Browsing by Author "González Sarmiento, Rogelio"

Now showing items 1-20 of 24

BAX and BCL‐2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: the Retina 4 project

Pastor Idoate, Salvador ; Rodríguez Hernández, Irene; Rojas, Jimena; Fernández Martínez, Itziar ; García Gutiérrez, María Teresa; Ruiz‐Moreno, Jose M.; Rocha Sousa, Amandio; Ramkissoon, Yashin D.; Harsum, Steven; MacLaren, Robert E.; Charteris, David G.; Van Meurs, Jan C.; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos (2015)
Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia

Díez Revuelta, Álvaro ; Cieza-Borrella, Clara; Suazo, Vanessa; González Sarmiento, Rogelio; Papiol, Sergi; Molina Rodríguez, Vicente (2014)
COL4A4 gene study of a European population: description of new mutations causing autosomal dominant Alport syndrome

Rosado, Consolación; Bueno Martínez, Elena ; Felipe, Carmen; González Sarmiento, Rogelio (2014)
Early‐onset acral basal cell carcinomas in Gorlin syndrome

Torrelo, A.; Vicente, A.; Navarro, L.; Planaguma, M.; González Sarmiento, Rogelio; Hernández‐Martín, A.; Noguera‐Morel, L.; Requena, L.; Colmenero, I.; Parareda, A.; González‐Enseñat, M.A.; Happle, R.; Bueno Martínez, Elena (2014)
Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series

Rodrigo-Nicolás, B.; Martín-Santiago, A.; Cañueto, J.; Vicente, A.; Torrelo, A.; Noguera-Morel, L.; Duat-Rodríguez, A.; Jorge Finnigan, Conrado ; Palacios-Álvarez, I.; García-Hernández, J.L.; Sebaratnam, Deshan; González Sarmiento, Rogelio; Hernández Martín, Ángela; Bueno Martínez, Elena (2018)
Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas

Bella Navarro, R.; García García, Ana Bárbara; González Sarmiento, Rogelio; Navarro, L.; Sánchez Sendra, B.; Revert, A.; Jordá, E.; Monteagudo, C.; Bueno Martínez, Elena (2017)
Functional characterization of rs2229094 (T>C) polymorphism in the tumor necrosis factor locus and lymphotoxin alpha expression in human retina: the Retina 4 project

Pastor Idoate, Salvador ; Rodríguez-Hernández, Irene; Rojas, Jimena; González-Buendía, Lucia; Delgado-Tirado, Santiago; López, Jose Carlos; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos (2017)
Genética en la inflamación, apoptosis y otras vías de muerte celular en el desprendimiento de retina y la vitreorretinopatía proliferante: Proyecto Retina-4

Pastor Idoate, Salvador (2015)
Immune system disorders, cancer and viral infections: A new treatment opportunity for the immune checkpoint inhibitors

Olivares Hernández, Alejandro; Figuero Pérez, Luis; MiRamóntes González, José Pablo ; López Gutiérrez, Álvaro; González Sarmiento, Rogelio; Cruz Hernández, Juan Jesús; Fonseca Sánchez, Emilio (2021)
Influence of DNA mismatch repair (MMR) system in survival and response to immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC): Retrospective analysis

Olivares Hernández, Alejandro; Barco Morillo, Edel del; Parra Pérez, Carmen; MiRamóntes González, José Pablo ; Figuero Pérez, Luis; Martín Gómez, Teresa ; Escala Cornejo, Roberto; Bellido Hernández, Lorena; González Sarmiento, Rogelio; Cruz Hernández, Juan Jesús; Ludeña de la Cruz, María Dolores (2022)
Matrix metalloproteinases in age-related macular degeneration (AMD)

García Onrubia, Luis; Valentín Bravo, Francisco Javier; Coco Martín, Rosa María ; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos ; Usategui Martín, Ricardo ; Pastor Idoate, Salvador (2020)
Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk

Usategui Martín, Ricardo ; Pastor Idoate, Salvador ; Chamorro, Antonio J.; Fernández Martínez, Itziar ; Fernández Bueno, Iván ; Marcos Martín, Miguel; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos (2019)
Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6

Citterio, Cintia E.; Morales, Cecilia M.; Bouhours-Nouet, Natacha; Machiavelli, Gloria A.; Gatelais, Frédérique; Coutant, Regis; González Sarmiento, Rogelio; Rivolta, Carina M.; Targovnik, Héctor M.; Bueno Martínez, Elena (2015)
Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone

Usategui Martín, Ricardo ; Gutiérrez-Cerrajero, Carlos; Jiménez-Vázquez, Sonia; Calero-Paniagua, Ismael; García-Aparicio, Judit; Corral Gudino, Luis ; del Pino-Montes, Javier; González Sarmiento, Rogelio (2018)
Predominantly pro-inflammatory phenotype with mixed M1/M2 polarization of peripheral blood classical monocytes and monocyte-derived macrophages among patients with excessive ethanol intake

Fernández Regueras, María; Carbonell, Cristina; Salete Granado, Daniel; García, Juan Luis; Gragera, Marcos; Pérez Nieto, María Ángeles; Morán Plata, Francisco Javier; Mayado, Andrea; Torres, Jorge Luis; Corchete Sánchez, Luis Antonio; Usategui Martín, Ricardo ; Bueno Martínez, Elena ; Rojas Pirela, Maura; Sabio, Guadalupe; González Sarmiento, Rogelio; Orfao, Alberto; Laso, Francisco Javier; Almeida, Julia; Marcos, Miguel (2023)
Programmed Cell Death and Autophagy in an in vitro Model of Spontaneous Neuroretinal Degeneration

Puertas Neyra, Kevin Louis ; Galindo Cabello, Nadia Regina ; Hernández Rodríguez, Leticia Adriána ; González Pérez, Fernando ; Rodríguez Cabello, José Carlos ; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos ; Usategui Martín, Ricardo ; Fernández Bueno, Iván (2022)
Resistance to immune checkpoint inhibitors secondary to myeloid-derived suppressor cells: A new therapeutic targeting of haematological malignancies

Olivares Hernández, Alejandro; Figuero Pérez, Luis; Terán Brage, Eduardo; López Gutiérrez, Álvaro; Tamayo Velasco, Álvaro ; González Sarmiento, Rogelio; Cruz Hernández, Juan Jesús; MiRamóntes González, José Pablo (2021)
Retinal neuroprotective effect of mesenchymal stem cells secretome through modulation of oxidative stress, autophagy, and programmed cell death

Usategui Martín, Ricardo ; Puertas Neyra, Kevin Louis ; Galindo Cabello, Nadia Regina ; Hernández Rodríguez, Leticia Adriána ; González Pérez, Fernando ; Rodríguez Cabello, José Carlos ; González Sarmiento, Rogelio; Pastor Jimeno, José Carlos ; Fernández Bueno, Iván (2022)
Rho-kinase inhibitors for the treatment of refractory diabetic macular oedema

Mateos Olivares, Milagros; García Onrubia, Luis; Valentín Bravo, Francisco Javier; González Sarmiento, Rogelio; López Gálvez, María Isabel ; Pastor Jimeno, José Carlos ; Usategui Martín, Ricardo ; Pastor Idoate, Salvador (2021)
Study of the true clinical progression of autosomal dominant alport syndrome in a european population

Rosado, Consolación; Bueno Martínez, Elena ; Felipe, Carmen; Valverde, Sebastián; González Sarmiento, Rogelio (2015)

Browsing by Author "González Sarmiento, Rogelio"

BAX and BCL‐2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: the Retina 4 project ﻿

Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia ﻿

COL4A4 gene study of a European population: description of new mutations causing autosomal dominant Alport syndrome ﻿

Early‐onset acral basal cell carcinomas in Gorlin syndrome ﻿

Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series ﻿

Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas ﻿

Functional characterization of rs2229094 (T&gt;C) polymorphism in the tumor necrosis factor locus and lymphotoxin alpha expression in human retina: the Retina 4 project ﻿

Genética en la inflamación, apoptosis y otras vías de muerte celular en el desprendimiento de retina y la vitreorretinopatía proliferante: Proyecto Retina-4 ﻿

Immune system disorders, cancer and viral infections: A new treatment opportunity for the immune checkpoint inhibitors ﻿

Influence of DNA mismatch repair (MMR) system in survival and response to immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC): Retrospective analysis ﻿

Matrix metalloproteinases in age-related macular degeneration (AMD) ﻿

Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk ﻿

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6 ﻿

Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone ﻿

Predominantly pro-inflammatory phenotype with mixed M1/M2 polarization of peripheral blood classical monocytes and monocyte-derived macrophages among patients with excessive ethanol intake ﻿

Programmed Cell Death and Autophagy in an in vitro Model of Spontaneous Neuroretinal Degeneration ﻿

Resistance to immune checkpoint inhibitors secondary to myeloid-derived suppressor cells: A new therapeutic targeting of haematological malignancies ﻿

Retinal neuroprotective effect of mesenchymal stem cells secretome through modulation of oxidative stress, autophagy, and programmed cell death ﻿

Rho-kinase inhibitors for the treatment of refractory diabetic macular oedema ﻿

Study of the true clinical progression of autosomal dominant alport syndrome in a european population ﻿

BAX and BCL‐2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: the Retina 4 project

Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia

COL4A4 gene study of a European population: description of new mutations causing autosomal dominant Alport syndrome

Early‐onset acral basal cell carcinomas in Gorlin syndrome

Evidence of the high prevalence of neurological disorders in nonsyndromic X-linked recessive ichthyosis: a retrospective case series

Familial seborrhoeic keratosis associated with multiple ‘pure reticulated acanthomas’ and infundibulocystic basal cell carcinomas

Functional characterization of rs2229094 (T>C) polymorphism in the tumor necrosis factor locus and lymphotoxin alpha expression in human retina: the Retina 4 project

Genética en la inflamación, apoptosis y otras vías de muerte celular en el desprendimiento de retina y la vitreorretinopatía proliferante: Proyecto Retina-4

Immune system disorders, cancer and viral infections: A new treatment opportunity for the immune checkpoint inhibitors

Influence of DNA mismatch repair (MMR) system in survival and response to immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC): Retrospective analysis

Matrix metalloproteinases in age-related macular degeneration (AMD)

Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6

Polymorphisms in genes implicated in base excision repair (BER) pathway are associated with susceptibility to Paget's disease of bone

Predominantly pro-inflammatory phenotype with mixed M1/M2 polarization of peripheral blood classical monocytes and monocyte-derived macrophages among patients with excessive ethanol intake

Programmed Cell Death and Autophagy in an in vitro Model of Spontaneous Neuroretinal Degeneration

Resistance to immune checkpoint inhibitors secondary to myeloid-derived suppressor cells: A new therapeutic targeting of haematological malignancies

Retinal neuroprotective effect of mesenchymal stem cells secretome through modulation of oxidative stress, autophagy, and programmed cell death

Rho-kinase inhibitors for the treatment of refractory diabetic macular oedema

Study of the true clinical progression of autosomal dominant alport syndrome in a european population