-
1
-
-
33749242599
-
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
-
Archer HL, Evans J, Edwards S, Colley J, Newbury-Ecob R, O'Callaghan F, Huyton M, O'Regan M, Tolmie J, Sampson J, Clarke A, Osborne J (2006) CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients. J Med Genet 43:729-734.
-
(2006)
J Med Genet
, vol.43
, pp. 729-734
-
-
Archer, H.L.1
Evans, J.2
Edwards, S.3
Colley, J.4
Newbury-Ecob, R.5
O'Callaghan, F.6
Huyton, M.7
O'Regan, M.8
Tolmie, J.9
Sampson, J.10
Clarke, A.11
Osborne, J.12
-
3
-
-
33845988053
-
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation
-
Bertani I, Rusconi L, Bolognese F, Forlani G, Conca B, De Monte L, Badaracco G, Landsberger N, Kilstrup-Nielsen C (2006) Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation. J Biol Chem 281:32048-32056.
-
(2006)
J Biol Chem
, vol.281
, pp. 32048-32056
-
-
Bertani, I.1
Rusconi, L.2
Bolognese, F.3
Forlani, G.4
Conca, B.5
De Monte, L.6
Badaracco, G.7
Landsberger, N.8
Kilstrup-Nielsen, C.9
-
4
-
-
0033646567
-
Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: Identification of several novel mutations and polymorphisms
-
Buyse IM, Fang P, Hoon KT, Amir RE, Zoghbi HY, Roa BB (2000) Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms. Am J Hum Genet 67:1428-1436.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1428-1436
-
-
Buyse, I.M.1
Fang, P.2
Hoon, K.T.3
Amir, R.E.4
Zoghbi, H.Y.5
Roa, B.B.6
-
5
-
-
31444434393
-
The disease progression mutant mice is affected of Mecp2 by the level of BDNF expression
-
Chang Q, Khare G, Dani V, Nelson S, Jaenisch R (2006) The disease progression mutant mice is affected of Mecp2 by the level of BDNF expression. Neuron 49:341-348.
-
(2006)
Neuron
, vol.49
, pp. 341-348
-
-
Chang, Q.1
Khare, G.2
Dani, V.3
Nelson, S.4
Jaenisch, R.5
-
6
-
-
18144443930
-
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: Correlation of disease severity with mutation type and location
-
Cheadle JP, Gill H, Fleming N, Maynard J, Kerr A, Leonard H, Krawczak M, Cooper DN, Lynch S, Thomas N, Hughes H, Hulten M, Ravine D, Sampson JR, Clarke A (2000) Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location. Hum Mol Genet 9:1119-1129.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1119-1129
-
-
Cheadle, J.P.1
Gill, H.2
Fleming, N.3
Maynard, J.4
Kerr, A.5
Leonard, H.6
Krawczak, M.7
Cooper, D.N.8
Lynch, S.9
Thomas, N.10
Hughes, H.11
Hulten, M.12
Ravine, D.13
Sampson, J.R.14
Clarke, A.15
-
7
-
-
0026583942
-
PDGF alpha- and beta-receptors activate unique and common signal transduction pathways
-
Eriksson A, Siegbahn A, Westermark B, Heldin CH, Claesson-Welsh L (1992) PDGF alpha- and beta-receptors activate unique and common signal transduction pathways. EMBO J 11:543-550.
-
(1992)
EMBO J
, vol.11
, pp. 543-550
-
-
Eriksson, A.1
Siegbahn, A.2
Westermark, B.3
Heldin, C.H.4
Claesson-Welsh, L.5
-
8
-
-
27144463130
-
Early onset seizures and Rett-like features associated with mutations in CDKL5
-
Evans JC, Archer HL, Colley JP, Ravn K, Nielsen JB, Kerr A, Williams E, Christodoulou J, Gécz J, Jardine PE, Wright MJ, Pilz DT, Lazarou L, Cooper DN, Sampson JR, Butler R, Whatley SD, Clarke AJ (2005) Early onset seizures and Rett-like features associated with mutations in CDKL5. Eur J Hum Genet 13:1113-1120.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 1113-1120
-
-
Evans, J.C.1
Archer, H.L.2
Colley, J.P.3
Ravn, K.4
Nielsen, J.B.5
Kerr, A.6
Williams, E.7
Christodoulou, J.8
Gécz, J.9
Jardine, P.E.10
Wright, M.J.11
Pilz, D.T.12
Lazarou, L.13
Cooper, D.N.14
Sampson, J.R.15
Butler, R.16
Whatley, S.D.17
Clarke, A.J.18
-
9
-
-
0037900881
-
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome
-
Gill H, Cheadle JP, Maynard J, Fleming N, Whatley S, Cranston T, Thompson EM, Leonard H, Davis M, Christodoulou J, Skjeldal O, Hanefeld F, Kerr A, Tandy A, Ravine D, Clarke A (2003) Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome. J Med Genet 40:380-384.
-
(2003)
J Med Genet
, vol.40
, pp. 380-384
-
-
Gill, H.1
Cheadle, J.P.2
Maynard, J.3
Fleming, N.4
Whatley, S.5
Cranston, T.6
Thompson, E.M.7
Leonard, H.8
Davis, M.9
Christodoulou, J.10
Skjeldal, O.11
Hanefeld, F.12
Kerr, A.13
Tandy, A.14
Ravine, D.15
Clarke, A.16
-
10
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA (1998) Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 92:63-72.
-
(1998)
Cell
, vol.92
, pp. 63-72
-
-
Gleeson, J.G.1
Allen, K.M.2
Fox, J.W.3
Lamperti, E.D.4
Berkovic, S.5
Scheffer, I.6
Cooper, E.C.7
Dobyns, W.B.8
Minnerath, S.R.9
Ross, M.E.10
Walsh, C.A.11
-
11
-
-
11844304062
-
The role of the Rho GTPases in neuronal development
-
Govek EE, Newey SE, Van Aelst L (2005) The role of the Rho GTPases in neuronal development. Genes Dev 19:1-49.
-
(2005)
Genes Dev
, vol.19
, pp. 1-49
-
-
Govek, E.E.1
Newey, S.E.2
Van Aelst, L.3
-
12
-
-
0021815213
-
Rett's syndrome: Prevalence and impact on progressive severe mental retardation in girls
-
Hagberg B (1985) Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls. Acta Paediatr Scand 74:405-408.
-
(1985)
Acta Paediatr Scand
, vol.74
, pp. 405-408
-
-
Hagberg, B.1
-
13
-
-
0020507697
-
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
-
Hagberg B, Aicardi J, Dias K, Ramos O (1983) A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann Neurol 14:471-479.
-
(1983)
Ann Neurol
, vol.14
, pp. 471-479
-
-
Hagberg, B.1
Aicardi, J.2
Dias, K.3
Ramos, O.4
-
14
-
-
0032559362
-
Rho GTPases and the actin cytoskeleton
-
Hall A (1998) Rho GTPases and the actin cytoskeleton. Science 279:509-514.
-
(1998)
Science
, vol.279
, pp. 509-514
-
-
Hall, A.1
-
15
-
-
0031214960
-
Involvement of phosphatidylinositide 3′-kinase and Rac in platelet-derived growth factor-induced actin reorganization and chemotaxis
-
Hooshmand-Rad R, Claesson-Welsh L, Wennström S, Yokote K, Siegbahn A, Heldin CH (1997) Involvement of phosphatidylinositide 3′-kinase and Rac in platelet-derived growth factor-induced actin reorganization and chemotaxis. Exp Cell Res 234:434-441.
-
(1997)
Exp Cell Res
, vol.234
, pp. 434-441
-
-
Hooshmand-Rad, R.1
Claesson-Welsh, L.2
Wennström, S.3
Yokote, K.4
Siegbahn, A.5
Heldin, C.H.6
-
16
-
-
0041488911
-
Trk receptors: Roles in neuronal signal transduction
-
Huang EJ, Reichardt LF (2003) Trk receptors: roles in neuronal signal transduction. Annu Rev Biochem 72:609-642.
-
(2003)
Annu Rev Biochem
, vol.72
, pp. 609-642
-
-
Huang, E.J.1
Reichardt, L.F.2
-
18
-
-
0031837109
-
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
-
Jones PL, Veenstra GJ, Wade PA, Vermaak D, Kass SU, Landsberger N, Strouboulis J, Wolffe AP (1998) Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat Genet 19:187-191.
-
(1998)
Nat Genet
, vol.19
, pp. 187-191
-
-
Jones, P.L.1
Veenstra, G.J.2
Wade, P.A.3
Vermaak, D.4
Kass, S.U.5
Landsberger, N.6
Strouboulis, J.7
Wolffe, A.P.8
-
19
-
-
0033797735
-
Dendritic anomalies in disorders associated with mental retardation
-
Kaufmann WE, Moser HW (2000) Dendritic anomalies in disorders associated with mental retardation. Cereb Cortex 10:981-991.
-
(2000)
Cereb Cortex
, vol.10
, pp. 981-991
-
-
Kaufmann, W.E.1
Moser, H.W.2
-
20
-
-
29644439879
-
CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disorders
-
Lin C, Franco B, Rosner MR (2005) CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disorders. Hum Mol Genet 14:3775-3786.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3775-3786
-
-
Lin, C.1
Franco, B.2
Rosner, M.R.3
-
21
-
-
0030599382
-
Axonal origin and purity of growth cones isolated from fetal rat brain
-
Lohse K, Helmke SM, Wood MR, Quiroga S, de la Houssaye BA, Miller VE, Negre-Aminou P, Pfenninger KH (1996) Axonal origin and purity of growth cones isolated from fetal rat brain. Brain Res Dev Brain Res 96:83-96.
-
(1996)
Brain Res Dev Brain Res
, vol.96
, pp. 83-96
-
-
Lohse, K.1
Helmke, S.M.2
Wood, M.R.3
Quiroga, S.4
De La Houssaye, B.A.5
Miller, V.E.6
Negre-Aminou, P.7
Pfenninger, K.H.8
-
22
-
-
0036468677
-
Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors
-
Lois C, Hong EJ, Pease S, Brown EJ, Baltimore D (2002) Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors. Science 295:868-872.
-
(2002)
Science
, vol.295
, pp. 868-872
-
-
Lois, C.1
Hong, E.J.2
Pease, S.3
Brown, E.J.4
Baltimore, D.5
-
23
-
-
0036441201
-
Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity
-
Luo L (2002) Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity. Annu Rev Cell Dev Biol 18:601-635.
-
(2002)
Annu Rev Cell Dev Biol
, vol.18
, pp. 601-635
-
-
Luo, L.1
-
24
-
-
26444495179
-
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
-
Mari F, Azimonti S, Bertani I, Bolognese F, Colombo E, Caselli R, Scala E, Longo I, Grosso S, Pescucci C, Ariani F, Hayek G, Balestri P, Bergo A, Badaracco G, Zappella M, Broccoli V, Renieri A, Kilstrup-Nielsen C, Landsberger N (2005) CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome. Hum Mol Genet 14:1935-1946.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1935-1946
-
-
Mari, F.1
Azimonti, S.2
Bertani, I.3
Bolognese, F.4
Colombo, E.5
Caselli, R.6
Scala, E.7
Longo, I.8
Grosso, S.9
Pescucci, C.10
Ariani, F.11
Hayek, G.12
Balestri, P.13
Bergo, A.14
Badaracco, G.15
Zappella, M.16
Broccoli, V.17
Renieri, A.18
Kilstrup-Nielsen, C.19
Landsberger, N.20
more..
-
25
-
-
0028858681
-
Neurotrophins regulate dendritic growth in developing visual cortex
-
McAllister AK, Lo DC, Katz LC (1995) Neurotrophins regulate dendritic growth in developing visual cortex. Neuron 15:791-803.
-
(1995)
Neuron
, vol.15
, pp. 791-803
-
-
McAllister, A.K.1
Lo, D.C.2
Katz, L.C.3
-
26
-
-
33745890228
-
TrkB binds and tyrosine-phosphorylates Tiam1, leading to activation of Rac1 and induction of changes in cellular morphology
-
Miyamoto Y, Yamauchi J, Tanoue A, Wu C, Mobley WC (2006) TrkB binds and tyrosine-phosphorylates Tiam1, leading to activation of Rac1 and induction of changes in cellular morphology. Proc Natl Acad Sci U S A 103:10444-10449.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 10444-10449
-
-
Miyamoto, Y.1
Yamauchi, J.2
Tanoue, A.3
Wu, C.4
Mobley, W.C.5
-
27
-
-
0032144185
-
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region
-
Montini E, Andolfi G, Caruso A, Buchner G, Walpole SM, Mariani M, Consalez G, Trump D, Ballabio A, Franco B (1998) Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region. Genomics 51:427-433.
-
(1998)
Genomics
, vol.51
, pp. 427-433
-
-
Montini, E.1
Andolfi, G.2
Caruso, A.3
Buchner, G.4
Walpole, S.M.5
Mariani, M.6
Consalez, G.7
Trump, D.8
Ballabio, A.9
Franco, B.10
-
28
-
-
0032574977
-
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
-
Nan X, Ng HH, Johnson CA, Laherty CD, Turner BM, Eisenman RN, Bird A (1998) Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature 393:386-389.
-
(1998)
Nature
, vol.393
, pp. 386-389
-
-
Nan, X.1
Ng, H.H.2
Johnson, C.A.3
Laherty, C.D.4
Turner, B.M.5
Eisenman, R.N.6
Bird, A.7
-
29
-
-
33746658154
-
FilGAP, a Rho- and ROCK-regulated GAP for Rac binds filamin A to control actin remodelling
-
Ohta Y, Hartwig JH, Stossel TP (2006) FilGAP, a Rho- and ROCK-regulated GAP for Rac binds filamin A to control actin remodelling. Nat Cell Biology 8:803-U835.
-
(2006)
Nat Cell Biology
, vol.8
-
-
Ohta, Y.1
Hartwig, J.H.2
Stossel, T.P.3
-
30
-
-
46149125934
-
Endocytic trafficking of Rac is required for the spatial restriction of signaling in cell migration
-
Palamidessi A, Frittoli E, Garré M, Faretta M, Mione M, Testa I, Diaspro A, Lanzetti L, Scita G, Di Fiore PP (2008) Endocytic trafficking of Rac is required for the spatial restriction of signaling in cell migration. Cell 134:135-147.
-
(2008)
Cell
, vol.134
, pp. 135-147
-
-
Palamidessi, A.1
Frittoli, E.2
Garré, M.3
Faretta, M.4
Mione, M.5
Testa, I.6
Diaspro, A.7
Lanzetti, L.8
Scita, G.9
Di Fiore, P.P.10
-
31
-
-
0036543312
-
Rho proteins, mental retardation and the cellular basis of cognition
-
Ramakers GJ (2002) Rho proteins, mental retardation and the cellular basis of cognition. Trends Neurosci 25:191-199.
-
(2002)
Trends Neurosci
, vol.25
, pp. 191-199
-
-
Ramakers, G.J.1
-
32
-
-
33749010358
-
Neurotrophin-regulated signalling pathways
-
Reichardt LF (2006) Neurotrophin-regulated signalling pathways. Philos Trans R Soc Lond B Biol Sci 361:1545-1564.
-
(2006)
Philos Trans R Soc Lond B Biol Sci
, vol.361
, pp. 1545-1564
-
-
Reichardt, L.F.1
-
33
-
-
0033081753
-
Regulation of the small GTPbinding protein Rho by cell adhesion and the cytoskeleton
-
Ren XD, Kiosses WB, Schwartz MA (1999) Regulation of the small GTPbinding protein Rho by cell adhesion and the cytoskeleton. EMBO J 18:578-585.
-
(1999)
EMBO J
, vol.18
, pp. 578-585
-
-
Ren, X.D.1
Kiosses, W.B.2
Schwartz, M.A.3
-
34
-
-
70449356630
-
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery
-
Ricciardi S, Kilstrup-Nielsen C, Bienvenu T, Jacquette A, Landsberger N, Broccoli V (2009) CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery. Human Molecular Genetics 18:4590-4602.
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 4590-4602
-
-
Ricciardi, S.1
Kilstrup-Nielsen, C.2
Bienvenu, T.3
Jacquette, A.4
Landsberger, N.5
Broccoli, V.6
-
35
-
-
57649148768
-
CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail
-
Rusconi L, Salvatoni L, Giudici L, Bertani I, Kilstrup-Nielsen C, Broccoli V, Landsberger N (2008) CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail. J Biol Chem 283:30101-30111.
-
(2008)
J Biol Chem
, vol.283
, pp. 30101-30111
-
-
Rusconi, L.1
Salvatoni, L.2
Giudici, L.3
Bertani, I.4
Kilstrup-Nielsen, C.5
Broccoli, V.6
Landsberger, N.7
-
36
-
-
0031975810
-
Platelet-derived growth factor (PDGF)-induced actin rearrangement is deregulated in cells expressing a mutant Y778F PDGF beta-receptor
-
Ruusala A, Sundberg C, Arvidsson AK, Rupp-Thuresson E, Heldin CH, Claesson-Welsh L (1998) Platelet-derived growth factor (PDGF)-induced actin rearrangement is deregulated in cells expressing a mutant Y778F PDGF beta-receptor. J Cell Sci 111:111-120.
-
(1998)
J Cell Sci
, vol.111
, pp. 111-120
-
-
Ruusala, A.1
Sundberg, C.2
Arvidsson, A.K.3
Rupp-Thuresson, E.4
Heldin, C.H.5
Claesson-Welsh, L.6
-
37
-
-
0035584249
-
Efficient gene transfer into the embryonic mouse brain using in vivo electroporation
-
Saito T, Nakatsuji N (2001) Efficient gene transfer into the embryonic mouse brain using in vivo electroporation. Dev Biol 240:237-246.
-
(2001)
Dev Biol
, vol.240
, pp. 237-246
-
-
Saito, T.1
Nakatsuji, N.2
-
38
-
-
13444263520
-
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
-
Scala E, Ariani F, Mari F, Caselli R, Pescucci C, Longo I, Meloni I, Giachino D, Bruttini M, Hayek G, Zappella M, Renieri A (2005) CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms. J Med Genet 42:103-107.
-
(2005)
J Med Genet
, vol.42
, pp. 103-107
-
-
Scala, E.1
Ariani, F.2
Mari, F.3
Caselli, R.4
Pescucci, C.5
Longo, I.6
Meloni, I.7
Giachino, D.8
Bruttini, M.9
Hayek, G.10
Zappella, M.11
Renieri, A.12
-
39
-
-
8844252981
-
Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation
-
Tao J, Van Esch H, Hagedorn-Greiwe M, Hoffmann K, Moser B, Raynaud M, Sperner J, Fryns JP, Schwinger E, Gécz J, Ropers HH, Kalscheuer VM (2004) Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation. Am J Hum Genet 75:1149-1154.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1149-1154
-
-
Tao, J.1
Van Esch, H.2
Hagedorn-Greiwe, M.3
Hoffmann, K.4
Moser, B.5
Raynaud, M.6
Sperner, J.7
Fryns, J.P.8
Schwinger, E.9
Gécz, J.10
Ropers, H.H.11
Kalscheuer, V.M.12
-
40
-
-
8844269073
-
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
-
Weaving LS, Christodoulou J, Williamson SL, Friend KL, McKenzie OL, Archer H, Evans J, Clarke A, Pelka GJ, Tam PP, Watson C, Lahooti H, Ellaway CJ, Bennetts B, Leonard H, Gécz J (2004) Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. Am J Hum Genet 75:1079-1093.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1079-1093
-
-
Weaving, L.S.1
Christodoulou, J.2
Williamson, S.L.3
Friend, K.L.4
McKenzie, O.L.5
Archer, H.6
Evans, J.7
Clarke, A.8
Pelka, G.J.9
Tam, P.P.10
Watson, C.11
Lahooti, H.12
Ellaway, C.J.13
Bennetts, B.14
Leonard, H.15
Gécz, J.16
-
41
-
-
0037223854
-
Signalling and crosstalk of Rho GTPases in mediating axon guidance
-
Yuan XB, Jin M, Xu X, Song YQ, Wu CP, Poo MM, Duan S (2003) Signalling and crosstalk of Rho GTPases in mediating axon guidance. Nat Cell Biol 5:38-45.
-
(2003)
Nat Cell Biol
, vol.5
, pp. 38-45
-
-
Yuan, X.B.1
Jin, M.2
Xu, X.3
Song, Y.Q.4
Wu, C.P.5
Poo, M.M.6
Duan, S.7
-
42
-
-
34250807034
-
Polarized signaling endosomes coordinate BDNF-induced chemotaxis of cerebellar precursors
-
Zhou P, Porcionatto M, Pilapil M, Chen Y, Choi Y, Tolias KF, Bikoff JB, Hong EJ, Greenberg ME, Segal RA (2007) Polarized signaling endosomes coordinate BDNF-induced chemotaxis of cerebellar precursors. Neuron 55:53-68.
-
(2007)
Neuron
, vol.55
, pp. 53-68
-
-
Zhou, P.1
Porcionatto, M.2
Pilapil, M.3
Chen, Y.4
Choi, Y.5
Tolias, K.F.6
Bikoff, J.B.7
Hong, E.J.8
Greenberg, M.E.9
Segal, R.A.10
-
43
-
-
55149088605
-
Requirement of TORC1 for late-phase long-term potentiation in the hippocampus
-
Zhou Y, Wu H, Li S, Chen Q, Cheng XW, Zheng J, Takemori H, Xiong ZQ (2006) Requirement of TORC1 for late-phase long-term potentiation in the hippocampus. PLoS One 1:e16.
-
(2006)
PLoS One
, vol.1
-
-
Zhou, Y.1
Wu, H.2
Li, S.3
Chen, Q.4
Cheng, X.W.5
Zheng, J.6
Takemori, H.7
Xiong, Z.Q.8
|