| Year |
Citation |
Score |
| 2015 |
Shen WC, Li HY, Chen GC, Chern Y, Tu PH. Mutations in the ubiquitin-binding domain of OPTN/optineurin interfere with autophagy-mediated degradation of misfolded proteins by a dominant-negative mechanism. Autophagy. 11: 685-700. PMID 25484089 DOI: 10.4161/Auto.36098 |
0.347 |
|
| 2015 |
Liu YJ, Ju TC, Chen HM, Jang YS, Lee LM, Lai HL, Tai HC, Fang JM, Lin YL, Tu PH, Chern Y. Activation of AMP-activated protein kinase α1 mediates mislocalization of TDP-43 in amyotrophic lateral sclerosis. Human Molecular Genetics. 24: 787-801. PMID 25256353 DOI: 10.1093/Hmg/Ddu497 |
0.328 |
|
| 2014 |
Wu HC, Lin YC, Liu CH, Chung HC, Wang YT, Lin YW, Ma HI, Tu PH, Lawler SE, Chen RH. USP11 regulates PML stability to control Notch-induced malignancy in brain tumours. Nature Communications. 5: 3214. PMID 24487962 DOI: 10.1038/Ncomms4214 |
0.301 |
|
| 2013 |
Huang YC, Lin KF, He RY, Tu PH, Koubek J, Hsu YC, Huang JJ. Inhibition of TDP-43 aggregation by nucleic acid binding. Plos One. 8: e64002. PMID 23737961 DOI: 10.1371/Journal.Pone.0064002 |
0.3 |
|
| 2013 |
Hsiao HY, Chen YC, Chen HM, Tu PH, Chern Y. A critical role of astrocyte-mediated nuclear factor-κB-dependent inflammation in Huntington's disease. Human Molecular Genetics. 22: 1826-42. PMID 23372043 DOI: 10.1093/Hmg/Ddt036 |
0.329 |
|
| 2012 |
Lo WL, Chu PY, Lee TH, Su TL, Chien Y, Chen YW, Huang PI, Tseng LM, Tu PH, Kao SY, Lo JF. A Combined DNA-Affinic Molecule and N-Mustard Alkylating Agent Has an Anti-Cancer Effect and Induces Autophagy in Oral Cancer Cells. International Journal of Molecular Sciences. 13: 3277-90. PMID 22489152 DOI: 10.3390/Ijms13033277 |
0.3 |
|
| 2007 |
Behrens MI, Mukherjee O, Tu PH, Liscic RM, Grinberg LT, Carter D, Paulsmeyer K, Taylor-Reinwald L, Gitcho M, Norton JB, Chakraverty S, Goate AM, Morris JC, Cairns NJ. Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation. Alzheimer Disease and Associated Disorders. 21: 1-7. PMID 17334266 DOI: 10.1097/Wad.0B013E31803083F2 |
0.319 |
|
| 2006 |
Forman MS, Mackenzie IR, Cairns NJ, Swanson E, Boyer PJ, Drachman DA, Jhaveri BS, Karlawish JH, Pestronk A, Smith TW, Tu PH, Watts GD, Markesbery WR, Smith CD, Kimonis VE. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. Journal of Neuropathology and Experimental Neurology. 65: 571-81. PMID 16783167 DOI: 10.1097/00005072-200606000-00005 |
0.331 |
|
| 1997 |
Zhang B, Tu P, Abtahian F, Trojanowski JQ, Lee VM. Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation. The Journal of Cell Biology. 139: 1307-15. PMID 9382875 DOI: 10.1083/Jcb.139.5.1307 |
0.335 |
|
| 1996 |
Tu PH, Raju P, Robinson KA, Gurney ME, Trojanowski JQ, Lee VM. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proceedings of the National Academy of Sciences of the United States of America. 93: 3155-60. PMID 8610185 DOI: 10.1073/Pnas.93.7.3155 |
0.35 |
|
| 1995 |
Tu PH, Elder G, Lazzarini RA, Nelson D, Trojanowski JQ, Lee VM. Overexpression of the human NFM subunit in transgenic mice modifies the level of endogenous NFL and the phosphorylation state of NFH subunits. The Journal of Cell Biology. 129: 1629-40. PMID 7790359 DOI: 10.1083/Jcb.129.6.1629 |
0.328 |
|
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