mismatch repair as antimutator and mutator: for better or for worse." Frontiers in genetics vol. 5 (2014): 287. doi: https://doi.org/10.3389/fgene.2014.00287
Bak ST, Sakellariou D, Pena-Diaz J. The dual nature of mismatch repair as antimutator and mutator: for better or for worse. Front Genet. 2014 Aug 21;5:287. doi: 10.3389/fgene.2014.00287. eCollection 2014. PMID: 25191341; PMCID: PMC4139959.
Copy Download .nbib Format: NLM
Expression of alternative NADH dehydrogenases (NDH-2) in the phytopathogenic fungus .

FEBS open bio

Matuz-Mares D, Matus-Ortega G, Cárdenas-Monroy C, Romero-Aguilar L, Villalobos-Rocha JC, Vázquez-Meza H, Guerra-Sánchez G, Peña-Díaz A, Pardo JP.
PMID: 30221129
FEBS Open Bio. 2018 Jul 05;8(8):1267-1279. doi: 10.1002/2211-5463.12475. eCollection 2018 Aug.

Type 2 alternative NADH dehydrogenases (NDH-2) participate indirectly in the generation of the electrochemical proton gradient by transferring electrons from NADH and NADPH into the ubiquinone pool. Due to their structural simplicity, alternative NADH dehydrogenases have been proposed as...

Cite
Matuz-Mares D, Matus-Ortega G, Cárdenas-Monroy C, et al. Expression of alternative NADH dehydrogenases (NDH-2) in the phytopathogenic fungus . FEBS Open Bio. 2018;8(8):1267-1279doi: 10.1002/2211-5463.12475.
Matuz-Mares, D., Matus-Ortega, G., Cárdenas-Monroy, C., Romero-Aguilar, L., Villalobos-Rocha, J. C., Vázquez-Meza, H., Guerra-Sánchez, G., Peña-Díaz, A., & Pardo, J. P. (2018). Expression of alternative NADH dehydrogenases (NDH-2) in the phytopathogenic fungus . FEBS open bio, 8(8), 1267-1279. https://doi.org/10.1002/2211-5463.12475
Matuz-Mares, Deyamira, et al. "Expression of alternative NADH dehydrogenases (NDH-2) in the phytopathogenic fungus ." FEBS open bio vol. 8,8 (2018): 1267-1279. doi: https://doi.org/10.1002/2211-5463.12475
Matuz-Mares D, Matus-Ortega G, Cárdenas-Monroy C, Romero-Aguilar L, Villalobos-Rocha JC, Vázquez-Meza H, Guerra-Sánchez G, Peña-Díaz A, Pardo JP. Expression of alternative NADH dehydrogenases (NDH-2) in the phytopathogenic fungus . FEBS Open Bio. 2018 Jul 05;8(8):1267-1279. doi: 10.1002/2211-5463.12475. eCollection 2018 Aug. PMID: 30221129; PMCID: PMC6134880.
Copy Download .nbib Format: NLM
Correction to: Fe-S cluster assembly in the supergroup Excavata.

Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry

Peña-Diaz P, Lukeš J.
PMID: 29845355
J Biol Inorg Chem. 2018 Jun;23(4):543. doi: 10.1007/s00775-018-1568-2.

The article "Fe-S cluster assembly in the supergroup Excavata", written by Priscila Peña‑Diaz, Julius Lukeš was originally published electronically on the publisher's internet portal (currently SpringerLink) without open access.

Cite
Peña-Diaz P, Lukeš J. Correction to: Fe-S cluster assembly in the supergroup Excavata. J Biol Inorg Chem. 2018;23(4):543doi: 10.1007/s00775-018-1568-2.
Peña-Diaz, P., & Lukeš, J. (2018). Correction to: Fe-S cluster assembly in the supergroup Excavata. Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 23(4), 543. https://doi.org/10.1007/s00775-018-1568-2
Peña-Diaz, Priscila, and Lukeš, Julius. "Correction to: Fe-S cluster assembly in the supergroup Excavata." Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry vol. 23,4 (2018): 543. doi: https://doi.org/10.1007/s00775-018-1568-2
Peña-Diaz P, Lukeš J. Correction to: Fe-S cluster assembly in the supergroup Excavata. J Biol Inorg Chem. 2018 Jun;23(4):543. doi: 10.1007/s00775-018-1568-2. PMID: 29845355; PMCID: PMC6006202.
Copy Download .nbib Format: NLM
Analysis of bacterial survival after exposure to reactive oxygen species or antibiotics.

Data in brief

van der Heijden J, Vogt SL, Reynolds LA, Peña-Díaz J, Tupin A, Aussel L, Finlay BB.
PMID: 27077092
Data Brief. 2016 Mar 22;7:894-9. doi: 10.1016/j.dib.2016.03.060. eCollection 2016 Jun.

The redox balance in a variety of Gram-negative bacteria was explored using redox sensitive GFP (roGFP2), J. van der Heijden et al. doi:10.1016/j.freeradbiomed.2015.11.029[1]. This data article provides Supporting material to further investigate the relationship between Salmonella typhimurium survival and...

Cite
van der Heijden J, Vogt SL, Reynolds LA, et al. Analysis of bacterial survival after exposure to reactive oxygen species or antibiotics. Data Brief. 2016;7:894-9doi: 10.1016/j.dib.2016.03.060.
van der Heijden, J., Vogt, S. L., Reynolds, L. A., Peña-Díaz, J., Tupin, A., Aussel, L., & Finlay, B. B. (2016). Analysis of bacterial survival after exposure to reactive oxygen species or antibiotics. Data in brief, 7894-9. https://doi.org/10.1016/j.dib.2016.03.060
van der Heijden, Joris, et al. "Analysis of bacterial survival after exposure to reactive oxygen species or antibiotics." Data in brief vol. 7 (2016): 894-9. doi: https://doi.org/10.1016/j.dib.2016.03.060
van der Heijden J, Vogt SL, Reynolds LA, Peña-Díaz J, Tupin A, Aussel L, Finlay BB. Analysis of bacterial survival after exposure to reactive oxygen species or antibiotics. Data Brief. 2016 Mar 22;7:894-9. doi: 10.1016/j.dib.2016.03.060. eCollection 2016 Jun. PMID: 27077092; PMCID: PMC4816907.
Copy Download .nbib Format: NLM
High quality genome assembly of the amitochondriate eukaryote .

Microbial genomics

Treitli SC, Peña-Diaz P, Hałakuc P, Karnkowska A, Hampl V.
PMID: 34951395
Microb Genom. 2021 Dec;7(12). doi: 10.1099/mgen.0.000745.

No abstract available.

Cite
Treitli SC, Peña-Diaz P, Hałakuc P, et al. High quality genome assembly of the amitochondriate eukaryote . Microb Genom. 2021;7(12)doi: 10.1099/mgen.0.000745.
Treitli, S. C., Peña-Diaz, P., Hałakuc, P., Karnkowska, A., & Hampl, V. (2021). High quality genome assembly of the amitochondriate eukaryote . Microbial genomics, 7(12), . https://doi.org/10.1099/mgen.0.000745
Treitli, Sebastian Cristian, et al. "High quality genome assembly of the amitochondriate eukaryote ." Microbial genomics vol. 7,12 (2021). doi: https://doi.org/10.1099/mgen.0.000745
Treitli SC, Peña-Diaz P, Hałakuc P, Karnkowska A, Hampl V. High quality genome assembly of the amitochondriate eukaryote . Microb Genom. 2021 Dec;7(12). doi: 10.1099/mgen.0.000745. PMID: 34951395.
Copy Download .nbib Format: NLM
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation.

Nucleic acids research

Quaglia F, Mészáros B, Salladini E, Hatos A, Pancsa R, Chemes LB, Pajkos M, Lazar T, Peña-Díaz S, Santos J, Ács V, Farahi N, Fichó E, Aspromonte MC, Bassot C, Chasapi A, Davey NE, Davidović R, Dobson L, Elofsson A, Erdős G, Gaudet P, Giglio M, Glavina J, Iserte J, Iglesias V, Kálmán Z, Lambrughi M, Leonardi E, Longhi S, Macedo-Ribeiro S, Maiani E, Marchetti J, Marino-Buslje C, Mészáros A, Monzon AM, Minervini G, Nadendla S, Nilsson JF, Novotný M, Ouzounis CA, Palopoli N, Papaleo E, Pereira PJB, Pozzati G, Promponas VJ, Pujols J, Rocha ACS, Salas M, Sawicki LR, Schad E, Shenoy A, Szaniszló T, Tsirigos KD, Veljkovic N, Parisi G, Ventura S, Dosztányi Z, Tompa P, Tosatto SCE, Piovesan D.
PMID: 34850135
Nucleic Acids Res. 2022 Jan 07;50:D480-D487. doi: 10.1093/nar/gkab1082.

The Database of Intrinsically Disordered Proteins (DisProt, URL: https://disprot.org) is the major repository of manually curated annotations of intrinsically disordered proteins and regions from the literature. We report here recent updates of DisProt version 9, including a restyled web...

Cite
Quaglia F, Mészáros B, Salladini E, et al. DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic Acids Res. 2022;50:D480-D487doi: 10.1093/nar/gkab1082.
Quaglia, F., Mészáros, B., Salladini, E., Hatos, A., Pancsa, R., Chemes, L. B., Pajkos, M., Lazar, T., Peña-Díaz, S., Santos, J., Ács, V., Farahi, N., Fichó, E., Aspromonte, M. C., Bassot, C., Chasapi, A., Davey, N. E., Davidović, R., Dobson, L., Elofsson, A., Erdős, G., Gaudet, P., Giglio, M., Glavina, J., Iserte, J., Iglesias, V., Kálmán, Z., Lambrughi, M., Leonardi, E., Longhi, S., Macedo-Ribeiro, S., Maiani, E., Marchetti, J., Marino-Buslje, C., Mészáros, A., Monzon, A. M., Minervini, G., Nadendla, S., Nilsson, J. F., Novotný, M., Ouzounis, C. A., Palopoli, N., Papaleo, E., Pereira, P. J. B., Pozzati, G., Promponas, V. J., Pujols, J., Rocha, A. C. S., Salas, M., Sawicki, L. R., Schad, E., Shenoy, A., Szaniszló, T., Tsirigos, K. D., Veljkovic, N., Parisi, G., Ventura, S., Dosztányi, Z., Tompa, P., Tosatto, S. C. E., & Piovesan, D. (2022). DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic acids research, 50D480-D487. https://doi.org/10.1093/nar/gkab1082
Quaglia, Federica, et al. "DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation." Nucleic acids research vol. 50 (2022): D480-D487. doi: https://doi.org/10.1093/nar/gkab1082
Quaglia F, Mészáros B, Salladini E, Hatos A, Pancsa R, Chemes LB, Pajkos M, Lazar T, Peña-Díaz S, Santos J, Ács V, Farahi N, Fichó E, Aspromonte MC, Bassot C, Chasapi A, Davey NE, Davidović R, Dobson L, Elofsson A, Erdős G, Gaudet P, Giglio M, Glavina J, Iserte J, Iglesias V, Kálmán Z, Lambrughi M, Leonardi E, Longhi S, Macedo-Ribeiro S, Maiani E, Marchetti J, Marino-Buslje C, Mészáros A, Monzon AM, Minervini G, Nadendla S, Nilsson JF, Novotný M, Ouzounis CA, Palopoli N, Papaleo E, Pereira PJB, Pozzati G, Promponas VJ, Pujols J, Rocha ACS, Salas M, Sawicki LR, Schad E, Shenoy A, Szaniszló T, Tsirigos KD, Veljkovic N, Parisi G, Ventura S, Dosztányi Z, Tompa P, Tosatto SCE, Piovesan D. DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic Acids Res. 2022 Jan 07;50:D480-D487. doi: 10.1093/nar/gkab1082. PMID: 34850135; PMCID: PMC8728214.
Copy Download .nbib Format: NLM
Cost-effectiveness analysis of the bevacizumab-irinotecan regimen in the treatment of primary glioblastoma multiforme recurrences.

Oncology letters

Ruiz-Sánchez D, Peinado II, Alaguero-Calero M, Sastre-Heres AJ, Diez BG, Peña-Díaz J.
PMID: 27588142
Oncol Lett. 2016 Sep;12(3):1935-1940. doi: 10.3892/ol.2016.4871. Epub 2016 Jul 15.

The purpose of the present study was to calculate the cost-effectiveness of the inclusion of the bevacizumab (BVZ) + irinotecan (CPT-11) regimen in the second-line of treatment for primary glioblastoma multiforme. A retrospective cohort study with a control group...

Cite
Ruiz-Sánchez D, Peinado II, Alaguero-Calero M, et al. Cost-effectiveness analysis of the bevacizumab-irinotecan regimen in the treatment of primary glioblastoma multiforme recurrences. Oncol Lett. 2016;12(3):1935-1940doi: 10.3892/ol.2016.4871.
Ruiz-Sánchez, D., Peinado, I. I., Alaguero-Calero, M., Sastre-Heres, A. J., Diez, B. G., & Peña-Díaz, J. (2016). Cost-effectiveness analysis of the bevacizumab-irinotecan regimen in the treatment of primary glioblastoma multiforme recurrences. Oncology letters, 12(3), 1935-1940. https://doi.org/10.3892/ol.2016.4871
Ruiz-Sánchez, Daniel, et al. "Cost-effectiveness analysis of the bevacizumab-irinotecan regimen in the treatment of primary glioblastoma multiforme recurrences." Oncology letters vol. 12,3 (2016): 1935-1940. doi: https://doi.org/10.3892/ol.2016.4871
Ruiz-Sánchez D, Peinado II, Alaguero-Calero M, Sastre-Heres AJ, Diez BG, Peña-Díaz J. Cost-effectiveness analysis of the bevacizumab-irinotecan regimen in the treatment of primary glioblastoma multiforme recurrences. Oncol Lett. 2016 Sep;12(3):1935-1940. doi: 10.3892/ol.2016.4871. Epub 2016 Jul 15. PMID: 27588142; PMCID: PMC4998143.
Copy Download .nbib Format: NLM
From simple to supercomplex: mitochondrial genomes of euglenozoan protists.

F1000Research

Faktorová D, Dobáková E, Peña-Diaz P, Lukeš J.
PMID: 27018240
F1000Res. 2016 Mar 23;5. doi: 10.12688/f1000research.8040.2. eCollection 2016.

Mitochondria are double membrane organelles of endosymbiotic origin, best known for constituting the centre of energetics of a eukaryotic cell. They contain their own mitochondrial genome, which as a consequence of gradual reduction during evolution typically contains less than...

Cite
Faktorová D, Dobáková E, Peña-Diaz P, et al. From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Res. 2016;5doi: 10.12688/f1000research.8040.2.
Faktorová, D., Dobáková, E., Peña-Diaz, P., & Lukeš, J. (2016). From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Research, 5. https://doi.org/10.12688/f1000research.8040.2
Faktorová, Drahomíra, et al. "From simple to supercomplex: mitochondrial genomes of euglenozoan protists." F1000Research vol. 5 (2016). doi: https://doi.org/10.12688/f1000research.8040.2
Faktorová D, Dobáková E, Peña-Diaz P, Lukeš J. From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Res. 2016 Mar 23;5. doi: 10.12688/f1000research.8040.2. eCollection 2016. PMID: 27018240; PMCID: PMC4806707.
Copy Download .nbib Format: NLM
From simple to supercomplex: mitochondrial genomes of euglenozoan protists.

F1000Research

Faktorová D, Dobáková E, Peña-Diaz P, Lukeš J.
PMID: 27018240
F1000Res. 2016 Mar 23;5. doi: 10.12688/f1000research.8040.2. eCollection 2016.

Mitochondria are double membrane organelles of endosymbiotic origin, best known for constituting the centre of energetics of a eukaryotic cell. They contain their own mitochondrial genome, which as a consequence of gradual reduction during evolution typically contains less than...

Cite
Faktorová D, Dobáková E, Peña-Diaz P, et al. From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Res. 2016;5doi: 10.12688/f1000research.8040.2.
Faktorová, D., Dobáková, E., Peña-Diaz, P., & Lukeš, J. (2016). From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Research, 5. https://doi.org/10.12688/f1000research.8040.2
Faktorová, Drahomíra, et al. "From simple to supercomplex: mitochondrial genomes of euglenozoan protists." F1000Research vol. 5 (2016). doi: https://doi.org/10.12688/f1000research.8040.2
Faktorová D, Dobáková E, Peña-Diaz P, Lukeš J. From simple to supercomplex: mitochondrial genomes of euglenozoan protists. F1000Res. 2016 Mar 23;5. doi: 10.12688/f1000research.8040.2. eCollection 2016. PMID: 27018240; PMCID: PMC4806707.
Copy Download .nbib Format: NLM
ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization.

Frontiers in molecular neuroscience

Peña-Díaz S, Pujols J, Conde-Giménez M, Čarija A, Dalfo E, García J, Navarro S, Pinheiro F, Santos J, Salvatella X, Sancho J, Ventura S.
PMID: 31920537
Front Mol Neurosci. 2019 Dec 17;12:306. doi: 10.3389/fnmol.2019.00306. eCollection 2019.

α-Synuclein (α-Syn) forms toxic intracellular protein inclusions and transmissible amyloid structures in Parkinson's disease (PD). Preventing α-Syn self-assembly has become one of the most promising approaches in the search for disease-modifying treatments for this neurodegenerative disorder. Here, we describe...

Cite
Peña-Díaz S, Pujols J, Conde-Giménez M, et al. ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization. Front Mol Neurosci. 2019;12:306doi: 10.3389/fnmol.2019.00306.
Peña-Díaz, S., Pujols, J., Conde-Giménez, M., Čarija, A., Dalfo, E., García, J., Navarro, S., Pinheiro, F., Santos, J., Salvatella, X., Sancho, J., & Ventura, S. (2019). ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization. Frontiers in molecular neuroscience, 12306. https://doi.org/10.3389/fnmol.2019.00306
Peña-Díaz, Samuel, et al. "ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization." Frontiers in molecular neuroscience vol. 12 (2019): 306. doi: https://doi.org/10.3389/fnmol.2019.00306
Peña-Díaz S, Pujols J, Conde-Giménez M, Čarija A, Dalfo E, García J, Navarro S, Pinheiro F, Santos J, Salvatella X, Sancho J, Ventura S. ZPD-2, a Small Compound That Inhibits α-Synuclein Amyloid Aggregation and Its Seeded Polymerization. Front Mol Neurosci. 2019 Dec 17;12:306. doi: 10.3389/fnmol.2019.00306. eCollection 2019. PMID: 31920537; PMCID: PMC6928008.
Copy Download .nbib Format: NLM
Apoptosis assessment in high-content and high-throughput screening assays.

BioTechniques

Rens C, Shapira T, Peña-Diaz S, Chao JD, Pfeifer T, Av-Gay Y.
PMID: 34114488
Biotechniques. 2021 Jun;70(6):309-318. doi: 10.2144/btn-2020-0164. Epub 2021 Jun 11.

Here the authors describe the development of AUTOptosis, an economical and rapid apoptosis monitoring method suitable for high-content and high-throughput screening assays. AUTOptosis is based on the quantification of nuclei intensity via staining with Hoechst 33342. First, the authors...

Cite
Rens C, Shapira T, Peña-Diaz S, et al. Apoptosis assessment in high-content and high-throughput screening assays. Biotechniques. 2021;70(6):309-318doi: 10.2144/btn-2020-0164.
Rens, C., Shapira, T., Peña-Diaz, S., Chao, J. D., Pfeifer, T., & Av-Gay, Y. (2021). Apoptosis assessment in high-content and high-throughput screening assays. BioTechniques, 70(6), 309-318. https://doi.org/10.2144/btn-2020-0164
Rens, Céline, et al. "Apoptosis assessment in high-content and high-throughput screening assays." BioTechniques vol. 70,6 (2021): 309-318. doi: https://doi.org/10.2144/btn-2020-0164
Rens C, Shapira T, Peña-Diaz S, Chao JD, Pfeifer T, Av-Gay Y. Apoptosis assessment in high-content and high-throughput screening assays. Biotechniques. 2021 Jun;70(6):309-318. doi: 10.2144/btn-2020-0164. Epub 2021 Jun 11. PMID: 34114488.
Copy Download .nbib Format: NLM
DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation.

Nucleic acids research

Quaglia F, Mészáros B, Salladini E, Hatos A, Pancsa R, Chemes LB, Pajkos M, Lazar T, Peña-Díaz S, Santos J, Ács V, Farahi N, Fichó E, Aspromonte MC, Bassot C, Chasapi A, Davey NE, Davidović R, Dobson L, Elofsson A, Erdős G, Gaudet P, Giglio M, Glavina J, Iserte J, Iglesias V, Kálmán Z, Lambrughi M, Leonardi E, Longhi S, Macedo-Ribeiro S, Maiani E, Marchetti J, Marino-Buslje C, Mészáros A, Monzon AM, Minervini G, Nadendla S, Nilsson JF, Novotný M, Ouzounis CA, Palopoli N, Papaleo E, Pereira PJB, Pozzati G, Promponas VJ, Pujols J, Rocha ACS, Salas M, Sawicki LR, Schad E, Shenoy A, Szaniszló T, Tsirigos KD, Veljkovic N, Parisi G, Ventura S, Dosztányi Z, Tompa P, Tosatto SCE, Piovesan D.
PMID: 34850135
Nucleic Acids Res. 2021 Nov 25; doi: 10.1093/nar/gkab1082. Epub 2021 Nov 25.

The Database of Intrinsically Disordered Proteins (DisProt, URL: https://disprot.org) is the major repository of manually curated annotations of intrinsically disordered proteins and regions from the literature. We report here recent updates of DisProt version 9, including a restyled web...

Cite
Quaglia F, Mészáros B, Salladini E, et al. DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic Acids Res. 2021;doi: 10.1093/nar/gkab1082.
Quaglia, F., Mészáros, B., Salladini, E., Hatos, A., Pancsa, R., Chemes, L. B., Pajkos, M., Lazar, T., Peña-Díaz, S., Santos, J., Ács, V., Farahi, N., Fichó, E., Aspromonte, M. C., Bassot, C., Chasapi, A., Davey, N. E., Davidović, R., Dobson, L., Elofsson, A., Erdős, G., Gaudet, P., Giglio, M., Glavina, J., Iserte, J., Iglesias, V., Kálmán, Z., Lambrughi, M., Leonardi, E., Longhi, S., Macedo-Ribeiro, S., Maiani, E., Marchetti, J., Marino-Buslje, C., Mészáros, A., Monzon, A. M., Minervini, G., Nadendla, S., Nilsson, J. F., Novotný, M., Ouzounis, C. A., Palopoli, N., Papaleo, E., Pereira, P. J. B., Pozzati, G., Promponas, V. J., Pujols, J., Rocha, A. C. S., Salas, M., Sawicki, L. R., Schad, E., Shenoy, A., Szaniszló, T., Tsirigos, K. D., Veljkovic, N., Parisi, G., Ventura, S., Dosztányi, Z., Tompa, P., Tosatto, S. C. E., & Piovesan, D. (2021). DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic acids research, . https://doi.org/10.1093/nar/gkab1082
Quaglia, Federica, et al. "DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation." Nucleic acids research vol. (2021). doi: https://doi.org/10.1093/nar/gkab1082
Quaglia F, Mészáros B, Salladini E, Hatos A, Pancsa R, Chemes LB, Pajkos M, Lazar T, Peña-Díaz S, Santos J, Ács V, Farahi N, Fichó E, Aspromonte MC, Bassot C, Chasapi A, Davey NE, Davidović R, Dobson L, Elofsson A, Erdős G, Gaudet P, Giglio M, Glavina J, Iserte J, Iglesias V, Kálmán Z, Lambrughi M, Leonardi E, Longhi S, Macedo-Ribeiro S, Maiani E, Marchetti J, Marino-Buslje C, Mészáros A, Monzon AM, Minervini G, Nadendla S, Nilsson JF, Novotný M, Ouzounis CA, Palopoli N, Papaleo E, Pereira PJB, Pozzati G, Promponas VJ, Pujols J, Rocha ACS, Salas M, Sawicki LR, Schad E, Shenoy A, Szaniszló T, Tsirigos KD, Veljkovic N, Parisi G, Ventura S, Dosztányi Z, Tompa P, Tosatto SCE, Piovesan D. DisProt in 2022: improved quality and accessibility of protein intrinsic disorder annotation. Nucleic Acids Res. 2021 Nov 25; doi: 10.1093/nar/gkab1082. Epub 2021 Nov 25. PMID: 34850135.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 23 entries