Ute Woehlbier

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Coauteurs

Patricio ManqueFull ProfessorAdresse e-mail validée de umayor.cl
Melissa NassifVicerrectoría de Investigación, Universidad MayorAdresse e-mail validée de umayor.cl
Danilo Bilches MedinasInstitute of Chemistry, University of Sao PauloAdresse e-mail validée de iq.usp.br
Catherine AndreuUniversitat de ValènciaAdresse e-mail validée de uv.es
Mauricio TorresResearch Investigator University of MichiganAdresse e-mail validée de med.umich.edu
Gregory BuckProfessor of Microbiology and Immunology, & Computer ScienceAdresse e-mail validée de vcuhealth.org
Sajid MalikHuman Genetics Program, Dept. of Zoology, Faculty of Biological Sci., Quaid-iAdresse e-mail validée de qau.edu.pk
Michael j BlackmanFrancis Crick InstituteAdresse e-mail validée de crick.ac.uk
Robert BrownAdresse e-mail validée de umassmed.edu
Rene Luis Vidal GomezUniversidad MayorAdresse e-mail validée de umayor.cl
Sebastián Beltrán VergaraUniversidad MayorAdresse e-mail validée de umayor.cl
Matthew A ChildImperial College LondonAdresse e-mail validée de imperial.ac.uk
Luiz JulianoAC Camargo Cancer CenterAdresse e-mail validée de accamargo.org.br
Ellen KnuepferPrinciple Laboratory Research Scientist, The Francis Crick InsituteAdresse e-mail validée de crick.ac.uk
konstantinos koussisThe Francis Crick InstituteAdresse e-mail validée de crick.ac.uk
Victor Hugo Cornejo CoronaPontificia Universidad Catolica de ChileAdresse e-mail validée de uc.cl
Fabiola OsorioAssociate ProfessorAdresse e-mail validée de med.uchile.cl
Maritza OñateAlbert Einstein College of MedicineAdresse e-mail validée de einsteinmed.edu
VALENTINA FERNANDA CASTILLOPontificia Universidad Católica de ChileAdresse e-mail validée de uc.cl
Zeleke Mekonnen (PhD)Professor of Medical Parasitology, Jimma UniversityAdresse e-mail validée de ju.edu.et

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Ute Woehlbier

Center for Integrative Biology (CIB), Faculty of Science, Universidad Mayor, Chile

Adresse e-mail validée de umayor.cl

neurodegeneration novel disease genes infectious disease amyotrophic lateral sclerosis


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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	10715	2021
Modulating stress responses by the UPRosome: A matter of life and death U Woehlbier, C Hetz Trends in Biochemical Sciences, 2011	332	2011
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	213	2009
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	118	2016
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	115	2006
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	113	2012
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	113	2006
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	106	2018
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	85	2015
The enigmatic role of C9ORF72 in autophagy M Nassif, U Woehlbier, PA Manque Frontiers in neuroscience 11, 267426, 2017	77	2017
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	77	2010
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	67	2011
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	64	2015
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	52	2015
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	50	2020
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	44	2012
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	42	2013
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	25	2019
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	16	2022

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