Search Results - "Cardenas, Paula P."

Double-strand break repair in bacteria: a view from Bacillus subtilis by Ayora, Silvia, Carrasco, Begoña, Cárdenas, Paula P., César, Carolina E., Cañas, Cristina, Yadav, Tribhuwan, Marchisone, Chiara, Alonso, Juan C.

“…Abstract In all living organisms, the response to double-strand breaks (DSBs) is critical for the maintenance of chromosome integrity. Homologous recombination…”
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RecX facilitates homologous recombination by modulating RecA activities by Cárdenas, Paula P, Carrasco, Begoña, Defeu Soufo, Clarisse, César, Carolina E, Herr, Katharina, Kaufenstein, Miriam, Graumann, Peter L, Alonso, Juan C

“…The Bacillus subtilis recH342 strain, which decreases interspecies recombination without significantly affecting the frequency of transformation with homogamic…”
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Lymphocyte integration of complement cues by Marin, Ana V., Cárdenas, Paula P., Jiménez-Reinoso, Anaïs, Muñoz-Ruiz, Miguel, Regueiro, Jose R.

“…We address current data, views and puzzles on the emerging topic of regulation of lymphocytes by complement proteins or fragments. Such regulation is believed…”
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Early steps of double-strand break repair in Bacillus subtilis by Alonso, Juan C., Cardenas, Paula P., Sanchez, Humberto, Hejna, James, Suzuki, Yuki, Takeyasu, Kunio

“…All organisms rely on integrated networks to repair DNA double-strand breaks (DSBs) in order to preserve the integrity of the genetic information, to…”
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Bacillus subtilis polynucleotide phosphorylase 3′-to-5′ DNase activity is involved in DNA repair by Cardenas, Paula P., Carrasco, Begoña, Sanchez, Humberto, Deikus, Gintaras, Bechhofer, David H, Alonso, Juan C

“…In the presence of Mn2+, an activity in a preparation of purified Bacillus subtilis RecN degrades single-stranded (ss) DNA with a 3′ → 5′ polarity. This…”
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Polynucleotide phosphorylase exonuclease and polymerase activities on single-stranded DNA ends are modulated by RecN, SsbA and RecA proteins by Cardenas, Paula P., Carzaniga, Thomas, Zangrossi, Sandro, Briani, Federica, Garcia-Tirado, Esther, Dehò, Gianni, Alonso, Juan C.

“…Bacillus subtilis pnpA gene product, polynucleotide phosphorylase (PNPase), is involved in double-strand break (DSB) repair via homologous recombination (HR)…”
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Detection of the Early Stage of Recombinational DNA Repair by Silicon Nanowire Transistors by Chiesa, Marco, Cardenas, Paula P, Otón, Francisco, Martinez, Javier, Mas-Torrent, Marta, Garcia, Fernando, Alonso, Juan C, Rovira, Concepció, Garcia, Ricardo

“…A silicon nanowire-based biosensor has been designed and applied for label-free and ultrasensitive detection of the early stage of recombinational DNA repair…”
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Dynamic structures of Bacillus subtilis RecN-DNA complexes by Sanchez, Humberto, Cardenas, Paula P, Yoshimura, Shige H, Takeyasu, Kunio, Alonso, Juan C

“…Genetic and cytological evidences suggest that Bacillus subtilis RecN acts prior to and after end-processing of DNA double-strand ends via homologous…”
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Nonsense CD247 mutations show dominant-negative features in T-cell receptor expression and function by Briones, Alejandro C., Megino, Rebeca F., Marin, Ana V., Chacón-Arguedas, Daniel, García-Martinez, Elena, Balastegui-Martín, Héctor, Reyburn, Hugh T., Henrickson, Sarah E., Rodríguez-Sainz, Carmen, Seoane-Reula, Elena, Sanchez-Mateos, Paloma, Cardenas, Paula P., Regueiro, Jose R.

“…[Display omitted] The invariant TCR ζ/CD247 homodimer is crucial for TCR/CD3 expression and signaling through its 3 immunoreceptor tyrosine-based activation…”
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DNA double strand break end-processing and RecA induce RecN expression levels in Bacillus subtilis by Cardenas, Paula P., Gándara, Carolina, Alonso, Juan C.

“…•Bacillus subtilis RecN is among the first responders to DNA double strand breaks (DSBs).•Two major signaling-related cascades (SOS and DSBR) are induced upon…”
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Bacillus subtilis RarA Acts as a Positive RecA Accessory Protein by Romero, Hector, Serrano, Ester, Hernández-Tamayo, Rogelio, Carrasco, Begoña, Cárdenas, Paula P, Ayora, Silvia, Graumann, Peter L, Alonso, Juan C

“…Ubiquitous RarA AAA ATPases play crucial roles in the cellular response to blocked replication forks in pro- and eukaryotes. Here, we provide evidence that…”
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CD3G or CD3D Knockdown in Mature, but Not Immature, T Lymphocytes Similarly Cripples the Human TCRαβ Complex by Garcillán, Beatriz, Fuentes, Patricia, Marin, Ana V., Megino, Rebeca F., Chacon-Arguedas, Daniel, Mazariegos, Marina S., Jiménez-Reinoso, Anaïs, Muñoz-Ruiz, Miguel, Laborda, Raquel G., Cárdenas, Paula P., Fernández-Malavé, Edgar, Toribio, Maria L., Regueiro, José R.

“…The human αβ T-cell receptor (TCR) is composed of a variable heterodimer (TCRαβ) and three invariant dimers (CD3γε, CD3δε, and ζζ/CD247 2 ). The role of each…”
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MHC class I genes in the owl monkey: mosaic organisation, convergence and loci diversity by Cardenas, Paula P, Suarez, Carlos F, Martinez, Pilar, Patarroyo, Manuel E, Patarroyo, Manuel A

“…The MHC class I molecule plays an important role in immune response, pathogen recognition and response against vaccines and self- versus non-self-recognition…”
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High level of conservation in Plasmodium vivax merozoite surface protein 4 (PvMSP4) by Martinez, Pilar, Suarez, Carlos F., Gomez, Andromeda, Cardenas, Paula P., Guerrero, Jose E., Patarroyo, Manuel A.

“…Plasmodium vivax merozoite surface protein 4 (PvMSP4) has been considered to be a promising malarial vaccine candidate. The antigenic diversity displayed by…”
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The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants by Materna, Marie, Delmonte, Ottavia M, Bosticardo, Marita, Momenilandi, Mana, Conrey, Peyton E, Charmeteau-De Muylder, Bénédicte, Bravetti, Clotilde, Bellworthy, Rebecca, Cederholm, Axel, Staels, Frederik, Ganoza, Christian A, Darko, Samuel, Sayed, Samir, Le Floc'h, Corentin, Ogishi, Masato, Rinchai, Darawan, Guenoun, Andrea, Bolze, Alexandre, Khan, Taushif, Gervais, Adrian, Krüger, Renate, Völler, Mirjam, Palterer, Boaz, Sadeghi-Shabestari, Mahnaz, Langlois de Septenville, Anne, Schramm, Chaim A, Shah, Sanjana, Tello-Cajiao, John J, Pala, Francesca, Amini, Kayla, Campos, Jose S, Lima, Noemia Santana, Eriksson, Daniel, Lévy, Romain, Seeleuthner, Yoann, Jyonouchi, Soma, Ata, Manar, Al Ali, Fatima, Stittrich, Anna, Deswarte, Caroline, Pereira, Anaïs, Mégret, Jérôme, Le Voyer, Tom, Bastard, Paul, Berteloot, Laureline, Dussiot, Michaël, Vladikine, Natasha, Cardenas, Paula P, Jouanguy, Emmanuelle, Alqahtani, Mashael, Hasan, Amal, Thanaraj, Thangavel Alphonse, Rosain, Jérémie, Al Qureshah, Fahd, Sabato, Vito, Alyanakian, Marie Alexandra, Leruez-Ville, Marianne, Rozenberg, Flore, Haddad, Elie, Regueiro, Jose R, Toribio, Maria L, Kelsen, Judith R, Salehi, Mansoor, Nasiri, Shahram, Torabizadeh, Mehdi, Rokni-Zadeh, Hassan, Changi-Ashtiani, Majid, Vatandoost, Nasimeh, Moravej, Hossein, Akrami, Seyed Mohammad, Mazloomrezaei, Mohsen, Cobat, Aurélie, Meyts, Isabelle, Toyofuku, Etsushi, Nishimura, Madoka, Moriya, Kunihiko, Mizukami, Tomoyuki, Imai, Kohsuke, Abel, Laurent, Malissen, Bernard, Al-Mulla, Fahd, Alkuraya, Fowzan Sami, Parvaneh, Nima, von Bernuth, Horst, Beetz, Christian, Davi, Frédéric, Douek, Daniel C, Cheynier, Rémi, Langlais, David, Landegren, Nils, Marr, Nico, Morio, Tomohiro, Shahrooei, Mohammad, Schrijvers, Rik, Henrickson, Sarah E, Luche, Hervé, Notarangelo, Luigi D, Casanova, Jean-Laurent, Béziat, Vivien

“…We describe humans with rare biallelic loss-of-function variants impairing pre-α T cell receptor (pre-TCRα) expression. Low circulating naive αβ T cell counts…”
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Nonsense CD247 mutations show dominant-negative features in TCR expression and function by Briones, Alejandro C, Megino, Rebeca F, Marin, Ana V, Chacón-Arguedas, Daniel, García-Martinez, Elena, Martín, Héctor Balastegui, Reyburn, Hugh T, Henrickson, Sarah E, Rodríguez-Sainz, Carmen, Seoane-Reula, Elena, Sanchez-Mateos, Paloma, Cardenas, Paula P, Regueiro, Jose R

“…The invariant TCRζ/CD247 homodimer is crucial for TCR/CD3 expression and signaling through its three immunoreceptor tyrosine-based activation motifs (ITAMs)…”
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New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy by Bravo García-Morato, María, Aracil Santos, Francisco Javier, Briones, Alejandro Contreras, Blázquez Moreno, Alfonso, del Pozo Maté, Ángela, Domínguez-Soto, Ángeles, Beato Merino, María José, del Pino Molina, Lucía, Torres Canizales, Juan, Marin, Ana Victoria, Vallespín García, Elena, Feito Rodríguez, Marta, Plaza López Sabando, Diego, Jiménez-Reinoso, Anaïs, Mozo del Castillo, Yasmina, Sanz Santaeufemia, Francisco José, de Lucas-Laguna, Raúl, Cárdenas, Paula P., Casamayor Polo, Laura, Coronel Díaz, María, Valés-Gómez, Mar, Roldán Santiago, Ernesto, Ferreira Cerdán, Antonio, Nevado Blanco, Julián, Corbí, Ángel L., Reyburn, Hugh T., Regueiro, José Ramón, López-Granados, Eduardo, Rodríguez Pena, Rebeca

“…Genetic analysis using a next-generation sequencing (NGS)–customized panel allowed us to exclude mutations in all previously reported PID-related genes…”
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New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy by Bravo García-Morato, María, Aracil Santos, Francisco Javier, Briones, Alejandro Contreras, Blázquez Moreno, Alfonso, Del Pozo Maté, Ángela, Domínguez-Soto, Ángeles, Beato Merino, María José, Del Pino Molina, Lucía, Torres Canizales, Juan, Marin, Ana Victoria, Vallespín García, Elena, Feito Rodríguez, Marta, Plaza López Sabando, Diego, Jiménez-Reinoso, Anaïs, Mozo Del Castillo, Yasmina, Sanz Santaeufemia, Francisco José, de Lucas-Laguna, Raúl, Cárdenas, Paula P, Casamayor Polo, Laura, Coronel Díaz, María, Valés-Gómez, Mar, Roldán Santiago, Ernesto, Ferreira Cerdán, Antonio, Nevado Blanco, Julián, Corbí, Ángel L, Reyburn, Hugh T, Regueiro, José Ramón, López-Granados, Eduardo, Rodríguez Pena, Rebeca

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