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Acta Pædiatrica(1)
American Journal of Medical Genetics, Part A(1)
Diabetologia(1)
Growth Hormone and IGF Research(1)
Human Mutation(1)
Despite higher body fat content, Ecuadorian subjects with Laron syndrome have less insulin resistance and lower incidence of diabetes than their relatives
ArticleAbstract: In the present pandemics of obesity and insulin resistant diabetes mellitus (DM), the specific contrPalabras claves:Growth hormone, Growth hormone receptor, Growth hormone receptor deficiency, Laron syndromeAutores:Carolina Guevara, Enrique Terán, Jaime Guevara-Aguirre, Marco Guevara-Aguirre, Procel P., Rosado V.Fuentes:googlescopusMutation creating a new splice site in the growth hormone receptor genes of 37 Ecuadorean patients with Laron syndrome
ArticleAbstract: Laron syndrome is an autosomal recessive condition characterized by resistance to growth hormone. WePalabras claves:Growth hormone receptor, Laron dwarfism, mutation, RNA splicingAutores:Berg M.A., Francke U., Jaime Guevara-Aguirre, Rosenbloom A.L., Rosenfeld R.G.Fuentes:scopusObesity, diabetes and cancer: insight into the relationship from a cohort with growth hormone receptor deficiency
ReviewAbstract: Obesity with insulin-resistant diabetes and increased cancer risk is a global problem. We consider tPalabras claves:apoptosis, Cáncer, DIABÉTES, Growth hormone receptor, IGF-1, Insulin, obesity, ReviewAutores:Jaime Guevara-Aguirre, Rosenbloom A.L.Fuentes:scopusIs there heterozygote expression of growth hormone receptor deficiency?
ArticleAbstract: Expression of heterozygosity for the defect in the growth hormone (GH) receptor has been proposed toPalabras claves:growth hormone binding protein, Growth hormone receptor, Growth hormone receptor deficiency, heterozygote expression, insulin‐like growth factor I, Laron syndromeAutores:Fielder P.J., Jaime Guevara-Aguirre, Rosenbloom A.L., Rosenfeld R.G.Fuentes:scopusThe E180splice mutation in the GHR gene causing laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
ArticleAbstract: Laron syndrome (LS) is a genetic disorder caused by mutations in the growth hormone receptor (GHR) gPalabras claves:Growth hormone insensitivity, Growth hormone receptor, Growth hormone receptor deficiency, Laron syndrome, Lineage markers, Mitochondrial haplogroups, Y-chromosome haplogroupsAutores:Arnhold I.J.P., Cassorla F., Damiani D., Fridman C., Gonçalves F.T., Hwa V., Jaime Guevara-Aguirre, Jorge A.A.L., Laron Z., Lins T.S.S., Pinto E.M., Rosembloom A.L., Rosenfeld R.G., Shevah O.Fuentes:scopus