-
2
-
-
0030589601
-
Platelet-activating factor acetylhydrolase expression and activity suggest a link between neuronal migration and platelet-activating factor
-
(1996)
Dev. Biol.
, vol.180
, pp. 579-593
-
-
Albrecht, U.1
Abu-Issa, R.2
Rätz, B.3
Hattori, M.4
Aoki, J.5
Arai, H.6
Inoue, K.7
Eichele, G.8
-
3
-
-
0002313476
-
Studying gene expression on tissue sections using in situ hybridization
-
Adolph K. (Ed.), Human Genome Methods, Boca Raton, FL: CRC Press
-
(1998)
, pp. 93-120
-
-
Albrecht, U.1
Lu, H.C.2
Revelli, J.P.3
Xu, X.C.4
Lotan, R.5
Eichele, G.6
-
5
-
-
0031018336
-
Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
-
(1997)
Neuron
, vol.18
, pp. 29-42
-
-
Chase, T.1
Kwon, Y.T.2
Bronson, R.3
Dikkes, P.4
Li, E.5
Tsai, L.H.6
-
8
-
-
0034618076
-
The Lis1-related NUDF protein of Aspergillus niduans interacts with the coiled-coil domain of the NUDE/RO11 protein
-
(2000)
J. Cell Biol.
, vol.150
, pp. 681-688
-
-
Efimov, V.P.1
Morris, N.R.2
-
10
-
-
0027264603
-
Secretion of a neuropeptide-metabolizing enzyme similar to endopeptidase 22.19 by glioma C6 cells
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.191
, pp. 275-281
-
-
Ferro, E.S.1
Tambourgi, D.V.2
Gobersztejn, F.3
Gomes, M.D.4
Sucupira, M.5
Armelin, M.C.6
Kipnis, T.L.7
Camargo, A.C.8
-
11
-
-
0033042045
-
Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly
-
(1999)
Ann. Neurol.
, vol.45
, pp. 154-161
-
-
Fogli, A.1
Guerrini, R.2
Moro, F.3
Fernandez-Alvarez, E.4
Livet, M.5
Renieri, A.6
Cioni, M.7
Pilz, D.8
Veggiotti, P.9
Rossi, E.10
Ballabio, A.11
Carrozzo, R.12
-
12
-
-
0029854139
-
Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein β subunit
-
(1996)
Biochemistry
, vol.35
, pp. 13985-13994
-
-
Garcia-Higuera, I.1
Fenoglio, J.2
Li, Y.3
Lewis, C.4
Panchenko, M.5
Reiner, O.6
Smith, T.7
Neer, E.8
-
13
-
-
0030297912
-
Crystal structure at 2.4 Å resolution of the complex of transducin βγ and its regulator, phosducin
-
(1996)
Cell
, vol.87
, pp. 577-588
-
-
Gaudet, R.1
Bohm, A.2
Sigler, P.3
-
14
-
-
13044317276
-
Ubiquitin-dependent degradation of IκBα is mediated by a ubiquitin ligase Skp1/Cul1/F-box protein FWD1
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 3859-3863
-
-
Hatakeyama, S.1
Kitagawa, M.2
Nakayama, K.3
Shirane, M.4
Matsumoto, M.5
Hattori, K.6
Higashi, H.7
Nakano, H.8
Okumura, K.9
Onoe, K.10
Good, R.A.11
Nakayama, K.I.12
-
17
-
-
0034607144
-
Molecular and immunochemical evidences demonstrate that endooligopeptidase A is the predominant cytosolic oligopeptidase of rabbit brain
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.269
, pp. 7-13
-
-
Hayashi, M.A.F.1
Portar, F.C.V.2
Tambourgi, D.V.3
Sucupira, M.4
Yamane, T.5
Fernandes, B.L.6
Ferro, E.S.7
Reboucas, N.A.8
Camargo, A.C.M.9
-
18
-
-
0031848149
-
Graded reduction of Pafah1b1 (mLis1) activity results in neuronal migration defects and early embryonic lethality
-
(1998)
Nat. Genet.
, vol.19
, pp. 333-339
-
-
Hirotsune, S.1
Fleck, M.W.2
Gambello, M.J.3
Bix, G.J.4
Chen, A.5
Clark, G.D.6
Ledbetter, D.H.7
McBain, C.J.8
Wynshaw-Boris, A.9
-
19
-
-
0031021088
-
Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer
-
(1997)
Nature
, vol.385
, pp. 89-93
-
-
Ho, Y.S.1
Swenson, L.2
Derewenda, U.3
Serre, L.4
Wei, Y.5
Dauter, Z.6
Hattori, M.7
Adachi, T.8
Aoki, J.9
Arai, H.10
Inoue, K.11
Derewenda, Z.S.12
-
21
-
-
0033522491
-
An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of β-catenin
-
(1999)
EMBO J.
, vol.18
, pp. 2401-2410
-
-
Kitagawa, M.1
Hatakeyama, S.2
Shirane, M.3
Matsumoto, M.4
Noriko, I.5
Hattori, K.6
Nakamichi, I.7
Kikuchi, A.8
Nakayama, K.I.9
Nakayama, K.10
-
22
-
-
0034637504
-
Direct association of Lis1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE
-
(2000)
FEBS Lett.
, vol.479
, pp. 57-62
-
-
Kitagawa, M.1
Umezu, M.2
Aoki, J.3
Koizumi, H.4
Arai, H.5
Inoue, K.6
-
24
-
-
0032693534
-
Lis1, the Drosophila homolog of a human lissencephaly disease gene, is required for germline cell division and oocyte differentiation
-
(1999)
Development
, vol.126
, pp. 4477-4488
-
-
Liu, Z.1
Xie, T.2
Steward, R.3
-
29
-
-
0032493049
-
The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC
-
(1998)
Curr. Biol.
, vol.8
, pp. 603-606
-
-
Morris, S.M.1
Albrecht, U.2
Reiner, O.3
Eichele, G.4
Yu-Lee, L.Y.5
-
31
-
-
0029768093
-
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11173-11178
-
-
Ohshima, 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
-
32
-
-
0028574348
-
Lissencephaly-1 is one of the most conserved proteins between mouse and human: a single amino-acid difference in 410 residues
-
(1994)
Gene
, vol.150
, pp. 415-416
-
-
Peterfy, M.1
Gyuris, T.2
Basu, R.3
-
34
-
-
7844223263
-
LIS1 and XLIS1(DCX) mutations cause most classical lissencephaly, but different patterns of malformation
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 2029-2037
-
-
Pilz, D.T.1
Matsumoto, N.2
Minnerath, S.3
Mills, P.4
Gleeson, J.G.5
Allen, K.M.6
Walsh, C.A.7
Barkovich, A.J.8
Dobyns, W.B.9
Ledbetter, D.H.10
Ross, M.E.11
-
35
-
-
0344423821
-
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1757-1760
-
-
Pilz, D.1
Kuc, J.2
Matsumoto, N.3
Bodurtha, J.4
Bernadi, B.5
Tassinari, C.6
Dobyns, W.7
Ledbetter, D.8
-
36
-
-
0029013985
-
Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration
-
(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
Eichele, G.11
-
39
-
-
0032860480
-
A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant
-
(1999)
Nat. Genet.
, vol.23
, pp. 104-107
-
-
Sidow, A.1
Bulotsk, M.S.2
Kerrebrock, A.W.3
Birren, B.4
Altshuler, D.5
Jaenisch, R.6
Johnson, K.R.7
Lander, E.S.8
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