Browsing by author "Iglesias, Sara"

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)

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)

Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis

Coto Segura, Pablo

; González Fernández, Daniel; Batalla, Alberto; Gómez de Oña, Juan

; González Lara, Leire; Queiro Silva, Rubén

; Alonso, Belén; Iglesias, Sara; Coto García, Eliecer

(2016)

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)

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 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)

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Martín Fernández, María

; Álvarez Martínez, María Victoria

; Alonso, Belén; Iglesias, Sara; Coto García, Eliecer

(2014)

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)

NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant

Coto Segura, Pablo

; González Lara, Leire; Gómez de Oña, Juan

; Eiris Salvado, Noemí; Batalla, Ana; Gómez, Celia; Requena, Sheila; Queiro Silva, Rubén

; Alonso, Belén; Iglesias, Sara; Coto García, Eliecer

(2017)

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)

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes among Tunisian Patients

Jaafar, N.; Gómez de Oña, Juan

; Kammoun, I.; Zairi, I.; Amara, W. B.; Kachboura, S.; Kraiem, S.; Hammami, M.; Iglesias, Sara; Alonso, Belén; Coto García, Eliecer

(2016)

Browsing by author "Iglesias, Sara"

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

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

Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis ﻿

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 ﻿

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 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 ﻿

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing ﻿

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 ﻿

NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant ﻿

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

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes among Tunisian Patients ﻿

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

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

Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis

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

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 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

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

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

NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant

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

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes among Tunisian Patients