Listar por autor "Alonso González, Belén"

ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: A Next Generation Sequencing approach

Tavira Iglesias, Beatriz

; Gómez de Oña, Juan

; Díaz Corte, María del Carmen

; Suárez, Beatriz; Coronel, Diego; Arias, Manuel; López Larrea, Carlos

; Iglesias, Sara; Alonso González, Belén

; Rodrigo, Emilio; Coto García, Eliecer

(2015)

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease

Miar Cuervo, Ana Belén

; Álvarez Martínez, María Victoria

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Alonso González, Belén

; Martínez Rodríguez, Carmen

; Calatayud Noguera, María Teresa

; Menéndez González, Manuel

; Morís de la Tassa, Germán

; Coto García, Eliecer

(2011)

CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients

Coto Segura, Pablo

; Batalla Cebey, Ana; González Fernández, Daniel; Gómez de Oña, Juan

; Santos-Juanes Jiménez, Jorge

; Queiro Silva, Rubén

; Alonso González, Belén

; Iglesias, Sara; Coto García, Eliecer

(2015)

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Coto García, Eliecer

; Calvo Temprano, David

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Rubín López, José Manuel

; Díaz Corte, María del Carmen

; Gil Peña, Helena

; Alonso González, Belén

; Iglesias, Sara; Gómez de Oña, Juan

(2017)

An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations

Coto García, Eliecer

; García Fernández, F. J.; Calvo Temprano, David

; Salgado Aranda, R.; Martín González, J.; Alonso González, Belén

; Iglesias, Sara; Gómez de Oña, Juan

(2016)

FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients

Mena Álvarez, Lorena de

; Fernández Cardo, Lucía

; Coto García, Eliecer

; Miar Cuervo, Ana Belén

; Díaz González, Marta Elvira

; Corao Trueba, Ana Isabel

; Alonso González, Belén

; Ribacoba Montero, Renée

; Salvador Aguiar, Carlos

; Menéndez González, Manuel

; Morís de la Tassa, Germán

; Álvarez Martínez, María Victoria

(2010)

Furin gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19

Coto García, Eliecer

; Muñiz Albaiceta, Guillermo

; Amado Rodríguez, Laura

; García Clemente, Marta María

; Cuesta Llavona, Elías; Vázquez Coto, Daniel; Alonso González, Belén

; Iglesias, Sara; Melón García, Santiago

(2022)

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Rodríguez Reguero, José Julián

; Gómez de Oña, Juan

; Martín Fernández, María

; Flórez Muñoz, Juan Pablo; Morís de la Tassa, César

; Iglesias, Sara; Alonso González, Belén

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2013)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

Coto García, Eliecer

; Rodríguez Reguero, José Julián

; Avanzas Fernández, Pablo

; Pascual Calleja, Isaac

; Martín, M.; Hevia Nava, Sergio

; Morís de la Tassa, César

; Díaz Molina, Beatriz

; Rodríguez Lambert, José Luis

; Alonso González, Belén

; Cuesta Llavona, Elías; Díaz Corte, María del Carmen

; Gómez, Juan (2019)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Alonso González, Belén

; Iglesias, Sara; Rodríguez Reguero, José Julián

; López Larrea, Carlos

; Coto Segura, Pablo

(2018)

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, José Julián

; Martín Fernández, María

; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Díaz Molina, Beatriz

; Avanzas Fernández, Pablo

; Coto García, Eliecer

(2018)

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Alonso González, Belén

; Iglesias, Sara; Gil Peña, Helena

; Yin, Xueqian; Coto Segura, Pablo

(2018-10-08)

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients

Tavira Iglesias, Beatriz

; Gómez de Oña, Juan

; Málaga Guerrero, Serafín

; Santos Rodríguez, Fernando

; Fernández Aracama, Javier; Alonso González, Belén

; Iglesias, Sara; Benavides, Ana; Hernando, Inés; Plasencia, Ana; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2015)

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease

Miar Cuervo, Ana Belén

; Álvarez Martínez, María Victoria

; Corao Trueba, Ana Isabel

; Alonso González, Belén

; Díaz González, Marta Elvira

; Menéndez, Manuel; Martínez, Carmen; Calatayud Noguera, María Teresa

; Morís de la Tassa, César

(2011)

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

Coto García, Eliecer

; Gómez de Oña, Juan

; Alonso González, Belén

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Menéndez González, Manuel

; Martínez Rodríguez, Carmen

; Calatayud Noguera, María Teresa

; Morís de la Tassa, Germán

; Álvarez Martínez, María Victoria

(2011)

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

Palacín Fernández, María

; Álvarez Martínez, María Victoria

; Martín Fernández, María

; Díaz González, Marta Elvira

; Corao Trueba, Ana Isabel

; Alonso González, Belén

; Díaz Molina, Beatriz

; Lozano Martínez-Luengas, Íñigo

; Avanzas Fernández, Pablo

; Morís de la Tassa, César

; Rodríguez Reguero, José Julián

; Rodríguez Fernández, Isabel

; López Larrea, Carlos

; Cannata Andía, Jorge Benito

; Batalla, Alberto; Ruiz Ortega, Marta; Martínez Camblor, Pablo

; Coto García, Eliecer

(2011)

Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients

Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Junquera, Manuel R.; Álvarez, Celso; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Coto García, Eliecer

(2016)

Next generation sequencing search for uromodulin gene variants related with impaired renal function

Gómez de Oña, Juan

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Álvarez, Fancisco; Iglesias, Sara; Alonso González, Belén

; Coto García, Eliecer

(2015)

A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients

Fernández, Ángela; Gómez de Oña, Juan

; Alonso González, Belén

; Iglesias, Sara; Coto García, Eliecer

(2015)

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy

Coto García, Eliecer

; Rodríguez Reguero, José Julián

; Palacín Fernández, María

; Gómez de Oña, Juan

; Alonso González, Belén

; Iglesias, Sara; Martín Fernández, María

; Tavira Iglesias, Beatriz

; Díaz Molina, Beatriz

; Morales Pérez, Carlos Alonso

; Morís de la Tassa, César

; Rodríguez Lambert, José Luis

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Álvarez Martínez, María Victoria

(2012)

Listar por autor "Alonso González, Belén"

ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: A Next Generation Sequencing approach ﻿

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease ﻿

CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients ﻿

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT ﻿

An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations ﻿

FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients ﻿

Furin gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19 ﻿

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain) ﻿

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease ﻿

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function ﻿

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy ﻿

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function ﻿

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients ﻿

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease ﻿

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy ﻿

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H ﻿

Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients ﻿

Next generation sequencing search for uromodulin gene variants related with impaired renal function ﻿

A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients ﻿

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy ﻿

ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: A Next Generation Sequencing approach

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease

CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations

FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients

Furin gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease

Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients

Next generation sequencing search for uromodulin gene variants related with impaired renal function

A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy