-
1
-
-
0025767294
-
The predictive value of microcephaly during the first year of life for mental retardation at seven years
-
Dolk H. The predictive value of microcephaly during the first year of life for mental retardation at seven years. Dev Med Child Neurol 1991, 33:974-983.
-
(1991)
Dev Med Child Neurol
, vol.33
, pp. 974-983
-
-
Dolk, H.1
-
2
-
-
78049336905
-
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
-
Bilguvar K, Ozturk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizoglu D, Tuysuz B, Caglayan AO, Gokben S, et al. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature 2010, 467:207-210.
-
(2010)
Nature
, vol.467
, pp. 207-210
-
-
Bilguvar, K.1
Ozturk, A.K.2
Louvi, A.3
Kwan, K.Y.4
Choi, M.5
Tatli, B.6
Yalnizoglu, D.7
Tuysuz, B.8
Caglayan, A.O.9
Gokben, S.10
-
3
-
-
78049332008
-
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture
-
Yu TW, Mochida GH, Tischfield DJ, Sgaier SK, Flores-Sarnat L, Sergi CM, Topcu M, McDonald MT, Barry BJ, Felie JM, et al. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat Genet 2010, 42:1015-1020.
-
(2010)
Nat Genet
, vol.42
, pp. 1015-1020
-
-
Yu, T.W.1
Mochida, G.H.2
Tischfield, D.J.3
Sgaier, S.K.4
Flores-Sarnat, L.5
Sergi, C.M.6
Topcu, M.7
McDonald, M.T.8
Barry, B.J.9
Felie, J.M.10
-
4
-
-
78049336070
-
WDR62 is associated with the spindle pole and is mutated in human microcephaly
-
Nicholas AK, Khurshid M, Desir J, Carvalho OP, Cox JJ, Thornton G, Kausar R, Ansar M, Ahmad W, Verloes A, et al. WDR62 is associated with the spindle pole and is mutated in human microcephaly. Nat Genet 2010, 42:1010-1014.
-
(2010)
Nat Genet
, vol.42
, pp. 1010-1014
-
-
Nicholas, A.K.1
Khurshid, M.2
Desir, J.3
Carvalho, O.P.4
Cox, J.J.5
Thornton, G.6
Kausar, R.7
Ansar, M.8
Ahmad, W.9
Verloes, A.10
-
5
-
-
22144497124
-
Retrospective birth dating of cells in humans
-
Spalding KL, Bhardwaj RD, Buchholz BA, Druid H, Frisen J. Retrospective birth dating of cells in humans. Cell 2005, 122:133-143.
-
(2005)
Cell
, vol.122
, pp. 133-143
-
-
Spalding, K.L.1
Bhardwaj, R.D.2
Buchholz, B.A.3
Druid, H.4
Frisen, J.5
-
6
-
-
33847677187
-
Cellular scaling rules for primate brains
-
Herculano-Houzel S, Collins CE, Wong P, Kaas JH. Cellular scaling rules for primate brains. Proc Natl Acad Sci USA 2007, 104:3562-3567.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 3562-3567
-
-
Herculano-Houzel, S.1
Collins, C.E.2
Wong, P.3
Kaas, J.H.4
-
7
-
-
0037297342
-
The changing number of cells in the human fetal forebrain and its subdivisions: a stereological analysis
-
Samuelsen GB, Larsen KB, Bogdanovic N, Laursen H, Graem N, Larsen JF, Pakkenberg B. The changing number of cells in the human fetal forebrain and its subdivisions: a stereological analysis. Cereb Cortex 2003, 13:115-122.
-
(2003)
Cereb Cortex
, vol.13
, pp. 115-122
-
-
Samuelsen, G.B.1
Larsen, K.B.2
Bogdanovic, N.3
Laursen, H.4
Graem, N.5
Larsen, J.F.6
Pakkenberg, B.7
-
8
-
-
0038324076
-
Developmental and evolutionary adaptations of cortical radial glia
-
Rakic P. Developmental and evolutionary adaptations of cortical radial glia. Cereb Cortex 2003, 13:541-549.
-
(2003)
Cereb Cortex
, vol.13
, pp. 541-549
-
-
Rakic, P.1
-
9
-
-
0035065006
-
Maturation of white matter in the human brain: a review of magnetic resonance studies
-
Paus T, Collins DL, Evans AC, Leonard G, Pike B, Zijdenbos A. Maturation of white matter in the human brain: a review of magnetic resonance studies. Brain Res Bull 2001, 54:255-266.
-
(2001)
Brain Res Bull
, vol.54
, pp. 255-266
-
-
Paus, T.1
Collins, D.L.2
Evans, A.C.3
Leonard, G.4
Pike, B.5
Zijdenbos, A.6
-
10
-
-
0025113285
-
Morphometric study of human cerebral cortex development
-
Huttenlocher PR. Morphometric study of human cerebral cortex development. Neuropsychologia 1990, 28:517-527.
-
(1990)
Neuropsychologia
, vol.28
, pp. 517-527
-
-
Huttenlocher, P.R.1
-
11
-
-
0020036478
-
Fetal head circumference: relation to menstrual age
-
Hadlock FP, Deter RL, Harrist RB, Park SK. Fetal head circumference: relation to menstrual age. AJR Am J Roentgenol 1982, 138:649-653.
-
(1982)
AJR Am J Roentgenol
, vol.138
, pp. 649-653
-
-
Hadlock, F.P.1
Deter, R.L.2
Harrist, R.B.3
Park, S.K.4
-
12
-
-
0023263516
-
Head circumference reference data: birth to 18 years
-
Roche AF, Mukherjee D, Guo SM, Moore WM. Head circumference reference data: birth to 18 years. Pediatrics 1987, 79:706-712.
-
(1987)
Pediatrics
, vol.79
, pp. 706-712
-
-
Roche, A.F.1
Mukherjee, D.2
Guo, S.M.3
Moore, W.M.4
-
13
-
-
0037030677
-
Origin of GABAergic neurons in the human neocortex
-
Letinic K, Zoncu R, Rakic P. Origin of GABAergic neurons in the human neocortex. Nature 2002, 417:645-649.
-
(2002)
Nature
, vol.417
, pp. 645-649
-
-
Letinic, K.1
Zoncu, R.2
Rakic, P.3
-
14
-
-
34347331316
-
Development of cortical GABAergic circuits and its implications for neurodevelopmental disorders
-
Di Cristo G. Development of cortical GABAergic circuits and its implications for neurodevelopmental disorders. Clin Genet 2007, 72:1-8.
-
(2007)
Clin Genet
, vol.72
, pp. 1-8
-
-
Di Cristo, G.1
-
15
-
-
78650041368
-
New insights into cortical interneurons development and classification: contribution of developmental studies
-
Vitalis T, Rossier J. New insights into cortical interneurons development and classification: contribution of developmental studies. Dev Neurobiol 2011, 71:34-44.
-
(2011)
Dev Neurobiol
, vol.71
, pp. 34-44
-
-
Vitalis, T.1
Rossier, J.2
-
16
-
-
79957590028
-
We have got you 'covered': how the meninges control brain development
-
Siegenthaler JA, Pleasure SJ. We have got you 'covered': how the meninges control brain development. Curr Opin Genet Dev 2010, 21:249-255.
-
(2010)
Curr Opin Genet Dev
, vol.21
, pp. 249-255
-
-
Siegenthaler, J.A.1
Pleasure, S.J.2
-
17
-
-
77956487199
-
Building a human cortex: the evolutionary differentiation of Cajal-Retzius cells and the cortical hem
-
Meyer G. Building a human cortex: the evolutionary differentiation of Cajal-Retzius cells and the cortical hem. J Anat 2010, 217:334-343.
-
(2010)
J Anat
, vol.217
, pp. 334-343
-
-
Meyer, G.1
-
18
-
-
0029080470
-
Cleavage orientation and the asymmetric inheritance of Notch1 immunoreactivity in mammalian neurogenesis
-
Chenn A, McConnell SK. Cleavage orientation and the asymmetric inheritance of Notch1 immunoreactivity in mammalian neurogenesis. Cell 1995, 82:631-641.
-
(1995)
Cell
, vol.82
, pp. 631-641
-
-
Chenn, A.1
McConnell, S.K.2
-
19
-
-
0344334400
-
Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse
-
Angevine JB, Jr, Sidman RL. Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature 1961, 192:766-768.
-
(1961)
Nature
, vol.192
, pp. 766-768
-
-
Angevine, J.B.1
Sidman, R.L.2
-
20
-
-
0032493910
-
Reduced apoptosis and cytochrome c-mediated caspase activation in mice lacking caspase 9
-
Kuida K, Haydar TF, Kuan CY, Gu Y, Taya C, Karasuyama H, Su MS, Rakic P, Flavell RA. Reduced apoptosis and cytochrome c-mediated caspase activation in mice lacking caspase 9. Cell 1998, 94:325-337.
-
(1998)
Cell
, vol.94
, pp. 325-337
-
-
Kuida, K.1
Haydar, T.F.2
Kuan, C.Y.3
Gu, Y.4
Taya, C.5
Karasuyama, H.6
Su, M.S.7
Rakic, P.8
Flavell, R.A.9
-
21
-
-
0032493870
-
Differential requirement for caspase 9 in apoptotic pathways in vivo
-
Hakem R, Hakem A, Duncan GS, Henderson JT, Woo M, Soengas MS, Elia A, de la Pompa JL, Kagi D, Khoo W, et al. Differential requirement for caspase 9 in apoptotic pathways in vivo. Cell 1998, 94:339-352.
-
(1998)
Cell
, vol.94
, pp. 339-352
-
-
Hakem, R.1
Hakem, A.2
Duncan, G.S.3
Henderson, J.T.4
Woo, M.5
Soengas, M.S.6
Elia, A.7
de la Pompa, J.L.8
Kagi, D.9
Khoo, W.10
-
22
-
-
0032544449
-
Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development
-
Cecconi F, Alvarez-Bolado G, Meyer BI, Roth KA, Gruss P. Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development. Cell 1998, 94:727-737.
-
(1998)
Cell
, vol.94
, pp. 727-737
-
-
Cecconi, F.1
Alvarez-Bolado, G.2
Meyer, B.I.3
Roth, K.A.4
Gruss, P.5
-
23
-
-
0032544564
-
Apaf1 is required for mitochondrial pathways of apoptosis and brain development
-
Yoshida H, Kong YY, Yoshida R, Elia AJ, Hakem A, Hakem R, Penninger JM, Mak TW. Apaf1 is required for mitochondrial pathways of apoptosis and brain development. Cell 1998, 94:739-750.
-
(1998)
Cell
, vol.94
, pp. 739-750
-
-
Yoshida, H.1
Kong, Y.Y.2
Yoshida, R.3
Elia, A.J.4
Hakem, A.5
Hakem, R.6
Penninger, J.M.7
Mak, T.W.8
-
24
-
-
79959924122
-
Development and evolution of the human neocortex
-
Lui JH, Hansen DV, Kriegstein AR. Development and evolution of the human neocortex. Cell 2011, 146:18-36.
-
(2011)
Cell
, vol.146
, pp. 18-36
-
-
Lui, J.H.1
Hansen, D.V.2
Kriegstein, A.R.3
-
25
-
-
0029095348
-
Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model
-
Caviness VS, Takahashi T, Nowakowski RS. Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model. Trends Neurosci 1995, 18:379-383.
-
(1995)
Trends Neurosci
, vol.18
, pp. 379-383
-
-
Caviness, V.S.1
Takahashi, T.2
Nowakowski, R.S.3
-
26
-
-
0037566738
-
Cell output, cell cycle duration and neuronal specification: a model of integrated mechanisms of the neocortical proliferative process
-
Caviness VS, Goto T, Tarui T, Takahashi T, Bhide PG, Nowakowski RS. Cell output, cell cycle duration and neuronal specification: a model of integrated mechanisms of the neocortical proliferative process. Cereb Cortex 2003, 13:592-598.
-
(2003)
Cereb Cortex
, vol.13
, pp. 592-598
-
-
Caviness, V.S.1
Goto, T.2
Tarui, T.3
Takahashi, T.4
Bhide, P.G.5
Nowakowski, R.S.6
-
27
-
-
1542297728
-
Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis
-
Haubensak W, Attardo A, Denk W, Huttner WB. Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis. Proc Natl Acad Sci USA 2004, 101:3196-3201.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 3196-3201
-
-
Haubensak, W.1
Attardo, A.2
Denk, W.3
Huttner, W.B.4
-
28
-
-
4043142765
-
Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells
-
Miyata T, Kawaguchi A, Saito K, Kawano M, Muto T, Ogawa M. Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells. Development 2004, 131:3133-3145.
-
(2004)
Development
, vol.131
, pp. 3133-3145
-
-
Miyata, T.1
Kawaguchi, A.2
Saito, K.3
Kawano, M.4
Muto, T.5
Ogawa, M.6
-
29
-
-
1642458489
-
Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases
-
Noctor SC, Martinez-Cerdeno V, Ivic L, Kriegstein AR. Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nat Neurosci 2004, 7:136-144.
-
(2004)
Nat Neurosci
, vol.7
, pp. 136-144
-
-
Noctor, S.C.1
Martinez-Cerdeno, V.2
Ivic, L.3
Kriegstein, A.R.4
-
30
-
-
33750375788
-
Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion
-
Kriegstein A, Noctor S, Martinez-Cerdeno V. Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion. Nat Rev Neurosci 2006, 7:883-890.
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 883-890
-
-
Kriegstein, A.1
Noctor, S.2
Martinez-Cerdeno, V.3
-
31
-
-
37149046732
-
Role of intermediate progenitor cells in cerebral cortex development
-
Pontious A, Kowalczyk T, Englund C, Hevner RF. Role of intermediate progenitor cells in cerebral cortex development. Dev Neurosci 2008, 30:24-32.
-
(2008)
Dev Neurosci
, vol.30
, pp. 24-32
-
-
Pontious, A.1
Kowalczyk, T.2
Englund, C.3
Hevner, R.F.4
-
32
-
-
77950076985
-
Neurogenic radial glia in the outer subventricular zone of human neocortex
-
Hansen DV, Lui JH, Parker PR, Kriegstein AR. Neurogenic radial glia in the outer subventricular zone of human neocortex. Nature 2010, 464:554-561.
-
(2010)
Nature
, vol.464
, pp. 554-561
-
-
Hansen, D.V.1
Lui, J.H.2
Parker, P.R.3
Kriegstein, A.R.4
-
33
-
-
79959426933
-
A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex
-
Reillo I, de Juan Romero C, Garcia-Cabezas MA, Borrell V. A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex. Cereb Cortex 2011, 21:1674-1694.
-
(2011)
Cereb Cortex
, vol.21
, pp. 1674-1694
-
-
Reillo, I.1
de Juan Romero, C.2
Garcia-Cabezas, M.A.3
Borrell, V.4
-
34
-
-
79955455586
-
A new subtype of progenitor cell in the mouse embryonic neocortex
-
Wang X, Tsai JW, LaMonica B, Kriegstein AR. A new subtype of progenitor cell in the mouse embryonic neocortex. Nat Neurosci 2011, 14:555-561.
-
(2011)
Nat Neurosci
, vol.14
, pp. 555-561
-
-
Wang, X.1
Tsai, J.W.2
LaMonica, B.3
Kriegstein, A.R.4
-
35
-
-
0036302105
-
Identification of microcephalin, a protein implicated in determining the size of the human brain
-
Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, et al. Identification of microcephalin, a protein implicated in determining the size of the human brain. Am J Hum Genet 2002, 71:136-142.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 136-142
-
-
Jackson, A.P.1
Eastwood, H.2
Bell, S.M.3
Adu, J.4
Toomes, C.5
Carr, I.M.6
Roberts, E.7
Hampshire, D.J.8
Crow, Y.J.9
Mighell, A.J.10
-
36
-
-
0036787796
-
ASPM is a major determinant of cerebral cortical size
-
Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham JM, Springell K, Mahadevan M, Crow YJ, Markham AF, et al. ASPM is a major determinant of cerebral cortical size. Nat Genet 2002, 32:316-320.
-
(2002)
Nat Genet
, vol.32
, pp. 316-320
-
-
Bond, J.1
Roberts, E.2
Mochida, G.H.3
Hampshire, D.J.4
Scott, S.5
Askham, J.M.6
Springell, K.7
Mahadevan, M.8
Crow, Y.J.9
Markham, A.F.10
-
37
-
-
20144386602
-
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
-
Bond J, Roberts E, Springell K, Lizarraga SB, Scott S, Higgins J, Hampshire DJ, Morrison EE, Leal GF, Silva EO, et al. A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nat Genet 2005, 37:353-355.
-
(2005)
Nat Genet
, vol.37
, pp. 353-355
-
-
Bond, J.1
Roberts, E.2
Springell, K.3
Lizarraga, S.B.4
Scott, S.5
Higgins, J.6
Hampshire, D.J.7
Morrison, E.E.8
Leal, G.F.9
Silva, E.O.10
-
38
-
-
62649118818
-
Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly
-
Kumar A, Girimaji SC, Duvvari MR, Blanton SH. Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. Am J Hum Genet 2009, 84:286-290.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 286-290
-
-
Kumar, A.1
Girimaji, S.C.2
Duvvari, M.R.3
Blanton, S.H.4
-
39
-
-
77955068270
-
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4
-
Guernsey DL, Jiang H, Hussin J, Arnold M, Bouyakdan K, Perry S, Babineau-Sturk T, Beis J, Dumas N, Evans SC, et al. Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. Am J Hum Genet 2010, 87:40-51.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 40-51
-
-
Guernsey, D.L.1
Jiang, H.2
Hussin, J.3
Arnold, M.4
Bouyakdan, K.5
Perry, S.6
Babineau-Sturk, T.7
Beis, J.8
Dumas, N.9
Evans, S.C.10
-
40
-
-
80054978334
-
A primary microcephaly protein complex forms a ring around parental centrioles
-
Sir JH, Barr AR, Nicholas AK, Carvalho OP, Khurshid M, Sossick A, Reichelt S, D'Santos C, Woods CG, Gergely F. A primary microcephaly protein complex forms a ring around parental centrioles. Nat Genet 2011.
-
(2011)
Nat Genet
-
-
Sir, J.H.1
Barr, A.R.2
Nicholas, A.K.3
Carvalho, O.P.4
Khurshid, M.5
Sossick, A.6
Reichelt, S.7
D'Santos, C.8
Woods, C.G.9
Gergely, F.10
-
41
-
-
80052424031
-
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly
-
Marchal JA, Ghani M, Schindler D, Gavvovidis I, Winkler T, Esquitino V, Sternberg N, Busche A, Krawitz P, Hecht J, et al. Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly. Cell Cycle 2011, 10:2967-2977.
-
(2011)
Cell Cycle
, vol.10
, pp. 2967-2977
-
-
Marchal, J.A.1
Ghani, M.2
Schindler, D.3
Gavvovidis, I.4
Winkler, T.5
Esquitino, V.6
Sternberg, N.7
Busche, A.8
Krawitz, P.9
Hecht, J.10
-
42
-
-
36549009913
-
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly
-
Kerjan G, Gleeson JG. Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly. Trends Genet 2007, 23:623-630.
-
(2007)
Trends Genet
, vol.23
, pp. 623-630
-
-
Kerjan, G.1
Gleeson, J.G.2
-
43
-
-
79957591321
-
What disorders of cortical development tell us about the cortex: one plus one does not always make two
-
Manzini MC, Walsh CA. What disorders of cortical development tell us about the cortex: one plus one does not always make two. Curr Opin Genet Dev 2011, 21:333-339.
-
(2011)
Curr Opin Genet Dev
, vol.21
, pp. 333-339
-
-
Manzini, M.C.1
Walsh, C.A.2
-
44
-
-
80053553994
-
The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries
-
Nigg EA, Stearns T. The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries. Nat Cell Biol 2011, 13:1154-1160.
-
(2011)
Nat Cell Biol
, vol.13
, pp. 1154-1160
-
-
Nigg, E.A.1
Stearns, T.2
-
45
-
-
70350228242
-
Primary microcephaly: do all roads lead to Rome?
-
Thornton GK, Woods CG. Primary microcephaly: do all roads lead to Rome?. Trends Genet 2009, 25:501-510.
-
(2009)
Trends Genet
, vol.25
, pp. 501-510
-
-
Thornton, G.K.1
Woods, C.G.2
-
46
-
-
38349078475
-
Cep68 and Cep215 (Cdk5rap2) are required for centrosome cohesion
-
Graser S, Stierhof YD, Nigg EA. Cep68 and Cep215 (Cdk5rap2) are required for centrosome cohesion. J Cell Sci 2007, 120:4321-4331.
-
(2007)
J Cell Sci
, vol.120
, pp. 4321-4331
-
-
Graser, S.1
Stierhof, Y.D.2
Nigg, E.A.3
-
48
-
-
76349104200
-
Drosophila Ana2 is a conserved centriole duplication factor
-
Stevens NR, Dobbelaere J, Brunk K, Franz A, Raff JW. Drosophila Ana2 is a conserved centriole duplication factor. J Cell Biol 2010, 188:313-323.
-
(2010)
J Cell Biol
, vol.188
, pp. 313-323
-
-
Stevens, N.R.1
Dobbelaere, J.2
Brunk, K.3
Franz, A.4
Raff, J.W.5
-
49
-
-
79951847409
-
The Stil protein regulates centrosome integrity and mitosis through suppression of Chfr
-
Castiel A, Danieli MM, David A, Moshkovitz S, Aplan PD, Kirsch IR, Brandeis M, Kramer A, Izraeli S. The Stil protein regulates centrosome integrity and mitosis through suppression of Chfr. J Cell Sci 2011, 124:532-539.
-
(2011)
J Cell Sci
, vol.124
, pp. 532-539
-
-
Castiel, A.1
Danieli, M.M.2
David, A.3
Moshkovitz, S.4
Aplan, P.D.5
Kirsch, I.R.6
Brandeis, M.7
Kramer, A.8
Izraeli, S.9
-
50
-
-
78349263512
-
Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome
-
Cizmecioglu O, Arnold M, Bahtz R, Settele F, Ehret L, Haselmann-Weiss U, Antony C, Hoffmann I. Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome. J Cell Biol 2010, 191:731-739.
-
(2010)
J Cell Biol
, vol.191
, pp. 731-739
-
-
Cizmecioglu, O.1
Arnold, M.2
Bahtz, R.3
Settele, F.4
Ehret, L.5
Haselmann-Weiss, U.6
Antony, C.7
Hoffmann, I.8
-
51
-
-
77957982182
-
Asterless is a scaffold for the onset of centriole assembly
-
Dzhindzhev NS, Yu QD, Weiskopf K, Tzolovsky G, Cunha-Ferreira I, Riparbelli M, Rodrigues-Martins A, Bettencourt-Dias M, Callaini G, Glover DM. Asterless is a scaffold for the onset of centriole assembly. Nature 2010, 467:714-718.
-
(2010)
Nature
, vol.467
, pp. 714-718
-
-
Dzhindzhev, N.S.1
Yu, Q.D.2
Weiskopf, K.3
Tzolovsky, G.4
Cunha-Ferreira, I.5
Riparbelli, M.6
Rodrigues-Martins, A.7
Bettencourt-Dias, M.8
Callaini, G.9
Glover, D.M.10
-
52
-
-
78349243322
-
Cep152 interacts with Plk4 and is required for centriole duplication
-
Hatch EM, Kulukian A, Holland AJ, Cleveland DW, Stearns T. Cep152 interacts with Plk4 and is required for centriole duplication. J Cell Biol 2010, 191:721-729.
-
(2010)
J Cell Biol
, vol.191
, pp. 721-729
-
-
Hatch, E.M.1
Kulukian, A.2
Holland, A.J.3
Cleveland, D.W.4
Stearns, T.5
-
53
-
-
67349228738
-
Overly long centrioles and defective cell division upon excess of the SAS-4-related protein CPAP
-
Kohlmaier G, Loncarek J, Meng X, McEwen BF, Mogensen MM, Spektor A, Dynlacht BD, Khodjakov A, Gonczy P. Overly long centrioles and defective cell division upon excess of the SAS-4-related protein CPAP. Curr Biol 2009, 19:1012-1018.
-
(2009)
Curr Biol
, vol.19
, pp. 1012-1018
-
-
Kohlmaier, G.1
Loncarek, J.2
Meng, X.3
McEwen, B.F.4
Mogensen, M.M.5
Spektor, A.6
Dynlacht, B.D.7
Khodjakov, A.8
Gonczy, P.9
-
54
-
-
67349233018
-
Control of centriole length by CPAP and CP110
-
Schmidt TI, Kleylein-Sohn J, Westendorf J, Le Clech M, Lavoie SB, Stierhof YD, Nigg EA. Control of centriole length by CPAP and CP110. Curr Biol 2009, 19:1005-1011.
-
(2009)
Curr Biol
, vol.19
, pp. 1005-1011
-
-
Schmidt, T.I.1
Kleylein-Sohn, J.2
Westendorf, J.3
Le Clech, M.4
Lavoie, S.B.5
Stierhof, Y.D.6
Nigg, E.A.7
-
55
-
-
67349279485
-
CPAP is a cell-cycle regulated protein that controls centriole length
-
Tang CJ, Fu RH, Wu KS, Hsu WB, Tang TK. CPAP is a cell-cycle regulated protein that controls centriole length. Nat Cell Biol 2009, 11:825-831.
-
(2009)
Nat Cell Biol
, vol.11
, pp. 825-831
-
-
Tang, C.J.1
Fu, R.H.2
Wu, K.S.3
Hsu, W.B.4
Tang, T.K.5
-
56
-
-
33745883798
-
Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
-
Fish JL, Kosodo Y, Enard W, Paabo S, Huttner WB. Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells. Proc Natl Acad Sci USA 2006, 103:10438-10443.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 10438-10443
-
-
Fish, J.L.1
Kosodo, Y.2
Enard, W.3
Paabo, S.4
Huttner, W.B.5
-
57
-
-
61849114654
-
NuMA-related LIN-5, ASPM-1, calmodulin and dynein promote meiotic spindle rotation independently of cortical LIN-5/GPR/Galpha
-
van der Voet M, Berends CW, Perreault A, Nguyen-Ngoc T, Gonczy P, Vidal M, Boxem M, van den Heuvel S. NuMA-related LIN-5, ASPM-1, calmodulin and dynein promote meiotic spindle rotation independently of cortical LIN-5/GPR/Galpha. Nat Cell Biol 2009, 11:269-277.
-
(2009)
Nat Cell Biol
, vol.11
, pp. 269-277
-
-
van der Voet, M.1
Berends, C.W.2
Perreault, A.3
Nguyen-Ngoc, T.4
Gonczy, P.5
Vidal, M.6
Boxem, M.7
van den Heuvel, S.8
-
58
-
-
77952201222
-
Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors
-
Lizarraga SB, Margossian SP, Harris MH, Campagna DR, Han AP, Blevins S, Mudbhary R, Barker JE, Walsh CA, Fleming MD. Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors. Development 2010, 137:1907-1917.
-
(2010)
Development
, vol.137
, pp. 1907-1917
-
-
Lizarraga, S.B.1
Margossian, S.P.2
Harris, M.H.3
Campagna, D.R.4
Han, A.P.5
Blevins, S.6
Mudbhary, R.7
Barker, J.E.8
Walsh, C.A.9
Fleming, M.D.10
-
59
-
-
5144222593
-
Mitotic spindle regulation by Nde1 controls cerebral cortical size
-
Feng Y, Walsh CA. Mitotic spindle regulation by Nde1 controls cerebral cortical size. Neuron 2004, 44:279-293.
-
(2004)
Neuron
, vol.44
, pp. 279-293
-
-
Feng, Y.1
Walsh, C.A.2
-
60
-
-
0035818519
-
Chromosomal variation in neurons of the developing and adult mammalian nervous system
-
Rehen SK, McConnell MJ, Kaushal D, Kingsbury MA, Yang AH, Chun J. Chromosomal variation in neurons of the developing and adult mammalian nervous system. Proc Natl Acad Sci USA 2001, 98:13361-13366.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 13361-13366
-
-
Rehen, S.K.1
McConnell, M.J.2
Kaushal, D.3
Kingsbury, M.A.4
Yang, A.H.5
Chun, J.6
-
61
-
-
0038045576
-
Alteration of gene expression by chromosome loss in the postnatal mouse brain
-
Kaushal D, Contos JJ, Treuner K, Yang AH, Kingsbury MA, Rehen SK, McConnell MJ, Okabe M, Barlow C, Chun J. Alteration of gene expression by chromosome loss in the postnatal mouse brain. J Neurosci 2003, 23:5599-5606.
-
(2003)
J Neurosci
, vol.23
, pp. 5599-5606
-
-
Kaushal, D.1
Contos, J.J.2
Treuner, K.3
Yang, A.H.4
Kingsbury, M.A.5
Rehen, S.K.6
McConnell, M.J.7
Okabe, M.8
Barlow, C.9
Chun, J.10
-
62
-
-
0344392982
-
Chromosome segregation defects contribute to aneuploidy in normal neural progenitor cells
-
Yang AH, Kaushal D, Rehen SK, Kriedt K, Kingsbury MA, McConnell MJ, Chun J. Chromosome segregation defects contribute to aneuploidy in normal neural progenitor cells. J Neurosci 2003, 23:10454-10462.
-
(2003)
J Neurosci
, vol.23
, pp. 10454-10462
-
-
Yang, A.H.1
Kaushal, D.2
Rehen, S.K.3
Kriedt, K.4
Kingsbury, M.A.5
McConnell, M.J.6
Chun, J.7
-
63
-
-
0027486966
-
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13
-
Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. JAMA 1993, 270:2838-2842.
-
(1993)
JAMA
, vol.270
, pp. 2838-2842
-
-
Dobyns, W.B.1
Reiner, O.2
Carrozzo, R.3
Ledbetter, D.H.4
-
64
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
-
des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrie A, Gelot A, Dupuis E, Motte J, Berwald-Netter Y, et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 1998, 92:51-61.
-
(1998)
Cell
, vol.92
, pp. 51-61
-
-
des Portes, V.1
Pinard, J.M.2
Billuart, P.3
Vinet, M.C.4
Koulakoff, A.5
Carrie, A.6
Gelot, A.7
Dupuis, E.8
Motte, J.9
Berwald-Netter, Y.10
-
65
-
-
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, et al. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 1998, 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
-
66
-
-
0031829069
-
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects
-
Sossey-Alaoui K, Hartung AJ, Guerrini R, Manchester DK, Posar A, Puche-Mira A, Andermann E, Dobyns WB, Srivastava AK. Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects. Hum Mol Genet 1998, 7:1327-1332.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1327-1332
-
-
Sossey-Alaoui, K.1
Hartung, A.J.2
Guerrini, R.3
Manchester, D.K.4
Posar, A.5
Puche-Mira, A.6
Andermann, E.7
Dobyns, W.B.8
Srivastava, A.K.9
-
67
-
-
0342906570
-
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
-
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat Genet 2000, 26:93-96.
-
(2000)
Nat Genet
, vol.26
, pp. 93-96
-
-
Hong, S.E.1
Shugart, Y.Y.2
Huang, D.T.3
Shahwan, S.A.4
Grant, P.E.5
Hourihane, J.O.6
Martin, N.D.7
Walsh, C.A.8
-
68
-
-
33846037932
-
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans
-
Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, Oliver PL, Fray M, Harvey RJ, Molnar Z, et al. Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell 2007, 128:45-57.
-
(2007)
Cell
, vol.128
, pp. 45-57
-
-
Keays, D.A.1
Tian, G.2
Poirier, K.3
Huang, G.J.4
Siebold, C.5
Cleak, J.6
Oliver, P.L.7
Fray, M.8
Harvey, R.J.9
Molnar, Z.10
-
69
-
-
79955824315
-
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]
-
Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, et al. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]. Am J Hum Genet 2011, 88:536-547.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 536-547
-
-
Alkuraya, F.S.1
Cai, X.2
Emery, C.3
Mochida, G.H.4
Al-Dosari, M.S.5
Felie, J.M.6
Hill, R.S.7
Barry, B.J.8
Partlow, J.N.9
Gascon, G.G.10
-
70
-
-
79955789917
-
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis
-
Bakircioglu M, Carvalho OP, Khurshid M, Cox JJ, Tuysuz B, Barak T, Yilmaz S, Caglayan O, Dincer A, Nicholas AK, et al. The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis. Am J Hum Genet 2011, 88:523-535.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 523-535
-
-
Bakircioglu, M.1
Carvalho, O.P.2
Khurshid, M.3
Cox, J.J.4
Tuysuz, B.5
Barak, T.6
Yilmaz, S.7
Caglayan, O.8
Dincer, A.9
Nicholas, A.K.10
-
71
-
-
38849091345
-
Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division
-
Yingling J, Youn YH, Darling D, Toyo-Oka K, Pramparo T, Hirotsune S, Wynshaw-Boris A. Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division. Cell 2008, 132:474-486.
-
(2008)
Cell
, vol.132
, pp. 474-486
-
-
Yingling, J.1
Youn, Y.H.2
Darling, D.3
Toyo-Oka, K.4
Pramparo, T.5
Hirotsune, S.6
Wynshaw-Boris, A.7
-
72
-
-
38649092988
-
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
-
Griffith E, Walker S, Martin CA, Vagnarelli P, Stiff T, Vernay B, Al Sanna N, Saggar A, Hamel B, Earnshaw WC, et al. Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling. Nat Genet 2008, 40:232-236.
-
(2008)
Nat Genet
, vol.40
, pp. 232-236
-
-
Griffith, E.1
Walker, S.2
Martin, C.A.3
Vagnarelli, P.4
Stiff, T.5
Vernay, B.6
Al Sanna, N.7
Saggar, A.8
Hamel, B.9
Earnshaw, W.C.10
-
73
-
-
0345073699
-
A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome
-
O'driscoll M, Ruiz-Perez V, Woods C, Jeggo P, Goodship J. A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome. Nat Genet 2003, 33:497-501.
-
(2003)
Nat Genet
, vol.33
, pp. 497-501
-
-
O'driscoll, M.1
Ruiz-Perez, V.2
Woods, C.3
Jeggo, P.4
Goodship, J.5
-
74
-
-
78651248502
-
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
-
Kalay E, Yigit G, Aslan Y, Brown KE, Pohl E, Bicknell LS, Kayserili H, Li Y, Tuysuz B, Nurnberg G, et al. CEP152 is a genome maintenance protein disrupted in Seckel syndrome. Nat Genet 2011, 43:23-26.
-
(2011)
Nat Genet
, vol.43
, pp. 23-26
-
-
Kalay, E.1
Yigit, G.2
Aslan, Y.3
Brown, K.E.4
Pohl, E.5
Bicknell, L.S.6
Kayserili, H.7
Li, Y.8
Tuysuz, B.9
Nurnberg, G.10
-
76
-
-
37749022460
-
Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis
-
Konno D, Shioi G, Shitamukai A, Mori A, Kiyonari H, Miyata T, Matsuzaki F. Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis. Nat Cell Biol 2008, 10:93-101.
-
(2008)
Nat Cell Biol
, vol.10
, pp. 93-101
-
-
Konno, D.1
Shioi, G.2
Shitamukai, A.3
Mori, A.4
Kiyonari, H.5
Miyata, T.6
Matsuzaki, F.7
-
77
-
-
79960207659
-
Mitotic spindle orientation in asymmetric and symmetric cell divisions during animal development
-
Morin X, Bellaiche Y. Mitotic spindle orientation in asymmetric and symmetric cell divisions during animal development. Dev Cell 2011, 21:102-119.
-
(2011)
Dev Cell
, vol.21
, pp. 102-119
-
-
Morin, X.1
Bellaiche, Y.2
-
78
-
-
38849199164
-
Par-complex proteins promote proliferative progenitor divisions in the developing mouse cerebral cortex
-
Costa MR, Wen G, Lepier A, Schroeder T, Gotz M. Par-complex proteins promote proliferative progenitor divisions in the developing mouse cerebral cortex. Development 2008, 135:11-22.
-
(2008)
Development
, vol.135
, pp. 11-22
-
-
Costa, M.R.1
Wen, G.2
Lepier, A.3
Schroeder, T.4
Gotz, M.5
-
79
-
-
67650898238
-
Mammalian Par3 regulates progenitor cell asymmetric division via notch signaling in the developing neocortex
-
Bultje RS, Castaneda-Castellanos DR, Jan LY, Jan YN, Kriegstein AR, Shi SH. Mammalian Par3 regulates progenitor cell asymmetric division via notch signaling in the developing neocortex. Neuron 2009, 63:189-202.
-
(2009)
Neuron
, vol.63
, pp. 189-202
-
-
Bultje, R.S.1
Castaneda-Castellanos, D.R.2
Jan, L.Y.3
Jan, Y.N.4
Kriegstein, A.R.5
Shi, S.H.6
-
80
-
-
0037135177
-
Regulation of cerebral cortical size by control of cell cycle exit in neural precursors
-
Chenn A, Walsh CA. Regulation of cerebral cortical size by control of cell cycle exit in neural precursors. Science 2002, 297:365-369.
-
(2002)
Science
, vol.297
, pp. 365-369
-
-
Chenn, A.1
Walsh, C.A.2
-
81
-
-
77951897491
-
The apical complex couples cell fate and cell survival to cerebral cortical development
-
Kim S, Lehtinen MK, Sessa A, Zappaterra MW, Cho SH, Gonzalez D, Boggan B, Austin CA, Wijnholds J, Gambello MJ, et al. The apical complex couples cell fate and cell survival to cerebral cortical development. Neuron 2010, 66:69-84.
-
(2010)
Neuron
, vol.66
, pp. 69-84
-
-
Kim, S.1
Lehtinen, M.K.2
Sessa, A.3
Zappaterra, M.W.4
Cho, S.H.5
Gonzalez, D.6
Boggan, B.7
Austin, C.A.8
Wijnholds, J.9
Gambello, M.J.10
-
82
-
-
0030200217
-
Asymmetric localization of a mammalian numb homolog during mouse cortical neurogenesis
-
Zhong W, Feder JN, Jiang MM, Jan LY, Jan YN. Asymmetric localization of a mammalian numb homolog during mouse cortical neurogenesis. Neuron 1996, 17:43-53.
-
(1996)
Neuron
, vol.17
, pp. 43-53
-
-
Zhong, W.1
Feder, J.N.2
Jiang, M.M.3
Jan, L.Y.4
Jan, Y.N.5
-
83
-
-
0037418320
-
Mitotic spindle rotation and mode of cell division in the developing telencephalon
-
Haydar TF, Ang E, Jr, Rakic P. Mitotic spindle rotation and mode of cell division in the developing telencephalon. Proc Natl Acad Sci USA 2003, 100:2890-2895.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 2890-2895
-
-
Haydar, T.F.1
Ang, E.2
Rakic, P.3
-
84
-
-
0033136704
-
NUMB localizes in the basal cortex of mitotic avian neuroepithelial cells and modulates neuronal differentiation by binding to NOTCH-1
-
Wakamatsu Y, Maynard TM, Jones SU, Weston JA. NUMB localizes in the basal cortex of mitotic avian neuroepithelial cells and modulates neuronal differentiation by binding to NOTCH-1. Neuron 1999, 23:71-81.
-
(1999)
Neuron
, vol.23
, pp. 71-81
-
-
Wakamatsu, Y.1
Maynard, T.M.2
Jones, S.U.3
Weston, J.A.4
-
85
-
-
42149188826
-
Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis
-
Noctor SC, Martinez-Cerdeno V, Kriegstein AR. Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis. J Comp Neurol 2008, 508:28-44.
-
(2008)
J Comp Neurol
, vol.508
, pp. 28-44
-
-
Noctor, S.C.1
Martinez-Cerdeno, V.2
Kriegstein, A.R.3
-
86
-
-
3042541528
-
Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells
-
Kosodo Y, Roper K, Haubensak W, Marzesco AM, Corbeil D, Huttner WB. Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells. EMBO J 2004, 23:2314-2324.
-
(2004)
EMBO J
, vol.23
, pp. 2314-2324
-
-
Kosodo, Y.1
Roper, K.2
Haubensak, W.3
Marzesco, A.M.4
Corbeil, D.5
Huttner, W.B.6
-
87
-
-
35548951453
-
Control of planar divisions by the G-protein regulator LGN maintains progenitors in the chick neuroepithelium
-
Morin X, Jaouen F, Durbec P. Control of planar divisions by the G-protein regulator LGN maintains progenitors in the chick neuroepithelium. Nat Neurosci 2007, 10:1440-1448.
-
(2007)
Nat Neurosci
, vol.10
, pp. 1440-1448
-
-
Morin, X.1
Jaouen, F.2
Durbec, P.3
-
88
-
-
80054841867
-
Mouse inscuteable induces apical-basal spindle orientation to facilitate intermediate progenitor generation in the developing neocortex
-
Postiglione MP, Juschke C, Xie Y, Haas GA, Charalambous C, Knoblich JA. Mouse inscuteable induces apical-basal spindle orientation to facilitate intermediate progenitor generation in the developing neocortex. Neuron 2011, 72:268-284.
-
(2011)
Neuron
, vol.72
, pp. 268-284
-
-
Postiglione, M.P.1
Juschke, C.2
Xie, Y.3
Haas, G.A.4
Charalambous, C.5
Knoblich, J.A.6
-
89
-
-
0034678396
-
The respective contributions of the mother and daughter centrioles to centrosome activity and behavior in vertebrate cells
-
Piel M, Meyer P, Khodjakov A, Rieder CL, Bornens M. The respective contributions of the mother and daughter centrioles to centrosome activity and behavior in vertebrate cells. J Cell Biol 2000, 149:317-330.
-
(2000)
J Cell Biol
, vol.149
, pp. 317-330
-
-
Piel, M.1
Meyer, P.2
Khodjakov, A.3
Rieder, C.L.4
Bornens, M.5
-
90
-
-
0036468420
-
Centrosome composition and microtubule anchoring mechanisms
-
Bornens M. Centrosome composition and microtubule anchoring mechanisms. Curr Opin Cell Biol 2002, 14:25-34.
-
(2002)
Curr Opin Cell Biol
, vol.14
, pp. 25-34
-
-
Bornens, M.1
-
91
-
-
70350061953
-
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
-
Wang X, Tsai JW, Imai JH, Lian WN, Vallee RB, Shi SH. Asymmetric centrosome inheritance maintains neural progenitors in the neocortex. Nature 2009, 461:947-955.
-
(2009)
Nature
, vol.461
, pp. 947-955
-
-
Wang, X.1
Tsai, J.W.2
Imai, J.H.3
Lian, W.N.4
Vallee, R.B.5
Shi, S.H.6
-
92
-
-
69949142444
-
Centriole age underlies asynchronous primary cilium growth in mammalian cells
-
Anderson CT, Stearns T. Centriole age underlies asynchronous primary cilium growth in mammalian cells. Curr Biol 2009, 19:1498-1502.
-
(2009)
Curr Biol
, vol.19
, pp. 1498-1502
-
-
Anderson, C.T.1
Stearns, T.2
-
93
-
-
35548974826
-
Cep164, a novel centriole appendage protein required for primary cilium formation
-
Graser S, Stierhof YD, Lavoie SB, Gassner OS, Lamla S, Le Clech M, Nigg EA. Cep164, a novel centriole appendage protein required for primary cilium formation. J Cell Biol 2007, 179:321-330.
-
(2007)
J Cell Biol
, vol.179
, pp. 321-330
-
-
Graser, S.1
Stierhof, Y.D.2
Lavoie, S.B.3
Gassner, O.S.4
Lamla, S.5
Le Clech, M.6
Nigg, E.A.7
-
94
-
-
58249087390
-
New regulators of Wnt/beta-catenin signaling revealed by integrative molecular screening
-
Major MB, Roberts BS, Berndt JD, Marine S, Anastas J, Chung N, Ferrer M, Yi X, Stoick-Cooper CL, von Haller PD, et al. New regulators of Wnt/beta-catenin signaling revealed by integrative molecular screening. Sci Signal 2008, 1:ra12.
-
(2008)
Sci Signal
, vol.1
-
-
Major, M.B.1
Roberts, B.S.2
Berndt, J.D.3
Marine, S.4
Anastas, J.5
Chung, N.6
Ferrer, M.7
Yi, X.8
Stoick-Cooper, C.L.9
von Haller, P.D.10
-
95
-
-
80053021310
-
ASPM regulates Wnt signaling pathway activity in the developing brain
-
Buchman JJ, Durak O, Tsai LH. ASPM regulates Wnt signaling pathway activity in the developing brain. Genes Dev 2011, 25:1909-1914.
-
(2011)
Genes Dev
, vol.25
, pp. 1909-1914
-
-
Buchman, J.J.1
Durak, O.2
Tsai, L.H.3
-
96
-
-
0001003110
-
XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos
-
Molenaar M, van de Wetering M, Oosterwegel M, Peterson-Maduro J, Godsave S, Korinek V, Roose J, Destree O, Clevers H. XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos. Cell 1996, 86:391-399.
-
(1996)
Cell
, vol.86
, pp. 391-399
-
-
Molenaar, M.1
van de Wetering, M.2
Oosterwegel, M.3
Peterson-Maduro, J.4
Godsave, S.5
Korinek, V.6
Roose, J.7
Destree, O.8
Clevers, H.9
-
97
-
-
0030999806
-
Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF
-
van de Wetering M, Cavallo R, Dooijes D, van Beest M, van Es J, Loureiro J, Ypma A, Hursh D, Jones T, Bejsovec A, et al. Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF. Cell 1997, 88:789-799.
-
(1997)
Cell
, vol.88
, pp. 789-799
-
-
van de Wetering, M.1
Cavallo, R.2
Dooijes, D.3
van Beest, M.4
van Es, J.5
Loureiro, J.6
Ypma, A.7
Hursh, D.8
Jones, T.9
Bejsovec, A.10
-
98
-
-
79953047750
-
Cilia in the nervous system: linking cilia function and neurodevelopmental disorders
-
Lee JE, Gleeson JG. Cilia in the nervous system: linking cilia function and neurodevelopmental disorders. Curr Opin Neurol 2011, 24:98-105.
-
(2011)
Curr Opin Neurol
, vol.24
, pp. 98-105
-
-
Lee, J.E.1
Gleeson, J.G.2
-
99
-
-
79551587194
-
Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia
-
Wallingford JB, Mitchell B. Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia. Genes Dev 2011, 25:201-213.
-
(2011)
Genes Dev
, vol.25
, pp. 201-213
-
-
Wallingford, J.B.1
Mitchell, B.2
-
101
-
-
84864584531
-
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
-
Chaki M, et al. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell 2012, 150:533-548.
-
(2012)
Cell
, vol.150
, pp. 533-548
-
-
Chaki, M.1
-
102
-
-
0028168856
-
A codon-based model of nucleotide substitution for protein-coding DNA sequences
-
Goldman N, Yang Z. A codon-based model of nucleotide substitution for protein-coding DNA sequences. Mol Biol Evol 1994, 11:725-736.
-
(1994)
Mol Biol Evol
, vol.11
, pp. 725-736
-
-
Goldman, N.1
Yang, Z.2
-
103
-
-
0347992009
-
Evolution of the human ASPM gene, a major determinant of brain size
-
Zhang J. Evolution of the human ASPM gene, a major determinant of brain size. Genetics 2003, 165:2063-2070.
-
(2003)
Genetics
, vol.165
, pp. 2063-2070
-
-
Zhang, J.1
-
104
-
-
1542329549
-
Adaptive evolution of ASPM, a major determinant of cerebral cortical size in humans
-
Evans PD, Anderson JR, Vallender EJ, Gilbert SL, Malcom CM, Dorus S, Lahn BT. Adaptive evolution of ASPM, a major determinant of cerebral cortical size in humans. Hum Mol Genet 2004, 13:489-494.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 489-494
-
-
Evans, P.D.1
Anderson, J.R.2
Vallender, E.J.3
Gilbert, S.L.4
Malcom, C.M.5
Dorus, S.6
Lahn, B.T.7
-
105
-
-
19344374302
-
Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion
-
Kouprina N, Pavlicek A, Mochida GH, Solomon G, Gersch W, Yoon YH, Collura R, Ruvolo M, Barrett JC, Woods CG, et al. Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion. PLoS Biol 2004, 2:E126.
-
(2004)
PLoS Biol
, vol.2
-
-
Kouprina, N.1
Pavlicek, A.2
Mochida, G.H.3
Solomon, G.4
Gersch, W.5
Yoon, Y.H.6
Collura, R.7
Ruvolo, M.8
Barrett, J.C.9
Woods, C.G.10
-
106
-
-
2942744749
-
Reconstructing the evolutionary history of microcephalin, a gene controlling human brain size
-
Evans PD, Anderson JR, Vallender EJ, Choi SS, Lahn BT. Reconstructing the evolutionary history of microcephalin, a gene controlling human brain size. Hum Mol Genet 2004, 13:1139-1145.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1139-1145
-
-
Evans, P.D.1
Anderson, J.R.2
Vallender, E.J.3
Choi, S.S.4
Lahn, B.T.5
-
107
-
-
2942737273
-
Molecular evolution of microcephalin, a gene determining human brain size
-
Wang YQ, Su B. Molecular evolution of microcephalin, a gene determining human brain size. Hum Mol Genet 2004, 13:1131-1137.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1131-1137
-
-
Wang, Y.Q.1
Su, B.2
-
108
-
-
33744513368
-
Molecular evolution of the brain size regulator genes CDK5RAP2 and CENPJ
-
Evans PD, Vallender EJ, Lahn BT. Molecular evolution of the brain size regulator genes CDK5RAP2 and CENPJ. Gene 2006, 375:75-79.
-
(2006)
Gene
, vol.375
, pp. 75-79
-
-
Evans, P.D.1
Vallender, E.J.2
Lahn, B.T.3
-
109
-
-
54149093564
-
Positive selection in ASPM is correlated with cerebral cortex evolution across primates but not with whole-brain size
-
Ali F, Meier R. Positive selection in ASPM is correlated with cerebral cortex evolution across primates but not with whole-brain size. Mol Biol Evol 2008, 25:2247-2250.
-
(2008)
Mol Biol Evol
, vol.25
, pp. 2247-2250
-
-
Ali, F.1
Meier, R.2
-
110
-
-
24344501297
-
Molecular insights into human brain evolution
-
Hill RS, Walsh CA. Molecular insights into human brain evolution. Nature 2005, 437:64-67.
-
(2005)
Nature
, vol.437
, pp. 64-67
-
-
Hill, R.S.1
Walsh, C.A.2
-
112
-
-
0037158715
-
Molecular evolution of FOXP2, a gene involved in speech and language
-
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Paabo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 2002, 418:869-872.
-
(2002)
Nature
, vol.418
, pp. 869-872
-
-
Enard, W.1
Przeworski, M.2
Fisher, S.E.3
Lai, C.S.4
Wiebe, V.5
Kitano, T.6
Monaco, A.P.7
Paabo, S.8
-
113
-
-
6944242766
-
Birth and adaptive evolution of a hominoid gene that supports high neurotransmitter flux
-
Burki F, Kaessmann H. Birth and adaptive evolution of a hominoid gene that supports high neurotransmitter flux. Nat Genet 2004, 36:1061-1063.
-
(2004)
Nat Genet
, vol.36
, pp. 1061-1063
-
-
Burki, F.1
Kaessmann, H.2
-
114
-
-
4444311117
-
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome
-
Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, et al. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nat Genet 2004, 36:1008-1013.
-
(2004)
Nat Genet
, vol.36
, pp. 1008-1013
-
-
Ferland, R.J.1
Eyaid, W.2
Collura, R.V.3
Tully, L.D.4
Hill, R.S.5
Al-Nouri, D.6
Al-Rumayyan, A.7
Topcu, M.8
Gascon, G.9
Bodell, A.10
-
115
-
-
22144441718
-
Accelerated evolution of the pituitary adenylate cyclase-activating polypeptide precursor gene during human origin
-
Wang YQ, Qian YP, Yang S, Shi H, Liao CH, Zheng HK, Wang J, Lin AA, Cavalli-Sforza LL, Underhill PA, et al. Accelerated evolution of the pituitary adenylate cyclase-activating polypeptide precursor gene during human origin. Genetics 2005, 170:801-806.
-
(2005)
Genetics
, vol.170
, pp. 801-806
-
-
Wang, Y.Q.1
Qian, Y.P.2
Yang, S.3
Shi, H.4
Liao, C.H.5
Zheng, H.K.6
Wang, J.7
Lin, A.A.8
Cavalli-Sforza, L.L.9
Underhill, P.A.10
-
116
-
-
33745268919
-
Sonic Hedgehog, a key development gene, experienced intensified molecular evolution in primates
-
Dorus S, Anderson JR, Vallender EJ, Gilbert SL, Zhang L, Chemnick LG, Ryder OA, Li W, Lahn BT. Sonic Hedgehog, a key development gene, experienced intensified molecular evolution in primates. Hum Mol Genet 2006, 15:2031-2037.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2031-2037
-
-
Dorus, S.1
Anderson, J.R.2
Vallender, E.J.3
Gilbert, S.L.4
Zhang, L.5
Chemnick, L.G.6
Ryder, O.A.7
Li, W.8
Lahn, B.T.9
-
117
-
-
33749551431
-
A primate-specific acceleration in the evolution of the caspase-dependent apoptosis pathway
-
Vallender EJ, Lahn BT. A primate-specific acceleration in the evolution of the caspase-dependent apoptosis pathway. Hum Mol Genet 2006, 15:3034-3040.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3034-3040
-
-
Vallender, E.J.1
Lahn, B.T.2
-
118
-
-
33750207992
-
Did brain-specific genes evolve faster in humans than in chimpanzees?
-
Shi P, Bakewell MA, Zhang J. Did brain-specific genes evolve faster in humans than in chimpanzees?. Trends Genet 2006, 22:608-613.
-
(2006)
Trends Genet
, vol.22
, pp. 608-613
-
-
Shi, P.1
Bakewell, M.A.2
Zhang, J.3
-
119
-
-
33846984255
-
Rate of evolution in brain-expressed genes in humans and other primates
-
Wang HY, Chien HC, Osada N, Hashimoto K, Sugano S, Gojobori T, Chou CK, Tsai SF, Wu CI, Shen CK. Rate of evolution in brain-expressed genes in humans and other primates. PLoS Biol 2007, 5:e13.
-
(2007)
PLoS Biol
, vol.5
-
-
Wang, H.Y.1
Chien, H.C.2
Osada, N.3
Hashimoto, K.4
Sugano, S.5
Gojobori, T.6
Chou, C.K.7
Tsai, S.F.8
Wu, C.I.9
Shen, C.K.10
-
120
-
-
42449158086
-
A common SNP of MCPH1 is associated with cranial volume variation in Chinese population
-
Wang JK, Li Y, Su B. A common SNP of MCPH1 is associated with cranial volume variation in Chinese population. Hum Mol Genet 2008, 17:1329-1335.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1329-1335
-
-
Wang, J.K.1
Li, Y.2
Su, B.3
-
121
-
-
76249096218
-
Sex-dependent association of common variants of microcephaly genes with brain structure
-
Rimol LM, Agartz I, Djurovic S, Brown AA, Roddey JC, Kahler AK, Mattingsdal M, Athanasiu L, Joyner AH, Schork NJ, et al. Sex-dependent association of common variants of microcephaly genes with brain structure. Proc Natl Acad Sci USA 2010, 107:384-388.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 384-388
-
-
Rimol, L.M.1
Agartz, I.2
Djurovic, S.3
Brown, A.A.4
Roddey, J.C.5
Kahler, A.K.6
Mattingsdal, M.7
Athanasiu, L.8
Joyner, A.H.9
Schork, N.J.10
-
122
-
-
84861526824
-
Checkpoint control and cancer
-
Medema RH, Macurek L. Checkpoint control and cancer. Oncogene 2012, 31:2601-2613.
-
(2012)
Oncogene
, vol.31
, pp. 2601-2613
-
-
Medema, R.H.1
Macurek, L.2
-
124
-
-
80053364894
-
Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations
-
Janssen A, van der Burg M, Szuhai K, Kops GJ, Medema RH. Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations. Science 2011, 333:1895-1898.
-
(2011)
Science
, vol.333
, pp. 1895-1898
-
-
Janssen, A.1
van der Burg, M.2
Szuhai, K.3
Kops, G.J.4
Medema, R.H.5
-
125
-
-
77953289301
-
New insights into p53 activation
-
Brooks CL, Gu W. New insights into p53 activation. Cell Res 2010, 20:614-621.
-
(2010)
Cell Res
, vol.20
, pp. 614-621
-
-
Brooks, C.L.1
Gu, W.2
-
126
-
-
0032511976
-
Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV
-
Frank KM, Sekiguchi JM, Seidl KJ, Swat W, Rathbun GA, Cheng HL, Davidson L, Kangaloo L, Alt FW. Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV. Nature 1998, 396:173-177.
-
(1998)
Nature
, vol.396
, pp. 173-177
-
-
Frank, K.M.1
Sekiguchi, J.M.2
Seidl, K.J.3
Swat, W.4
Rathbun, G.A.5
Cheng, H.L.6
Davidson, L.7
Kangaloo, L.8
Alt, F.W.9
-
127
-
-
0032585526
-
Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice
-
Barnes DE, Stamp G, Rosewell I, Denzel A, Lindahl T. Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice. Curr Biol 1998, 8:1395-1398.
-
(1998)
Curr Biol
, vol.8
, pp. 1395-1398
-
-
Barnes, D.E.1
Stamp, G.2
Rosewell, I.3
Denzel, A.4
Lindahl, T.5
-
128
-
-
0032417640
-
A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis
-
Gao Y, Sun Y, Frank KM, Dikkes P, Fujiwara Y, Seidl KJ, Sekiguchi JM, Rathbun GA, Swat W, Wang J, et al. A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis. Cell 1998, 95:891-902.
-
(1998)
Cell
, vol.95
, pp. 891-902
-
-
Gao, Y.1
Sun, Y.2
Frank, K.M.3
Dikkes, P.4
Fujiwara, Y.5
Seidl, K.J.6
Sekiguchi, J.M.7
Rathbun, G.A.8
Swat, W.9
Wang, J.10
-
129
-
-
0034646304
-
Defective embryonic neurogenesis in Ku-deficient but not DNA-dependent protein kinase catalytic subunit-deficient mice
-
Gu Y, Sekiguchi J, Gao Y, Dikkes P, Frank K, Ferguson D, Hasty P, Chun J, Alt FW. Defective embryonic neurogenesis in Ku-deficient but not DNA-dependent protein kinase catalytic subunit-deficient mice. Proc Natl Acad Sci USA 2000, 97:2668-2673.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 2668-2673
-
-
Gu, Y.1
Sekiguchi, J.2
Gao, Y.3
Dikkes, P.4
Frank, K.5
Ferguson, D.6
Hasty, P.7
Chun, J.8
Alt, F.W.9
-
130
-
-
0035072744
-
Elevated DNA double strand breaks and apoptosis in the CNS of scid mutant mice
-
Vemuri MC, Schiller E, Naegele JR. Elevated DNA double strand breaks and apoptosis in the CNS of scid mutant mice. Cell Death Differ 2001, 8:245-255.
-
(2001)
Cell Death Differ
, vol.8
, pp. 245-255
-
-
Vemuri, M.C.1
Schiller, E.2
Naegele, J.R.3
-
131
-
-
0036210178
-
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive condition
-
Neitzel H, Neumann LM, Schindler D, Wirges A, Tonnies H, Trimborn M, Krebsova A, Richter R, Sperling K. Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive condition. Am J Hum Genet 2002, 70:1015-1022.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1015-1022
-
-
Neitzel, H.1
Neumann, L.M.2
Schindler, D.3
Wirges, A.4
Tonnies, H.5
Trimborn, M.6
Krebsova, A.7
Richter, R.8
Sperling, K.9
-
132
-
-
3242657086
-
Mutations in microcephalin cause aberrant regulation of chromosome condensation
-
Trimborn M, Bell SM, Felix C, Rashid Y, Jafri H, Griffiths PD, Neumann LM, Krebs A, Reis A, Sperling K, et al. Mutations in microcephalin cause aberrant regulation of chromosome condensation. Am J Hum Genet 2004, 75:261-266.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 261-266
-
-
Trimborn, M.1
Bell, S.M.2
Felix, C.3
Rashid, Y.4
Jafri, H.5
Griffiths, P.D.6
Neumann, L.M.7
Krebs, A.8
Reis, A.9
Sperling, K.10
-
133
-
-
27244445051
-
BRIT1/MCPH1 is a DNA damage responsive protein that regulates the Brca1-Chk1 pathway, implicating checkpoint dysfunction in microcephaly
-
Lin SY, Rai R, Li K, Xu ZX, Elledge SJ. BRIT1/MCPH1 is a DNA damage responsive protein that regulates the Brca1-Chk1 pathway, implicating checkpoint dysfunction in microcephaly. Proc Natl Acad Sci USA 2005, 102:15105-15109.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 15105-15109
-
-
Lin, S.Y.1
Rai, R.2
Li, K.3
Xu, Z.X.4
Elledge, S.J.5
-
134
-
-
33745763425
-
Regulation of mitotic entry by microcephalin and its overlap with ATR signalling
-
Alderton G, Galbiati L, Griffith E, Surinya K, Neitzel H, Jackson A, Jeggo P, O'driscoll M. Regulation of mitotic entry by microcephalin and its overlap with ATR signalling. Nat Cell Biol 2006, 8:725-733.
-
(2006)
Nat Cell Biol
, vol.8
, pp. 725-733
-
-
Alderton, G.1
Galbiati, L.2
Griffith, E.3
Surinya, K.4
Neitzel, H.5
Jackson, A.6
Jeggo, P.7
O'driscoll, M.8
-
135
-
-
33746857684
-
BRIT1 regulates early DNA damage response, chromosomal integrity, and cancer
-
Rai R, Dai H, Multani AS, Li K, Chin K, Gray J, Lahad JP, Liang J, Mills GB, Meric-Bernstam F, et al. BRIT1 regulates early DNA damage response, chromosomal integrity, and cancer. Cancer Cell 2006, 10:145-157.
-
(2006)
Cancer Cell
, vol.10
, pp. 145-157
-
-
Rai, R.1
Dai, H.2
Multani, A.S.3
Li, K.4
Chin, K.5
Gray, J.6
Lahad, J.P.7
Liang, J.8
Mills, G.B.9
Meric-Bernstam, F.10
-
136
-
-
36849000716
-
MCPH1 functions in an H2AX-dependent but MDC1-independent pathway in response to DNA damage
-
Wood JL, Singh N, Mer G, Chen J. MCPH1 functions in an H2AX-dependent but MDC1-independent pathway in response to DNA damage. J Biol Chem 2007, 282:35416-35423.
-
(2007)
J Biol Chem
, vol.282
, pp. 35416-35423
-
-
Wood, J.L.1
Singh, N.2
Mer, G.3
Chen, J.4
-
137
-
-
57649223685
-
Microcephalin/MCPH1 associates with the Condensin II complex to function in homologous recombination repair
-
Wood JL, Liang Y, Li K, Chen J. Microcephalin/MCPH1 associates with the Condensin II complex to function in homologous recombination repair. J Biol Chem 2008, 283:29586-29592.
-
(2008)
J Biol Chem
, vol.283
, pp. 29586-29592
-
-
Wood, J.L.1
Liang, Y.2
Li, K.3
Chen, J.4
-
138
-
-
76749170775
-
BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice
-
Liang Y, Gao H, Lin SY, Peng G, Huang X, Zhang P, Goss JA, Brunicardi FC, Multani AS, Chang S, et al. BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice. PLoS Genet 2010, 6:e1000826.
-
(2010)
PLoS Genet
, vol.6
-
-
Liang, Y.1
Gao, H.2
Lin, S.Y.3
Peng, G.4
Huang, X.5
Zhang, P.6
Goss, J.A.7
Brunicardi, F.C.8
Multani, A.S.9
Chang, S.10
-
139
-
-
77949532680
-
Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function
-
Trimborn M, Ghani M, Walther DJ, Dopatka M, Dutrannoy V, Busche A, Meyer F, Nowak S, Nowak J, Zabel C, et al. Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function. PLoS One 2010, 5:e9242.
-
(2010)
PLoS One
, vol.5
-
-
Trimborn, M.1
Ghani, M.2
Walther, D.J.3
Dopatka, M.4
Dutrannoy, V.5
Busche, A.6
Meyer, F.7
Nowak, S.8
Nowak, J.9
Zabel, C.10
-
140
-
-
80455177095
-
MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway
-
Gruber R, Zhou Z, Sukchev M, Joerss T, Frappart PO, Wang ZQ. MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway. Nat Cell Biol 2011, 13:1325-1334.
-
(2011)
Nat Cell Biol
, vol.13
, pp. 1325-1334
-
-
Gruber, R.1
Zhou, Z.2
Sukchev, M.3
Joerss, T.4
Frappart, P.O.5
Wang, Z.Q.6
-
141
-
-
77950862610
-
Immunoglobulin class switch recombination deficiencies
-
Kracker S, Gardes P, Mazerolles F, Durandy A. Immunoglobulin class switch recombination deficiencies. Clin Immunol 2010, 135:193-203.
-
(2010)
Clin Immunol
, vol.135
, pp. 193-203
-
-
Kracker, S.1
Gardes, P.2
Mazerolles, F.3
Durandy, A.4
-
143
-
-
79953032797
-
Mechanisms that promote and suppress chromosomal translocations in lymphocytes
-
Gostissa M, Alt FW, Chiarle R. Mechanisms that promote and suppress chromosomal translocations in lymphocytes. Annu Rev Immunol 2011, 29:319-350.
-
(2011)
Annu Rev Immunol
, vol.29
, pp. 319-350
-
-
Gostissa, M.1
Alt, F.W.2
Chiarle, R.3
-
144
-
-
80052146061
-
Chromatin and the DNA damage response: The cancer connection
-
Luijsterburg MS, van Attikum H. Chromatin and the DNA damage response: The cancer connection. Mol Oncol 2011, 5:349-367.
-
(2011)
Mol Oncol
, vol.5
, pp. 349-367
-
-
Luijsterburg, M.S.1
van Attikum, H.2
-
145
-
-
17344372572
-
Positional cloning of the gene for Nijmegen breakage syndrome
-
Matsuura S, Tauchi H, Nakamura A, Kondo N, Sakamoto S, Endo S, Smeets D, Solder B, Belohradsky BH, Der Kaloustian VM, et al. Positional cloning of the gene for Nijmegen breakage syndrome. Nat Genet 1998, 19:179-181.
-
(1998)
Nat Genet
, vol.19
, pp. 179-181
-
-
Matsuura, S.1
Tauchi, H.2
Nakamura, A.3
Kondo, N.4
Sakamoto, S.5
Endo, S.6
Smeets, D.7
Solder, B.8
Belohradsky, B.H.9
Der Kaloustian, V.M.10
-
146
-
-
0032076248
-
The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response
-
Carney JP, Maser RS, Olivares H, Davis EM, Le Beau M, Yates JR 3rd, Hays L, Morgan WF, Petrini JH. The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. Cell 1998, 93:477-486.
-
(1998)
Cell
, vol.93
, pp. 477-486
-
-
Carney, J.P.1
Maser, R.S.2
Olivares, H.3
Davis, E.M.4
Le Beau, M.5
Yates, J.R.6
Hays, L.7
Morgan, W.F.8
Petrini, J.H.9
-
147
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanova E, Cooper PR, Nowak NJ, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 1998, 93:467-476.
-
(1998)
Cell
, vol.93
, pp. 467-476
-
-
Varon, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanova, E.8
Cooper, P.R.9
Nowak, N.J.10
-
148
-
-
18244362081
-
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency
-
O'Driscoll M, Cerosaletti KM, Girard PM, Dai Y, Stumm M, Kysela B, Hirsch B, Gennery A, Palmer SE, Seidel J, et al. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency. Mol Cell 2001, 8:1175-1185.
-
(2001)
Mol Cell
, vol.8
, pp. 1175-1185
-
-
O'Driscoll, M.1
Cerosaletti, K.M.2
Girard, P.M.3
Dai, Y.4
Stumm, M.5
Kysela, B.6
Hirsch, B.7
Gennery, A.8
Palmer, S.E.9
Seidel, J.10
-
149
-
-
30944455282
-
Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV
-
Buck D, Moshous D. DeChasseval R, Ma Y, LeDeist F, Cavazzana-Calvo M, Fischer A, Casanova J, Lieber M, DeVillartay J. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV. Eur J Immunol 2006, 36:224-235.
-
(2006)
Eur J Immunol
, vol.36
, pp. 224-235
-
-
Buck, D.1
Moshous, D.2
DeChasseval, R.3
Ma, Y.4
LeDeist, F.5
Cavazzana-Calvo, M.6
Fischer, A.7
Casanova, J.8
Lieber, M.9
DeVillartay, J.10
-
150
-
-
31044440630
-
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly
-
Buck D, Malivert L, de Chasseval R, Barraud A, Fondaneche MC, Sanal O, Plebani A, Stephan JL, Hufnagel M, le Deist F, et al. Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly. Cell 2006, 124:287-299.
-
(2006)
Cell
, vol.124
, pp. 287-299
-
-
Buck, D.1
Malivert, L.2
de Chasseval, R.3
Barraud, A.4
Fondaneche, M.C.5
Sanal, O.6
Plebani, A.7
Stephan, J.L.8
Hufnagel, M.9
le Deist, F.10
-
151
-
-
65149095154
-
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder
-
Waltes R, Kalb R, Gatei M, Kijas AW, Stumm M, Sobeck A, Wieland B, Varon R, Lerenthal Y, Lavin MF, et al. Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am J Hum Genet 2009, 84:605-616.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 605-616
-
-
Waltes, R.1
Kalb, R.2
Gatei, M.3
Kijas, A.W.4
Stumm, M.5
Sobeck, A.6
Wieland, B.7
Varon, R.8
Lerenthal, Y.9
Lavin, M.F.10
-
152
-
-
77649188409
-
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
-
Shen J, Gilmore EC, Marshall CA, Haddadin M, Reynolds JJ, Eyaid W, Bodell A, Barry B, Gleason D, Allen K, et al. Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nat Genet 2010, 42:245-249.
-
(2010)
Nat Genet
, vol.42
, pp. 245-249
-
-
Shen, J.1
Gilmore, E.C.2
Marshall, C.A.3
Haddadin, M.4
Reynolds, J.J.5
Eyaid, W.6
Bodell, A.7
Barry, B.8
Gleason, D.9
Allen, K.10
-
153
-
-
79951852632
-
Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly
-
Matsumoto Y, Miyamoto T, Sakamoto H, Izumi H, Nakazawa Y, Ogi T, Tahara H, Oku S, Hiramoto A, Shiiki T, et al. Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly. DNA Repair (Amst) 2011, 10:314-321.
-
(2011)
DNA Repair (Amst)
, vol.10
, pp. 314-321
-
-
Matsumoto, Y.1
Miyamoto, T.2
Sakamoto, H.3
Izumi, H.4
Nakazawa, Y.5
Ogi, T.6
Tahara, H.7
Oku, S.8
Hiramoto, A.9
Shiiki, T.10
-
154
-
-
0942268166
-
DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
-
Lehmann A. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Biochimie 2003, 85:1101-1111.
-
(2003)
Biochimie
, vol.85
, pp. 1101-1111
-
-
Lehmann, A.1
-
155
-
-
0029057336
-
A single ataxia telangiectasia gene with a product similar to PI-3 kinase
-
Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, et al. A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 1995, 268:1749-1753.
-
(1995)
Science
, vol.268
, pp. 1749-1753
-
-
Savitsky, K.1
Bar-Shira, A.2
Gilad, S.3
Rotman, G.4
Ziv, Y.5
Vanagaite, L.6
Tagle, D.A.7
Smith, S.8
Uziel, T.9
Sfez, S.10
-
156
-
-
0033544724
-
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
-
Stewart GS, Maser RS, Stankovic T, Bressan DA, Kaplan MI, Jaspers NG, Raams A, Byrd PJ, Petrini JH, Taylor AM. The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder. Cell 1999, 99:577-587.
-
(1999)
Cell
, vol.99
, pp. 577-587
-
-
Stewart, G.S.1
Maser, R.S.2
Stankovic, T.3
Bressan, D.A.4
Kaplan, M.I.5
Jaspers, N.G.6
Raams, A.7
Byrd, P.J.8
Petrini, J.H.9
Taylor, A.M.10
-
157
-
-
0034785531
-
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
-
Moreira MC, Barbot C, Tachi N, Kozuka N, Uchida E, Gibson T, Mendonça P, Costa M, Barros J, Yanagisawa T, et al. The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin. Nat Genet 2001, 29:189-193.
-
(2001)
Nat Genet
, vol.29
, pp. 189-193
-
-
Moreira, M.C.1
Barbot, C.2
Tachi, N.3
Kozuka, N.4
Uchida, E.5
Gibson, T.6
Mendonça, P.7
Costa, M.8
Barros, J.9
Yanagisawa, T.10
-
158
-
-
18644386254
-
Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy
-
Takashima H, Boerkoel C, John J, Saifi G, Salih M, Armstrong D, Mao Y, Quiocho F, Roa B, Nakagawa M, et al. Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy. Nat Genet 2002, 32:267-272.
-
(2002)
Nat Genet
, vol.32
, pp. 267-272
-
-
Takashima, H.1
Boerkoel, C.2
John, J.3
Saifi, G.4
Salih, M.5
Armstrong, D.6
Mao, Y.7
Quiocho, F.8
Roa, B.9
Nakagawa, M.10
-
159
-
-
10744230604
-
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
-
Moreira MC, Klur S, Watanabe M, Nemeth AH, Le Ber I, Moniz JC, Tranchant C, Aubourg P, Tazir M, Schols L, et al. Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nat Genet 2004, 36:225-227.
-
(2004)
Nat Genet
, vol.36
, pp. 225-227
-
-
Moreira, M.C.1
Klur, S.2
Watanabe, M.3
Nemeth, A.H.4
Le Ber, I.5
Moniz, J.C.6
Tranchant, C.7
Aubourg, P.8
Tazir, M.9
Schols, L.10
-
160
-
-
14544268980
-
Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1
-
El-Khamisy SF, Saifi GM, Weinfeld M, Johansson F, Helleday T, Lupski JR, Caldecott KW. Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1. Nature 2005, 434:108-113.
-
(2005)
Nature
, vol.434
, pp. 108-113
-
-
El-Khamisy, S.F.1
Saifi, G.M.2
Weinfeld, M.3
Johansson, F.4
Helleday, T.5
Lupski, J.R.6
Caldecott, K.W.7
-
161
-
-
48249095920
-
Single-strand break repair and genetic disease
-
Caldecott KW. Single-strand break repair and genetic disease. Nat Rev Genet 2008, 9:619-631.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 619-631
-
-
Caldecott, K.W.1
-
162
-
-
58549092574
-
DNA repair deficiency and neurological disease
-
McKinnon PJ. DNA repair deficiency and neurological disease. Nat Rev Neurosci 2009, 10:100-112.
-
(2009)
Nat Rev Neurosci
, vol.10
, pp. 100-112
-
-
McKinnon, P.J.1
-
163
-
-
36949026694
-
Activation and regulation of ATM kinase activity in response to DNA double-strand breaks
-
Lee JH, Paull TT. Activation and regulation of ATM kinase activity in response to DNA double-strand breaks. Oncogene 2007, 26:7741-7748.
-
(2007)
Oncogene
, vol.26
, pp. 7741-7748
-
-
Lee, J.H.1
Paull, T.T.2
-
164
-
-
47749141560
-
ATR: an essential regulator of genome integrity
-
Cimprich KA, Cortez D. ATR: an essential regulator of genome integrity. Nat Rev Mol Cell Biol 2008, 9:616-627.
-
(2008)
Nat Rev Mol Cell Biol
, vol.9
, pp. 616-627
-
-
Cimprich, K.A.1
Cortez, D.2
-
165
-
-
77955841725
-
The MRN complex in double-strand break repair and telomere maintenance
-
Lamarche BJ, Orazio NI, Weitzman MD. The MRN complex in double-strand break repair and telomere maintenance. FEBS Lett 2010, 584:3682-3695.
-
(2010)
FEBS Lett
, vol.584
, pp. 3682-3695
-
-
Lamarche, B.J.1
Orazio, N.I.2
Weitzman, M.D.3
-
167
-
-
34249947699
-
ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage
-
3rd
-
Matsuoka S, Ballif BA, Smogorzewska A, McDonald ER, 3rd Hurov KE, Luo J, Bakalarski CE, Zhao Z, Solimini N, Lerenthal Y, et al. ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage. Science 2007, 316:1160-1166.
-
(2007)
Science
, vol.316
, pp. 1160-1166
-
-
Matsuoka, S.1
Ballif, B.A.2
Smogorzewska, A.3
McDonald, E.R.4
Hurov, K.E.5
Luo, J.6
Bakalarski, C.E.7
Zhao, Z.8
Solimini, N.9
Lerenthal, Y.10
-
168
-
-
84855834154
-
Differential function of NBS1 and ATR in neurogenesis
-
Zhou Z, Bruhn C, Wang ZQ. Differential function of NBS1 and ATR in neurogenesis. DNA Repair (Amst) 2012, 11:210-221.
-
(2012)
DNA Repair (Amst)
, vol.11
, pp. 210-221
-
-
Zhou, Z.1
Bruhn, C.2
Wang, Z.Q.3
-
169
-
-
24344461251
-
A patient with mutations in DNA Ligase IV: Clinical features and overlap with Nijmegen breakage syndrome
-
Ben-Omran T, Cerosaletti K, Concannon P, Weitzman S, Nezarati M. A patient with mutations in DNA Ligase IV: Clinical features and overlap with Nijmegen breakage syndrome. Am J Med Genet 2005, 137A:283-287.
-
(2005)
Am J Med Genet
, vol.137 A
, pp. 283-287
-
-
Ben-Omran, T.1
Cerosaletti, K.2
Concannon, P.3
Weitzman, S.4
Nezarati, M.5
-
170
-
-
38049125555
-
The endless tale of non-homologous end-joining
-
Weterings E, Chen DJ. The endless tale of non-homologous end-joining. Cell Res 2008, 18:114-124.
-
(2008)
Cell Res
, vol.18
, pp. 114-124
-
-
Weterings, E.1
Chen, D.J.2
-
171
-
-
70350088548
-
Mechanisms of double-strand break repair in somatic mammalian cells
-
Hartlerode AJ, Scully R. Mechanisms of double-strand break repair in somatic mammalian cells. Biochem J 2009, 423:157-168.
-
(2009)
Biochem J
, vol.423
, pp. 157-168
-
-
Hartlerode, A.J.1
Scully, R.2
-
172
-
-
0033634973
-
DNA ligase IV deficiency in mice leads to defective neurogenesis and embryonic lethality via the p53 pathway
-
Frank KM, Sharpless NE, Gao Y, Sekiguchi JM, Ferguson DO, Zhu C, Manis JP, Horner J, DePinho RA, Alt FW. DNA ligase IV deficiency in mice leads to defective neurogenesis and embryonic lethality via the p53 pathway. Mol Cell 2000, 5:993-1002.
-
(2000)
Mol Cell
, vol.5
, pp. 993-1002
-
-
Frank, K.M.1
Sharpless, N.E.2
Gao, Y.3
Sekiguchi, J.M.4
Ferguson, D.O.5
Zhu, C.6
Manis, J.P.7
Horner, J.8
DePinho, R.A.9
Alt, F.W.10
-
173
-
-
0034668060
-
Defective neurogenesis resulting from DNA ligase IV deficiency requires Atm
-
Lee Y, Barnes DE, Lindahl T, McKinnon PJ. Defective neurogenesis resulting from DNA ligase IV deficiency requires Atm. Genes Dev 2000, 14:2576-2580.
-
(2000)
Genes Dev
, vol.14
, pp. 2576-2580
-
-
Lee, Y.1
Barnes, D.E.2
Lindahl, T.3
McKinnon, P.J.4
-
174
-
-
0035853127
-
Genetic interactions between ATM and the nonhomologous end-joining factors in genomic stability and development
-
Sekiguchi J, Ferguson DO, Chen HT, Yang EM, Earle J, Frank K, Whitlow S, Gu Y, Xu Y, Nussenzweig A, et al. Genetic interactions between ATM and the nonhomologous end-joining factors in genomic stability and development. Proc Natl Acad Sci USA 2001, 98:3243-3248.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 3243-3248
-
-
Sekiguchi, J.1
Ferguson, D.O.2
Chen, H.T.3
Yang, E.M.4
Earle, J.5
Frank, K.6
Whitlow, S.7
Gu, Y.8
Xu, Y.9
Nussenzweig, A.10
-
175
-
-
33745628782
-
Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development
-
Orii KE, Lee Y, Kondo N, McKinnon PJ. Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development. Proc Natl Acad Sci USA 2006, 103:10017-10022.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 10017-10022
-
-
Orii, K.E.1
Lee, Y.2
Kondo, N.3
McKinnon, P.J.4
-
176
-
-
34250001115
-
BRCA2 is required for neurogenesis and suppression of medulloblastoma
-
Frappart PO, Lee Y, Lamont J, McKinnon PJ. BRCA2 is required for neurogenesis and suppression of medulloblastoma. EMBO J 2007, 26:2732-2742.
-
(2007)
EMBO J
, vol.26
, pp. 2732-2742
-
-
Frappart, P.O.1
Lee, Y.2
Lamont, J.3
McKinnon, P.J.4
-
177
-
-
0035846899
-
XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair
-
Whitehouse CJ, Taylor RM, Thistlethwaite A, Zhang H, Karimi-Busheri F, Lasko DD, Weinfeld M, Caldecott KW. XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair. Cell 2001, 104:107-117.
-
(2001)
Cell
, vol.104
, pp. 107-117
-
-
Whitehouse, C.J.1
Taylor, R.M.2
Thistlethwaite, A.3
Zhang, H.4
Karimi-Busheri, F.5
Lasko, D.D.6
Weinfeld, M.7
Caldecott, K.W.8
-
178
-
-
6344238643
-
Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV
-
Koch CA, Agyei R, Galicia S, Metalnikov P, O'Donnell P, Starostine A, Weinfeld M, Durocher D. Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV. EMBO J 2004, 23:3874-3885.
-
(2004)
EMBO J
, vol.23
, pp. 3874-3885
-
-
Koch, C.A.1
Agyei, R.2
Galicia, S.3
Metalnikov, P.4
O'Donnell, P.5
Starostine, A.6
Weinfeld, M.7
Durocher, D.8
-
179
-
-
68149161604
-
The genesis of cerebellar interneurons and the prevention of neural DNA damage require XRCC1
-
Lee Y, Katyal S, Li Y, El-Khamisy SF, Russell HR, Caldecott KW, McKinnon PJ. The genesis of cerebellar interneurons and the prevention of neural DNA damage require XRCC1. Nat Neurosci 2009, 12:973-980.
-
(2009)
Nat Neurosci
, vol.12
, pp. 973-980
-
-
Lee, Y.1
Katyal, S.2
Li, Y.3
El-Khamisy, S.F.4
Russell, H.R.5
Caldecott, K.W.6
McKinnon, P.J.7
|