Lista de

Sequence Deletion
14
"Fertilization defects in sperm from Cysteine-rich secretory protein 2 (Crisp2) knockout mice: Implications for fertility disorders" (2016) Brukman, N.G.;Miyata, H.;Torres, P. (...)Cuasnicú, P.S. Molecular Human Reproduction. 22(4):240-251
"Application of BRED technology to construct recombinant D29 reporter phage expressing EGFP" (2013) da Silva, J.L.;Piuri, M.;Broussard, G. (...)Hirata, M.H. FEMS Microbiology Letters. 344(2):166-172
"Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system" (2012) Bidart, G.N.;Ruiz, J.A.;de Almeida, A. (...)Nikel, P.I. Applied and Environmental Microbiology. 78(24):8784-8794
"Molecular analysis of the UROD gene in 17 Argentinean patients with familial porphyria cutanea tarda: Characterization of four novel mutations" (2012) Méndez, M.;Rossetti, M.V.;Gómez-Abecia, S. (...)Enríquez de Salamanca, R. Molecular Genetics and Metabolism. 105(4):629-633
"Role of pre-A motif in nitric oxide scavenging by truncated hemoglobin, HbN, of Mycobacterium tuberculosis" (2009) Lama, A.;Pawaria, S.;Bidon-Chanal, A. (...)Dikshit, K.L. Journal of Biological Chemistry. 284(21):14457-14468
"Ancient exaptation of a CORE-SINE retroposon into a highly conserved mammalian neuronal enhancer of the proopiomelanocortin gene" (2007) Santangelo, A.M.;De Souza, F.S.J.;Franchini, L.F. (...)Rubinstein, M. PLoS Genetics. 3(10):1813-1826
"Xanthan induces plant susceptibility by suppressing callose deposition" (2006) Yun, M.H.;Torres, P.S.;El Oirdi, M. (...)Vojnov, A.A. Plant Physiology. 141(1):178-187
"Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients" (2005) Dalamón, V.;Béhèran, A.;Diamante, F. (...)Elgoyhen, A.B. Hearing Research. 207(1-2):43-49
"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
"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