Follow
Huu Phuc Nguyen
Huu Phuc Nguyen
University of Tuebingen, Institute of Medical Genetics and Applied Genomics
Verified email at med.uni-tuebingen.de - Homepage
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
13184*2021
Transgenic rat model of Huntington's disease
S von Hörsten, I Schmitt, HP Nguyen, C Holzmann, T Schmidt, T Walther, ...
Human molecular genetics 12 (6), 617-624, 2003
4182003
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
TR Rebbeck, TM Friebel, E Friedman, U Hamann, D Huo, A Kwong, ...
Human mutation 39 (5), 593-620, 2018
2912018
Lawson criterion for ignition exceeded in an inertial fusion experiment
H Abu-Shawareb, R Acree, P Adams, J Adams, B Addis, R Aden, P Adrian, ...
Physical review letters 129 (7), 075001, 2022
2512022
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease
S Nuber, E Petrasch-Parwez, B Winner, J Winkler, S von Hörsten, ...
Journal of Neuroscience 28 (10), 2471-2484, 2008
2162008
Huntingtin forms toxic NH2-terminal fragment complexes that are promoted by the age-dependent decrease in proteasome activity
H Zhou, F Cao, Z Wang, ZX Yu, HP Nguyen, J Evans, SH Li, XJ Li
The Journal of cell biology 163 (1), 109-118, 2003
1832003
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes
M Valenza, V Leoni, JM Karasinska, L Petricca, J Fan, J Carroll, ...
Journal of Neuroscience 30 (32), 10844-10850, 2010
1712010
Lack of huntingtin-associated protein-1 causes neuronal death resembling hypothalamic degeneration in Huntington's disease
SH Li, ZX Yu, CL Li, HP Nguyen, YX Zhou, C Deng, XJ Li
Journal of Neuroscience 23 (17), 6956-6964, 2003
1572003
Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities
K Grundmann, B Reischmann, G Vanhoutte, J Hübener, P Teismann, ...
Neurobiology of disease 27 (2), 190-206, 2007
1522007
The regulation of OXPHOS by extramitochondrial calcium
FN Gellerich, Z Gizatullina, S Trumbeckaite, HP Nguyen, T Pallas, ...
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (6-7), 1018-1027, 2010
1512010
Huntingtin inclusions do not deplete polyglutamine-containing transcription factors in HD mice
ZX Yu, SH Li, HP Nguyen, XJ Li
Human molecular genetics 11 (8), 905-914, 2002
1462002
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease
HP Nguyen, P Kobbe, H Rahne, T Wörpel, B Jäger, M Stephan, R Pabst, ...
Human Molecular Genetics 15 (21), 3177-3194, 2006
1382006
Sex differences in a transgenic rat model of Huntington's disease: decreased 17β-estradiol levels correlate with reduced numbers of DARPP32+ neurons in males
FJ Bode, M Stephan, H Suhling, R Pabst, RH Straub, KA Raber, M Bonin, ...
Human molecular genetics 17 (17), 2595-2609, 2008
1362008
A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease
L Yu-Taeger, E Petrasch-Parwez, AP Osmand, A Redensek, S Metzger, ...
Journal of Neuroscience 32 (44), 15426-15438, 2012
1212012
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-β signaling in an animal model of Huntington disease
M Kandasamy, S Couillard-Despres, KA Raber, M Stephan, B Lehner, ...
Journal of Neuropathology & Experimental Neurology 69 (7), 717-728, 2010
1182010
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)
J Hübener, JJ Weber, C Richter, L Honold, A Weiss, F Murad, P Breuer, ...
Human molecular genetics 22 (3), 508-518, 2013
1152013
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease
S Metzger, J Rong, HP Nguyen, A Cape, J Tomiuk, AS Soehn, P Propping, ...
Human molecular genetics 17 (8), 1137-1146, 2008
1112008
Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7
S Metzger, M Saukko, H Van Che, L Tong, Y Puder, O Riess, HP Nguyen
Human genetics 128, 453-459, 2010
1102010
Mitochondria and energetic depression in cell pathophysiology
E Seppet, M Gruno, A Peetsalu, Z Gizatullina, HP Nguyen, S Vielhaber, ...
International journal of molecular sciences 10 (5), 2252-2303, 2009
1102009
Cellular and subcellular localization of Huntington aggregates in the brain of a rat transgenic for Huntington disease
E Petrasch‐Parwez, HP Nguyen, M Löbbecke‐Schumacher, HW Habbes, ...
Journal of Comparative Neurology 501 (5), 716-730, 2007
1092007
The system can't perform the operation now. Try again later.
Articles 1–20