Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gessami Sanchez"'
Autor:
Julie Kanter, R. Clark Brown, Cynthia Norris, Santosh M. Nair, Abdullah Kutlar, Deepa Manwani, Nirmish Shah, Chiaki Tanaka, Shankaranand Bodla, Gessami Sanchez-Olle, Urs Albers, Darla Liles
Publikováno v:
Blood Advances. 7:943-952
Crizanlizumab is an anti–P-selectin monoclonal antibody indicated to reduce the frequency/prevent recurrence of vaso-occlusive crises (VOCs) in patients with sickle cell disease (SCD) aged ≥16 years. This analysis of an ongoing phase 2, nonrandom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a0d8d9b6bc44660774018cebf9778b2
https://doi.org/10.1182/bloodadvances.2022008209
https://doi.org/10.1182/bloodadvances.2022008209
Autor:
Santosh M Nair, Shankaranand Bodla, Gessami Sanchez-Olle, R. Clark Brown, Kim Smith-Whitley, Darla K. Liles, Chiaki Tanaka, Julie Kanter, Nirmish Shah, Urs Albers
Publikováno v:
Blood. 136:17-19
Background: SCD is an inherited blood disorder characterized by hemolytic anemia, endothelial damage and acutely painful VOCs that cause chronic and potentially life-threatening complications. P-selectin is an adhesion protein that plays a key role i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b08e3658bb16e6db023000a793cb54e5
https://doi.org/10.1182/blood-2020-137434
https://doi.org/10.1182/blood-2020-137434
Autor:
Katherine Stemke-Hale, Mathew S. Maurer, Ana Vivancos, Yuker Wang, Gessami Sanchez, Violeta Serra, Gordon B. Mills, Yasir H. Ibrahim, Cristina Saura, Jordi Rodon, Ramon Parsons, Ludmila Prudkin, José Baselga, José Antonio Jiménez, Javier Hernandez, Claudia Aura, Santiago Ramón y Cajal, Rodrigo Dienstmann, Hanina Hibshoosh, Josep Tabernero, Vicente Peg
Publikováno v:
Cancer Research. 72:683-683
PTEN and PIK3CA status are potential predictors of response to PI3K-pathway inhibitors. Therefore, we searched the most reliable platform to assess both PTEN expression and PIK3CA mutations in primary and metastatic breast cancer (BC). Cross-validati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dc5e589baf1a6a4b3bad01cc58fb500
https://doi.org/10.1158/1538-7445.am2012-683
https://doi.org/10.1158/1538-7445.am2012-683
Autor:
Gessami Sanchez, Raül Santamaria, Daniel Grinberg, Amparo Chabás, Laura Gort, Evagelia Dimitriou, Lluïsa Vilageliu, Helen Michelakakis, Spyros Fotopoulos, Maria Dassopoulou, Marina Moraitou
Publikováno v:
Journal of Inherited Metabolic Disease. 29:591-591
Homozygosity for D409H has been associated with a unique type III subtype of the disease with a phenotype dominated by severe cardiovascular involvement, whereas neurological findings, if present, are restricted to oculomotor apraxia and features suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bc6f38c342d9a64bd3f4d87b211a81a
https://doi.org/10.1007/s10545-006-0316-x
https://doi.org/10.1007/s10545-006-0316-x