-
1
-
-
0034044563
-
The Shank family of scaffold proteins
-
The Shank family of scaffold proteins. Sheng M, Kim E, J Cell Sci 2000 113 Pt 11 1851 1856 10806096 (Pubitemid 30386489)
-
(2000)
Journal of Cell Science
, vol.113
, Issue.11
, pp. 1851-1856
-
-
Sheng, M.1
Kim, E.2
-
2
-
-
0033581830
-
Synapse structure: Glutamate receptors connected by the shanks
-
10.1016/S0960-9822(00)80043-3 10574750
-
Synapse structure: glutamate receptors connected by the shanks. Ehlers MD, Curr Biol 1999 9 848 R850 10.1016/S0960-9822(00)80043-3 10574750
-
(1999)
Curr Biol
, vol.9
-
-
Ehlers, M.D.1
-
3
-
-
80053101302
-
Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies
-
10.1016/j.tcb.2011.07.003 21840719
-
Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies. Grabrucker AM, Schmeisser MJ, Schoen M, Boeckers TM, Trends Cell Biol 2011 21 594 603 10.1016/j.tcb.2011.07.003 21840719
-
(2011)
Trends Cell Biol
, vol.21
, pp. 594-603
-
-
Grabrucker, A.M.1
Schmeisser, M.J.2
Schoen, M.3
Boeckers, T.M.4
-
4
-
-
0033166537
-
Coupling of mGluR/Homer and PSD-95 complexes by the Shank family of postsynaptic density proteins
-
DOI 10.1016/S0896-6273(00)80810-7
-
Coupling of mGluR/homer and PSD-95 complexes by the Shank family of postsynaptic density proteins. Tu JC, Xiao B, Naisbitt S, Yuan JP, Petralia RS, Brakeman P, Doan A, Aakalu VK, Lanahan AA, Sheng M, Worley PF, Neuron 1999 23 583 592 10.1016/S0896-6273(00)80810-7 10433269 (Pubitemid 29359928)
-
(1999)
Neuron
, vol.23
, Issue.3
, pp. 583-592
-
-
Tu, J.C.1
Xiao, B.2
Naisbitt, S.3
Yuan, J.P.4
Petralia, R.S.5
Brakeman, P.6
Doan, A.7
Aakalu, V.K.8
Lanahan, A.A.9
Sheng, M.10
Worley, P.F.11
-
5
-
-
0033165926
-
Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin
-
DOI 10.1016/S0896-6273(00)80809-0
-
Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin. Naisbitt S, Kim E, Tu JC, Xiao B, Sala C, Valtschanoff J, Weinberg RJ, Worley PF, Sheng M, Neuron 1999 23 569 582 10.1016/S0896-6273(00)80809-0 10433268 (Pubitemid 29359927)
-
(1999)
Neuron
, vol.23
, Issue.3
, pp. 569-582
-
-
Naisbitt, S.1
Eunjoon, K.2
Tu, J.C.3
Xiao, B.4
Sala, C.5
Valtschanoff, J.6
Weinberg, R.J.7
Worley, P.F.8
Sheng, M.9
-
6
-
-
33646115168
-
Direct interaction of post-synaptic density-95/Dlg/ZO-1 domain-containing synaptic molecule Shank3 with GluR1 alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor
-
10.1111/j.1471-4159.2006.03831.x 16606358
-
Direct interaction of post-synaptic density-95/Dlg/ZO-1 domain-containing synaptic molecule Shank3 with GluR1 alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor. Uchino S, Wada H, Honda S, Nakamura Y, Ondo Y, Uchiyama T, Tsutsumi M, Suzuki E, Hirasawa T, Kohsaka S, J Neurochem 2006 97 1203 1214 10.1111/j.1471-4159.2006.03831.x 16606358
-
(2006)
J Neurochem
, vol.97
, pp. 1203-1214
-
-
Uchino, S.1
Wada, H.2
Honda, S.3
Nakamura, Y.4
Ondo, Y.5
Uchiyama, T.6
Tsutsumi, M.7
Suzuki, E.8
Hirasawa, T.9
Kohsaka, S.10
-
7
-
-
80053423590
-
Importance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapses
-
10.1074/jbc.M111.258384 21795692
-
Importance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapses. Verpelli C, Dvoretskova E, Vicidomini C, Rossi F, Chiappalone M, Schoen M, Di Stefano B, Mantegazza R, Broccoli V, Bockers TM, Dityatev A, Sala C, J Biol Chem 2011 286 34839 34850 10.1074/jbc.M111.258384 21795692
-
(2011)
J Biol Chem
, vol.286
, pp. 34839-34850
-
-
Verpelli, C.1
Dvoretskova, E.2
Vicidomini, C.3
Rossi, F.4
Chiappalone, M.5
Schoen, M.6
Di Stefano, B.7
Mantegazza, R.8
Broccoli, V.9
Bockers, T.M.10
Dityatev, A.11
Sala, C.12
-
8
-
-
84876070991
-
Modeling autism by SHANK gene mutations in mice
-
10.1016/j.neuron.2013.03.016 23583105
-
Modeling autism by SHANK gene mutations in mice. Jiang YH, Ehlers MD, Neuron 2013 78 8 27 10.1016/j.neuron.2013.03.016 23583105
-
(2013)
Neuron
, vol.78
, pp. 8-27
-
-
Jiang, Y.H.1
Ehlers, M.D.2
-
9
-
-
0042828948
-
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
-
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms. Wilson HL, Wong AC, Shaw SR, Tse WY, Stapleton GA, Phelan MC, Hu S, Marshall J, McDermid HE, J Med Genet 2003 40 575 584 10.1136/jmg.40.8.575 12920066 (Pubitemid 37046910)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.8
, pp. 575-584
-
-
Wilson, H.L.1
Wong, A.C.C.2
Shaw, S.R.3
Tse, W.-Y.4
Stapleton, G.A.5
Phelan, M.C.6
Hu, S.7
Marshall, J.8
McDermid, H.E.9
-
10
-
-
79952484202
-
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
-
10.1016/j.ajhg.2011.02.001 21376300
-
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. Hamdan FF, Gauthier J, Araki Y, Lin DT, Yoshizawa Y, Higashi K, Park AR, Spiegelman D, Dobrzeniecka S, Piton A, Tomitori H, Daoud H, Massicotte C, Henrion E, Diallo O, S2D Group, Shekarabi M, Marineau C, Shevell M, Maranda B, Mitchell G, Nadeau A, D'Anjou G, Vanasse M, Srour M, Lafrenière RG, Drapeau P, Lacaille JC, Kim E, Lee JR, et al. Am J Hum Genet 2011 88 306 316 10.1016/j.ajhg.2011.02.001 21376300
-
(2011)
Am J Hum Genet
, vol.88
, pp. 306-316
-
-
Hamdan, F.F.1
Gauthier, J.2
Araki, Y.3
Lin, D.T.4
Yoshizawa, Y.5
Higashi, K.6
Park, A.R.7
Spiegelman, D.8
Dobrzeniecka, S.9
Piton, A.10
Tomitori, H.11
Daoud, H.12
Massicotte, C.13
Henrion, E.14
Diallo, O.15
Shekarabi, M.16
Marineau, C.17
Shevell, M.18
Maranda, B.19
Mitchell, G.20
Nadeau, A.21
D'Anjou, G.22
Vanasse, M.23
Srour, M.24
Lafrenière, R.G.25
Drapeau, P.26
Lacaille, J.C.27
Kim, E.28
Lee, J.R.29
more..
-
11
-
-
36749040875
-
Contribution of SHANK3 mutations to autism spectrum disorder
-
DOI 10.1086/522590
-
Contribution of SHANK3 mutations to autism spectrum disorder. Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW, Am J Hum Genet 2007 81 1289 1297 10.1086/522590 17999366 (Pubitemid 350211458)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1289-1297
-
-
Moessner, R.1
Marshall, C.R.2
Sutcliffe, J.S.3
Skaug, J.4
Pinto, D.5
Vincent, J.6
Zwaigenbaum, L.7
Fernandez, B.8
Roberts, W.9
Szatmari, P.10
Scherer, S.W.11
-
12
-
-
33845889998
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
-
DOI 10.1038/ng1933, PII NG1933
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsater H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T, Nat Genet 2007 39 25 27 10.1038/ng1933 17173049 (Pubitemid 46026497)
-
(2007)
Nature Genetics
, vol.39
, Issue.1
, pp. 25-27
-
-
Durand, C.M.1
Betancur, C.2
Boeckers, T.M.3
Bockmann, J.4
Chaste, P.5
Fauchereau, F.6
Nygren, G.7
Rastam, M.8
Gillberg, I.C.9
Anckarsater, H.10
Sponheim, E.11
Goubran-Botros, H.12
Delorme, R.13
Chabane, N.14
Mouren-Simeoni, M.-C.15
De Mas, P.16
Bieth, E.17
Roge, B.18
Heron, D.19
Burglen, L.20
Gillberg, C.21
Leboyer, M.22
Bourgeron, T.23
more..
-
13
-
-
80051674258
-
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorder
-
10.1093/hmg/ddr243 21624971
-
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorder. Schaaf CP, Sabo A, Sakai Y, Crosby J, Muzny D, Hawes A, Lewis L, Akbar H, Varghese R, Boerwinkle E, Gibbs RA, Zoghbi HY, Hum Mol Genet 2011 20 17 3366 3375 10.1093/hmg/ddr243 21624971
-
(2011)
Hum Mol Genet
, vol.20
, Issue.17
, pp. 3366-3375
-
-
Schaaf, C.P.1
Sabo, A.2
Sakai, Y.3
Crosby, J.4
Muzny, D.5
Hawes, A.6
Lewis, L.7
Akbar, H.8
Varghese, R.9
Boerwinkle, E.10
Gibbs, R.A.11
Zoghbi, H.Y.12
-
14
-
-
85027958692
-
Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development
-
10.1097/YPG.0b013e328341e069 21378602
-
Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development. Waga C, Okamoto N, Ondo Y, Fukumura-Kato R, Goto Y, Kohsaka S, Uchino S, Psychiatr Genet 2011 21 208 211 10.1097/YPG.0b013e328341e069 21378602
-
(2011)
Psychiatr Genet
, vol.21
, pp. 208-211
-
-
Waga, C.1
Okamoto, N.2
Ondo, Y.3
Fukumura-Kato, R.4
Goto, Y.5
Kohsaka, S.6
Uchino, S.7
-
15
-
-
77952374703
-
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
-
10.1073/pnas.0906232107 20385823
-
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Gauthier J, Champagne N, Lafreniere RG, Xiong L, Spiegelman D, Brustein E, Lapointe M, Peng H, Cote M, Noreau A, Hamdan FF, Addington AM, Rapoport JL, Delisi LE, Krebs MO, Joober R, Fathalli F, Mouaffak F, Haghighi AP, Néri C, Dubé MP, Samuels ME, Marineau C, Stone EA, Awadalla P, Barker PA, Carbonetto S, Drapeau P, Rouleau GA, S2D Team, Proc Natl Acad Sci U S A 2010 107 7863 7868 10.1073/pnas. 0906232107 20385823
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 7863-7868
-
-
Gauthier, J.1
Champagne, N.2
Lafreniere, R.G.3
Xiong, L.4
Spiegelman, D.5
Brustein, E.6
Lapointe, M.7
Peng, H.8
Cote, M.9
Noreau, A.10
Hamdan, F.F.11
Addington, A.M.12
Rapoport, J.L.13
Delisi, L.E.14
Krebs, M.O.15
Joober, R.16
Fathalli, F.17
Mouaffak, F.18
Haghighi, A.P.19
Néri, C.20
Dubé, M.P.21
Samuels, M.E.22
Marineau, C.23
Stone, E.A.24
Awadalla, P.25
Barker, P.A.26
Carbonetto, S.27
Drapeau, P.28
Rouleau, G.A.29
more..
-
16
-
-
80054889797
-
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
-
10.1186/2040-2392-1-15 21167025
-
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Bozdagi O, Sakurai T, Papapetrou D, Wang X, Dickstein DL, Takahashi N, Kajiwara Y, Yang M, Katz AM, Scattoni ML, Harris MJ, Saxena R, Silverman JL, Crawley JN, Zhou Q, Hof PR, Buxbaum JD, Molecular Autism 2010 1 15 10.1186/2040-2392-1-15 21167025
-
(2010)
Molecular Autism
, vol.1
, pp. 15
-
-
Bozdagi, O.1
Sakurai, T.2
Papapetrou, D.3
Wang, X.4
Dickstein, D.L.5
Takahashi, N.6
Kajiwara, Y.7
Yang, M.8
Katz, A.M.9
Scattoni, M.L.10
Harris, M.J.11
Saxena, R.12
Silverman, J.L.13
Crawley, J.N.14
Zhou, Q.15
Hof, P.R.16
Buxbaum, J.D.17
-
17
-
-
79955536349
-
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction
-
10.1038/nature09965 21423165
-
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction. Peca J, Feliciano C, Ting JT, Wang W, Wells MF, Venkatraman TN, Lascola CD, Fu Z, Feng G, Nature 2011 472 437 442 10.1038/nature09965 21423165
-
(2011)
Nature
, vol.472
, pp. 437-442
-
-
Peca, J.1
Feliciano, C.2
Ting, J.T.3
Wang, W.4
Wells, M.F.5
Venkatraman, T.N.6
Lascola, C.D.7
Fu, Z.8
Feng, G.9
-
18
-
-
79960111638
-
Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3
-
10.1093/hmg/ddr212 21558424
-
Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3. Wang X, McCoy PA, Rodriguiz RM, Pan Y, Je HS, Roberts AC, Kim CJ, Berrios J, Colvin JS, Bousquet-Moore D, Lorenzo I, Wu G, Weinberg RJ, Ehlers MD, Philpot BD, Beaudet AL, Wetsel WC, Jiang YH, Hum Mol Genet 2011 20 3093 3108 10.1093/hmg/ddr212 21558424
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3093-3108
-
-
Wang, X.1
McCoy, P.A.2
Rodriguiz, R.M.3
Pan, Y.4
Je, H.S.5
Roberts, A.C.6
Kim, C.J.7
Berrios, J.8
Colvin, J.S.9
Bousquet-Moore, D.10
Lorenzo, I.11
Wu, G.12
Weinberg, R.J.13
Ehlers, M.D.14
Philpot, B.D.15
Beaudet, A.L.16
Wetsel, W.C.17
Jiang, Y.H.18
-
19
-
-
84862274500
-
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2
-
22699619
-
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2. Schmeisser MJ, Ey E, Wegener S, Bockmann J, Stempel AV, Kuebler A, Janssen AL, Udvardi PT, Shiban E, Spilker C, Balschun D, Skryabin BV, Dieck S, Smalla KH, Montag D, Leblond CS, Faure P, Torquet N, Le Sourd AM, Toro R, Grabrucker AM, Shoichet SA, Schmitz D, Kreutz MR, Bourgeron T, Gundelfinger ED, Boeckers TM, Nature 2012 486 256 260 22699619
-
(2012)
Nature
, vol.486
, pp. 256-260
-
-
Schmeisser, M.J.1
Ey, E.2
Wegener, S.3
Bockmann, J.4
Stempel, A.V.5
Kuebler, A.6
Janssen, A.L.7
Udvardi, P.T.8
Shiban, E.9
Spilker, C.10
Balschun, D.11
Skryabin, B.V.12
Dieck, S.13
Smalla, K.H.14
Montag, D.15
Leblond, C.S.16
Faure, P.17
Torquet, N.18
Le Sourd, A.M.19
Toro, R.20
Grabrucker, A.M.21
Shoichet, S.A.22
Schmitz, D.23
Kreutz, M.R.24
Bourgeron, T.25
Gundelfinger, E.D.26
Boeckers, T.M.27
more..
-
20
-
-
84887841772
-
Loss of predominant shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission
-
10.1523/JNEUROSCI.3017-13.2013 24259569
-
Loss of predominant shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission. Kouser M, Speed HE, Dewey CM, Reimers JM, Widman AJ, Gupta N, Liu S, Jaramillo TC, Bangash M, Xiao B, Worley PF, Powell CM, J Neurosci 2013 33 18448 18468 10.1523/JNEUROSCI.3017-13.2013 24259569
-
(2013)
J Neurosci
, vol.33
, pp. 18448-18468
-
-
Kouser, M.1
Speed, H.E.2
Dewey, C.M.3
Reimers, J.M.4
Widman, A.J.5
Gupta, N.6
Liu, S.7
Jaramillo, T.C.8
Bangash, M.9
Xiao, B.10
Worley, P.F.11
Powell, C.M.12
-
21
-
-
0032830935
-
Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development
-
DOI 10.1074/jbc.274.41.29510
-
Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development. Lim S, Naisbitt S, Yoon J, Hwang JI, Suh PG, Sheng M, Kim E, J Biol Chem 1999 274 29510 29518 10.1074/jbc.274.41.29510 10506216 (Pubitemid 29477125)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.41
, pp. 29510-29518
-
-
Lim, S.1
Naisbitt, S.2
Yoon, J.3
Hwang, J.-I.4
Suh, P.-G.5
Sheng, M.6
Eunjoon, K.7
-
22
-
-
84859066832
-
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
-
10.1371/journal.pgen.1002521 22346768
-
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, et al. PLoS Genet 2012 8 1002521 10.1371/journal.pgen.1002521 22346768
-
(2012)
PLoS Genet
, vol.8
, pp. 51002521
-
-
Leblond, C.S.1
Heinrich, J.2
Delorme, R.3
Proepper, C.4
Betancur, C.5
Huguet, G.6
Konyukh, M.7
Chaste, P.8
Ey, E.9
Rastam, M.10
Anckarsäter, H.11
Nygren, G.12
Gillberg, I.C.13
Melke, J.14
Toro, R.15
Regnault, B.16
Fauchereau, F.17
Mercati, O.18
Lemière, N.19
Skuse, D.20
Poot, M.21
Holt, R.22
Monaco, A.P.23
Järvelä, I.24
Kantojärvi, K.25
Vanhala, R.26
Curran, S.27
Collier, D.A.28
Bolton, P.29
Chiocchetti, A.30
more..
-
23
-
-
77954504873
-
Conserved role of intragenic DNA methylation in regulating alternative promoters
-
10.1038/nature09165 20613842
-
Conserved role of intragenic DNA methylation in regulating alternative promoters. Maunakea AK, Nagarajan RP, Bilenky M, Ballinger TJ, D'Souza C, Fouse SD, Johnson BE, Hong C, Nielsen C, Zhao Y, Turecki G, Delaney A, Varhol R, Thiessen N, Shchors K, Heine VM, Rowitch DH, Xing X, Fiore C, Schillebeeckx M, Jones SJ, Haussler D, Marra MA, Hirst M, Wang T, Costello JF, Nature 2010 466 253 257 10.1038/nature09165 20613842
-
(2010)
Nature
, vol.466
, pp. 253-257
-
-
Maunakea, A.K.1
Nagarajan, R.P.2
Bilenky, M.3
Ballinger, T.J.4
D'Souza, C.5
Fouse, S.D.6
Johnson, B.E.7
Hong, C.8
Nielsen, C.9
Zhao, Y.10
Turecki, G.11
Delaney, A.12
Varhol, R.13
Thiessen, N.14
Shchors, K.15
Heine, V.M.16
Rowitch, D.H.17
Xing, X.18
Fiore, C.19
Schillebeeckx, M.20
Jones, S.J.21
Haussler, D.22
Marra, M.A.23
Hirst, M.24
Wang, T.25
Costello, J.F.26
more..
-
24
-
-
84891829149
-
Identification of two novel Shank3 transcripts in the developing mouse neocortex
-
10.1111/jnc.12505 24164323
-
Identification of two novel Shank3 transcripts in the developing mouse neocortex. Waga C, Asano H, Sanagi T, Suzuki E, Nakamura Y, Tsuchiya A, Itoh M, Goto YI, Kohsaka S, Uchino S, J Neurochem 2014 128 2 280 293 10.1111/jnc.12505 24164323
-
(2014)
J Neurochem
, vol.128
, Issue.2
, pp. 280-293
-
-
Waga, C.1
Asano, H.2
Sanagi, T.3
Suzuki, E.4
Nakamura, Y.5
Tsuchiya, A.6
Itoh, M.7
Goto, Y.I.8
Kohsaka, S.9
Uchino, S.10
-
25
-
-
84894535118
-
Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders
-
10.1093/hmg/ddt547 24186872
-
Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders. Zhu L, Wang X, Li XL, Towers A, Cao X, Wang P, Bowman R, Yang H, Goldstein J, Li YJ, Jiang YH, Hum Mol Genet 2014 23 6 1563 1783 10.1093/hmg/ddt547 24186872
-
(2014)
Hum Mol Genet
, vol.23
, Issue.6
, pp. 1563-1783
-
-
Zhu, L.1
Wang, X.2
Li, X.L.3
Towers, A.4
Cao, X.5
Wang, P.6
Bowman, R.7
Yang, H.8
Goldstein, J.9
Li, Y.J.10
Jiang, Y.H.11
-
26
-
-
84891903357
-
Therapeutic approaches for shankopathies
-
10.1002/dneu.22084 23536326
-
Therapeutic approaches for shankopathies. Wang X, Bey AL, Chung L, Krystal AD, Jiang YH, Dev Neurobiol 2014 74 123 135 10.1002/dneu.22084 23536326
-
(2014)
Dev Neurobiol
, vol.74
, pp. 123-135
-
-
Wang, X.1
Bey, A.L.2
Chung, L.3
Krystal, A.D.4
Jiang, Y.H.5
-
27
-
-
80054744496
-
Isolation and culture of neurons and astrocytes from the mouse brain cortex
-
10.1007/978-1-61779-328-8-4 21913093
-
Isolation and culture of neurons and astrocytes from the mouse brain cortex. Kim HJ, Magrane J, Methods Mol Biol 2011 793 63 75 10.1007/978-1-61779- 328-8-4 21913093
-
(2011)
Methods Mol Biol
, vol.793
, pp. 63-75
-
-
Kim, H.J.1
Magrane, J.2
-
28
-
-
84863205849
-
NIH Image to ImageJ: 25 years of image analysis
-
10.1038/nmeth.2089 22930834
-
NIH Image to ImageJ: 25 years of image analysis. Schneider CA, Rasband WS, Eliceiri KW, Nat Methods 2012 9 671 675 10.1038/nmeth.2089 22930834
-
(2012)
Nat Methods
, vol.9
, pp. 671-675
-
-
Schneider, C.A.1
Rasband, W.S.2
Eliceiri, K.W.3
-
29
-
-
46949094761
-
Involvement of the role of Chk1 in lithium-induced G2/M phase cell cycle arrest in hepatocellular carcinoma cells
-
DOI 10.1002/jcb.21693
-
Involvement of the role of Chk1 in lithium-induced G2/M phase cell cycle arrest in hepatocellular carcinoma cells. Wang XM, Li J, Feng XC, Wang Q, Guan DY, Shen ZH, J Cell Biochem 2008 104 1181 1191 10.1002/jcb.21693 18247328 (Pubitemid 351961693)
-
(2008)
Journal of Cellular Biochemistry
, vol.104
, Issue.4
, pp. 1181-1191
-
-
Wang, X.-M.1
Li, J.2
Feng, X.-C.3
Wang, Q.4
Guan, D.-Y.5
Shen, Z.-H.6
-
30
-
-
0035955643
-
Synaptic scaffolding proteins in rat brain. Ankyrin repeats of the multidomain Shank protein family interact with the cytoskeletal protein alpha-fodrin
-
10.1074/jbc.M102454200 11509555
-
Synaptic scaffolding proteins in rat brain. Ankyrin repeats of the multidomain Shank protein family interact with the cytoskeletal protein alpha-fodrin. Bockers TM, Mameza MG, Kreutz MR, Bockmann J, Weise C, Buck F, Richter D, Gundelfinger ED, Kreienkamp HJ, J Biol Chem 2001 276 40104 40112 10.1074/jbc.M102454200 11509555
-
(2001)
J Biol Chem
, vol.276
, pp. 40104-40112
-
-
Bockers, T.M.1
Mameza, M.G.2
Kreutz, M.R.3
Bockmann, J.4
Weise, C.5
Buck, F.6
Richter, D.7
Gundelfinger, E.D.8
Kreienkamp, H.J.9
-
31
-
-
0037374587
-
Activity level controls postsynaptic composition and signaling via the ubiquitin-proteasome system
-
DOI 10.1038/nn1013
-
Activity level controls postsynaptic composition and signaling via the ubiquitin-proteasome system. Ehlers MD, Nat Neurosci 2003 6 231 242 10.1038/nn1013 12577062 (Pubitemid 36278281)
-
(2003)
Nature Neuroscience
, vol.6
, Issue.3
, pp. 231-242
-
-
Ehlers, M.D.1
-
32
-
-
46149096244
-
Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system
-
10.1146/annurev.neuro.31.060407.125631 18558867
-
Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system. Flavell SW, Greenberg ME, Annu Rev Neurosci 2008 31 563 590 10.1146/annurev.neuro.31.060407.125631 18558867
-
(2008)
Annu Rev Neurosci
, vol.31
, pp. 563-590
-
-
Flavell, S.W.1
Greenberg, M.E.2
-
33
-
-
78449288141
-
Targeting the correct HDAC(s) to treat cognitive disorders
-
10.1016/j.tips.2010.09.003 20980063
-
Targeting the correct HDAC(s) to treat cognitive disorders. Fischer A, Sananbenesi F, Mungenast A, Tsai LH, Trends Pharmacol Sci 2010 31 605 617 10.1016/j.tips.2010.09.003 20980063
-
(2010)
Trends Pharmacol Sci
, vol.31
, pp. 605-617
-
-
Fischer, A.1
Sananbenesi, F.2
Mungenast, A.3
Tsai, L.H.4
-
34
-
-
63149192174
-
Neuronal cell depolarization induces intragenic chromatin modifications affecting NCAM alternative splicing
-
10.1073/pnas.0810666106 19251664
-
Neuronal cell depolarization induces intragenic chromatin modifications affecting NCAM alternative splicing. Schor IE, Rascovan N, Pelisch F, Allo M, Kornblihtt AR, Proc Natl Acad Sci U S A 2009 106 4325 4330 10.1073/pnas. 0810666106 19251664
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 4325-4330
-
-
Schor, I.E.1
Rascovan, N.2
Pelisch, F.3
Allo, M.4
Kornblihtt, A.R.5
-
35
-
-
34248209169
-
DNA methylation regulates tissue-speci.c expression of Shank3
-
DOI 10.1111/j.1471-4159.2007.04539.x
-
DNA methylation regulates tissue-specific expression of Shank3. Beri S, Tonna N, Menozzi G, Bonaglia MC, Sala C, Giorda R, J Neurochem 2007 101 1380 1391 10.1111/j.1471-4159.2007.04539.x 17419801 (Pubitemid 46718829)
-
(2007)
Journal of Neurochemistry
, vol.101
, Issue.5
, pp. 1380-1391
-
-
Beri, S.1
Tonna, N.2
Menozzi, G.3
Bonaglia, M.C.4
Sala, C.5
Giorda, R.6
-
36
-
-
0035110856
-
Sharpin, a novel postsynaptic density protein that directly interacts with the shank family of proteins
-
DOI 10.1006/mcne.2000.0940
-
Sharpin, a novel postsynaptic density protein that directly interacts with the shank family of proteins. Lim S, Sala C, Yoon J, Park S, Kuroda S, Sheng M, Kim E, Mol Cell Neurosci 2001 17 385 397 10.1006/mcne.2000.0940 11178875 (Pubitemid 32176494)
-
(2001)
Molecular and Cellular Neuroscience
, vol.17
, Issue.2
, pp. 385-397
-
-
Lim, S.1
Sala, C.2
Yoon, J.3
Park, S.4
Kuroda, S.5
Sheng, M.6
Kim, E.7
-
37
-
-
0035341508
-
An NMDA receptor ER retention signal regulated by phosphorylation and alternative splicing
-
An NMDA receptor ER retention signal regulated by phosphorylation and alternative splicing. Scott DB, Blanpied TA, Swanson GT, Zhang C, Ehlers MD, J Neurosci 2001 21 3063 3072 11312291 (Pubitemid 32323488)
-
(2001)
Journal of Neuroscience
, vol.21
, Issue.9
, pp. 3063-3072
-
-
Scott, D.B.1
Blanpied, T.A.2
Swanson, G.T.3
Zhang, C.4
Ehlers, M.D.5
-
38
-
-
0031983653
-
Neurexins: Three genes and 1001 products
-
DOI 10.1016/S0168-9525(97)01324-3
-
Neurexins: three genes and 1001 products. Missler M, Sudhof TC, Trends Genet 1998 14 20 26 10.1016/S0168-9525(97)01324-3 9448462 (Pubitemid 28034298)
-
(1998)
Trends in Genetics
, vol.14
, Issue.1
, pp. 20-26
-
-
Missler, M.1
Sudhof, T.C.2
-
39
-
-
33847250395
-
Mouse and rat BDNF gene structure and expression revisited
-
10.1002/jnr.21139 17149751
-
Mouse and rat BDNF gene structure and expression revisited. Aid T, Kazantseva A, Piirsoo M, Palm K, Timmusk T, J Neurosci Res 2007 85 525 535 10.1002/jnr.21139 17149751
-
(2007)
J Neurosci Res
, vol.85
, pp. 525-535
-
-
Aid, T.1
Kazantseva, A.2
Piirsoo, M.3
Palm, K.4
Timmusk, T.5
-
40
-
-
84887882471
-
Heterogeneity within autism spectrum disorders: What have We learned from neuroimaging studies?
-
24198778
-
Heterogeneity within autism spectrum disorders: what have We learned from neuroimaging studies? Lenroot RK, Yeung PK, Front Hum Neurosci 2013 7 733 24198778
-
(2013)
Front Hum Neurosci
, vol.7
, pp. 733
-
-
Lenroot, R.K.1
Yeung, P.K.2
-
41
-
-
84857609997
-
Parsing heterogeneity in autism spectrum disorders: Visual scanning of dynamic social scenes in school-aged children
-
10.1016/j.jaac.2011.12.017 22365460
-
Parsing heterogeneity in autism spectrum disorders: visual scanning of dynamic social scenes in school-aged children. Rice K, Moriuchi JM, Jones W, Klin A, J Am Acad Child Adolesc Psychiatry 2012 51 238 248 10.1016/j.jaac.2011. 12.017 22365460
-
(2012)
J Am Acad Child Adolesc Psychiatry
, vol.51
, pp. 238-248
-
-
Rice, K.1
Moriuchi, J.M.2
Jones, W.3
Klin, A.4
-
42
-
-
79952313620
-
Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting
-
21129364
-
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Betancur C, Brain Res 2011 1380 42 77 21129364
-
(2011)
Brain Res
, vol.1380
, pp. 42-77
-
-
Betancur, C.1
-
43
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
DOI 10.1038/nrg2346, PII NRG2346
-
Advances in autism genetics: on the threshold of a new neurobiology. Abrahams BS, Geschwind DH, Nat Rev Genet 2008 9 341 355 10.1038/nrg2346 18414403 (Pubitemid 351556064)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
44
-
-
0033094318
-
Heterogeneity and the genetics of autism
-
10212560
-
Heterogeneity and the genetics of autism. Szatmari P, J Psychiatry Neurosci 1999 24 159 165 10212560
-
(1999)
J Psychiatry Neurosci
, vol.24
, pp. 159-165
-
-
Szatmari, P.1
-
45
-
-
84881664021
-
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing
-
10.1016/j.ajhg.2013.06.012 23849776
-
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. Jiang YH, Yuen RK, Jin X, Wang M, Chen N, Wu X, Ju J, Mei J, Shi Y, He M, Wang G, Liang J, Wang Z, Cao D, Carter MT, Chrysler C, Drmic IE, Howe JL, Lau L, Marshall CR, Merico D, Nalpathamkalam T, Thiruvahindrapuram B, Thompson A, Uddin M, Walker S, Luo J, Anagnostou E, Zwaigenbaum L, Ring RH, et al. Am J Hum Genet 2013 93 249 263 10.1016/j.ajhg.2013.06.012 23849776
-
(2013)
Am J Hum Genet
, vol.93
, pp. 249-263
-
-
Jiang, Y.H.1
Yuen, R.K.2
Jin, X.3
Wang, M.4
Chen, N.5
Wu, X.6
Ju, J.7
Mei, J.8
Shi, Y.9
He, M.10
Wang, G.11
Liang, J.12
Wang, Z.13
Cao, D.14
Carter, M.T.15
Chrysler, C.16
Drmic, I.E.17
Howe, J.L.18
Lau, L.19
Marshall, C.R.20
Merico, D.21
Nalpathamkalam, T.22
Thiruvahindrapuram, B.23
Thompson, A.24
Uddin, M.25
Walker, S.26
Luo, J.27
Anagnostou, E.28
Zwaigenbaum, L.29
Ring, R.H.30
more..
-
46
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
10.1038/nature10945 22495306
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW, Nature 2012 485 237 241 10.1038/nature10945 22495306
-
(2012)
Nature
, vol.485
, pp. 237-241
-
-
Sanders, S.J.1
Murtha, M.T.2
Gupta, A.R.3
Murdoch, J.D.4
Raubeson, M.J.5
Willsey, A.J.6
Ercan-Sencicek, A.G.7
Dilullo, N.M.8
Parikshak, N.N.9
Stein, J.L.10
Walker, M.F.11
Ober, G.T.12
Teran, N.A.13
Song, Y.14
El-Fishawy, P.15
Murtha, R.C.16
Choi, M.17
Overton, J.D.18
Bjornson, R.D.19
Carriero, N.J.20
Meyer, K.A.21
Bilguvar, K.22
Mane, S.M.23
Sestan, N.24
Lifton, R.P.25
Günel, M.26
Roeder, K.27
Geschwind, D.H.28
Devlin, B.29
State, M.W.30
more..
-
47
-
-
84860297457
-
De novo gene disruptions in children on the autistic spectrum
-
10.1016/j.neuron.2012.04.009 22542183
-
De novo gene disruptions in children on the autistic spectrum. Iossifov I, Ronemus M, Levy D, Wang Z, Hakker I, Rosenbaum J, Yamrom B, Lee YH, Narzisi G, Leotta A, Kendall J, Grabowska E, Ma B, Marks S, Rodgers L, Stepansky A, Troge J, Andrews P, Bekritsky M, Pradhan K, Ghiban E, Kramer M, Parla J, Demeter R, Fulton LL, Fulton RS, Magrini VJ, Ye K, Darnell JC, Darnell RB, et al. Neuron 2012 74 285 299 10.1016/j.neuron.2012.04.009 22542183
-
(2012)
Neuron
, vol.74
, pp. 285-299
-
-
Iossifov, I.1
Ronemus, M.2
Levy, D.3
Wang, Z.4
Hakker, I.5
Rosenbaum, J.6
Yamrom, B.7
Lee, Y.H.8
Narzisi, G.9
Leotta, A.10
Kendall, J.11
Grabowska, E.12
Ma, B.13
Marks, S.14
Rodgers, L.15
Stepansky, A.16
Troge, J.17
Andrews, P.18
Bekritsky, M.19
Pradhan, K.20
Ghiban, E.21
Kramer, M.22
Parla, J.23
Demeter, R.24
Fulton, L.L.25
Fulton, R.S.26
Magrini, V.J.27
Ye, K.28
Darnell, J.C.29
Darnell, R.B.30
more..
-
48
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
10.1038/nature11011 22495311
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders. Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Schafer C, Liu H, Zhao T, Cai G, Lihm J, Dannenfelser R, Jabado O, Peralta Z, Nagaswamy U, Muzny D, Reid JG, Newsham I, Wu Y, et al. Nature 2012 485 242 245 10.1038/nature11011 22495311
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'Ayan, A.4
Samocha, K.E.5
Sabo, A.6
Lin, C.F.7
Stevens, C.8
Wang, L.S.9
Makarov, V.10
Polak, P.11
Yoon, S.12
Maguire, J.13
Crawford, E.L.14
Campbell, N.G.15
Geller, E.T.16
Valladares, O.17
Schafer, C.18
Liu, H.19
Zhao, T.20
Cai, G.21
Lihm, J.22
Dannenfelser, R.23
Jabado, O.24
Peralta, Z.25
Nagaswamy, U.26
Muzny, D.27
Reid, J.G.28
Newsham, I.29
Wu, Y.30
more..
|