Zobrazeno 1 - 10
of 310
pro vyhledávání: '"Eduardo Salido"'
Autor:
Virginia Nieto-Romero, Aida García-Torralba, Andrea Molinos-Vicente, Francisco José Moya, Sandra Rodríguez-Perales, Ramón García-Escudero, Eduardo Salido, José-Carlos Segovia, María García-Bravo
Publikováno v:
iScience, Vol 27, Iss 4, Pp 109530- (2024)
Summary: Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder characterized by oxalate overproduction in the liver, resulting in renal damage. It is caused by mutations in the AGXT gene. Combined liver and kidney transplantation
Externí odkaz:
https://doaj.org/article/411c37ce7ba4439a93a3142a4e678f12
Autor:
Asunción Beltrán, María Sánchez-Villalobos, Eduardo Salido, Carmen Algueró, Eulalia Campos, Ana Belén Pérez-Oliva, Miguel Blanquer, José M. Moraleda
Publikováno v:
Biomedicines, Vol 12, Iss 7, p 1607 (2024)
Hereditary spherocytosis (HS) is a membranopathy that impacts the vertical junctions between the cytoskeleton and the plasma membrane of erythrocytes. The gold standard method for diagnosing it is osmotic gradient ektacytometry (OGE). However, access
Externí odkaz:
https://doaj.org/article/02a23b33cbf84477aff34ea6ccf1c1d3
Autor:
Martyna Krupinska, Carmen León, Rocío López Henríquez, Beatriz Esquivel Vázquez, Rosa Nieves Rodríguez Rodríguez, Patricia Marrero Marrero, Luciano Delgado Plasencia, Eduardo Salido
Publikováno v:
Polish Journal of Pathology, Vol 73, Iss 4, Pp 364-370 (2023)
Atypical spindle cell lipomatous tumour (ASCLT) is a benign neoplasm that presents a variable proportion of atypical spindle and adipocytic cells, frequently expressing CD34, and embedded in myxoid or collagenous matrix. An important feature is a con
Externí odkaz:
https://doaj.org/article/c96bf6b0199340f2a3bf3f98091c11cb
Autor:
Lucia Castilla, Jose Aspa, Jorge Martínez Nieto, Ángel Zúñiga Cabrera, Marta Santiago, Ana Garcia Feria, Josefa Esperanza Marco Buades, María Argüello Marina, Rosa María Ayala Diaz, Ricardo Sanchez, Rafael Del Orbe Barreto, Ana Lobo Olmedo, Julio Dávila-Valls, Sonia Martín-Pérez, Cristina Jativa Saez, Inés Hernández Rodriguez, Eduardo Salido, Valle Recasens, Lucía Guerrero Fernández, Maria Belén Moreno Risco, Ataulfo González Fernández, Montserrat Lopez Rubio
Publikováno v:
HemaSphere, Vol 7, p e6313050 (2023)
Externí odkaz:
https://doaj.org/article/eda95f35d3a94157acf2603bc7cba2c6
Autor:
Domingo Hernández, Teresa Vázquez-Sánchez, Eugenia Sola, Veronica Lopez, Pedro Ruiz-Esteban, Abelardo Caballero, Eduardo Salido, Myriam Leon, Aurelio Rodriguez, Nuria Serra, Consuelo Rodriguez, Carme Facundo, Manel Perello, Irene Silva, Domingo Marrero-Miranda, Ignacio Cidraque, Francesc Moreso, Luis Guirado, Daniel Serón, Armando Torres
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Subclinical inflammation, including borderline lesions (BL), is very common (30–40%) after kidney transplantation (KT), even in low immunological risk patients, and can lead to interstitial fibrosis/tubular atrophy (IFTA) and wo
Externí odkaz:
https://doaj.org/article/f3dd443430a94f4380cfa6f11e3346e2
Autor:
María Sánchez Villalobos, Eduardo Salido Fiérrez, Jorge Martínez Nieto, Mª Carmen García Garay, Asunción Beltrán Videla, Ana Belen Pérez Oliva, Miguel Blanquer Blanquer, José María Moraleda Jiménez
Publikováno v:
Hematology Reports, Vol 14, Iss 4, Pp 300-304 (2022)
Hereditary pyropoikilocytosis (HPP) is characterised by severe hemolytic anemia due to membrane instability. We report the case of a 13-day-old boy with neonatal jaundice and severe hemolytic anemia. A peripheral smear examination showed severe aniso
Externí odkaz:
https://doaj.org/article/0a1b763d9cd44a2f82caace5345ab164
Autor:
Rebeca Martinez-Turrillas, Angel Martin-Mallo, Saray Rodriguez-Diaz, Natalia Zapata-Linares, Paula Rodriguez-Marquez, Patxi San Martin-Uriz, Amaia Vilas-Zornoza, María E. Calleja-Cervantes, Eduardo Salido, Felipe Prosper, Juan R. Rodriguez-Madoz
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 25, Iss , Pp 137-146 (2022)
Genome-editing strategies, especially CRISPR-Cas9 systems, have substantially increased the efficiency of innovative therapeutic approaches for monogenic diseases such as primary hyperoxalurias (PHs). We have previously demonstrated that inhibition o
Externí odkaz:
https://doaj.org/article/bd677a9b29c243f29edb333113c24eef
Autor:
María Sánchez-Villalobos, Eulalia Campos Baños, María Jesús Juan Fita, José María Egea Mellado, Inmaculada Gonzalez Gallego, Asunción Beltrán Videla, Mercedes Berenguer Piqueras, Mar Bermúdez Cortés, José María Moraleda Jiménez, Encarna Guillen Navarro, Eduardo Salido Fierrez, Ana B. Pérez-Oliva
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 4, p 55 (2023)
Sickle cell disease (SCD) is an inherited autosomal recessive hemoglobin disorder caused by the presence of hemoglobin S, a mutant abnormal hemoglobin caused by a nucleotide change in codon 6 of the β-globin chain gene. SCD involves a chronic inflam
Externí odkaz:
https://doaj.org/article/9546bdae6acb46e69273e85dad40b1a2
Autor:
Juan Luis Pacheco-Garcia, Matteo Cagiada, Kelly Tienne-Matos, Eduardo Salido, Kresten Lindorff-Larsen, Angel L. Pey
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Recent advances in DNA sequencing technologies are revealing a large individual variability of the human genome. Our capacity to establish genotype-phenotype correlations in such large-scale is, however, limited. This task is particularly challenging
Externí odkaz:
https://doaj.org/article/ac7e3935ec344ca1bc48f1470a5bf2f1
Publikováno v:
Molecules, Vol 27, Iss 24, p 8762 (2022)
The mutations G170R and I244T are the most common disease cause in primary hyperoxaluria type I (PH1). These mutations cause the misfolding of the AGT protein in the minor allele AGT-LM that contains the P11L polymorphism, which may affect the foldin
Externí odkaz:
https://doaj.org/article/70acc055b13a40a58a70307115ca250f