-
1
-
-
0026876196
-
The gene for X-linked Kallmann syndrome: A human neuronal migration defect
-
Ballabio A., Camerino G. The gene for X-linked Kallmann syndrome: A human neuronal migration defect. Curr. Opin. Genet. Dev. 2:1992;417-421.
-
(1992)
Curr. Opin. Genet. Dev.
, vol.2
, pp. 417-421
-
-
Ballabio, A.1
Camerino, G.2
-
2
-
-
0002389440
-
The reeler Malformation
-
Plenum Press, New York
-
V.S.J. Caviness, J.E. Crandall, M.A. Edwards, The reeler Malformation. Implications for Neocortical Histogenesis, vol. 7, Plenum Press, New York, 1988.
-
(1988)
Implications for Neocortical Histogenesis
, vol.7
-
-
Caviness, V.S.J.1
Crandall, J.E.2
Edwards, M.A.3
-
3
-
-
0018244387
-
Mechanisms of cortical development: A view from mutations in mice
-
Caviness V.S.J., Rakic P. Mechanisms of cortical development: A view from mutations in mice. Ann. Rev. Neurosci. 1:1978;297-326.
-
(1978)
Ann. Rev. Neurosci.
, vol.1
, pp. 297-326
-
-
Caviness, V.S.J.1
Rakic, P.2
-
4
-
-
0031018336
-
Mice lacking p35, a neuronal activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
-
Chae T., Kwon Y.T., Bronson R., Dikkes P., Li E., Tsai L.H. Mice lacking p35, a neuronal activator of Cdk5, display cortical lamination defects, seizures, and adult lethality. Neuron. 18:1997;29-42.
-
(1997)
Neuron
, vol.18
, pp. 29-42
-
-
Chae, T.1
Kwon, Y.T.2
Bronson, R.3
Dikkes, P.4
Li, E.5
Tsai, L.H.6
-
5
-
-
0029065329
-
The axonal chemoattractant netrin-1 is also a chemorepellent for trochlear motor axons
-
Colamarino S.A., Tessier-Lavigne M. The axonal chemoattractant netrin-1 is also a chemorepellent for trochlear motor axons. Cell. 81:1995;621-629.
-
(1995)
Cell
, vol.81
, pp. 621-629
-
-
Colamarino, S.A.1
Tessier-Lavigne, M.2
-
6
-
-
0029971793
-
Functions of netrins and semaphorins in axon guidance
-
Culotti J.G., Kolodkin A.L. Functions of netrins and semaphorins in axon guidance. Curr. Opin. Neurobiol. 6:1996;81-88.
-
(1996)
Curr. Opin. Neurobiol.
, vol.6
, pp. 81-88
-
-
Culotti, J.G.1
Kolodkin, A.L.2
-
8
-
-
0028940096
-
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
-
D'Arcangelo G., Miao G.G., Chen S.-C., Soares H.D., Morgan J.I., Curran T. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature. 374:1995;719-723.
-
(1995)
Nature
, vol.374
, pp. 719-723
-
-
D'Arcangelo, G.1
Miao, G.G.2
Chen, S.-C.3
Soares, H.D.4
Morgan, J.I.5
Curran, T.6
-
9
-
-
0030001226
-
Detection of the reelin breakpoint in reeler mice
-
D'Arcangelo G., Miao G.G., Curran T. Detection of the reelin breakpoint in reeler mice. Mol. Brain Res. 39:1996;234-236.
-
(1996)
Mol. Brain Res.
, vol.39
, pp. 234-236
-
-
D'Arcangelo, G.1
Miao, G.G.2
Curran, T.3
-
10
-
-
0031031005
-
Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody
-
D'Arcangelo G., Nakajima K., Miyata T., Ogawa M., Mikoshiba K., Curran T. Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody. J. Neurosci. 17:1997;23-31.
-
(1997)
J. Neurosci.
, vol.17
, pp. 23-31
-
-
D'Arcangelo, G.1
Nakajima, K.2
Miyata, T.3
Ogawa, M.4
Mikoshiba, K.5
Curran, T.6
-
11
-
-
0030902291
-
Cajal-Retzius cells regulate the radial glia phenotype in the adult and developing cerebellum and alter granule cell migration
-
Soriano E., Alvarado-Mallrt R.M., Dumesnil N., Del Rio J.A., Sotelo C. Cajal-Retzius cells regulate the radial glia phenotype in the adult and developing cerebellum and alter granule cell migration. Neuron. 18:1997;563-577.
-
(1997)
Neuron
, vol.18
, pp. 563-577
-
-
Soriano, E.1
Alvarado-Mallrt, R.M.2
Dumesnil, N.3
Del Rio, J.A.4
Sotelo, C.5
-
12
-
-
0018428074
-
Evidence for the occurrence of early modifications in the 'glia limitans' layer of the neocortex of the reeler mouse
-
Derer P. Evidence for the occurrence of early modifications in the 'glia limitans' layer of the neocortex of the reeler mouse. Neurosci. Lett. 13:1979;195-202.
-
(1979)
Neurosci. Lett.
, vol.13
, pp. 195-202
-
-
Derer, P.1
-
13
-
-
0025166679
-
Cajal-Retzius cell ontogenesis and death in mouse brain visualized by HRP and electron microscopy
-
Derer P., Derer M. Cajal-Retzius cell ontogenesis and death in mouse brain visualized by HRP and electron microscopy. Neuroscience. 36:1990;839-856.
-
(1990)
Neuroscience
, vol.36
, pp. 839-856
-
-
Derer, P.1
Derer, M.2
-
14
-
-
0026331140
-
Estimation of genetic distances between 'reeler' and nearby loci on mouse chromosome 5
-
Dernoncourt C., Ruelle D., Goffinet A.M. Estimation of genetic distances between 'reeler' and nearby loci on mouse chromosome 5. Genomics. 11:1991;1167-1169.
-
(1991)
Genomics
, vol.11
, pp. 1167-1169
-
-
Dernoncourt, C.1
Ruelle, D.2
Goffinet, A.M.3
-
15
-
-
65749318026
-
Two new mutants 'trembler' and 'reeler', with neurological actions in the house mouse
-
Falconer D.S. Two new mutants 'trembler' and 'reeler', with neurological actions in the house mouse. J. Genet. 50:1951;192-201.
-
(1951)
J. Genet.
, vol.50
, pp. 192-201
-
-
Falconer, D.S.1
-
16
-
-
0025938481
-
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
-
Franco B., Guioli S., Pragliola A., Incerti B., Bardoni B., Tonlorenzi R., Carrozzo R., Maestrini E., Pieretti M., Taillon-Miller P.et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature. 353:1991;529-536.
-
(1991)
Nature
, vol.353
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
Incerti, B.4
Bardoni, B.5
Tonlorenzi, R.6
Carrozzo, R.7
Maestrini, E.8
Pieretti, M.9
Taillon-Miller, P.10
-
17
-
-
0027379724
-
Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin
-
George E.L., Georges-Labouesse E.N., Patel-King R.S., Rayburn H., Hynes R.O. Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin. Development. 119:1993;1079-1091.
-
(1993)
Development
, vol.119
, pp. 1079-1091
-
-
George, E.L.1
Georges-Labouesse, E.N.2
Patel-King, R.S.3
Rayburn, H.4
Hynes, R.O.5
-
18
-
-
0018640776
-
An early developmental defect in the cerebral cortex of the reeler mouse
-
Goffinet A.M. An early developmental defect in the cerebral cortex of the reeler mouse. Anat. Embryol. 157:1997;205-216.
-
(1997)
Anat. Embryol.
, vol.157
, pp. 205-216
-
-
Goffinet, A.M.1
-
19
-
-
0021168726
-
Events governing organization of postmigratory neurons: Studies on brain development in normal and reeler mice
-
Goffinet A.M. Events governing organization of postmigratory neurons: Studies on brain development in normal and reeler mice. Brain Res. 319:1984;261-296.
-
(1984)
Brain Res.
, vol.319
, pp. 261-296
-
-
Goffinet, A.M.1
-
20
-
-
0026591491
-
The reeler gene: A clue to brain development and evolution
-
Goffinet A.M. The reeler gene: A clue to brain development and evolution. Int. J. Dev. Biol. 36:1992;101-107.
-
(1992)
Int. J. Dev. Biol.
, vol.36
, pp. 101-107
-
-
Goffinet, A.M.1
-
21
-
-
0021709654
-
Architectonic and hodological organization of the cerebellum in reeler mutant mice
-
Goffinet A.M., So K.F., Yamamoto M., Edwards M., Caviness V. Jr. Architectonic and hodological organization of the cerebellum in reeler mutant mice. Brain Res. 318:1984;263-276.
-
(1984)
Brain Res.
, vol.318
, pp. 263-276
-
-
Goffinet, A.M.1
So, K.F.2
Yamamoto, M.3
Edwards, M.4
Caviness V., Jr.5
-
23
-
-
0028023599
-
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase
-
Hattori M., Adachi H., Tsujimoto M., Arai N., Inoue K. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase. Nature. 370:1994;216-218.
-
(1994)
Nature
, vol.370
, pp. 216-218
-
-
Hattori, M.1
Adachi, H.2
Tsujimoto, M.3
Arai, N.4
Inoue, K.5
-
24
-
-
0029072876
-
The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons
-
Hirotsune S., Takahara T., Sasaki N., Hirose K., Yoshiki A., Ohashi T., Kusakabe M., Murakami Y., Muramatsu M., Watanabe S., Nakao K., Katsuki M., Hayashizaki Y. The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Nat. Genet. 10:1995;77-83.
-
(1995)
Nat. Genet.
, vol.10
, pp. 77-83
-
-
Hirotsune, S.1
Takahara, T.2
Sasaki, N.3
Hirose, K.4
Yoshiki, A.5
Ohashi, T.6
Kusakabe, M.7
Murakami, Y.8
Muramatsu, M.9
Watanabe, S.10
Nakao, K.11
Katsuki, M.12
Hayashizaki, Y.13
-
25
-
-
0029008963
-
The mouse mutation Reeler causes increased adhesion within a subpopulation of early postmitotic cortical neurons
-
Hoffarth R.M., Johnston J.G., Krushel L.A., van der Kooy D. The mouse mutation Reeler causes increased adhesion within a subpopulation of early postmitotic cortical neurons. J. Neurosci. 15:1995;4838-4850.
-
(1995)
J. Neurosci.
, vol.15
, pp. 4838-4850
-
-
Hoffarth, R.M.1
Johnston, J.G.2
Krushel, L.A.3
Van Der Kooy, D.4
-
26
-
-
0026503656
-
Contact and adhesive specificities in the associations, migrations and targeting of cells and axons
-
Hynes R.O., Lander A.D. Contact and adhesive specificities in the associations, migrations and targeting of cells and axons. Cell. 68:1992;303-322.
-
(1992)
Cell
, vol.68
, pp. 303-322
-
-
Hynes, R.O.1
Lander, A.D.2
-
27
-
-
0028061313
-
Netrins are diffusible chemotropic factors for commissural axons in the embryonic spinal cord
-
Kennedy T.E., Serafini T., de la Torre J.R., Tessier-Lavigne M. Netrins are diffusible chemotropic factors for commissural axons in the embryonic spinal cord. Cell. 78:1994;425-435.
-
(1994)
Cell
, vol.78
, pp. 425-435
-
-
Kennedy, T.E.1
Serafini, T.2
De La Torre, J.R.3
Tessier-Lavigne, M.4
-
28
-
-
0026770381
-
F-spondin: A gene expressed at high levels in the floor plate encodes a secreted protein that promotes neural cell adhesion and neurite extension
-
Klar A., Baldassare M., Jessel T.M. F-spondin: A gene expressed at high levels in the floor plate encodes a secreted protein that promotes neural cell adhesion and neurite extension. Cell. 69:1992;95-110.
-
(1992)
Cell
, vol.69
, pp. 95-110
-
-
Klar, A.1
Baldassare, M.2
Jessel, T.M.3
-
29
-
-
0021800963
-
The J1 glycoprotein: A novel nervous system cell adhesion molecule of the L2/HNK-1 family
-
Kruse J., Keilhauer G., Faissner A., Timpl R., Schachner M. The J1 glycoprotein: A novel nervous system cell adhesion molecule of the L2/HNK-1 family. Nature. 316:1995;146-148.
-
(1995)
Nature
, vol.316
, pp. 146-148
-
-
Kruse, J.1
Keilhauer, G.2
Faissner, A.3
Timpl, R.4
Schachner, M.5
-
30
-
-
0028286753
-
Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome
-
Legouis R., Cohen-Salmon M., Del Castillo I., Petit C. Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome. Biomed. Pharmacother. 48:1994;241-246.
-
(1994)
Biomed. Pharmacother.
, vol.48
, pp. 241-246
-
-
Legouis, R.1
Cohen-Salmon, M.2
Del Castillo, I.3
Petit, C.4
-
31
-
-
0017847944
-
Dual origin of the mammalian neocortex and evolution of the cortical plate
-
Marin-Padilla M. Dual origin of the mammalian neocortex and evolution of the cortical plate. Anat. Embryol. 152:1978;109-126.
-
(1978)
Anat. Embryol.
, vol.152
, pp. 109-126
-
-
Marin-Padilla, M.1
-
32
-
-
0019942737
-
Origin, prenatal development and structural organization of layer I of the human cerebral (motor) cortex. A Golgi study
-
Marin-Padilla M., Marin-Padilla T.M. Origin, prenatal development and structural organization of layer I of the human cerebral (motor) cortex. A Golgi study. Anat. Embryol. 164:1982;164-206.
-
(1982)
Anat. Embryol.
, vol.164
, pp. 164-206
-
-
Marin-Padilla, M.1
Marin-Padilla, T.M.2
-
33
-
-
0027997112
-
Isolation of an allele of reeler by insertional mutagenesis
-
Miao G.G., Smeyne R.J., D'Arcangelo G., Copeland N.G., Jenkins N.A., Morgan J.I., Curran T. Isolation of an allele of reeler by insertional mutagenesis. Proc. Natl. Acad. Sci. USA. 91:1994;11050-11054.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 11050-11054
-
-
Miao, G.G.1
Smeyne, R.J.2
D'Arcangelo, G.3
Copeland, N.G.4
Jenkins, N.A.5
Morgan, J.I.6
Curran, T.7
-
34
-
-
0028917340
-
Cerebral cortical dysplasia associated with pediatric epilepsy. Review of neuropathologic features and proposal for a grading system
-
Mischel P.S., Nguyen L.P., Vinters H.V. Cerebral cortical dysplasia associated with pediatric epilepsy. Review of neuropathologic features and proposal for a grading system. J. Neuropathol. Exp. Neurol. 54:1995;137-153.
-
(1995)
J. Neuropathol. Exp. Neurol.
, vol.54
, pp. 137-153
-
-
Mischel, P.S.1
Nguyen, L.P.2
Vinters, H.V.3
-
35
-
-
0029789652
-
Distribution of the reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogenic antibody CR-50 on normal and reeler mice
-
Miyata T., Nakajima K., Aruga J., Takahashi S., Ikenaka K., Mikoshiba K., Ogawa M. Distribution of the reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogenic antibody CR-50 on normal and reeler mice. J. Comp. Neurol. 372:1996;215-228.
-
(1996)
J. Comp. Neurol.
, vol.372
, pp. 215-228
-
-
Miyata, T.1
Nakajima, K.2
Aruga, J.3
Takahashi, S.4
Ikenaka, K.5
Mikoshiba, K.6
Ogawa, M.7
-
36
-
-
0030908070
-
Regulation of purkinje cell alignment by reelin as revealed with CR-50 antibody
-
Miyata T., Nakajima K., Mikoshiba K., Ogawa M. Regulation of purkinje cell alignment by reelin as revealed with CR-50 antibody. J. Neurosci. 17:1997;3599-3609.
-
(1997)
J. Neurosci.
, vol.17
, pp. 3599-3609
-
-
Miyata, T.1
Nakajima, K.2
Mikoshiba, K.3
Ogawa, M.4
-
37
-
-
0029008666
-
The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons
-
Ogawa M., Miyata T., Nakajima K., Yagyu K., Seike M., Ikenaka K., Yamamoto H., Mikoshiba K. The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron. 14:1995;899-912.
-
(1995)
Neuron
, vol.14
, pp. 899-912
-
-
Ogawa, M.1
Miyata, T.2
Nakajima, K.3
Yagyu, K.4
Seike, M.5
Ikenaka, K.6
Yamamoto, H.7
Mikoshiba, K.8
-
38
-
-
0029768093
-
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death
-
Oshima T., Ward J.M., Huh C.-G., Longenecker G., Veeranna, Pant H.C., Brady R.O., Martin L.J., Kulkarni A.B. Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Proc. Natl. Acad. Sci. USA. 93:1996;11173-11178.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11173-11178
-
-
Oshima, T.1
Ward, J.M.2
Huh, C.-G.3
Longenecker, G.4
Veeranna5
Pant, H.C.6
Brady, R.O.7
Martin, L.J.8
Kulkarni, A.B.9
-
39
-
-
0028085307
-
Recognition, adhesion, transmembrane signaling and cell motility in guided neuronal migration
-
Rakic P., Cameron R.S., Komuro H. Recognition, adhesion, transmembrane signaling and cell motility in guided neuronal migration. Curr. Biol. 4:1994;63-69.
-
(1994)
Curr. Biol.
, vol.4
, pp. 63-69
-
-
Rakic, P.1
Cameron, R.S.2
Komuro, H.3
-
40
-
-
0029013985
-
Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration
-
Reiner O., Albrecht U., Gordon M., Chianese K.A., Wong C., Gal-Gerber O., Sapir T., Siracusa L.D., Buchberg A.M., Caskey C.T.et al. Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration. J. Neurosci. 15:1995;3730-3738.
-
(1995)
J. Neurosci.
, vol.15
, pp. 3730-3738
-
-
Reiner, O.1
Albrecht, U.2
Gordon, M.3
Chianese, K.A.4
Wong, C.5
Gal-Gerber, O.6
Sapir, T.7
Siracusa, L.D.8
Buchberg, A.M.9
Caskey, C.T.10
-
41
-
-
0027176708
-
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
-
Reiner O., Carrozzo R., Shen Y., Wehnert M., Faustinella F., Dobyns W.B., Caskey C.T., Ledbetter D.H. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature. 364:1993;717-721.
-
(1993)
Nature
, vol.364
, pp. 717-721
-
-
Reiner, O.1
Carrozzo, R.2
Shen, Y.3
Wehnert, M.4
Faustinella, F.5
Dobyns, W.B.6
Caskey, C.T.7
Ledbetter, D.H.8
-
42
-
-
0029876529
-
Schizophrenia, the heteromodal association neocortex and development: Potential for a neurogenetic approach
-
Ross C.A., Pearlson G.D. Schizophrenia, the heteromodal association neocortex and development: Potential for a neurogenetic approach. Trends Neurosci. 19:1996;171-176.
-
(1996)
Trends Neurosci.
, vol.19
, pp. 171-176
-
-
Ross, C.A.1
Pearlson, G.D.2
-
43
-
-
0029797416
-
The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yeald a diffusible component
-
Rugarli E.I., Ghezzi C., Valsecchi V., Ballabio A. The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yeald a diffusible component. Hum. Mol. Genet. 5:1996;1109-1115.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1109-1115
-
-
Rugarli, E.I.1
Ghezzi, C.2
Valsecchi, V.3
Ballabio, A.4
-
44
-
-
0027278607
-
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting
-
Rugarli E.I., Lutz B., Kuratani S.C., Wawersik S., Borsani G., Ballabio A., Eichele G. Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting. Nat. Genet. 4:1993;19-26.
-
(1993)
Nat. Genet.
, vol.4
, pp. 19-26
-
-
Rugarli, E.I.1
Lutz, B.2
Kuratani, S.C.3
Wawersik, S.4
Borsani, G.5
Ballabio, A.6
Eichele, G.7
-
45
-
-
0026666302
-
Mice develop normally without tenascin
-
Saga Y., Yagi T., Ikawa Y., Sakakura T., Aizawa S. Mice develop normally without tenascin. Genes. Dev. 6:1992;1821-1831.
-
(1992)
Genes. Dev.
, vol.6
, pp. 1821-1831
-
-
Saga, Y.1
Yagi, T.2
Ikawa, Y.3
Sakakura, T.4
Aizawa, S.5
-
46
-
-
0028138219
-
The netrins define a family of axon outgrowth-promoting proteins homologous to elegans UNC-6
-
Serafini T., Kennedy T.E., Galko M.J., Mirzayan C., Jessell T.M., Tessier-Lavigne M.C. The netrins define a family of axon outgrowth-promoting proteins homologous to elegans UNC-6. Cell. 78:1994;409-442.
-
(1994)
Cell
, vol.78
, pp. 409-442
-
-
Serafini, T.1
Kennedy, T.E.2
Galko, M.J.3
Mirzayan, C.4
Jessell, T.M.5
Tessier-Lavigne, M.C.6
-
49
-
-
0018757238
-
The development of the hippocampus and dentate gyrus in normal and reeler mice
-
Stanfield B.B., Cowan W.M. The development of the hippocampus and dentate gyrus in normal and reeler mice. J. Comp. Neurol. 185:1979;461-484.
-
(1979)
J. Comp. Neurol.
, vol.185
, pp. 461-484
-
-
Stanfield, B.B.1
Cowan, W.M.2
-
50
-
-
0030281598
-
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
-
Sweet H.O., Bronson R.T., Johnson K.R., Cook S.A., Davisson M.T. Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration. Mamm. Genome. 7:1996;798-802.
-
(1996)
Mamm. Genome.
, vol.7
, pp. 798-802
-
-
Sweet, H.O.1
Bronson, R.T.2
Johnson, K.R.3
Cook, S.A.4
Davisson, M.T.5
-
51
-
-
8944258929
-
Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon
-
Takahara T.et al. Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon. Hum. Mol. Genet. 5:1996;989-993.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 989-993
-
-
Takahara, T.1
-
52
-
-
0023030039
-
Observations on the cerebellum of normal-reeler mutant mouse chimera
-
Terashima T., Inoue K., Inoue Y., Yokoyama M., Mikoshiba K. Observations on the cerebellum of normal-reeler mutant mouse chimera. J. Comp. Neurol. 252:1986;264-278.
-
(1986)
J. Comp. Neurol.
, vol.252
, pp. 264-278
-
-
Terashima, T.1
Inoue, K.2
Inoue, Y.3
Yokoyama, M.4
Mikoshiba, K.5
-
53
-
-
0018864346
-
Structural abnormalities in the olfactory bulb of the Reeler mouse
-
Wyss J.M., Stanfield B.B., Cowan W.M. Structural abnormalities in the olfactory bulb of the Reeler mouse. Brain Res. 188:1980;566-571.
-
(1980)
Brain Res.
, vol.188
, pp. 566-571
-
-
Wyss, J.M.1
Stanfield, B.B.2
Cowan, W.M.3
-
54
-
-
0010486618
-
A novel neurological mutation of mouse, yotari, which exhibits reeler-like phenotype but expresses reelin
-
in press.
-
H. Yoneshima, E. Nagata, M. Matsumoto, M. Yomada, K. Nakajima, T. Miyata, M. Ogawa, K. Mikoshiba, A novel neurological mutation of mouse, yotari, which exhibits reeler-like phenotype but expresses reelin, Neurosci. Res., in press.
-
Neurosci. Res.
-
-
Yoneshima, H.1
Nagata, E.2
Matsumoto, M.3
Yomada, M.4
Nakajima, K.5
Miyata, T.6
Ogawa, M.7
Mikoshiba, K.8
-
55
-
-
85085844590
-
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of Reelin
-
in press.
-
D. Goldowitz, R.C. Cushing, E. Laywell, G. D'Arcangelo, M. Sheldon, H.O. Sweet, M. Davisson, D. Steindler, T. Curran, Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of Reelin, J. Neurosci. in press.
-
J. Neurosci.
-
-
Goldowitz, D.1
Cushing, R.C.2
Laywell, E.3
D'Arcangelo, G.4
Sheldon, M.5
Sweet, H.O.6
Davisson, M.7
Steindler, D.8
Curran, T.9
-
56
-
-
0030717493
-
Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice
-
Sheldon M., Rice D.S., D'Arcangelo G., Yoneshima H., Nakajima K., Mikoshiba K., Howell B.W., Cooper J.A., Goldowitz D., Curran T. Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice. Nature. 389:1997;730-733.
-
(1997)
Nature
, vol.389
, pp. 730-733
-
-
Sheldon, M.1
Rice, D.S.2
D'Arcangelo, G.3
Yoneshima, H.4
Nakajima, K.5
Mikoshiba, K.6
Howell, B.W.7
Cooper, J.A.8
Goldowitz, D.9
Curran, T.10
-
57
-
-
0031035703
-
Mouse disabled (mDab1): A Scr binding protein implicated in neuronal development
-
Howell B.W., Gertler F.B., Cooper J.A. Mouse disabled (mDab1): a Scr binding protein implicated in neuronal development. EMBO J. 16:1997;121-132.
-
(1997)
EMBO J.
, vol.16
, pp. 121-132
-
-
Howell, B.W.1
Gertler, F.B.2
Cooper, J.A.3
-
58
-
-
0030704354
-
Neuronal migrations in the developing mouse brain are regulated by mDab1 p80
-
Howell B.W., Hawkes R., Soriano P., Cooper J.A. Neuronal migrations in the developing mouse brain are regulated by mDab1 p80. Nature. 389:1997;733-736.
-
(1997)
Nature
, vol.389
, pp. 733-736
-
-
Howell, B.W.1
Hawkes, R.2
Soriano, P.3
Cooper, J.A.4
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