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Navegar por autor "Carracedo Álvarez, Ángel"

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Mostrando ítems 41-59 de 59

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      Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders 

      2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]
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      Next-generation sequencing data strengthens the involvement of cardiac structural diseases in Sudden Infant Death Syndrome (SIDS) 

      2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio [et al.]
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      Nucleocytoplasmic transport and gene expression in patients with heart failure 

      2012- González Juanatey, José Ramón; Carracedo Álvarez, Ángel; Vidal Figueroa, Anxo
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      P3.23 Characterization of a new mutation in the GADP1 gene causing axonal autosomal dominant Charcot-Marie-Tooth disease (CMT2K) 

      2011- Carracedo Álvarez, Ángel; Blanco Arias, Patricia; Arias Gómez, Manuel; Pardo Fernández, Julio; Guijarro del Amo, Mónica [et al.]
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      Patterns of Y-STR variation in Italy 

      2012- Carracedo Álvarez, Ángel
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      Pharmacogenetics of OATP transporters reveals that SLCO1B1 c.388a>G variant is determinant of increased atorvastatin response 

      2011- Carracedo Álvarez, Ángel; Salas Ellacuriaga, Antonio; Phillips, Cristopher Paul; Rodrigues, AC; Rodrigues, Alice C; [et al.]
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      Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration. 

      2013- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Candamio Folgar, Sonia; [et al.]
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      Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients 

      2013- Carracedo Álvarez, Ángel; Brión Martínez, María José; Iñiguez Romo, Andres; Bravo Amaro, Marisol; Bastos Fernández, Guillermo [et al.]
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      Population genetics of 17 Y-STR markers in West Libya (Tripoli region) 

      2013- Carracedo Álvarez, Ángel; Sánchez Diz, Paula; Rey González, Daniel
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      Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables 

      2015- Carracedo Álvarez, Ángel; Brión Martínez, María José
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      Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases. 

      2011- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]
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      Sarcomeric gene mutations in sudden infant death syndrome (SIDS) 

      2012- Carracedo Álvarez, Ángel; Brión Martínez, María José; Santori Gómez, Montserrat; Blanco Verea, Alejandro José; Gil Torres, Rocio; [et al.]
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      SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests? 

      2012- Carracedo Álvarez, Ángel; Salas Ellacuriaga, Antonio
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      SNPS in DNA repair and damage detection genes and acute normal tissue toxicity in prostate cancer patients 

      2012- Fachal Vilar, Laura; Vega Gliemmo, Ana; Carracedo Álvarez, Ángel; Sanchez Garcia, Manuel; Lobato Busto, Ramón; [et al.]
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      The CYP1A2 -163C>A polymorphism is associated with clozapine-induced generalized tonic-clonic seizures in Brazilian schizophrenia patients 

      2013- Carracedo Álvarez, Ángel
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      The value of genetic polymorphisms to predict toxicity in metastatic colorectal patients with irinotecan-based regimens 

      2012- Carracedo Álvarez, Ángel; Mosquera Leal, Ana; Candamio Folgar, Sonia; López López, Rafael; Barros Angueira, Francisco; [et al.]
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      Tumor Profiling at the Service of Cancer Therapy 

      2021- Fernández Rozadilla, Ceres; Santos Simoes, Ana Rita; Lleonart, M. E.; Carnero, A.; Carracedo Álvarez, Ángel [et al.]
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      Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage 

      2012- Carracedo Álvarez, Ángel
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      Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease 

      2014- Carracedo Álvarez, Ángel; Brión Martínez, María José; Blanco Verea, Alejandro José; Sobrino Rey, Beatríz; Amigo Lechuga, Jorge; [et al.]
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