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Ute Woehlbier
Ute Woehlbier
Center for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Chile
Verified email at umayor.cl
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
106962021
Modulating stress responses by the UPRosome: A matter of life and death
U Woehlbier, C Hetz
Trends in Biochemical Sciences, 2011
3302011
A multifunctional serine protease primes the malaria parasite for red blood cell invasion
K Koussis, C Withers-Martinez, S Yeoh, M Child, F Hackett, E Knuepfer, ...
The EMBO journal 28 (6), 725-735, 2009
2132009
ALS‐linked protein disulfide isomerase variants cause motor dysfunction
U Woehlbier, A Colombo, MJ Saaranen, V Pérez, J Ojeda, FJ Bustos, ...
The EMBO journal 35 (8), 845-865, 2016
1182016
Interactions between merozoite surface proteins 1, 6, and 7 of the malaria parasite Plasmodium falciparum
CW Kauth, U Woehlbier, M Kern, Z Mekonnen, R Lutz, N Mücke, ...
Journal of Biological Chemistry 281 (42), 31517-31527, 2006
1152006
Protein disulfide isomerases in neurodegeneration: from disease mechanisms to biomedical applications
CI Andreu, U Woehlbier, M Torres, C Hetz
FEBS letters 586 (18), 2826-2834, 2012
1132012
Analysis of Antibodies Directed against Merozoite Surface Protein 1 of the Human Malaria Parasite Plasmodium falciparum
U Woehlbier, C Epp, CW Kauth, R Lutz, CA Long, B Coulibaly, B Kouyaté, ...
Infection and immunity 74 (2), 1313-1322, 2006
1132006
Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosis
DB Medinas, P Rozas, F Martínez Traub, U Woehlbier, RH Brown, ...
Proceedings of the National Academy of Sciences 115 (32), 8209-8214, 2018
1042018
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients
P Gonzalez-Perez, U Woehlbier, RJ Chian, P Sapp, GA Rouleau, ...
Gene 566 (2), 158-165, 2015
852015
The enigmatic role of C9ORF72 in autophagy
M Nassif, U Woehlbier, PA Manque
Frontiers in neuroscience 11, 267426, 2017
772017
Antibodies against multiple merozoite surface antigens of the human malaria parasite Plasmodium falciparum inhibit parasite maturation and red blood cell invasion
U Woehlbier, C Epp, F Hackett, MJ Blackman, H Bujard
Malaria journal 9, 1-12, 2010
772010
Identification and immunological characterization of three potential vaccinogens against Cryptosporidium species
PA Manque, F Tenjo, U Woehlbier, AM Lara, MG Serrano, P Xu, JM Alves, ...
Clinical and Vaccine Immunology 18 (11), 1796-1802, 2011
672011
The protein-disulfide isomerase ERp57 regulates the steady-state levels of the prion protein
M Torres, DB Medinas, JM Matamala, U Woehlbier, VH Cornejo, T Solda, ...
Journal of Biological Chemistry 290 (39), 23631-23645, 2015
642015
Functional role of the disulfide isomerase ERp57 in axonal regeneration
V Castillo, M Oñate, U Woehlbier, P Rozas, C Andreu, D Medinas, ...
PLoS One 10 (9), e0136620, 2015
522015
Implications of Selective Autophagy Dysfunction for ALS Pathology
E Vicencio, S Beltrán, L Labrador, P Manque, M Nassif, U Woehlbier
Cells 9 (2), 381, 2020
492020
Altered prion protein expression pattern in CSF as a biomarker for Creutzfeldt-Jakob disease
M Torres, L Cartier, JM Matamala, N Hernández, U Woehlbier, C Hetz
PLoS One 7 (4), e36159, 2012
442012
Intranasal vaccination in mice with an attenuated Salmonella enterica Serovar 908htr A expressing Cp15 of Cryptosporidium: impact of malnutrition with preservation of cytokine …
JK Roche, AL Rojo, LB Costa, R Smeltz, P Manque, U Woehlbier, ...
Vaccine 31 (6), 912-918, 2013
422013
Homozygous mutation in CEP19, a gene mutated in morbid obesity
E Yıldız Bölükbaşı, S Mumtaz, M Afzal, U Woehlbier, S Malik, A Tolun
Bardet-Biedl syndrome with predominant postaxial polydactyly. J Med Genet 55 …, 2018
36*2018
Network approach identifies Pacer as an autophagy protein involved in ALS pathogenesis
S Beltran, M Nassif, E Vicencio, J Arcos, L Labrador, BI Cortes, C Cortez, ...
Molecular Neurodegeneration 14, 1-18, 2019
252019
Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis
D Bilches Medinas, S Malik, E Yıldız‐Bölükbaşı, J Borgonovo, ...
The EMBO Journal 41 (2), e105531, 2022
162022
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