INVESTIGADORES
BISTUE MILLON Maria Beatriz
artículos
MILLON, MARIA BEATRIZ BISTUE; BRUNO, MARTIN A.
Single cell transcriptomic heterogeneity between sporadic early and late‐onset of Alzheimer’s disease
ALZHEIMERS & DEMENTIA; Lugar: Amsterdam; Año: 2023
NAVAS GUIMARAES, MARÍA EUGENIA; LOPEZ-BLANCO, ROI; CORREA, JUAN; FERNANDEZ-VILLAMARIN, MARCOS; BISTUÉ, MARÍA BEATRIZ; MARTINO-ADAMI, PAMELA; MORELLI, LAURA; KUMAR, VIJAY; WEMPE, MICHAEL F.; CUELLO, A.C.; FERNANDEZ-MEGIA, EDUARDO; BRUNO, MARTIN A.
Liver X Receptor Activation with an Intranasal Polymer Therapeutic Prevents Cognitive Decline without Altering Lipid Levels
ACS NANO; Año: 2021 vol. 15 p. 4678 - 4687
ASTEGGIANO, CARLA GABRIELA; PAPAZOGLU, MAGALI; BISTUÉ MILLÓN, MARÍA BEATRIZ; PERALTA, MARÍA FERNANDA; AZAR, NYDIA BEATRIZ; SPÉCOLA, NORMA SPÉCOLA; GUELBERT, NORBERTO; SULDRUP, NIELS SULDRUP; PEREYRA, MARCELA; DODELSON DE KREMER, RAQUEL
Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls
PEDIATRIC RESEARCH; Año: 2018 vol. 84 p. 837 - 841
BISTUÉ MILLÓN MARÍA BEATRIZ; CYNTIA AMOROSI; MAGALÍ PAPAZOGLUA; SYRAVIGNA MYRIAM; GRACIELA ELSO-BERBERIAN; CARLA GABRIELA ASTEGGIANO
New insights on Na + /Ca 2+ exchangers and protein glycosylation in human cells
Trends in Cell & Molecular Biology; Año: 2017 vol. 12 p. 17 - 32
BISTUÉ MILLÓN, M. BEATRIZ; IULITA, M. FLORENCIA; PENTZ, ROWAN; AGUILAR, LISI FLORES; DO CARMO, SONIA; ALLARD, SIMON; MICHALSKI, BERNADETA; WILSON, EDWARD N.; DUCATENZEILER, ADRIANA; BRUNO, MARTIN A.; FAHNESTOCK, MARGARET; CUELLO, A. CLAUDIO
Differential deregulation of NGF and BDNF neurotrophins in a transgenic rat model of Alzheimer's disease
NEUROBIOLOGY OF DISEASE; Año: 2017 vol. 108 p. 307 - 323
DAISY RYMEN; ROMAIN PEANNE; MARÍA BEATRIZ BISTUE MILLÓN; FRANÇOIS FOULQUIER; GERT MATTHIJS
MAN1B1 Deficiency: An Unexpected CDG-II
PLOS GENETICS; Lugar: San Francisco; Año: 2013 vol. 9 p. 1 - 13
GERT MATTHIJS, DAISY RYMEN, MARIA BEATRIZ BISTUE MILLON, ERIKA SOUCHE, VALÉRIE RACE
Approaches of homozygosity mapping and exome sequencing for the identification of novel types of CDG
GLYCOCONJUGATE JOURNAL; Año: 2013 vol. 30 p. 67 - 76
M.B. BISTUE MILLON, ; M.A. DELGADO, N.B. AZAR, N. GUELBERT, L. STURIALE, D. GAROZZO, G. MATTHIJS, J. JAEKEN, RAQUEL DODELSON DE KREMER, AND C.G. ASTEGGIANO
Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?
JOURNAL OF INHERITED METABOLIC DISEASE; Año: 2011 p. 65 - 72