关注
Michele Christine Landemberger
Michele Christine Landemberger
Pesquisadora Científica - A.C. Camargo Cancer Center; Professora Titular Universidade Paulista
在 cipe.accamargo.org.br 的电子邮件经过验证
标题
引用次数
引用次数
年份
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant
R Walz, R Castro, TR Velasco, V Alexandre Jr, MH Lopes, JP Leite, ...
Neurology 61 (9), 1204-1210, 2003
662003
PrPC displays an essential protective role from oxidative stress in an astrocyte cell line derived from PrPC knockout mice
FR Bertuchi, DMG Bourgeon, MC Landemberger, VR Martins, ...
Biochemical and biophysical research communications 418 (1), 27-32, 2012
532012
Cellular prion protein modulates defensive attention and innate fear-induced behaviour evoked in transgenic mice submitted to an agonistic encounter with the tropical coral …
B Lobão-Soares, R Walz, RDS Prediger, RL Freitas, F Calvo, ...
Behavioural brain research 194 (2), 129-137, 2008
532008
High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC
RMRPS Castro, MC Landemberger, R Walz, CG Carlotti Jr, N Huang, ...
Journal of neuroscience methods 139 (2), 263-269, 2004
242004
Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein
PBC Nico, B Lobão-Soares, MC Landemberger, W Marques Jr, CI Tasca, ...
Neuroscience letters 388 (1), 21-26, 2005
232005
Rab5C enhances resistance to ionizing radiation in rectal cancer
AR Baptistella, MC Landemberger, MVS Dias, FS Giudice, BR Rodrigues, ...
Journal of Molecular Medicine 97, 855-869, 2019
202019
Complex movement disorders in fatal familial insomnia: a clinical and genetic discussion
JL Pedroso, WBVR Pinto, PVS Souza, IF Ricarte, MC Landemberger, ...
Neurology 81 (12), 1098-1099, 2013
192013
High phenotypic variability in Gerstmann-Sträussler-Scheinker disease
J Smid, A Studart, MC Landemberger, CF Machado, PR Nóbrega, ...
Arquivos de neuro-psiquiatria 75, 331-338, 2017
182017
Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171
ER Coimbra, K Rezek, S Escorsi-Rosset, MC Landemberger, RM Castro, ...
Epilepsy & Behavior 8 (3), 635-642, 2006
172006
Prion diseases are under compulsory notification in Brazil: surveillance of cases evaluated by biochemical and/or genetic markers from 2005 to 2007
VR Martins, HR Gomes, L Chimelli, S Rosemberg, MC Landemberger
Dementia & Neuropsychologia 1 (4), 347-355, 2007
122007
Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survival
CF Machado, FH Beraldo, TG Santos, D Bourgeon, MC Landemberger, ...
Journal of Biological Chemistry 287 (52), 43777-43788, 2012
112012
Cortical malformations are associated with a rare polymorphism of cellular prion protein
R Walz, R Castro, MC Landemberger, TR Velasco, VC Terra-Bustamante, ...
Neurology 63 (3), 557-560, 2004
112004
Transmissible spongiform encephalopathies
CA Hart
Journal of medical microbiology 42 (3), 153-155, 1995
11*1995
Asymmetric cortical high signal on diffusion weighted-MRI in a case of Creutzfeldt-Jakob disease
R Nitrini, R Areza-Fegyveres, VR Martins, RMRPS Castro, ...
Arquivos de neuro-psiquiatria 63, 519-522, 2005
92005
Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease
J Smid, MC Landemberger, VS Bahia, VR Martins, R Nitrini
Arquivos de neuro-psiquiatria 71 (7), 423-427, 2013
82013
Second-generation RT-QuIC assay for the diagnosis of Creutzfeldt-Jakob disease patients in Brazil
BJAP Barbosa, BB Castrillo, RP Alvim, MH De Brito, HR Gomes, ...
Frontiers in bioengineering and biotechnology 8, 929, 2020
72020
Sexual disinhibition and agrypnia excitata in fatal familial insomnia
LC De Souza, AL Teixeira, FL Rocha, MC Landemberger, VR Martins, ...
Journal of the neurological sciences 367, 140-142, 2016
72016
Loss of STI 1‐mediated neuronal survival and differentiation in disease‐associated mutations of prion protein
MC Landemberger, GP de Oliveira, CF Machado, KJ Gollob, VR Martins
Journal of neurochemistry 145 (5), 409-416, 2018
52018
First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease
RKM De Souza, ND Josviak, MS Batistela, PSF Santos, ...
Prion 11 (6), 465-468, 2017
42017
Genomics and epidemiology for gastric adenocarcinomas
Applied Cancer Research 37 (1), 7, 2017
42017
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