-
1
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann, M. et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130-133 (2006).
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
-
2
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Arai, T. et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem. Biophys. Res. Commun. 351, 602-611 (2006).
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.351
, pp. 602-611
-
-
Arai, T.1
-
3
-
-
77950867149
-
TAR DNA-binding protein 43 in neurodegenerative disease
-
Chen-Plotkin, A. S., Lee, V. M. & Trojanowski, J. Q. TAR DNA-binding protein 43 in neurodegenerative disease. Nat. Rev. Neurol. 6, 211-220 (2010).
-
(2010)
Nat. Rev. Neurol.
, vol.6
, pp. 211-220
-
-
Chen-Plotkin, A.S.1
Lee, V.M.2
Trojanowski, J.Q.3
-
4
-
-
33744781515
-
Frontotemporal dementia: Clinicopathological correlations
-
Forman, M. S. et al. Frontotemporal dementia: clinicopathological correlations. Ann. Neurol. 59, 952-962 (2006).
-
(2006)
Ann. Neurol.
, vol.59
, pp. 952-962
-
-
Forman, M.S.1
-
5
-
-
0036160338
-
Frontotemporal dementia
-
Snowden, J. S., Neary, D. & Mann, D. M. Frontotemporal dementia. Br. J. Psychiatry 180, 140-143 (2002).
-
(2002)
Br. J. Psychiatry
, vol.180
, pp. 140-143
-
-
Snowden, J.S.1
Neary, D.2
Mann, D.M.3
-
6
-
-
37349039461
-
TDP-43 proteinopathies: Neurodegenerative protein misfolding diseases without amyloidosis
-
Kwong, L. K., Uryu, K., Trojanowski, J. Q. & Lee, V. M. TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis. Neurosignals 16, 41-51 (2008).
-
(2008)
Neurosignals
, vol.16
, pp. 41-51
-
-
Kwong, L.K.1
Uryu, K.2
Trojanowski, J.Q.3
Lee, V.M.4
-
7
-
-
84877970597
-
A 43-kDa TDP-43 species is present in aggregates associated with frontotemporal lobar degeneration
-
Bosque, P. J., Boyer, P. J. & Mishra, P. A 43-kDa TDP-43 species is present in aggregates associated with frontotemporal lobar degeneration. PLoS ONE 8, e62301 (2013).
-
(2013)
PLoS ONE
, vol.8
, pp. e62301
-
-
Bosque, P.J.1
Boyer, P.J.2
Mishra, P.3
-
8
-
-
34249751076
-
TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein
-
Strong, M. J. et al. TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein. Mol. Cell Neurosci. 35, 320-327 (2007).
-
(2007)
Mol. Cell Neurosci.
, vol.35
, pp. 320-327
-
-
Strong, M.J.1
-
9
-
-
84878873344
-
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid
-
Bigio, E. H. et al. Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid. Acta Neuropathol. 125, 463-465 (2013).
-
(2013)
Acta Neuropathol.
, vol.125
, pp. 463-465
-
-
Bigio, E.H.1
-
10
-
-
65649133114
-
Amyloid fibrils: Abnormal protein assembly
-
Rambaran, R. N. & Serpell, L. C. Amyloid fibrils: abnormal protein assembly. Prion 2, 112-117 (2008).
-
(2008)
Prion
, vol.2
, pp. 112-117
-
-
Rambaran, R.N.1
Serpell, L.C.2
-
11
-
-
33847662852
-
Soluble protein oligomers in neurodegeneration: Lessons from the Alzheimer's amyloid beta-peptide
-
Haass, C. & Selkoe, D. J. Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid beta-peptide. Nat. Rev. Mol. Cell. Biol. 8, 101-112 (2007).
-
(2007)
Nat. Rev. Mol. Cell. Biol.
, vol.8
, pp. 101-112
-
-
Haass, C.1
Selkoe, D.J.2
-
12
-
-
79955044494
-
Soluble amyloid beta-protein dimers isolated from Alzheimer cortex directly induce Tau hyperphosphorylation and neuritic degeneration
-
Jin, M. et al. Soluble amyloid beta-protein dimers isolated from Alzheimer cortex directly induce Tau hyperphosphorylation and neuritic degeneration. Proc. Natl Acad. Sci. USA 108, 5819-5824 (2011).
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 5819-5824
-
-
Jin, M.1
-
13
-
-
0242668337
-
Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis
-
Kayed, R. et al. Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486-489 (2003).
-
(2003)
Science
, vol.300
, pp. 486-489
-
-
Kayed, R.1
-
14
-
-
33344463679
-
Common mechanisms of amyloid oligomer pathogenesis in degenerative disease
-
Glabe, C. G. Common mechanisms of amyloid oligomer pathogenesis in degenerative disease. Neurobiol. Aging 27, 570-575 (2006).
-
(2006)
Neurobiol. Aging
, vol.27
, pp. 570-575
-
-
Glabe, C.G.1
-
15
-
-
33644861975
-
Common structure and toxic function of amyloid oligomers implies a common mechanism of pathogenesis
-
Glabe, C. G. & Kayed, R. Common structure and toxic function of amyloid oligomers implies a common mechanism of pathogenesis. Neurology 66, S74-S78 (2006).
-
(2006)
Neurology
, vol.66
, pp. S74-S78
-
-
Glabe, C.G.1
Kayed, R.2
-
16
-
-
54249100481
-
TDP-43: An emerging new player in neurodegenerative diseases
-
Wang, I. F., Wu, L. S. & Shen, C. K. TDP-43: an emerging new player in neurodegenerative diseases. Trends Mol. Med. 14, 479-485 (2008).
-
(2008)
Trends Mol. Med.
, vol.14
, pp. 479-485
-
-
Wang, I.F.1
Wu, L.S.2
Shen, C.K.3
-
17
-
-
64549100193
-
Structural insights into TDP-43 in nucleic-acid binding and domain interactions
-
Kuo, P. H., Doudeva, L. G., Wang, Y. T., Shen, C. K. & Yuan, H. S. Structural insights into TDP-43 in nucleic-acid binding and domain interactions. Nucleic Acids Res. 37, 1799-1808 (2009).
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. 1799-1808
-
-
Kuo, P.H.1
Doudeva, L.G.2
Wang, Y.T.3
Shen, C.K.4
Yuan, H.S.5
-
18
-
-
0029066110
-
Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs
-
Ou, S. H., Wu, F., Harrich, D., Garcia-Martinez, L. F. & Gaynor, R. B. Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs. J. Virol. 69, 3584-3596 (1995).
-
(1995)
J. Virol.
, vol.69
, pp. 3584-3596
-
-
Ou, S.H.1
Wu, F.2
Harrich, D.3
Garcia-Martinez, L.F.4
Gaynor, R.B.5
-
19
-
-
77950377360
-
Induction of amyloid fibrils by the C-terminal fragments of TDP-43 in amyotrophic lateral sclerosis
-
Chen, A. K. et al. Induction of amyloid fibrils by the C-terminal fragments of TDP-43 in amyotrophic lateral sclerosis. J. Am. Chem. Soc. 132, 1186-1187 (2010).
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 1186-1187
-
-
Chen, A.K.1
-
20
-
-
84865028374
-
Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice
-
Wu, L. S., Cheng, W. C. & Shen, C. K. J. Targeted depletion of TDP-43 expression in the spinal cord motor neurons leads to the development of amyotrophic lateral sclerosis-like phenotypes in mice. J. Biol. Chem. 287, 27335-27344 (2012).
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 27335-27344
-
-
Wu, L.S.1
Cheng, W.C.2
Shen, C.K.J.3
-
21
-
-
73249152831
-
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
-
Wegorzewska, I., Bell, S., Cairns, N. J., Miller, T. M. & Baloh, R. H. TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration. Proc. Natl Acad. Sci. USA 106, 18809-18814 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 18809-18814
-
-
Wegorzewska, I.1
Bell, S.2
Cairns, N.J.3
Miller, T.M.4
Baloh, R.H.5
-
22
-
-
44049097065
-
A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity
-
Johnson, B. S., McCaffery, J. M., Lindquist, S. & Gitler, A. D. A yeast TDP-43 proteinopathy model: exploring the molecular determinants of TDP-43 aggregation and cellular toxicity. Proc. Natl Acad. Sci. USA 105, 6439-6444 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 6439-6444
-
-
Johnson, B.S.1
McCaffery, J.M.2
Lindquist, S.3
Gitler, A.D.4
-
23
-
-
63949083624
-
Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression
-
Tatom, J. B. et al. Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression. Mol. Ther. 17, 607-613 (2009).
-
(2009)
Mol. Ther.
, vol.17
, pp. 607-613
-
-
Tatom, J.B.1
-
24
-
-
77649269011
-
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
-
Wils, H. et al. TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration. Proc. Natl Acad. Sci. USA 107, 3858-3863 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 3858-3863
-
-
Wils, H.1
-
25
-
-
77955395385
-
Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLDU
-
Tsai, K. J. et al. Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLDU. J. Exp. Med. 207, 1661-1673 (2010).
-
(2010)
J. Exp. Med.
, vol.207
, pp. 1661-1673
-
-
Tsai, K.J.1
-
26
-
-
84878224074
-
Aberrant assembly of RNA recognition motif 1 links to pathogenic conversion of TAR DNA-binding protein of 43 kDa (TDP-43)
-
Shodai, A. et al. Aberrant assembly of RNA recognition motif 1 links to pathogenic conversion of TAR DNA-binding protein of 43 kDa (TDP-43). J. Biol. Chem. 288, 14886-14905 (2013).
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 14886-14905
-
-
Shodai, A.1
-
27
-
-
84875228800
-
Molecular mechanism of oxidation-induced TDP-43 RRM1 aggregation and loss of function
-
Chang, C. K., Chiang, M. H., Toh, E. K., Chang, C. F. & Huang, T. H. Molecular mechanism of oxidation-induced TDP-43 RRM1 aggregation and loss of function. FEBS Lett. 587, 575-582 (2013).
-
(2013)
FEBS Lett.
, vol.587
, pp. 575-582
-
-
Chang, C.K.1
Chiang, M.H.2
Toh, E.K.3
Chang, C.F.4
Huang, T.H.5
-
28
-
-
84875985444
-
The truncated C-terminal RNA recognition motif of TDP-43 protein plays a key role in forming proteinaceous aggregates
-
Wang, Y. T. et al. The truncated C-terminal RNA recognition motif of TDP-43 protein plays a key role in forming proteinaceous aggregates. J. Biol. Chem. 288, 9049-9057 (2013).
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 9049-9057
-
-
Wang, Y.T.1
-
29
-
-
84880073331
-
Structural transformation of the amyloidogenic core region of TAR DNA binding protein of 43 kDa (TDP-43) initiates its aggregation and cytoplasmic inclusion
-
Jiang, L. L. et al. Structural transformation of the amyloidogenic core region of TAR DNA binding protein of 43 kDa (TDP-43) initiates its aggregation and cytoplasmic inclusion. J. Biol. Chem. 288, 19614-19624 (2013).
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 19614-19624
-
-
Jiang, L.L.1
-
30
-
-
84857410934
-
Delineation of the core aggregation sequences of TDP-43 C-terminal fragment
-
Saini, A. & Chauhan, V. S. Delineation of the core aggregation sequences of TDP-43 C-terminal fragment. Chembiochem 12, 2495-2501 (2011).
-
(2011)
Chembiochem
, vol.12
, pp. 2495-2501
-
-
Saini, A.1
Chauhan, V.S.2
-
31
-
-
33750365052
-
Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins?
-
Lashuel, H. A. & Lansbury, Jr P. T. Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins? Q. Rev. Biophys. 39, 167-201 (2006).
-
(2006)
Q. Rev. Biophys.
, vol.39
, pp. 167-201
-
-
Lashuel, H.A.1
Lansbury, P.T.2
-
32
-
-
67749133873
-
TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity
-
Johnson, B. S. et al. TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity. J. Biol. Chem. 284, 20329-20339 (2009).
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 20329-20339
-
-
Johnson, B.S.1
-
33
-
-
0029115374
-
Kinetics of interaction of partially folded proteins with a hydrophobic dye: Evidence that molten globule character is maximal in early folding intermediates
-
Engelhard, M. & Evans, P. A. Kinetics of interaction of partially folded proteins with a hydrophobic dye: evidence that molten globule character is maximal in early folding intermediates. Protein Sci. 4, 1553-1562 (1995).
-
(1995)
Protein Sci.
, vol.4
, pp. 1553-1562
-
-
Engelhard, M.1
Evans, P.A.2
-
35
-
-
12244249201
-
Self-propagating, molecular-level polymorphism in Alzheimer's beta-amyloid fibrils
-
Petkova, A. T. et al. Self-propagating, molecular-level polymorphism in Alzheimer's beta-amyloid fibrils. Science 307, 262-265 (2005).
-
(2005)
Science
, vol.307
, pp. 262-265
-
-
Petkova, A.T.1
-
36
-
-
63849197629
-
Amyloid beta-protein assembly and Alzheimer disease
-
Roychaudhuri, R., Yang, M., Hoshi, M. M. & Teplow, D. B. Amyloid beta-protein assembly and Alzheimer disease. J. Biol. Chem. 284, 4749-4753 (2009).
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 4749-4753
-
-
Roychaudhuri, R.1
Yang, M.2
Hoshi, M.M.3
Teplow, D.B.4
-
37
-
-
84860171314
-
The E. coli CsgB nucleator of curli assembles to beta-sheet oligomers that alter the CsgA fibrillization mechanism
-
Shu, Q. et al. The E. coli CsgB nucleator of curli assembles to beta-sheet oligomers that alter the CsgA fibrillization mechanism. Proc. Natl Acad. Sci. USA 109, 6502-6507 (2012).
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. 6502-6507
-
-
Shu, Q.1
-
38
-
-
78649503285
-
Preparation and characterization of neurotoxic tau oligomers
-
Lasagna-Reeves, C. A., Castillo-Carranza, D. L., Guerrero-Muoz, M. J., Jackson, G. R. & Kayed, R. Preparation and characterization of neurotoxic tau oligomers. Biochemistry 49, 10039-10041 (2010).
-
(2010)
Biochemistry
, vol.49
, pp. 10039-10041
-
-
Lasagna-Reeves, C.A.1
Castillo-Carranza, D.L.2
Guerrero-Muoz, M.J.3
Jackson, G.R.4
Kayed, R.5
-
39
-
-
7044238416
-
Neurodegenerative diseases: A decade of discoveries paves the way for therapeutic breakthroughs
-
Forman, M. S., Trojanowski, J. Q. & Lee, V. M. Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs. Nat. Med. 10, 1055-1063 (2004).
-
(2004)
Nat. Med.
, vol.10
, pp. 1055-1063
-
-
Forman, M.S.1
Trojanowski, J.Q.2
Lee, V.M.3
-
40
-
-
84857642949
-
The toxic Abeta oligomer and Alzheimer's disease: An emperor in need of clothes
-
Benilova, I., Karran, E. & De Strooper, B. The toxic Abeta oligomer and Alzheimer's disease: an emperor in need of clothes. Nat. Neurosci. 15, 349-357 (2012).
-
(2012)
Nat. Neurosci.
, vol.15
, pp. 349-357
-
-
Benilova, I.1
Karran, E.2
De Strooper, B.3
-
41
-
-
34547203205
-
Amyloid beta ion channel: 3D structure and relevance to amyloid channel paradigm
-
Lal, R., Lin, H. & Quist, A. P. Amyloid beta ion channel: 3D structure and relevance to amyloid channel paradigm. Biochim. Biophys. Acta 1768, 1966-1975 (2007).
-
(2007)
Biochim. Biophys. Acta
, vol.1768
, pp. 1966-1975
-
-
Lal, R.1
Lin, H.2
Quist, A.P.3
-
42
-
-
33750365052
-
Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins?
-
Lashuel, H. A. & Lansbury, P. T. Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins? Q. Rev. Biophys. 39, 167-201 (2006).
-
(2006)
Q. Rev. Biophys.
, vol.39
, pp. 167-201
-
-
Lashuel, H.A.1
Lansbury, P.T.2
-
43
-
-
47949093588
-
Ultrastructural localization of TDP-43 in filamentous neuronal inclusions in various neurodegenerative diseases
-
Lin, W. L. & Dickson, D. W. Ultrastructural localization of TDP-43 in filamentous neuronal inclusions in various neurodegenerative diseases. Acta Neuropathol. 116, 205-213 (2008).
-
(2008)
Acta Neuropathol.
, vol.116
, pp. 205-213
-
-
Lin, W.L.1
Dickson, D.W.2
-
44
-
-
47949086625
-
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Hasegawa, M. et al. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann. Neurol. 64, 60-70 (2008).
-
(2008)
Ann. Neurol.
, vol.64
, pp. 60-70
-
-
Hasegawa, M.1
-
45
-
-
84857997227
-
Redox signalling directly regulates TDP-43 via cysteine oxidation and disulphide cross-linking
-
Cohen, T. J., Hwang, A. W., Unger, T., Trojanowski, J. Q. & Lee, V. M. Redox signalling directly regulates TDP-43 via cysteine oxidation and disulphide cross-linking. EMBO J. 31, 1241-1252 (2012).
-
(2012)
EMBO J.
, vol.31
, pp. 1241-1252
-
-
Cohen, T.J.1
Hwang, A.W.2
Unger, T.3
Trojanowski, J.Q.4
Lee, V.M.5
-
46
-
-
36348972414
-
Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies
-
Higashi, S. et al. Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies. Brain Res. 1184, 284-294 (2007).
-
(2007)
Brain Res.
, vol.1184
, pp. 284-294
-
-
Higashi, S.1
-
47
-
-
82355181107
-
TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: Association with age, hippocampal sclerosis and clinical phenotype
-
Davidson, Y. S. et al. TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype. Acta Neuropathol. 122, 703-713 (2011).
-
(2011)
Acta Neuropathol.
, vol.122
, pp. 703-713
-
-
Davidson, Y.S.1
-
48
-
-
34249949338
-
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
-
Amador-Ortiz, C. et al. TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease. Ann. Neurol. 61, 435-445 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 435-445
-
-
Amador-Ortiz, C.1
-
49
-
-
84885484356
-
Prion-like properties of pathological TDP-43 aggregates from diseased brains
-
Nonaka, T. et al. Prion-like properties of pathological TDP-43 aggregates from diseased brains. Cell Rep. 4, 124-134 (2013).
-
(2013)
Cell Rep.
, vol.4
, pp. 124-134
-
-
Nonaka, T.1
-
50
-
-
78649750391
-
Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy
-
Liachko, N. F., Guthrie, C. R. & Kraemer, B. C. Phosphorylation promotes neurotoxicity in a Caenorhabditis elegans model of TDP-43 proteinopathy. J. Neurosci. 30, 16208-16219 (2010).
-
(2010)
J. Neurosci.
, vol.30
, pp. 16208-16219
-
-
Liachko, N.F.1
Guthrie, C.R.2
Kraemer, B.C.3
-
51
-
-
0028871804
-
How to measure and predict the molar absorption coefficient of a protein
-
Pace, C. N., Vajdos, F., Fee, L., Grimsley, G. & Gray, T. How to measure and predict the molar absorption coefficient of a protein. Protein Sci. 4, 2411-2423 (1995).
-
(1995)
Protein Sci.
, vol.4
, pp. 2411-2423
-
-
Pace, C.N.1
Vajdos, F.2
Fee, L.3
Grimsley, G.4
Gray, T.5
-
52
-
-
33747652958
-
Distinct early folding and aggregation properties of Alzheimer amyloid-beta peptides Abeta40 and Abeta42: Stable trimer or tetramer formation by Abeta42
-
Chen, Y. R. & Glabe, C. G. Distinct early folding and aggregation properties of Alzheimer amyloid-beta peptides Abeta40 and Abeta42: stable trimer or tetramer formation by Abeta42. J. Biol. Chem. 281, 24414-24422 (2006).
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 24414-24422
-
-
Chen, Y.R.1
Glabe, C.G.2
-
53
-
-
3342901587
-
Kinetic traps in the folding/unfolding of procaspase-1 CARD domain
-
Chen, Y. R. & Clark, A. C. Kinetic traps in the folding/unfolding of procaspase-1 CARD domain. Protein Sci. 13, 2196-2206 (2004).
-
(2004)
Protein Sci.
, vol.13
, pp. 2196-2206
-
-
Chen, Y.R.1
Clark, A.C.2
-
54
-
-
79953225854
-
Distinct effects of Zn2+, Cu2+, Fe3+, and Al3+ on amyloid-β stability, oligomerization, and aggregation: Amyloid-β destabilization promotes annular protofibril formation
-
Chen, W. T., Liao, Y. H., Yu, H. M., Cheng, I. H. & Chen, Y. R. Distinct effects of Zn2+, Cu2+, Fe3+, and Al3+ on amyloid-β stability, oligomerization, and aggregation: amyloid-β destabilization promotes annular protofibril formation. J. Biol. Chem. 286, 9646-9656 (2011).
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 9646-9656
-
-
Chen, W.T.1
Liao, Y.H.2
Yu, H.M.3
Cheng, I.H.4
Chen, Y.R.5
-
55
-
-
79954613385
-
Folding stability of amyloid-{beta} 40 monomer is an important determinant of the nucleation kinetics in fibrillization
-
Ni, C. L., Shi, H. P., Yu, H. M., Chang, Y. C. & Chen, Y. R. Folding stability of amyloid-{beta} 40 monomer is an important determinant of the nucleation kinetics in fibrillization. FASEB J. 25, 1390-1401 (2011).
-
(2011)
FASEB J.
, vol.25
, pp. 1390-1401
-
-
Ni, C.L.1
Shi, H.P.2
Yu, H.M.3
Chang, Y.C.4
Chen, Y.R.5
-
56
-
-
0035860781
-
Amyloid beta-protein oligomerization: Prenucleation interactions revealed by photo-induced cross-linking of unmodified proteins
-
Bitan, G., Lomakin, A. & Teplow, D. B. Amyloid beta-protein oligomerization: prenucleation interactions revealed by photo-induced cross-linking of unmodified proteins. J. Biol. Chem. 276, 35176-35184 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 35176-35184
-
-
Bitan, G.1
Lomakin, A.2
Teplow, D.B.3
|