Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Miguel Ángel López-Martínez"'
Autor:
Tamara Carrizosa-Molina, Natalia Casillas-Díaz, Iris Pérez-Nadador, Claudia Vales-Villamarín, Miguel Ángel López-Martínez, Rosa Riveiro-Álvarez, Larry Wilhelm, Rita Cervera-Juanes, Carmen Garcés, Alejandro Lomniczi, Leandro Soriano-Guillén
Publikováno v:
Clinical Epigenetics, Vol 15, Iss 1, Pp 1-16 (2023)
Abstract Background In 1990, David Barker proposed that prenatal nutrition is directly linked to adult cardiovascular disease. Since then, the relationship between adult cardiovascular risk, metabolic syndrome and birth weight has been widely documen
Externí odkaz:
https://doaj.org/article/064832d6e85c4a79bd8740221a102d45
Autor:
Nelmar Valentina, Ortiz-Cabrera, Rosa, Riveiro-Álvarez, Miguel Ángel, López-Martínez, Pilar, Pérez-Segura, Isabel, Aragón-Gómez, María José, Trujillo-Tiebas, Leandro, Soriano-Guillén
Publikováno v:
Hormone research in paediatrics. 87(2)
Idiopathic central precocious puberty (ICPP) is the premature activation of the hypothalamic-pituitary-gonadal axis in the absence of organic disease. Up to now, just gain-of-function mutations of KISS1/KISS1R and loss-of-function mutations of the ma
Autor:
Rocio Sanchez-Alcudia, Maria Garcia-Hoyos, Miguel Angel Lopez-Martinez, Noelia Sanchez-Bolivar, Olga Zurita, Ascension Gimenez, Cristina Villaverde, Luciana Rodrigues-Jacy da Silva, Marta Corton, Raquel Perez-Carro, Simona Torriano, Vasiliki Kalatzis, Carlo Rivolta, Almudena Avila-Fernandez, Isabel Lorda, Maria J Trujillo-Tiebas, Blanca Garcia-Sandoval, Maria Isabel Lopez-Molina, Fiona Blanco-Kelly, Rosa Riveiro-Alvarez, Carmen Ayuso
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0151943 (2016)
Choroideremia (CHM) is a rare X-linked disease leading to progressive retinal degeneration resulting in blindness. The disorder is caused by mutations in the CHM gene encoding REP-1 protein, an essential component of the Rab geranylgeranyltransferase
Externí odkaz:
https://doaj.org/article/ae448938b8a44fa087fe836d56714519