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Your search keyword '"Fajardo‐Ramirez, Oscar R."' showing total 7 results
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7 results on '"Fajardo‐Ramirez, Oscar R."'

3. Fibroblast activation in response to TGFβ1 is modulated by co-culture with endothelial cells in a vascular organ-on-chip platform

Author

Luu, Rebeccah J., primary, Hoefler, B. Christopher, additional, Gard, Ashley L., additional, Ritenour, Casey R., additional, Rogers, Miles T., additional, Kim, Ernest S., additional, Coppeta, Jonathan R., additional, Cain, Brian P., additional, Isenberg, Brett C., additional, Azizgolshani, Hesham, additional, Fajardo-Ramirez, Oscar R., additional, García-Cardeña, Guillermo, additional, Lech, Matthew P., additional, Tomlinson, Lindsay, additional, Charest, Joseph L., additional, and Williams, Corin, additional

Published
2023
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4. T‐cell activation and bacterial infection in skin wounds of recessive dystrophic epidermolysis bullosa patients

Author

Alexeev, Vitali, primary, Huitema, Leonie, additional, Phillips, Taylor, additional, Cepeda, Rodrigo, additional, de los Cobos, Diego, additional, Perez, Regina Isabella Matus, additional, Salas‐Garza, Mauricio, additional, Fajardo‐Ramirez, Oscar R., additional, Ringpfeil, Franziska, additional, Uitto, Jouni, additional, Salas‐Alanis, Julio Cesar, additional, and Igoucheva, Olga, additional

Published
2022
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7. Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 Mutation.

Author

Esmer C, Salas-Alanis JC, Fajardo-Ramirez OR, Ramírez B, Hua R, and Choate K

Subjects
Fatal Outcome, Female, Humans, Infant, Newborn, Keratitis physiopathology, Mutation, Connexin 26 genetics, Keratitis genetics, Sepsis mortality
Abstract

Keratitis-ichthyosis-deafness syndrome is a well-characterized disease that has been related to mutations in the GJB6 gene. Clinical features such as erythrokeratoderma, palmoplantar keratoderma, alopecia, and progressive vascularizing keratitis, among others, are well known in this entity. In this report we describe a newborn female patient diagnosed with keratitis-ichthyosis-deafness syndrome with a lethal outcome due to sepsis. The patient harbored the mutation A88V that has been previously reported in lethal cases.

Published
2016

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