Exploration of a Collaborative Self-Directed Learning Model in Medical Education

por Kemp, Kyeorda, Baxa, Dwayne, Cortes, Claudio
Publicado 2022

The Challenges and Opportunities of Sustaining Academia-Sponsored Community Service Programs for Latinx Youth During the COVID-19 Pandemic

por Kim, Cheryne M., Silverman, Brittany R., Cortes, Claudio
Publicado 2021

EPySeg: a coding-free solution for automated segmentation of epithelia using deep learning

por Aigouy, Benoit, Cortes, Claudio, Liu, Shanda, Prud'Homme, Benjamin
Publicado 2020

Local release of properdin in the cellular microenvironment: role in pattern recognition and amplification of the alternative pathway of complement

por Cortes, Claudio, Ohtola, Jennifer A., Saggu, Gurpanna, Ferreira, Viviana P.
Publicado 2013

Hijacking Factor H for Complement Immune Evasion

por Moore, Sara R., Menon, Smrithi S., Cortes, Claudio, Ferreira, Viviana P.
Publicado 2021

An Integrated Mycobacterium tuberculosis Infection Session: Utilizing an Online Collaborative Platform in a Synchronous Classroom Setting

por Jackman, Trent D., Dersch, Anne M., Taylor, Tracey A. H., Cortes, Claudio
Publicado 2021

Characterization of Binding Properties of Individual Functional Sites of Human Complement Factor H

por Haque, Aftabul, Cortes, Claudio, Alam, M. Nurul, Sreedhar, Maladi, Ferreira, Viviana P., Pangburn, Michael K.
Publicado 2020

Yeast-based assay identifies novel Shh/Gli target genes in vertebrate development

por Milla, Luis A, Cortés, Claudio R, Hodar Q, Christian, Oñate, Maritza G, Cambiazo, Veronica, Burgess, Shawn M, Palma, Verónica
Publicado 2012

Factor H C-Terminal Domains Are Critical for Regulation of Platelet/Granulocyte Aggregate Formation

por Blatt, Adam Z., Saggu, Gurpanna, Cortes, Claudio, Herbert, Andrew P., Kavanagh, David, Ricklin, Daniel, Lambris, John D., Ferreira, Viviana P.
Publicado 2017

Properdin Is a Key Player in Lysis of Red Blood Cells and Complement Activation on Endothelial Cells in Hemolytic Anemias Caused by Complement Dysregulation

por Chen, Jin Y., Galwankar, Neeti S., Emch, Heather N., Menon, Smrithi S., Cortes, Claudio, Thurman, Joshua M., Merrill, Samuel A., Brodsky, Robert A., Ferreira, Viviana P.
Publicado 2020

COVID-19 severity is related to poor executive function in people with post-COVID conditions

por Ariza, Mar, Cano, Neus, Segura, Bàrbara, Adan, Ana, Bargalló, Núria, Caldú, Xavier, Campabadal, Anna, Jurado, Maria Angeles, Mataró, Maria, Pueyo, Roser, Sala-Llonch, Roser, Barrué, Cristian, Bejar, Javier, Cortés, Claudio Ulises, Garolera, Maite, Junqué, Carme
Publicado 2023

Neuropsychological impairment in post-COVID condition individuals with and without cognitive complaints

por Ariza, Mar, Cano, Neus, Segura, Bàrbara, Adan, Ana, Bargalló, Núria, Caldú, Xavier, Campabadal, Anna, Jurado, Maria Angeles, Mataró, Maria, Pueyo, Roser, Sala-Llonch, Roser, Barrué, Cristian, Bejar, Javier, Cortés, Claudio Ulises, Junqué, Carme, Garolera, Maite
Publicado 2022

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function

por Cortés, Claudio R., McInerney-Leo, Aideen M., Vogel, Ida, Rondón Galeano, Maria C., Leo, Paul J., Harris, Jessica E., Anderson, Lisa K., Keith, Patricia A., Brown, Matthew A., Ramsing, Mette, Duncan, Emma L., Zankl, Andreas, Wicking, Carol
Publicado 2016

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

por Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteboer, Stef J. F., Taylor, S. Paige, Herridge, Warren, Johnson, Colin A., Scambler, Peter J., Ueffing, Marius, Kayserili, Hulya, Krakow, Deborah, King, Stephen M., Beales, Philip L., Al-Gazali, Lihadh, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Mitchison, Hannah M., Witman, George B.
Publicado 2015

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

por Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteboer, Stef J. F., Taylor, S. Paige, Herridge, Warren, Johnson, Colin A., Scambler, Peter J., Ueffing, Marius, Kayserili, Hulya, Krakow, Deborah, King, Stephen M., Beales, Philip L., Al-Gazali, Lihadh, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Mitchison, Hannah M., Witman, George B.
Publicado 2016