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Dimitri Krainc
Dimitri Krainc
Adresse e-mail validée de northwestern.edu
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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
13162*2021
Apoptosis and necrosis: two distinct events induced, respectively, by mild and intense insults with N-methyl-D-aspartate or nitric oxide/superoxide in cortical cell cultures.
E Bonfoco, D Krainc, M Ankarcrona, P Nicotera, SA Lipton
Proceedings of the National Academy of Sciences 92 (16), 7162-7166, 1995
26721995
Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1α null mice
J Lin, PH Wu, PT Tarr, KS Lindenberg, J St-Pierre, C Zhang, VK Mootha, ...
Cell 119 (1), 121-135, 2004
14232004
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies
JR Mazzulli, YH Xu, Y Sun, AL Knight, PJ McLean, GA Caldwell, ...
Cell 146 (1), 37-52, 2011
13962011
Transcriptional repression of PGC-1α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration
L Cui, H Jeong, F Borovecki, CN Parkhurst, N Tanese, D Krainc
Cell 127 (1), 59-69, 2006
12072006
A call for transparent reporting to optimize the predictive value of preclinical research
SC Landis, SG Amara, K Asadullah, CP Austin, R Blumenstein, ...
Nature 490 (7419), 187-191, 2012
11732012
Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
AW Dunah, H Jeong, A Griffin, YM Kim, DG Standaert, SM Hersch, ...
Science 296 (5576), 2238-2243, 2002
8502002
Human iPSC-based modeling of late-onset disease via progerin-induced aging
JD Miller, YM Ganat, S Kishinevsky, RL Bowman, B Liu, EY Tu, ...
Cell stem cell 13 (6), 691-705, 2013
7812013
Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1α muscle-specific knock-out animals
C Handschin, S Chin, P Li, F Liu, E Maratos-Flier, NK LeBrasseur, Z Yan, ...
Journal of Biological Chemistry 282 (41), 30014-30021, 2007
7412007
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease
LF Burbulla, P Song, JR Mazzulli, E Zampese, YC Wong, S Jeon, ...
Science 357 (6357), 1255-1261, 2017
7262017
α-synuclein toxicity in neurodegeneration: mechanism and therapeutic strategies
YC Wong, D Krainc
Nature medicine 23 (2), 1-13, 2017
6792017
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1α in Huntington's disease neurodegeneration
P Weydt, VV Pineda, AE Torrence, RT Libby, TF Satterfield, ...
Cell metabolism 4 (5), 349-362, 2006
6672006
Mitochondria–lysosome contacts regulate mitochondrial fission via RAB7 GTP hydrolysis
YC Wong, D Ysselstein, D Krainc
Nature 554 (7692), 382-386, 2018
6512018
Classification and phylogeny of the MADS-box multigene family suggest defined roles of MADS-box gene subfamilies in the morphological evolution of eukaryotes
G Theißen, JT Kim, H Saedler
Journal of Molecular Evolution 43, 484-516, 1996
5661996
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson’s disease
O Cooper, H Seo, S Andrabi, C Guardia-Laguarta, J Graziotto, ...
Science translational medicine 4 (141), 141ra90-141ra90, 2012
5572012
Identification and rescue of α-synuclein toxicity in Parkinson patient–derived neurons
CY Chung, V Khurana, PK Auluck, DF Tardiff, JR Mazzulli, F Soldner, ...
Science 342 (6161), 983-987, 2013
5122013
Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease
F Borovecki, L Lovrecic, J Zhou, H Jeong, F Then, HD Rosas, SM Hersch, ...
Proceedings of the National Academy of Sciences 102 (31), 11023-11028, 2005
4972005
Acetylation targets mutant huntingtin to autophagosomes for degradation
H Jeong, F Then, TJ Melia, JR Mazzulli, L Cui, JN Savas, C Voisine, ...
Cell 137 (1), 60-72, 2009
4832009
Mice deficient for soluble adenylyl cyclase are infertile because of a severe sperm-motility defect
G Esposito, BS Jaiswal, F Xie, MAM Krajnc-Franken, TJAA Robben, ...
Proceedings of the National Academy of Sciences 101 (9), 2993-2998, 2004
4762004
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ...
JAMA neurology 70 (6), 727-735, 2013
4742013
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