Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Saa, Laura"'
Autor:
Reifs, Antonio, Fernandez-Calvo, Alba, Alonso-Lerma, Borja, Schönfelder, Jörg, Franco, David, Ortega-Muñoz, Mariano, Casares, Salvador, Jimenez-Lopez, Concepcion, Saa, Laura, Cortajarena, Aitziber L., De Sancho, David, San Sebastian, Eider, Perez-Jimenez, Raul
Publikováno v:
In Journal of Biological Chemistry April 2024 300(4)
Autor:
Khatami, Neda, Guerrero, Pedro, Martín, Pablo, Quintela, Eztizen, Ramos, Viviana, Saa, Laura, Cortajarena, Aitziber L., de la Caba, Koro, Camarero-Espinosa, Sandra, Abarrategi, Ander
Publikováno v:
In Carbohydrate Polymers 15 January 2024 324
Publikováno v:
In Talanta 1 April 2021 225
Autor:
Fernandez‐Calvo, Alba, Reifs, Antonio, Saa, Laura, Cortajarena, Aitziber L., De Sancho, David, Perez‐Jimenez, Raul
Publikováno v:
Protein Science: A Publication of the Protein Society; Jul2024, Vol. 33 Issue 7, p1-11, 11p
Autor:
Alberto Velasco-Benítez, Carlos1 carlos.velasco@correounivalle.edu.co, Isabel Collazos-Saa, Laura1, Andres García-Perdomo, Herney2
Publikováno v:
Pediatric Gastroenterology, Hepatology & Nutrition. Sep2022, Vol. 25 Issue 5, p376-386. 11p.
Autor:
Barroso, Javier, Díez-Buitrago, Beatriz, Saa, Laura, Möller, Marco, Briz, Nerea, Pavlov, Valeri
Publikováno v:
In Biosensors and Bioelectronics 15 March 2018 101:116-122
Autor:
Grinyte, Ruta, Barroso, Javier, Díez-Buitrago, Beatriz, Saa, Laura, Möller, Marco, Pavlov, Valeri
Publikováno v:
In Analytica Chimica Acta 15 September 2017 986:42-47
Publikováno v:
Iatreia, Vol 30, Iss 4, Pp 455-462 (2017)
Cohen syndrome (CS) is an uncommon autosomal recessive genetic disorder attributed to damage on VPS13B gene, locus 8q22-q23. Characteristic phenotype consists of intellectual disability, microcephaly, facial dysmorphism, ophthalmic abnormalities, tru
Externí odkaz:
https://doaj.org/article/16093809e49e4754afcd153b9d41b612
Publikováno v:
In Analytica Chimica Acta 30 June 2015 881:131-138
Publikováno v:
In Nano Today October 2013 8(5):461-468