-
1
-
-
82955220477
-
Alzheimer's disease: Pathological mechanisms and recent insights
-
Niedowicz DM, Nelson PT, Murphy MP (2011) Alzheimer's disease: Pathological mechanisms and recent insights. Curr Neuropharmacol 9, 674-684.
-
(2011)
Curr Neuropharmacol
, vol.9
, pp. 674-684
-
-
Niedowicz, D.M.1
Nelson, P.T.2
Murphy, M.P.3
-
2
-
-
70349558522
-
Genome-wide association study identifies variantsat CLU and PICALM associated with Alzheimer's disease
-
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schurmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dich-gans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J (2009) Genome-wide association study identifies variantsat CLU and PICALM associated with Alzheimer's disease. Nat Genet 41, 1088-1093.
-
(2009)
Nat Genet
, vol.41
, pp. 1088-1093
-
-
Harold, D.1
Abraham, R.2
Hollingworth, P.3
Sims, R.4
Gerrish, A.5
Hamshere, M.L.6
Pahwa, J.S.7
Moskvina, V.8
Dowzell, K.9
Williams, A.10
Jones, N.11
Thomas, C.12
Stretton, A.13
Morgan, A.R.14
Lovestone, S.15
Powell, J.16
Proitsi, P.17
Lupton, M.K.18
Brayne, C.19
Rubinsztein, D.C.20
Gill, M.21
Lawlor, B.22
Lynch, A.23
Morgan, K.24
Brown, K.S.25
Passmore, P.A.26
Craig, D.27
McGuinness, B.28
Todd, S.29
Holmes, C.30
Mann, D.31
Smith, A.D.32
Love, S.33
Kehoe, P.G.34
Hardy, J.35
Mead, S.36
Fox, N.37
Rossor, M.38
Collinge, J.39
Maier, W.40
Jessen, F.41
Schurmann, B.42
Van Den Bussche, H.43
Heuser, I.44
Kornhuber, J.45
Wiltfang, J.46
Dich-Gans, M.47
Frolich, L.48
Hampel, H.49
Hull, M.50
Rujescu, D.51
Goate, A.M.52
Kauwe, J.S.53
Cruchaga, C.54
Nowotny, P.55
Morris, J.C.56
Mayo, K.57
Sleegers, K.58
Bettens, K.59
Engelborghs, S.60
De Deyn, P.P.61
Van Broeckhoven, C.62
Livingston, G.63
Bass, N.J.64
Gurling, H.65
McQuillin, A.66
Gwilliam, R.67
Deloukas, P.68
Al-Chalabi, A.69
Shaw, C.E.70
Tsolaki, M.71
Singleton, A.B.72
Guerreiro, R.73
Muhleisen, T.W.74
Nothen, M.M.75
Moebus, S.76
Jockel, K.H.77
Klopp, N.78
Wichmann, H.E.79
Carrasquillo, M.M.80
Pankratz, V.S.81
Younkin, S.G.82
Holmans, P.A.83
O'Donovan, M.84
Owen, M.J.85
Williams, J.86
more..
-
3
-
-
78549264026
-
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tav-ernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fievet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossu P, Pic-cardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanche H, Dartigues JF, Tzourio C, Gut I, Van Broeckhoven C, Alperovitch A, Lathrop M, Amouyel P (2009) Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nat Genet 41, 1094-1099.
-
(2009)
Nat Genet
, vol.41
, pp. 1094-1099
-
-
Lambert, J.C.1
Heath, S.2
Even, G.3
Campion, D.4
Sleegers, K.5
Hiltunen, M.6
Combarros, O.7
Zelenika, D.8
Bullido, M.J.9
Tav-Ernier, B.10
Letenneur, L.11
Bettens, K.12
Berr, C.13
Pasquier, F.14
Fievet, N.15
Barberger-Gateau, P.16
Engelborghs, S.17
De Deyn, P.18
Mateo, I.19
Franck, A.20
Helisalmi, S.21
Porcellini, E.22
Hanon, O.23
De Pancorbo, M.M.24
Lendon, C.25
Dufouil, C.26
Jaillard, C.27
Leveillard, T.28
Alvarez, V.29
Bosco, P.30
Mancuso, M.31
Panza, F.32
Nacmias, B.33
Bossu, P.34
Pic-Cardi, P.35
Annoni, G.36
Seripa, D.37
Galimberti, D.38
Hannequin, D.39
Licastro, F.40
Soininen, H.41
Ritchie, K.42
Blanche, H.43
Dartigues, J.F.44
Tzourio, C.45
Gut, I.46
Van Broeckhoven, C.47
Alperovitch, A.48
Lathrop, M.49
Amouyel, P.50
more..
-
4
-
-
77952307991
-
Genome-wide analysis of genetic loci associated with Alzheimer disease
-
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gud-nason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT Jr, Janssens AC, Pankratz VS, Dar-tigues JF, Hollingworth P, Aspelund T, Hernandez I, Beiser A, Kuller LH, Koudstaal PJ, Dickson DW, Tzourio C, Abraham R, Antunez C, Du Y, Rotter JI, Aulchenko YS, Harris TB, Petersen RC, Berr C, Owen MJ, Lopez-Arrieta J, Varadara-jan BN, Becker JT, Rivadeneira F, Nalls MA, Graff-Radford NR, Campion D, Auerbach S, Rice K, Hofman A, Jonsson PV, Schmidt H, Lathrop M, Mosley TH, Au R, Psaty BM, Uitterlinden AG, Farrer LA, Lumley T, Ruiz A, Williams J, Amouyel P, Younkin SG, Wolf PA, Launer LJ, Lopez OL, van Duijn CM, Breteler MM (2010) Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 303, 1832-1840.
-
(2010)
JAMA
, vol.303
, pp. 1832-1840
-
-
Seshadri, S.1
Fitzpatrick, A.L.2
Ikram, M.A.3
Destefano, A.L.4
Gud-Nason, V.5
Boada, M.6
Bis, J.C.7
Smith, A.V.8
Carassquillo, M.M.9
Lambert, J.C.10
Harold, D.11
Schrijvers, E.M.12
Ramirez-Lorca, R.13
Debette, S.14
Longstreth, W.T.15
Janssens, A.C.16
Pankratz, V.S.17
Dar-Tigues, J.F.18
Hollingworth, P.19
Aspelund, T.20
Hernandez, I.21
Beiser, A.22
Kuller, L.H.23
Koudstaal, P.J.24
Dickson, D.W.25
Tzourio, C.26
Abraham, R.27
Antunez, C.28
Du, Y.29
Rotter, J.I.30
Aulchenko, Y.S.31
Harris, T.B.32
Petersen, R.C.33
Berr, C.34
Owen, M.J.35
Lopez-Arrieta, J.36
Varadara-Jan, B.N.37
Becker, J.T.38
Rivadeneira, F.39
Nalls, M.A.40
Graff-Radford, N.R.41
Campion, D.42
Auerbach, S.43
Rice, K.44
Hofman, A.45
Jonsson, P.V.46
Schmidt, H.47
Lathrop, M.48
Mosley, T.H.49
Au, R.50
Psaty, B.M.51
Uitterlinden, A.G.52
Farrer, L.A.53
Lumley, T.54
Ruiz, A.55
Williams, J.56
Amouyel, P.57
Younkin, S.G.58
Wolf, P.A.59
Launer, L.J.60
Lopez, O.L.61
Van Duijn, C.M.62
Breteler, M.M.63
more..
-
5
-
-
0029741917
-
BIN1isa novel MYC-interacting protein with features of a tumour suppressor
-
Sakamuro D, Elliott KJ, Wechsler-Reya R, Prendergast GC (1996) BIN1isa novel MYC-interacting protein with features of a tumour suppressor. Nat Genet 14, 69-77.
-
(1996)
Nat Genet
, vol.14
, pp. 69-77
-
-
Sakamuro, D.1
Elliott, K.J.2
Wechsler-Reya, R.3
Prendergast, G.C.4
-
6
-
-
0029997010
-
Genetic alterations in untreated metastases and androgen-independent prostate cancer detected by comparative genomic hybridization and allelotyping
-
Cher ML, Bova GS, Moore DH, Small EJ, Carroll PR, Pin SS, Epstein JI, Isaacs WB, Jensen RH (1996) Genetic alterations in untreated metastases and androgen-independent prostate cancer detected by comparative genomic hybridization and allelotyping. Cancer Res 56, 3091-3102.
-
(1996)
Cancer Res
, vol.56
, pp. 3091-3102
-
-
Cher, M.L.1
Bova, G.S.2
Moore, D.H.3
Small, E.J.4
Carroll, P.R.5
Pin, S.S.6
Epstein, J.I.7
Isaacs, W.B.8
Jensen, R.H.9
-
7
-
-
33645129695
-
The BAR domain proteins: Molding membranes in fission, fusion, and phagy
-
Ren G, Vajjhala P, Lee JS, Winsor B, Munn AL (2006) The BAR domain proteins: Molding membranes in fission, fusion, and phagy. Microbiol Mol Biol Rev 70, 37-120.
-
(2006)
Microbiol Mol Biol Rev
, vol.70
, pp. 37-120
-
-
Ren, G.1
Vajjhala, P.2
Lee, J.S.3
Winsor, B.4
Munn, A.L.5
-
8
-
-
33748288113
-
BAR, F-BAR (EFC) and ENTH/ANTH domains in the regulation of membrane-cytosol interfaces and membrane curvature
-
Itoh T, De Camilli P (2006) BAR, F-BAR (EFC) and ENTH/ANTH domains in the regulation of membrane-cytosol interfaces and membrane curvature. Biochim Biophys Acta 1761, 897-912.
-
(2006)
Biochim Biophys Acta
, vol.1761
, pp. 897-912
-
-
Itoh, T.1
De Camilli, P.2
-
9
-
-
46349097361
-
Membrane traffic and muscle: Lessons from human disease
-
Dowling JJ, Gibbs EM, Feldman EL (2008) Membrane traffic and muscle: Lessons from human disease. Traffic 9, 1035-1043.
-
(2008)
Traffic
, vol.9
, pp. 1035-1043
-
-
Dowling, J.J.1
Gibbs, E.M.2
Feldman, E.L.3
-
10
-
-
84886914118
-
BIN1Is decreasedin sporadic but not familial Alzheimer's disease or in aging
-
Glennon EB, Whitehouse IJ, Miners JS, Kehoe PG, Love S, Kellett KA, Hooper NM (2013) BIN1Is decreasedin sporadic but not familial Alzheimer's disease or in aging. PLoS One 8, e78806.
-
(2013)
PLoS One
, vol.8
, pp. e78806
-
-
Glennon, E.B.1
Whitehouse, I.J.2
Miners, J.S.3
Kehoe, P.G.4
Love, S.5
Kellett, K.A.6
Hooper, N.M.7
-
11
-
-
84888306100
-
Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology
-
Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Van Cauwenberghe C, Kolen KV, Geller F, Sottejeau Y, Harold D, Dourlen P, Grenier-Boley B, Kamatani Y, Delepine B, Demi-autte F, Zelenika D, Zommer N, Hamdane M, Bellenguez C, Dartigues JF, Hauw JJ, Letronne F, Ayral AM, Sleegers K, Schellens A, Broeck LV, Engelborghs S, De Deyn PP, Van-denberghe R, O'Donovan M, Owen M, Epelbaum J, Mercken M, Karran E, Bantscheff M, Drewes G, Joberty G, Campion D, Octave JN, Berr C, Lathrop M, Callaerts P, Mann D, Williams J, Buee L, Dewachter I, Van Broeckhoven C, Amouyel P, Moechars D, Dermaut B, Lambert JC (2013) Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Mol Psychiatry 18, 1225-1234.
-
(2013)
Mol Psychiatry
, vol.18
, pp. 1225-1234
-
-
Chapuis, J.1
Hansmannel, F.2
Gistelinck, M.3
Mounier, A.4
Van Cauwenberghe, C.5
Kolen, K.V.6
Geller, F.7
Sottejeau, Y.8
Harold, D.9
Dourlen, P.10
Grenier-Boley, B.11
Kamatani, Y.12
Delepine, B.13
Demi-Autte, F.14
Zelenika, D.15
Zommer, N.16
Hamdane, M.17
Bellenguez, C.18
Dartigues, J.F.19
Hauw, J.J.20
Letronne, F.21
Ayral, A.M.22
Sleegers, K.23
Schellens, A.24
Broeck, L.V.25
Engelborghs, S.26
De Deyn, P.P.27
Van-Denberghe, R.28
O'Donovan, M.29
Owen, M.30
Epelbaum, J.31
Mercken, M.32
Karran, E.33
Bantscheff, M.34
Drewes, G.35
Joberty, G.36
Campion, D.37
Octave, J.N.38
Berr, C.39
Lathrop, M.40
Callaerts, P.41
Mann, D.42
Williams, J.43
Buee, L.44
Dewachter, I.45
Van Broeckhoven, C.46
Amouyel, P.47
Moechars, D.48
Dermaut, B.49
Lambert, J.C.50
more..
-
12
-
-
79958101846
-
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
-
Fugier C, Klein AF, Hammer C, Vassilopoulos S, Ivarsson Y, Toussaint A, Tosch V, Vignaud A, Ferry A, Messaddeq N, Kokunai Y, Tsuburaya R, delaGrange P, Dembele D, Francois V, Precigout G, Boulade-Ladame C, Hummel MC, deMunain AL, Sergeant N, Laquerriere A, Thibault C, Deryckere F, Auboeuf D, Garcia L, Zimmermann P, Udd B, Schoser B, Takahashi MP, Nishino I, Bassez G, Laporte J, Furling D, Charlet-Berguerand N (2011) Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy. Nat Med 17, 720-725.
-
(2011)
Nat Med
, vol.17
, pp. 720-725
-
-
Fugier, C.1
Klein, A.F.2
Hammer, C.3
Vassilopoulos, S.4
Ivarsson, Y.5
Toussaint, A.6
Tosch, V.7
Vignaud, A.8
Ferry, A.9
Messaddeq, N.10
Kokunai, Y.11
Tsuburaya, R.12
Delagrange, P.13
Dembele, D.14
Francois, V.15
Precigout, G.16
Boulade-Ladame, C.17
Hummel, M.C.18
Demunain, A.L.19
Sergeant, N.20
Laquerriere, A.21
Thibault, C.22
Deryckere, F.23
Auboeuf, D.24
Garcia, L.25
Zimmermann, P.26
Udd, B.27
Schoser, B.28
Takahashi, M.P.29
Nishino, I.30
Bassez, G.31
Laporte, J.32
Furling, D.33
Charlet-Berguerand, N.34
more..
-
13
-
-
17144427268
-
Tau exons 2 and 10, which are misregulated in neurodegenerative diseases, are partly regulated by silencers which bind a SRp30c. SRp55 complex that either recruits or antagonizes htra2beta1
-
Wang Y, Wang J, Gao L, Lafyatis R, Stamm S, Andreadis A (2005) Tau exons 2 and 10, which are misregulated in neurodegenerative diseases, are partly regulated by silencers which bind a SRp30c. SRp55 complex that either recruits or antagonizes htra2beta1. J Biol Chem 280, 14230-14239.
-
(2005)
J Biol Chem
, vol.280
, pp. 14230-14239
-
-
Wang, Y.1
Wang, J.2
Gao, L.3
Lafyatis, R.4
Stamm, S.5
Andreadis, A.6
-
14
-
-
33644779759
-
Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1
-
Leroy O, Wang J, Maurage CA, Parent M, Cooper T, Buee L, Sergeant N, Andreadis A, Caillet-Boudin ML (2006) Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1. Biochim Biophys Acta 1762, 460-467.
-
(2006)
Biochim Biophys Acta
, vol.1762
, pp. 460-467
-
-
Leroy, O.1
Wang, J.2
Maurage, C.A.3
Parent, M.4
Cooper, T.5
Buee, L.6
Sergeant, N.7
Andreadis, A.8
Caillet-Boudin, M.L.9
-
15
-
-
79955609313
-
Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpres-sionofCELF2 but notbyMBNL1 silencing
-
Dhaenens CM, Tran H, Frandemiche ML, Carpentier C, Schraen-Maschke S, Sistiaga A, Goicoechea M, Eddarkaoui S, Van Brussels E, Obriot H, Labudeck A, Gevaert MH, Fernandez-Gomez F, Charlet-Berguerand N, Deramecourt V, Maurage CA, Buee L, de Munain AL, Sablonniere B, Caillet-Boudin ML, Sergeant N (2011) Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpres-sionofCELF2 but notbyMBNL1 silencing. Biochim Biophys Acta 1812, 732-742.
-
(2011)
Biochim Biophys Acta
, vol.1812
, pp. 732-742
-
-
Dhaenens, C.M.1
Tran, H.2
Frandemiche, M.L.3
Carpentier, C.4
Schraen-Maschke, S.5
Sistiaga, A.6
Goicoechea, M.7
Eddarkaoui, S.8
Van Brussels, E.9
Obriot, H.10
Labudeck, A.11
Gevaert, M.H.12
Fernandez-Gomez, F.13
Charlet-Berguerand, N.14
Deramecourt, V.15
Maurage, C.A.16
Buee, L.17
De Munain, A.L.18
Sablonniere, B.19
Caillet-Boudin, M.L.20
Sergeant, N.21
more..
-
17
-
-
28044436700
-
Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease
-
Maurage CA, Udd B, Ruchoux MM, Vermersch P, Kalimo H, Krahe R, Delacourte A, Sergeant N (2005) Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease. Neurology 65, 1636-1638.
-
(2005)
Neurology
, vol.65
, pp. 1636-1638
-
-
Maurage, C.A.1
Udd, B.2
Ruchoux, M.M.3
Vermersch, P.4
Kalimo, H.5
Krahe, R.6
Delacourte, A.7
Sergeant, N.8
-
18
-
-
83755185685
-
The brain in myotonic dystrophy 1 and 2: Evidence for a predominant white matter disease
-
Minnerop M, Weber B, Schoene-Bake JC, Roeske S, Mirbach S, Anspach C, Schneider-Gold C, Betz RC, Helmstaedter C, Tittgemeyer M, Klockgether T, Kornblum C (2011) The brain in myotonic dystrophy 1 and 2: Evidence for a predominant white matter disease. Brain 134, 3530-3546.
-
(2011)
Brain
, vol.134
, pp. 3530-3546
-
-
Minnerop, M.1
Weber, B.2
Schoene-Bake, J.C.3
Roeske, S.4
Mirbach, S.5
Anspach, C.6
Schneider-Gold, C.7
Betz, R.C.8
Helmstaedter, C.9
Tittgemeyer, M.10
Klockgether, T.11
Kornblum, C.12
-
19
-
-
0025052939
-
Mapping of the gene for CNBP, a finger protein, tohuman chromosome 3q13.3-q24
-
Lusis AJ, Rajavashisth TB, Klisak I, Heinzmann C, Mohandas T, Sparkes RS (1990) Mapping of the gene for CNBP, a finger protein, tohuman chromosome 3q13.3-q24.Genomics 8, 411-414.
-
(1990)
Genomics
, vol.8
, pp. 411-414
-
-
Lusis, A.J.1
Rajavashisth, T.B.2
Klisak, I.3
Heinzmann, C.4
Mohandas, T.5
Sparkes, R.S.6
-
20
-
-
83455164148
-
BACE2 expressionincreasesinhuman neurodegenerative disease
-
Holler CJ, Webb RL, Laux AL, Beckett TL, Niedowicz DM, Ahmed RR, Liu Y, Simmons CR, Dowling AL, Spinelli A, Khurgel M, Estus S, Head E, Hersh LB, Murphy MP (2012) BACE2 expressionincreasesinhuman neurodegenerative disease. Am J Pathol 180, 337-350.
-
(2012)
Am J Pathol
, vol.180
, pp. 337-350
-
-
Holler, C.J.1
Webb, R.L.2
Laux, A.L.3
Beckett, T.L.4
Niedowicz, D.M.5
Ahmed, R.R.6
Liu, Y.7
Simmons, C.R.8
Dowling, A.L.9
Spinelli, A.10
Khurgel, M.11
Estus, S.12
Head, E.13
Hersh, L.B.14
Murphy, M.P.15
-
21
-
-
84867518259
-
Postmortem Pittsburgh compound B (PiB) binding increases with Alzheimer's disease progression
-
Beckett TL, Webb RL, Niedowicz DM, Holler CJ, Matveev S, Baig I, LeVine H, 3rd, Keller JN, Murphy MP (2012) Postmortem Pittsburgh compound B (PiB) binding increases with Alzheimer's disease progression. J Alzheimers Dis 32, 127-138.
-
(2012)
J Alzheimers Dis
, vol.32
, pp. 127-138
-
-
Beckett, T.L.1
Webb, R.L.2
Niedowicz, D.M.3
Holler, C.J.4
Matveev, S.5
Baig, I.6
Levine, H.7
Keller, J.N.8
Murphy, M.P.9
-
22
-
-
84868117094
-
Pittsburgh compound B and the postmortem diagnosis of Alzheimer disease
-
Niedowicz DM, Beckett TL, Matveev S, Weidner AM, Baig I, Kryscio RJ, Mendiondo MS, LeVine H, 3rd, Keller JN, Murphy MP (2012) Pittsburgh compound B and the postmortem diagnosis of Alzheimer disease. Ann Neurol 72, 564-570.
-
(2012)
Ann Neurol
, vol.72
, pp. 564-570
-
-
Niedowicz, D.M.1
Beckett, T.L.2
Matveev, S.3
Weidner, A.M.4
Baig, I.5
Kryscio, R.J.6
Mendiondo, M.S.7
Levine, H.8
Keller, J.N.9
Murphy, M.P.10
-
23
-
-
34548253353
-
Abeta solubility and deposition during AD progression and in APPxPS-1 knock-in mice
-
Murphy MP, Beckett TL, Ding Q, Patel E, Markesbery WR, St Clair DK, LeVine H, 3rd, Keller JN (2007) Abeta solubility and deposition during AD progression and in APPxPS-1 knock-in mice. Neurobiol Dis 27, 301-311.
-
(2007)
Neurobiol Dis
, vol.27
, pp. 301-311
-
-
Murphy, M.P.1
Beckett, T.L.2
Ding, Q.3
Patel, E.4
Markesbery, W.R.5
St Clair, D.K.6
Levine, H.7
Keller, J.N.8
-
24
-
-
77955549972
-
APP (DeltaNL695) expression in murine tissue downregulates CNBP expression
-
Niedowicz DM, Beckett TL, Holler CJ, Weidner AM, Murphy MP (2010) APP (DeltaNL695) expression in murine tissue downregulates CNBP expression. Neurosci Lett 482, 57-61.
-
(2010)
Neurosci Lett
, vol.482
, pp. 57-61
-
-
Niedowicz, D.M.1
Beckett, T.L.2
Holler, C.J.3
Weidner, A.M.4
Murphy, M.P.5
-
25
-
-
84859904759
-
Frontal cortex neuropathology in dementia pugilistica
-
Saing T, Dick M, Nelson PT, Kim RC, Cribbs DH, Head E (2012) Frontal cortex neuropathology in dementia pugilistica. J Neurotrauma 29, 1054-1070.
-
(2012)
J Neurotrauma
, vol.29
, pp. 1054-1070
-
-
Saing, T.1
Dick, M.2
Nelson, P.T.3
Kim, R.C.4
Cribbs, D.H.5
Head, E.6
-
26
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm S (1979) A simple sequentially rejective multiple test procedure. Scand J Statist 6, 65-70.
-
(1979)
Scand J Statist
, vol.6
, pp. 65-70
-
-
Holm, S.1
-
27
-
-
0035800434
-
Mytotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
-
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, NAylor SL, Day JW, Ranum LPW (2001) Mytotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 293, 864-867.
-
(2001)
Science
, vol.293
, pp. 864-867
-
-
Liquori, C.L.1
Ricker, K.2
Moseley, M.L.3
Jacobsen, J.F.4
Kress, W.5
Naylor, S.L.6
Day, J.W.7
Ranum, L.P.W.8
-
28
-
-
80055006740
-
RNA Foci, CUGBP1, and ZNF9 are the primary targets of the mutant CUG and CCUG repeats expanded in myotonic dystrophies type 1 and type 2
-
Jones K, Jin B, Iakova P, Huichalaf C, Sarkar P, Schneider-Gold C, Schoser B, Meola G, Shyu AB, Timchenko N, Timchenko L (2011) RNA Foci, CUGBP1, and ZNF9 are the primary targets of the mutant CUG and CCUG repeats expanded in myotonic dystrophies type 1 and type 2. Am J Pathol 179, 2475-2489.
-
(2011)
Am J Pathol
, vol.179
, pp. 2475-2489
-
-
Jones, K.1
Jin, B.2
Iakova, P.3
Huichalaf, C.4
Sarkar, P.5
Schneider-Gold, C.6
Schoser, B.7
Meola, G.8
Shyu, A.B.9
Timchenko, N.10
Timchenko, L.11
-
29
-
-
77957322887
-
ZNF9 activationofIRES-mediated translation of the human ODC mRNAisdecreased in myotonic dystrophy type 2
-
Sammons MA, Antons AK, Bendjennat M, Udd B, Krahe R, Link AJ (2010) ZNF9 activationofIRES-mediated translation of the human ODC mRNAisdecreased in myotonic dystrophy type 2. PloS One 5, e9301.
-
(2010)
PloS One
, vol.5
, pp. e9301
-
-
Sammons, M.A.1
Antons, A.K.2
Bendjennat, M.3
Udd, B.4
Krahe, R.5
Link, A.J.6
-
30
-
-
67650742030
-
Reduction of the rate of protein translation in patients with myotonic dystrophy 2
-
Huichalaf C, Schoser B, Schneider-Gold C, Jin B, Sarkar P, Timchenko L (2009) Reduction of the rate of protein translation in patients with myotonic dystrophy 2. J Neurosci 29, 9042-9049.
-
(2009)
J Neurosci
, vol.29
, pp. 9042-9049
-
-
Huichalaf, C.1
Schoser, B.2
Schneider-Gold, C.3
Jin, B.4
Sarkar, P.5
Timchenko, L.6
-
31
-
-
34347393270
-
The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation
-
Gerbasi VR, Link AJ (2007) The myotonic dystrophy type 2 protein ZNF9 is part of an ITAF complex that promotes cap-independent translation. Mol Cell Proteomics 6, 1049-1058.
-
(2007)
Mol Cell Proteomics
, vol.6
, pp. 1049-1058
-
-
Gerbasi, V.R.1
Link, A.J.2
-
32
-
-
84870584668
-
Expression of novel Alzheimer's disease risk genes in control and Alzheimer's disease brains
-
Karch CM, Jeng AT, Nowotny P, Cady J, Cruchaga C, Goate AM (2012) Expression of novel Alzheimer's disease risk genes in control and Alzheimer's disease brains. PLoS One 7, e50976.
-
(2012)
PLoS One
, vol.7
, pp. e50976
-
-
Karch, C.M.1
Jeng, A.T.2
Nowotny, P.3
Cady, J.4
Cruchaga, C.5
Goate, A.M.6
-
33
-
-
84883771184
-
Exploring the value of plasma BIN1 as a potential biomarker for Alzheimer's disease
-
Sun L, Tan MS, Hu N, Yu JT, Tan L (2013) Exploring the value of plasma BIN1 as a potential biomarker for Alzheimer's disease. J Alzheimers Dis 37, 291-295.
-
(2013)
J Alzheimers Dis
, vol.37
, pp. 291-295
-
-
Sun, L.1
Tan, M.S.2
Hu, N.3
Yu, J.T.4
Tan, L.5
-
34
-
-
79951798741
-
Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease
-
Kauwe JS, Cruchaga C, Karch CM, Sadler B, Lee M, Mayo K, Latu W, Su'a M, Fagan AM, Holtzman DM, Morris JC, Alzheimer's Disease Neuroimaging I, Goate AM (2011) Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease. PLoS One 6, e15918.
-
(2011)
PLoS One
, vol.6
, pp. e15918
-
-
Kauwe, J.S.1
Cruchaga, C.2
Karch, C.M.3
Sadler, B.4
Lee, M.5
Mayo, K.6
Latu, W.7
Su'A, M.8
Fagan, A.M.9
Holtzman, D.M.10
Morris, J.C.11
Alzheimer'S Disease Neuroimaging, I.12
Goate, A.M.13
-
35
-
-
84855896677
-
Clathrin-mediated endocytic proteins are upregulated in the cortex of the Tg2576 mouse model ofAlzheimer's disease-like amyloid pathology
-
Thomas RS, Lelos MJ, Good MA, Kidd EJ (2011) Clathrin-mediated endocytic proteins are upregulated in the cortex of the Tg2576 mouse model ofAlzheimer's disease-like amyloid pathology. Biochem Biophys Res Commun 415, 656-661.
-
(2011)
Biochem Biophys Res Commun
, vol.415
, pp. 656-661
-
-
Thomas, R.S.1
Lelos, M.J.2
Good, M.A.3
Kidd, E.J.4
-
36
-
-
73349097586
-
AMPH-1/Amphiphysin/Bin1 functions with RME-1/Ehd1 in endocytic recycling
-
Pant S, Sharma M, Patel K, Caplan S, Carr CM, Grant BD (2009) AMPH-1/Amphiphysin/Bin1 functions with RME-1/Ehd1 in endocytic recycling. Nat Cell Biol 11, 1399-1410.
-
(2009)
Nat Cell Biol
, vol.11
, pp. 1399-1410
-
-
Pant, S.1
Sharma, M.2
Patel, K.3
Caplan, S.4
Carr, C.M.5
Grant, B.D.6
-
37
-
-
57649096298
-
The membrane-tubulating potential of amphiphysin 2/BIN1 is dependent on the microtubule-binding cytoplasmic linker protein 170 (CLIP-170)
-
Meunier B, Quaranta M, Daviet L, Hatzoglou A, Leprince C (2009) The membrane-tubulating potential of amphiphysin 2/BIN1 is dependent on the microtubule-binding cytoplasmic linker protein 170 (CLIP-170). Eur J Cell Biol 88, 91-102.
-
(2009)
Eur J Cell Biol
, vol.88
, pp. 91-102
-
-
Meunier, B.1
Quaranta, M.2
Daviet, L.3
Hatzoglou, A.4
Leprince, C.5
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