-
2
-
-
0029872978
-
Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey A, Phillips W, Rutter M (1996) Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J Child Psychol Psychiatry 37: 89-126.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
4
-
-
0030977686
-
Genetic influences in childhood-onset psychiatric disorders: Autism and attention-deficit/hyperactivity disorder
-
Smalley SL (1997) Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder. Am J Hum Genet 60: 1276-1282.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1276-1282
-
-
Smalley, S.L.1
-
5
-
-
0036112271
-
The behavioral disorders in epilepsy
-
Dravet C (2002) [The behavioral disorders in epilepsy]. Revue neurologique 158: 4S33-38.
-
(2002)
Revue Neurologique
, vol.158
-
-
Dravet, C.1
-
6
-
-
0038185246
-
Exploring new gene discoveries in idiopathic generalized epilepsy
-
Noebels JL (2003) Exploring new gene discoveries in idiopathic generalized epilepsy. Epilepsia 44 Suppl 2: 16-21.
-
(2003)
Epilepsia
, vol.44
, Issue.SUPPL. 2
, pp. 16-21
-
-
Noebels, J.L.1
-
7
-
-
55049083176
-
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome
-
Bassuk AG, Wallace RH, Buhr A, Buller AR, Afawi Z, et al. (2008) A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. American journal of human genetics 83: 572-581.
-
(2008)
American Journal of Human Genetics
, vol.83
, pp. 572-581
-
-
Bassuk, A.G.1
Wallace, R.H.2
Buhr, A.3
Buller, A.R.4
Afawi, Z.5
-
8
-
-
0344373791
-
Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements
-
Veeman MT, Slusarski DC, Kaykas A, Louie SH, Moon RT (2003) Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. Curr Biol 13: 680-685.
-
(2003)
Curr Biol
, vol.13
, pp. 680-685
-
-
Veeman, M.T.1
Slusarski, D.C.2
Kaykas, A.3
Louie, S.H.4
Moon, R.T.5
-
9
-
-
0033200334
-
The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs
-
Gubb D, Green C, Huen D, Coulson D, Johnson G, et al. (1999) The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs. Genes Dev 13: 2315-2327.
-
(1999)
Genes Dev
, vol.13
, pp. 2315-2327
-
-
Gubb, D.1
Green, C.2
Huen, D.3
Coulson, D.4
Johnson, G.5
-
10
-
-
57049170205
-
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
-
Piton A, Michaud JL, Peng H, Aradhya S, Gauthier J, et al. (2008) Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Hum Mol Genet 17: 3965-3974.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3965-3974
-
-
Piton, A.1
Michaud, J.L.2
Peng, H.3
Aradhya, S.4
Gauthier, J.5
-
11
-
-
77349112962
-
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism
-
Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, et al. (2010) A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. J Med Genet 47: 81-90.
-
(2010)
J Med Genet
, vol.47
, pp. 81-90
-
-
Kumar, R.A.1
Sudi, J.2
Babatz, T.D.3
Brune, C.W.4
Oswald, D.5
-
12
-
-
79957456437
-
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function
-
Fassio A, Patry L, Congia S, Onofri F, Piton A, et al. (2011) SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function. Hum Mol Genet 20: 2297-2307.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2297-2307
-
-
Fassio, A.1
Patry, L.2
Congia, S.3
Onofri, F.4
Piton, A.5
-
13
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain S, Quach H, Betancur C, Rastam M, Colineaux C, et al. (2003) Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 34: 27-29.
-
(2003)
Nat Genet
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
-
14
-
-
70149123667
-
Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity
-
Tao H, Suzuki M, Kiyonari H, Abe T, Sasaoka T, et al. (2009) Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity. Proceedings of the National Academy of Sciences of the United States of America 106: 14426-14431.
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, pp. 14426-14431
-
-
Tao, H.1
Suzuki, M.2
Kiyonari, H.3
Abe, T.4
Sasaoka, T.5
-
15
-
-
67651151005
-
Comprehensive behavioral phenotyping of calpastatin-knockout mice
-
Nakajima R, Takao K, Huang SM, Takano J, Iwata N, et al. (2008) Comprehensive behavioral phenotyping of calpastatin-knockout mice. Mol Brain 1: 7.
-
(2008)
Mol Brain
, vol.1
, pp. 7
-
-
Nakajima, R.1
Takao, K.2
Huang, S.M.3
Takano, J.4
Iwata, N.5
-
16
-
-
0042202625
-
Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia
-
Miyakawa T, Leiter LM, Gerber DJ, Gainetdinov RR, Sotnikova TD, et al. (2003) Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia. Proc Natl Acad Sci U S A 100: 8987-8992.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 8987-8992
-
-
Miyakawa, T.1
Leiter, L.M.2
Gerber, D.J.3
Gainetdinov, R.R.4
Sotnikova, T.D.5
-
17
-
-
1542267746
-
The role of the dorsal hippocampus in the acquisition and retrieval of context memory representations
-
Matus-Amat P, Higgins EA, Barrientos RM, Rudy JW (2004) The role of the dorsal hippocampus in the acquisition and retrieval of context memory representations. J Neurosci 24: 2431-2439.
-
(2004)
J Neurosci
, vol.24
, pp. 2431-2439
-
-
Matus-Amat, P.1
Higgins, E.A.2
Barrientos, R.M.3
Rudy, J.W.4
-
18
-
-
35648992042
-
Targeting ASIC1a reduces innate fear and alters neuronal activity in the fear circuit
-
Coryell MW, Ziemann AE, Westmoreland PJ, Haenfler JM, Kurjakovic Z, et al. (2007) Targeting ASIC1a reduces innate fear and alters neuronal activity in the fear circuit. Biol Psychiatry 62: 1140-1148.
-
(2007)
Biol Psychiatry
, vol.62
, pp. 1140-1148
-
-
Coryell, M.W.1
Ziemann, A.E.2
Westmoreland, P.J.3
Haenfler, J.M.4
Kurjakovic, Z.5
-
19
-
-
0030963019
-
Toward a functional analysis of the yeast genome through exhaustive two-hybrid screens
-
Fromont-Racine M, Rain JC, Legrain P (1997) Toward a functional analysis of the yeast genome through exhaustive two-hybrid screens. Nature genetics 16: 277-282.
-
(1997)
Nature Genetics
, vol.16
, pp. 277-282
-
-
Fromont-Racine, M.1
Rain, J.C.2
Legrain, P.3
-
20
-
-
20144379646
-
Protein interaction mapping: A Drosophila case study
-
Formstecher E, Aresta S, Collura V, Hamburger A, Meil A, et al. (2005) Protein interaction mapping: a Drosophila case study. Genome research 15: 376-384.
-
(2005)
Genome Research
, vol.15
, pp. 376-384
-
-
Formstecher, E.1
Aresta, S.2
Collura, V.3
Hamburger, A.4
Meil, A.5
-
21
-
-
0035843145
-
The protein-protein interaction map of Helicobacter pylori
-
Rain JC, Selig L, De Reuse H, Battaglia V, Reverdy C, et al. (2001) The protein-protein interaction map of Helicobacter pylori. Nature 409: 211-215.
-
(2001)
Nature
, vol.409
, pp. 211-215
-
-
Rain, J.C.1
Selig, L.2
De Reuse, H.3
Battaglia, V.4
Reverdy, C.5
-
22
-
-
0036974250
-
Prediction, assessment and validation of protein interaction maps in bacteria
-
Wojcik J, Boneca IG, Legrain P (2002) Prediction, assessment and validation of protein interaction maps in bacteria. Journal of molecular biology 323: 763-770.
-
(2002)
Journal of Molecular Biology
, vol.323
, pp. 763-770
-
-
Wojcik, J.1
Boneca, I.G.2
Legrain, P.3
-
23
-
-
0017710978
-
Characteristics of a human cell line transformed by DNA from human adenovirus type 5
-
Graham FL, Smiley J, Russell WC, Nairn R (1977) Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J Gen Virol 36: 59-74.
-
(1977)
J Gen Virol
, vol.36
, pp. 59-74
-
-
Graham, F.L.1
Smiley, J.2
Russell, W.C.3
Nairn, R.4
-
24
-
-
79851516501
-
Mutations in prickle orthologs cause seizures in flies, mice, and humans
-
Tao H, Manak JR, Sowers L, Mei X, Kiyonari H, et al. (2011) Mutations in prickle orthologs cause seizures in flies, mice, and humans. American journal of human genetics 88: 138-149.
-
(2011)
American Journal of Human Genetics
, vol.88
, pp. 138-149
-
-
Tao, H.1
Manak, J.R.2
Sowers, L.3
Mei, X.4
Kiyonari, H.5
-
25
-
-
77957190328
-
RNG105 deficiency impairs the dendritic localization of mRNAs for Na +/K+ ATPase subunit isoforms and leads to the degeneration of neuronal networks
-
Shiina N, Yamaguchi K, Tokunaga M (2010) RNG105 deficiency impairs the dendritic localization of mRNAs for Na +/K+ ATPase subunit isoforms and leads to the degeneration of neuronal networks. The Journal of neuroscience : the official journal of the Society for Neuroscience 30: 12816-12830.
-
(2010)
The Journal of Neuroscience: The Official Journal of the Society for Neuroscience
, vol.30
, pp. 12816-12830
-
-
Shiina, N.1
Yamaguchi, K.2
Tokunaga, M.3
-
28
-
-
0037320081
-
The coxsackie B virus and adenovirus receptor resides in a distinct membrane microdomain
-
Ashbourne Excoffon KJ, Moninger T, Zabner J (2003) The coxsackie B virus and adenovirus receptor resides in a distinct membrane microdomain. Journal of virology 77: 2559-2567.
-
(2003)
Journal of Virology
, vol.77
, pp. 2559-2567
-
-
Ashbourne Excoffon, K.J.1
Moninger, T.2
Zabner, J.3
-
29
-
-
42549096459
-
Expression of the neurosecretory process in PC12 cells is governed by REST
-
D'Alessandro R, Klajn A, Stucchi L, Podini P, Malosio ML, et al. (2008) Expression of the neurosecretory process in PC12 cells is governed by REST. J Neurochem 105: 1369-1383.
-
(2008)
J Neurochem
, vol.105
, pp. 1369-1383
-
-
D'Alessandro, R.1
Klajn, A.2
Stucchi, L.3
Podini, P.4
Malosio, M.L.5
-
30
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
Abrahams BS, Geschwind DH (2008) Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet 9: 341-355.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
31
-
-
80053064177
-
Mouse model of Timothy syndrome recapitulates triad of autistic traits
-
Bader PL, Faizi M, Kim LH, Owen SF, Tadross MR, et al. (2011) Mouse model of Timothy syndrome recapitulates triad of autistic traits. Proc Natl Acad Sci U S A 108: 15432-15437.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 15432-15437
-
-
Bader, P.L.1
Faizi, M.2
Kim, L.H.3
Owen, S.F.4
Tadross, M.R.5
-
32
-
-
4644373224
-
Sociability and preference for social novelty in five inbred strains: An approach to assess autistic-like behavior in mice
-
Moy SS, Nadler JJ, Perez A, Barbaro RP, Johns JM, et al. (2004) Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice. Genes Brain Behav 3: 287-302.
-
(2004)
Genes Brain Behav
, vol.3
, pp. 287-302
-
-
Moy, S.S.1
Nadler, J.J.2
Perez, A.3
Barbaro, R.P.4
Johns, J.M.5
-
33
-
-
35148821488
-
Mouse behavioral assays relevant to the symptoms of autism
-
Crawley JN (2007) Mouse behavioral assays relevant to the symptoms of autism. Brain pathology 17: 448-459.
-
(2007)
Brain Pathology
, vol.17
, pp. 448-459
-
-
Crawley, J.N.1
-
34
-
-
77649336870
-
Circadian rhythms and sleep in children with autism
-
Glickman G (2010) Circadian rhythms and sleep in children with autism. Neurosci Biobehav Rev 34: 755-768.
-
(2010)
Neurosci Biobehav Rev
, vol.34
, pp. 755-768
-
-
Glickman, G.1
-
35
-
-
33846588399
-
Abnormality of circadian rhythm accompanied by an increase in frontal cortex serotonin in animal model of autism
-
Tsujino N, Nakatani Y, Seki Y, Nakasato A, Nakamura M, et al. (2007) Abnormality of circadian rhythm accompanied by an increase in frontal cortex serotonin in animal model of autism. Neurosci Res 57: 289-295.
-
(2007)
Neurosci Res
, vol.57
, pp. 289-295
-
-
Tsujino, N.1
Nakatani, Y.2
Seki, Y.3
Nakasato, A.4
Nakamura, M.5
-
36
-
-
0345491828
-
REST/NRSF-interacting LIM domain protein, a putative nuclear translocation receptor
-
Shimojo M, Hersh LB (2003) REST/NRSF-interacting LIM domain protein, a putative nuclear translocation receptor. Molecular and cellular biology 23: 9025-9031.
-
(2003)
Molecular and Cellular Biology
, vol.23
, pp. 9025-9031
-
-
Shimojo, M.1
Hersh, L.B.2
-
37
-
-
67649663886
-
Yeast two-hybrid, a powerful tool for systems biology
-
Bruckner A, Polge C, Lentze N, Auerbach D, Schlattner U (2009) Yeast two-hybrid, a powerful tool for systems biology. Int J Mol Sci 10: 2763-2788.
-
(2009)
Int J Mol Sci
, vol.10
, pp. 2763-2788
-
-
Bruckner, A.1
Polge, C.2
Lentze, N.3
Auerbach, D.4
Schlattner, U.5
-
38
-
-
0031966041
-
LIM domains: Multiple roles as adapters and functional modifiers in protein interactions
-
Dawid IB, Breen JJ, Toyama R (1998) LIM domains: multiple roles as adapters and functional modifiers in protein interactions. Trends Genet 14: 156-162.
-
(1998)
Trends Genet
, vol.14
, pp. 156-162
-
-
Dawid, I.B.1
Breen, J.J.2
Toyama, R.3
-
39
-
-
0041701648
-
Identification and characterization of human PRICKLE1 and PRICKLE2 genes as well as mouse Prickle1 and Prickle2 genes homologous to Drosophila tissue polarity gene prickle
-
Katoh M (2003) Identification and characterization of human PRICKLE1 and PRICKLE2 genes as well as mouse Prickle1 and Prickle2 genes homologous to Drosophila tissue polarity gene prickle. Int J Mol Med 11: 249-256.
-
(2003)
Int J Mol Med
, vol.11
, pp. 249-256
-
-
Katoh, M.1
-
42
-
-
67349203862
-
Common increase of GATA-3 level in PC-12 cells by three teratogens causing autism spectrum disorders
-
Rout UK, Clausen P (2009) Common increase of GATA-3 level in PC-12 cells by three teratogens causing autism spectrum disorders. Neurosci Res 64: 162-169.
-
(2009)
Neurosci Res
, vol.64
, pp. 162-169
-
-
Rout, U.K.1
Clausen, P.2
-
43
-
-
57349193484
-
Valproic acid regulates catecholaminergic pathways by concentration-dependent threshold effects on TH mRNA synthesis and degradation
-
D'Souza A, Onem E, Patel P, La Gamma EF, Nankova BB (2009) Valproic acid regulates catecholaminergic pathways by concentration-dependent threshold effects on TH mRNA synthesis and degradation. Brain Res 1247: 1-10.
-
(2009)
Brain Res
, vol.1247
, pp. 1-10
-
-
D'Souza, A.1
Onem, E.2
Patel, P.3
La Gamma, E.F.4
Nankova, B.B.5
-
44
-
-
78649420524
-
Neurites from PC12 cells are connected to each other by synapse-like structures
-
Jeon CY, Jin JK, Koh YH, Chun W, Choi IG, et al. (2010) Neurites from PC12 cells are connected to each other by synapse-like structures. Synapse 64: 765-772.
-
(2010)
Synapse
, vol.64
, pp. 765-772
-
-
Jeon, C.Y.1
Jin, J.K.2
Koh, Y.H.3
Chun, W.4
Choi, I.G.5
-
45
-
-
18044377786
-
Regulation of dense core vesicle release from PC12 cells by interaction between the D2 dopamine receptor and calcium-dependent activator protein for secretion (CAPS)
-
Binda AV, Kabbani N, Levenson R (2005) Regulation of dense core vesicle release from PC12 cells by interaction between the D2 dopamine receptor and calcium-dependent activator protein for secretion (CAPS). Biochem Pharmacol 69: 1451-1461.
-
(2005)
Biochem Pharmacol
, vol.69
, pp. 1451-1461
-
-
Binda, A.V.1
Kabbani, N.2
Levenson, R.3
-
46
-
-
78349299390
-
PRICKLE1 progressive myoclonus epilepsy in Southern Italy
-
Criscuolo C, de Leva MF, Sorrentino P, Piro R, Carbone R, et al. (2010) PRICKLE1 progressive myoclonus epilepsy in Southern Italy. Movement disorders : official journal of the Movement Disorder Society 25: 2686-2687.
-
(2010)
Movement Disorders: Official Journal of the Movement Disorder Society
, vol.25
, pp. 2686-2687
-
-
Criscuolo, C.1
De Leva, M.F.2
Sorrentino, P.3
Piro, R.4
Carbone, R.5
-
47
-
-
33645415686
-
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2
-
Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, et al. (2006) Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. N Engl J Med 354: 1370-1377.
-
(2006)
N Engl J Med
, vol.354
, pp. 1370-1377
-
-
Strauss, K.A.1
Puffenberger, E.G.2
Huentelman, M.J.3
Gottlieb, S.4
Dobrin, S.E.5
-
48
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
Alarcon M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, et al. (2008) Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet 82: 150-159.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 150-159
-
-
Alarcon, M.1
Abrahams, B.S.2
Stone, J.L.3
Duvall, J.A.4
Perederiy, J.V.5
-
49
-
-
38749096303
-
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
-
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, et al. (2008) A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet 82: 160-164.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 160-164
-
-
Arking, D.E.1
Cutler, D.J.2
Brune, C.W.3
Teslovich, T.M.4
West, K.5
-
50
-
-
80053002788
-
Dystrophic serotonin axons in postmortem brains from young autism patients
-
Azmitia EC, Singh JS, Hou XP, Wegiel J (2011) Dystrophic serotonin axons in postmortem brains from young autism patients. Anat Rec (Hoboken) 294: 1653-1662.
-
(2011)
Anat Rec (Hoboken)
, vol.294
, pp. 1653-1662
-
-
Azmitia, E.C.1
Singh, J.S.2
Hou, X.P.3
Wegiel, J.4
-
51
-
-
84874118636
-
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders
-
Boccuto L, Lauri M, Sarasua SM, Skinner CD, Buccella D, et al. (2012) Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. Eur J Hum Genet.
-
(2012)
Eur J Hum Genet
-
-
Boccuto, L.1
Lauri, M.2
Sarasua, S.M.3
Skinner, C.D.4
Buccella, D.5
-
52
-
-
84880332828
-
Autism-related behavioral abnormalities in synapsin knockout mice
-
Greco B, Manago F, Tucci V, Kao HT, Valtorta F, et al. (2012) Autism-related behavioral abnormalities in synapsin knockout mice. Behav Brain Res.
-
(2012)
Behav Brain Res
-
-
Greco, B.1
Manago, F.2
Tucci, V.3
Kao, H.T.4
Valtorta, F.5
-
53
-
-
84860484751
-
Neuroethologically delineated differences in the seizure behavior of Synapsin 1 and Synapsin 2 knock-out mice
-
Etholm L, Bahonjic E, Walaas SI, Kao HT, Heggelund P (2012) Neuroethologically delineated differences in the seizure behavior of Synapsin 1 and Synapsin 2 knock-out mice. Epilepsy research 99: 252-259.
-
(2012)
Epilepsy Research
, vol.99
, pp. 252-259
-
-
Etholm, L.1
Bahonjic, E.2
Walaas, S.I.3
Kao, H.T.4
Heggelund, P.5
-
54
-
-
48249145132
-
The possible interplay of synaptic and clock genes in autism spectrum disorders
-
Bourgeron T (2007) The possible interplay of synaptic and clock genes in autism spectrum disorders. Cold Spring Harb Symp Quant Biol 72: 645-654.
-
(2007)
Cold Spring Harb Symp Quant Biol
, vol.72
, pp. 645-654
-
-
Bourgeron, T.1
-
55
-
-
1542407037
-
Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy
-
Garcia CC, Blair HJ, Seager M, Coulthard A, Tennant S, et al. (2004) Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy. Journal of medical genetics 41: 183-186.
-
(2004)
Journal of Medical Genetics
, vol.41
, pp. 183-186
-
-
Garcia, C.C.1
Blair, H.J.2
Seager, M.3
Coulthard, A.4
Tennant, S.5
-
56
-
-
78649753616
-
Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome
-
Feyder M, Karlsson RM, Mathur P, Lyman M, Bock R, et al. (2010) Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome. Am J Psychiatry 167: 1508-1517.
-
(2010)
Am J Psychiatry
, vol.167
, pp. 1508-1517
-
-
Feyder, M.1
Karlsson, R.M.2
Mathur, P.3
Lyman, M.4
Bock, R.5
-
57
-
-
0029962955
-
PSD-95 is associated with the postsynaptic density and not with the presynaptic membrane at forebrain synapses
-
Hunt CA, Schenker LJ, Kennedy MB (1996) PSD-95 is associated with the postsynaptic density and not with the presynaptic membrane at forebrain synapses. J Neurosci 16: 1380-1388.
-
(1996)
J Neurosci
, vol.16
, pp. 1380-1388
-
-
Hunt, C.A.1
Schenker, L.J.2
Kennedy, M.B.3
-
58
-
-
84856329927
-
Role of Prickle1 and Prickle2 in neurite outgrowth in murine neuroblastoma cells
-
Fujimura L, Hatano M (2012) Role of Prickle1 and Prickle2 in neurite outgrowth in murine neuroblastoma cells. Methods Mol Biol 839: 173-185.
-
(2012)
Methods Mol Biol
, vol.839
, pp. 173-185
-
-
Fujimura, L.1
Hatano, M.2
-
59
-
-
34548684134
-
Mouse Prickle1 and Prickle2 are expressed in postmitotic neurons and promote neurite outgrowth
-
Okuda H, Miyata S, Mori Y, Tohyama M (2007) Mouse Prickle1 and Prickle2 are expressed in postmitotic neurons and promote neurite outgrowth. FEBS Lett 581: 4754-4760.
-
(2007)
FEBS Lett
, vol.581
, pp. 4754-4760
-
-
Okuda, H.1
Miyata, S.2
Mori, Y.3
Tohyama, M.4
|