Year |
Citation |
Score |
2012 |
Yao J, Ho D, Calingasan NY, Pipalia NH, Lin MT, Beal MF. Neuroprotection by cyclodextrin in cell and mouse models of Alzheimer disease. The Journal of Experimental Medicine. 209: 2501-13. PMID 23209315 DOI: 10.1084/Jem.20121239 |
0.508 |
|
2012 |
Lin MT, Cantuti-Castelvetri I, Zheng K, Jackson KE, Tan YB, Arzberger T, Lees AJ, Betensky RA, Beal MF, Simon DK. Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease. Annals of Neurology. 71: 850-4. PMID 22718549 DOI: 10.1002/Ana.23568 |
0.531 |
|
2011 |
Tampellini D, Rahman N, Lin MT, Capetillo-Zarate E, Gouras GK. Impaired β-amyloid secretion in Alzheimer's disease pathogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 15384-90. PMID 22031884 DOI: 10.1523/Jneurosci.2986-11.2011 |
0.315 |
|
2011 |
Capetillo-Zarate E, Gracia L, Yu F, Banfelder JR, Lin MT, Tampellini D, Gouras GK. High-resolution 3D reconstruction reveals intra-synaptic amyloid fibrils. The American Journal of Pathology. 179: 2551-8. PMID 21925470 DOI: 10.1016/J.Ajpath.2011.07.045 |
0.301 |
|
2011 |
Dumont M, Kipiani K, Yu F, Wille E, Katz M, Calingasan NY, Gouras GK, Lin MT, Beal MF. Coenzyme Q10 decreases amyloid pathology and improves behavior in a transgenic mouse model of Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 27: 211-23. PMID 21799249 DOI: 10.3233/Jad-2011-110209 |
0.739 |
|
2011 |
Gouras G, Gracia L, Milner T, Banfelder J, Lin M, Tampellini D, Capetillo-Zarate E. P4-382: High-resolution 3-dimensional reconstruction reveals early intra-synaptic amyloid fibrils in Alzheimer's transgenic mice Alzheimer's & Dementia. 7: e46-e47. DOI: 10.1016/J.Jalz.2011.09.196 |
0.375 |
|
2011 |
Yao J, Beal F, Lin M. P3-171: MicroRNA related cofilin abnormality and the pathological consequences in a transgenic mouse model of Alzheimer's disease Alzheimer's & Dementia. 7: S572-S572. DOI: 10.1016/J.Jalz.2011.05.1612 |
0.358 |
|
2010 |
Yao J, Hennessey T, Flynt A, Lai E, Beal MF, Lin MT. MicroRNA-related cofilin abnormality in Alzheimer's disease. Plos One. 5: e15546. PMID 21179570 DOI: 10.1371/Journal.Pone.0015546 |
0.531 |
|
2010 |
Tampellini D, Capetillo-Zarate E, Dumont M, Huang Z, Yu F, Lin MT, Gouras GK. Effects of synaptic modulation on beta-amyloid, synaptophysin, and memory performance in Alzheimer's disease transgenic mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 14299-304. PMID 20980585 DOI: 10.1523/Jneurosci.3383-10.2010 |
0.489 |
|
2010 |
Yin F, Dumont M, Banerjee R, Ma Y, Li H, Lin MT, Beal MF, Nathan C, Thomas B, Ding A. Behavioral deficits and progressive neuropathology in progranulin-deficient mice: a mouse model of frontotemporal dementia. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 4639-47. PMID 20667979 DOI: 10.1096/fj.10.161471 |
0.631 |
|
2010 |
Dumont M, Lin MT, Beal MF. Mitochondria and antioxidant targeted therapeutic strategies for Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 20: S633-43. PMID 20421689 DOI: 10.3233/Jad-2010-100507 |
0.633 |
|
2010 |
Dumont M, Wille E, Calingasan NY, Nathan C, Flint Beal M, Lin MT. N-iminoethyl-L-lysine improves memory and reduces amyloid pathology in a transgenic mouse model of amyloid deposition. Neurochemistry International. 56: 345-51. PMID 19914323 DOI: 10.1016/J.Neuint.2009.11.006 |
0.548 |
|
2010 |
Takahashi RH, Capetillo-Zarate E, Lin MT, Milner TA, Gouras GK. Co-occurrence of Alzheimer's disease ß-amyloid and τ pathologies at synapses. Neurobiology of Aging. 31: 1145-52. PMID 18771816 DOI: 10.1016/J.Neurobiolaging.2008.07.021 |
0.34 |
|
2009 |
Tampellini D, Rahman N, Gallo EF, Huang Z, Dumont M, Capetillo-Zarate E, Ma T, Zheng R, Lu B, Nanus DM, Lin MT, Gouras GK. Synaptic activity reduces intraneuronal Abeta, promotes APP transport to synapses, and protects against Abeta-related synaptic alterations. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 9704-13. PMID 19657023 DOI: 10.1523/Jneurosci.2292-09.2009 |
0.458 |
|
2009 |
Dumont M, Wille E, Stack C, Calingasan NY, Beal MF, Lin MT. Reduction of oxidative stress, amyloid deposition, and memory deficit by manganese superoxide dismutase overexpression in a transgenic mouse model of Alzheimer's disease. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 23: 2459-66. PMID 19346295 DOI: 10.1096/Fj.09-132928 |
0.643 |
|
2009 |
Dumont M, Wille E, Calingasan NY, Tampellini D, Williams C, Gouras GK, Liby K, Sporn M, Nathan C, Flint Beal M, Lin MT. Triterpenoid CDDO-methylamide improves memory and decreases amyloid plaques in a transgenic mouse model of Alzheimer's disease. Journal of Neurochemistry. 109: 502-12. PMID 19200343 DOI: 10.1111/J.1471-4159.2009.05970.X |
0.567 |
|
2006 |
Lin MT, Beal MF. Alzheimer's APP mangles mitochondria. Nature Medicine. 12: 1241-3. PMID 17088888 DOI: 10.1038/Nm1106-1241 |
0.481 |
|
2006 |
Lin MT, Beal MF. Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature. 443: 787-95. PMID 17051205 DOI: 10.1038/Nature05292 |
0.459 |
|
2006 |
Hersch SM, Gevorkian S, Marder K, Moskowitz C, Feigin A, Cox M, Como P, Zimmerman C, Lin M, Zhang L, Ulug AM, Beal MF, Matson W, Bogdanov M, Ebbel E, et al. Creatine in Huntington disease is safe, tolerable, bioavailable in brain and reduces serum 8OH2'dG. Neurology. 66: 250-2. PMID 16434666 DOI: 10.1212/01.Wnl.0000194318.74946.B6 |
0.469 |
|
2005 |
Nathan C, Calingasan N, Nezezon J, Ding A, Lucia MS, La Perle K, Fuortes M, Lin M, Ehrt S, Kwon NS, Chen J, Vodovotz Y, Kipiani K, Beal MF. Protection from Alzheimer's-like disease in the mouse by genetic ablation of inducible nitric oxide synthase. The Journal of Experimental Medicine. 202: 1163-9. PMID 16260491 DOI: 10.1084/Jem.20051529 |
0.731 |
|
2005 |
Cantuti-Castelvetri I, Lin MT, Zheng K, Keller-McGandy CE, Betensky RA, Johns DR, Beal MF, Standaert DG, Simon DK. Somatic mitochondrial DNA mutations in single neurons and glia. Neurobiology of Aging. 26: 1343-55. PMID 16243605 DOI: 10.1016/J.Neurobiolaging.2004.11.008 |
0.533 |
|
2005 |
Lin MT, Simon DK. No evidence for heritability of Parkinson disease in Swedish twins. Neurology. 64: 932; author reply 93. PMID 15753453 DOI: 10.1212/WNL.64.5.932 |
0.405 |
|
2004 |
Li F, Calingasan NY, Yu F, Mauck WM, Toidze M, Almeida CG, Takahashi RH, Carlson GA, Flint Beal M, Lin MT, Gouras GK. Increased plaque burden in brains of APP mutant MnSOD heterozygous knockout mice. Journal of Neurochemistry. 89: 1308-12. PMID 15147524 DOI: 10.1111/J.1471-4159.2004.02455.X |
0.373 |
|
2004 |
Takahashi RH, Almeida CG, Kearney PF, Yu F, Lin MT, Milner TA, Gouras GK. Oligomerization of Alzheimer's beta-amyloid within processes and synapses of cultured neurons and brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 3592-9. PMID 15071107 DOI: 10.1523/Jneurosci.5167-03.2004 |
0.307 |
|
2004 |
Uluğ AM, Grünewald T, Lin MT, Kamal AK, Filippi CG, Zimmerman RD, Beal MF. Diffusion tensor imaging in the diagnosis of primary lateral sclerosis. Journal of Magnetic Resonance Imaging : Jmri. 19: 34-9. PMID 14696218 DOI: 10.1002/Jmri.10433 |
0.311 |
|
2004 |
Simon DK, Lin MT, Zheng L, Liu GJ, Ahn CH, Kim LM, Mauck WM, Twu F, Beal MF, Johns DR. Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease. Neurobiology of Aging. 25: 71-81. PMID 14675733 DOI: 10.1016/S0197-4580(03)00037-X |
0.571 |
|
2003 |
Zhang L, Ulug AM, Zimmerman RD, Lin MT, Rubin M, Beal MF. The diagnostic utility of FLAIR imaging in clinically verified amyotrophic lateral sclerosis. Journal of Magnetic Resonance Imaging : Jmri. 17: 521-7. PMID 12720261 DOI: 10.1002/Jmri.10293 |
0.34 |
|
2003 |
Gajewski CD, Lin MT, Cudkowicz ME, Beal MF, Manfredi G. Mitochondrial DNA from platelets of sporadic ALS patients restores normal respiratory functions in rho(0) cells. Experimental Neurology. 179: 229-35. PMID 12618129 DOI: 10.1016/S0014-4886(02)00022-5 |
0.4 |
|
2002 |
Simon DK, Lin MT, Pascual-Leone A. "Nature versus nurture" and incompletely penetrant mutations. Journal of Neurology, Neurosurgery, and Psychiatry. 72: 686-9. PMID 12023405 DOI: 10.1136/Jnnp.72.6.686 |
0.471 |
|
2002 |
Vives-Bauza C, Andreu AL, Manfredi G, Beal MF, Janetzky B, Gruenewald TH, Lin MT. Sequence analysis of the entire mitochondrial genome in Parkinson's disease. Biochemical and Biophysical Research Communications. 290: 1593-601. PMID 11820805 DOI: 10.1006/Bbrc.2002.6388 |
0.4 |
|
2002 |
Lin MT, Simon DK, Ahn CH, Kim LM, Beal MF. High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain. Human Molecular Genetics. 11: 133-45. PMID 11809722 DOI: 10.1093/Hmg/11.2.133 |
0.578 |
|
2001 |
Simon DK, Lin MT, Ahn CH, Liu GJ, Gibson GE, Beal MF, Johns DR. Low mutational burden of individual acquired mitochondrial DNA mutations in brain. Genomics. 73: 113-6. PMID 11352572 DOI: 10.1006/Geno.2001.6515 |
0.564 |
|
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