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DNA Mutational Analysis
10
"Structural Insights into the HWE Histidine Kinase Family: The Brucella Blue Light-Activated Histidine Kinase Domain" (2016) Rinaldi, J.;Arrar, M.;Sycz, G. (...)Goldbaum, F.A. Journal of Molecular Biology. 428(6):1165-1179
"Structural Insights into the HWE Histidine Kinase Family: The Brucella Blue Light-Activated Histidine Kinase Domain" (2016) Rinaldi, J.;Arrar, M.;Sycz, G. (...)Goldbaum, F.A. Journal of Molecular Biology. 428(6):1165-1179
"Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder" (2015) Nemirovsky, S.I.;Córdoba, M.;Zaiat, J.J. (...)Kauffman, M.A. PLoS ONE. 10(2)
"Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder" (2015) Nemirovsky, S.I.;Córdoba, M.;Zaiat, J.J. (...)Kauffman, M.A. PLoS ONE. 10(2)
"Genetic architecture of olfactory behavior in drosophila melanogaster: Differences and similarities across development" (2013) Lavagnino, N.J.; Arya, G.H.; Korovaichuk, A.; Fanara, J.J. Behavior Genetics. 43(4):348-359
"The very first description of a patient with hepatoerythropoietic porphyria in Argentina. Biochemical and Molecular Studies" (2009) Granata, B.X.;Parera, V.E.;Melito, V.A. (...)Rossetti, M.V. Cellular and Molecular Biology. 55(1):61-65
"Identification of neuronal enhancers of the proopiomelanocortin gene by transgenic mouse analysis and phylogenetic footprinting" (2005) De Souza, F.S.J.;Santangelo, A.M.;Bumaschny, V. (...)Rubinstein, M. Molecular and Cellular Biology. 25(8):3076-3086
"Mutations in familial porphyria cutanea tarda: Two novel and two previously described for hepatoerythropoietic porphyria" (2000) Mendez, M.;Rossetti, M.V.;De Siervi, A. (...)Parera, V. Human mutation. 16(3):269-270
"Mutation 1091delC is highly prevalent in Spanish Sanfilippo syndrome type A patients" (1998) Montfort, M.;Vilageliu, L.;Garcia-Giralt, N. (...)Grinberg, D. Human Mutation. 12(4):274-279