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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)
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)
Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

Alonso, N.; Cañueto, J.; Ciria, S.; Palacios‐Alvarez, I.; Alegre, M.; Badenas, C.; Barreiro, A.; Pena, L.; Maldonado, C.; Nespeira‐Jato, M.V.; Peña‐Penabad, C.; Azon, A.; Gavrilova, M.; Ferrer, I.; Sanmartin, O.; Robles, L.; Hernandez‐Martin, A.; Urioste, M.; Puig, S.; Puig, L.; González Sarmiento, Rogelio; Bueno Martínez, Elena (2017)
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)
Transcriptional Basis of Ca2+ Remodeling Reversal Induced by Polyamine Synthesis Inhibition in Colorectal Cancer Cells

Pérez-Riesgo, Enrique; Hernando Pérez, María Elena ; Feijóo Salgado, Verónica; Tajada Esteban, Sendoa ; Núñez Llorente, Lucía ; Villalobos Jorge, Carlos (2023)

DEP06 - Artículos de revista: Envíos recientes

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 ﻿

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

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome ﻿

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

Transcriptional Basis of Ca2+ Remodeling Reversal Induced by Polyamine Synthesis Inhibition in Colorectal Cancer Cells ﻿

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

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

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

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

Transcriptional Basis of Ca2+ Remodeling Reversal Induced by Polyamine Synthesis Inhibition in Colorectal Cancer Cells