Listar por autor "Ramsay, Andrew John"

Aging and chronic DNA damage response activate a regulatory pathway involving miR-29 and p53

Piñeiro Ugalde, Alejandro

; Ramsay, Andrew John

; Rosa de Sáa, Jorge de la; Varela Egocheaga, Ignacio Alejandro

; Mariño García, Guillermo

; Cadiñanos Bañales, Juan; Lu, Jun; Pérez Freije, José María

; López Otín, Carlos

(EMBO, 2011)

Cell-cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas

Fanjul Fernández, Miriam

; Quesada Fernández, Víctor

; Cabanillas Farpón, Rubén

; Cadiñanos Bañales, Juan; Fontanil López, Tania

; Obaya González, Álvaro Jesús

; Ramsay, Andrew John

; Llorente Pendás, José Luis

; Astudillo González, María Aurora

; Cal Miguel, Santiago Jesús

; López Otín, Carlos

(2013)

Chronic Lymphocytic Leukemia with SF3B1 Mutation

Quesada Fernández, Víctor

; Ramsay, Andrew John

; López Otín, Carlos

(2012)

A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction

Wallace, Daniel F.; Secondes, Eriza S.; Rishi, Gautam; Ostini, L.; Mcdonald, C. J.; Lane, Steven W.; Vu, Therese; Hooper, John D.; Velasco, Gloria; Ramsay, Andrew John

; López Otín, Carlos

; Subramaniam, V. Nathan (2015)

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Quesada Fernández, Víctor

; Conde del Campo, Laura; Villamor Casas, Neus; Rodríguez Ordóñez, Gonzalo

; Ramsay, Andrew John

; Álvarez Puente, Diana

; Velasco Cotarelo, María Gloria

; Pérez Freije, José María

; Suárez Puente, Xosé Antón

; López Otín, Carlos

(2012)

Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia

Ramsay, Andrew John

; Rodríguez Martínez, David

; Villamor Casas, Neus; Kwarciak, Agnieszka

; Tejedor Vaquero, Juan Ramón

; Valcárcel, Juan; López Guillermo, Armando; Martínez Trillos, Alejandra; Suárez Puente, Xosé Antón

; Campo, Elías; López Otín, Carlos

; Quesada Fernández, Víctor

(2013)

Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients

Rodríguez Martínez, David

; Ramsay, Andrew John

; Quesada Fernández, Víctor

; Garabaya Fernández, Cecilia

; Campo, Elías; Pérez Freije, José María

; López Otín, Carlos

(2013)

The genomic landscape of chronic lymphocytic leukemia: clinical implications

Quesada Fernández, Víctor

; Ramsay, Andrew John

; Rodríguez Martínez, David

; Suárez Puente, Xosé Antón

; Campo, Elías; López Otín, Carlos

(2013)

Iron-deficiency anemia from matriptase-2 inactivation is dependent on the presence of functional Bmp6

Lenoir, Anne; Deschemin, Jean-Christophe; Kautz, Leon; Ramsay, Andrew John

; Roth, Marie-Paule; López Otín, Carlos

; Vaulont, Sophie; Nicolas, Gaël (2011)

Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency?

Nicolas, Gaël; Deschemin, Jean-Christophe; Ramsay, Andrew John

; Mayeux, Patrick; Grandchamp, Bernard; Beaumont, Carole; Velasco Cotarelo, María Gloria

; Vaulont, Sophie (2011)

Liver hemojuvelin protein levels in mice deficient in matriptase-2 (Tmprss6)

Krijt, Jan; Fujikura, Yuzo; Ramsay, Andrew John

; Velasco Cotarelo, María Gloria

; Necas, Emanuel (Elsevier, 2011)

Loss of mitochondrial protease OMA1 alters processing of the GTPase OPA1 and causes obesity and defective thermogenesis in mice

Moral Quirós, Pedro

; Ramsay, Andrew John

; Sala, David; Fernández-Vizarra, Erika; Rodríguez, Francisco; Peinado Mena, Juan Ramón; Fernández García, María de la Soledad

; Vega Álvarez, José Antonio

; Enríquez, José Antonio; Zorzano, Antonio; López Otín, Carlos

(EMBO, 2012)

Matriptase-2

Ramsay, Andrew John

; Kwarciak, A.; Hooper, J. D.; López Otín, Carlos

; Velasco Cotarelo, María Gloria

(2013)

Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis

Ramsay, Andrew John

; Hooper, John D.; Rodríguez Folgueras, Alicia

; Velasco Cotarelo, María Gloria

; López Otín, Carlos

(2009)

Matriptase-2 deficiency protects from obesity by modulating iron homeostasis

Rodríguez Folgueras, Alicia

; Freitas Rodríguez, Sandra

; Ramsay, Andrew John

; Garabaya Fernández, Cecilia

; Rodríguez Díaz, Francisco José

; Velasco Cotarelo, María Gloria

; López Otín, Carlos

(2018)

Matriptase-2 is essential for hepcidin repression during fetal life and postnatal development in mice to maintain iron homeostasis

Willemetz, Alexandra; Lenoir, Anne; Deschemin, Jean-Christophe; López Otín, Carlos

; Ramsay, Andrew John

; Vaulont, Sophie; Nicolas, Gaël (2014)

Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms

Ramsay, Andrew John

; Quesada Fernández, Víctor

; Sánchez, Maika; Garabaya Fernández, Cecilia

; Sardà, María P.; Baiget, Monserrat; Remacha, Ángel; Velasco Cotarelo, María Gloria

; López Otín, Carlos

(Oxford University Press, 2009)

Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia

Rodríguez Martínez, David

; Bretones Sánchez, Gabriel

; Quesada Fernández, Víctor

; Ramsay, Andrew John

; Moral Quirós, Pedro

; López Otín, Carlos

(2015)

Next-generation sequencing reveals the secrets of the chronic lymphocytic leukemia genome

Ramsay, Andrew John

; Martínez Trillos, Alejandra; Jares, Pedro; Rodríguez Martínez, David

; Kwarciak, Agnieszka

; Quesada Fernández, Víctor

(2013)

Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma

Aoude, Lauren G.; Pritchard, Antonia L.; Robles Espinoza, Carla Daniela; Quesada Fernández, Víctor

; López Otín, Carlos

; Ramsay, Andrew John

(2015)

Listar por autor "Ramsay, Andrew John"

Aging and chronic DNA damage response activate a regulatory pathway involving miR-29 and p53 ﻿

Cell-cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas ﻿

Chronic Lymphocytic Leukemia with SF3B1 Mutation ﻿

A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction ﻿

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia ﻿

Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia ﻿

Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients ﻿

The genomic landscape of chronic lymphocytic leukemia: clinical implications ﻿

Iron-deficiency anemia from matriptase-2 inactivation is dependent on the presence of functional Bmp6 ﻿

Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency? ﻿

Liver hemojuvelin protein levels in mice deficient in matriptase-2 (Tmprss6) ﻿

Loss of mitochondrial protease OMA1 alters processing of the GTPase OPA1 and causes obesity and defective thermogenesis in mice ﻿

Matriptase-2 ﻿

Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis ﻿

Matriptase-2 deficiency protects from obesity by modulating iron homeostasis ﻿

Matriptase-2 is essential for hepcidin repression during fetal life and postnatal development in mice to maintain iron homeostasis ﻿

Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms ﻿

Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia ﻿

Next-generation sequencing reveals the secrets of the chronic lymphocytic leukemia genome ﻿

Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma ﻿

Aging and chronic DNA damage response activate a regulatory pathway involving miR-29 and p53

Cell-cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas

Chronic Lymphocytic Leukemia with SF3B1 Mutation

A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia

Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients

The genomic landscape of chronic lymphocytic leukemia: clinical implications

Iron-deficiency anemia from matriptase-2 inactivation is dependent on the presence of functional Bmp6

Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency?

Liver hemojuvelin protein levels in mice deficient in matriptase-2 (Tmprss6)

Loss of mitochondrial protease OMA1 alters processing of the GTPase OPA1 and causes obesity and defective thermogenesis in mice

Matriptase-2

Matriptase-2 (TMPRSS6): A proteolytic regulator of iron homeostasis

Matriptase-2 deficiency protects from obesity by modulating iron homeostasis

Matriptase-2 is essential for hepcidin repression during fetal life and postnatal development in mice to maintain iron homeostasis

Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms

Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia

Next-generation sequencing reveals the secrets of the chronic lymphocytic leukemia genome

Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma