-
1
-
-
34047152928
-
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1
-
Hennah W, Tomppo L, Hiekkalinna T, Palo OM, Kilpinen H, Ekelund J, Tuulio-Henriksson A, Silander K, Partonen T, Paunio T, Terwilliger JD, Lonnqvist J, Peltonen L. Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. Hum Mol Genet. 2007;16(5):453-462.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.5
, pp. 453-462
-
-
Hennah, W.1
Tomppo, L.2
Hiekkalinna, T.3
Palo, O.M.4
Kilpinen, H.5
Ekelund, J.6
Tuulio-Henriksson, A.7
Silander, K.8
Partonen, T.9
Paunio, T.10
Terwilliger, J.D.11
Lonnqvist, J.12
Peltonen, L.13
-
2
-
-
33746899307
-
-
Gurling HM, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, Curtis D, Blackwood D, MuirW, Malhotra AK, Buchanan RW, Good CD, Frackowiak RS, Dolan RJ. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Arch Gen Psychiatry. 2006;63(8):844-854.
-
Gurling HM, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, Curtis D, Blackwood D, MuirW, Malhotra AK, Buchanan RW, Good CD, Frackowiak RS, Dolan RJ. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Arch Gen Psychiatry. 2006;63(8):844-854.
-
-
-
-
3
-
-
33745221854
-
A review of disrupted-in- schizophrenia-1 (DISC1):neurodevelopment, cognition, and mental conditions
-
Ishizuka K, Paek M, Kamiya A, Sawa A. A review of disrupted-in- schizophrenia-1 (DISC1):neurodevelopment, cognition, and mental conditions. Biol Psychiatry. 2006; 59(12)1189-1197.
-
(2006)
Biol Psychiatry
, vol.59
, Issue.12
, pp. 1189-1197
-
-
Ishizuka, K.1
Paek, M.2
Kamiya, A.3
Sawa, A.4
-
4
-
-
33745712343
-
The genetics and biology of DISC1-an emerging role in psychosis and cognition
-
Porteous DJ, Thomson P, Brandon NJ, Millar JK. The genetics and biology of DISC1-an emerging role in psychosis and cognition. Biol Psychiatry. 2006; 60(2):123-131.
-
(2006)
Biol Psychiatry
, vol.60
, Issue.2
, pp. 123-131
-
-
Porteous, D.J.1
Thomson, P.2
Brandon, N.J.3
Millar, J.K.4
-
5
-
-
0038003196
-
-
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lonnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR. Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoega T, Helgason T. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: schizophrenia. Am J Hum Genet. 2003;73(1):34-48.
-
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lonnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR. Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoega T, Helgason T. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: schizophrenia. Am J Hum Genet. 2003;73(1):34-48.
-
-
-
-
6
-
-
0036024272
-
Genetic heterogeneity in schizophrenia II: Conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q
-
Chiu YF, McGrath JA, Thomquist MH, Wolyniec PS, Nestadt G, Swartz KL, Lasseter VK, Liang KY, Pulver AE. Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q. Mol Psychiatry. 2002; 7(6):658-664.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.6
, pp. 658-664
-
-
Chiu, Y.F.1
McGrath, J.A.2
Thomquist, M.H.3
Wolyniec, P.S.4
Nestadt, G.5
Swartz, K.L.6
Lasseter, V.K.7
Liang, K.Y.8
Pulver, A.E.9
-
7
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thomquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Pa-padimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Housman DE, Kazazian HH, Antonarakis S, Pulver AE. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet. 1998;20(1):70-73.
-
(1998)
Nat Genet
, vol.20
, Issue.1
, pp. 70-73
-
-
Blouin, J.L.1
Dombroski, B.A.2
Nath, S.K.3
Lasseter, V.K.4
Wolyniec, P.S.5
Nestadt, G.6
Thomquist, M.7
Ullrich, G.8
McGrath, J.9
Kasch, L.10
Lamacz, M.11
Thomas, M.G.12
Gehrig, C.13
Radhakrishna, U.14
Snyder, S.E.15
Balk, K.G.16
Neufeld, K.17
Swartz, K.L.18
DeMarchi, N.19
Pa-padimitriou, G.N.20
Dikeos, D.G.21
Stefanis, C.N.22
Chakravarti, A.23
Childs, B.24
Housman, D.E.25
Kazazian, H.H.26
Antonarakis, S.27
Pulver, A.E.28
more..
-
8
-
-
19944428702
-
Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia
-
Park N, Juo SH, Cheng R, Liu J, Loth JE, Lilliston B, Nee J, Grunn A, Kanyas K, Lerer B, Endicott J, Gilliam TC, Baron M. Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia. Mol Psychiatry. 2004;9(12):1091-1099.
-
(2004)
Mol Psychiatry
, vol.9
, Issue.12
, pp. 1091-1099
-
-
Park, N.1
Juo, S.H.2
Cheng, R.3
Liu, J.4
Loth, J.E.5
Lilliston, B.6
Nee, J.7
Grunn, A.8
Kanyas, K.9
Lerer, B.10
Endicott, J.11
Gilliam, T.C.12
Baron, M.13
-
10
-
-
0035478337
-
The centrosome in vertebrates: More than a microtubule-organizing center
-
Rieder CL, Faruki S, Khodjakov A. The centrosome in vertebrates: more than a microtubule-organizing center. Trends Cell Biol. 2001;11(10):413-419.
-
(2001)
Trends Cell Biol
, vol.11
, Issue.10
, pp. 413-419
-
-
Rieder, C.L.1
Faruki, S.2
Khodjakov, A.3
-
11
-
-
0036468420
-
Centrosome composition and microtubule anchoring mechanisms
-
Bornens M. Centrosome composition and microtubule anchoring mechanisms. Curr Opin Cell Biol. 2002;14(1):25-34.
-
(2002)
Curr Opin Cell Biol
, vol.14
, Issue.1
, pp. 25-34
-
-
Bornens, M.1
-
12
-
-
0035462382
-
Re-evaluating centrosome function
-
Doxsey S. Re-evaluating centrosome function. Nat Rev Mot Cell Biol. 2001;2(9): 688-698.
-
(2001)
Nat Rev Mot Cell Biol
, vol.2
, Issue.9
, pp. 688-698
-
-
Doxsey, S.1
-
13
-
-
33846040831
-
Trekking across the brain: The journey of neuronal migration
-
Ayala R,Shu T,Tsai LH. Trekking across the brain: the journey of neuronal migration. Cell. 2007;128(1):29-43.
-
(2007)
Cell
, vol.128
, Issue.1
, pp. 29-43
-
-
Ayala, R.1
Shu, T.2
Tsai, L.H.3
-
14
-
-
18144364317
-
-
Tsai LH, Gleeson JG. Nucleokinesis in neuronal migration. Neuron. 2005;46(3): 383-388.
-
Tsai LH, Gleeson JG. Nucleokinesis in neuronal migration. Neuron. 2005;46(3): 383-388.
-
-
-
-
16
-
-
0036250810
-
Life is a journey: A genetic look at neocortical development
-
Gupta A, Tsai LH, Wynshaw-Boris A. Life is a journey: a genetic look at neocortical development, Nat Rev Genet. 2002;3(5):342-355.
-
(2002)
Nat Rev Genet
, vol.3
, Issue.5
, pp. 342-355
-
-
Gupta, A.1
Tsai, L.H.2
Wynshaw-Boris, A.3
-
17
-
-
2442576086
-
Genetic basis of developmental malformations of the cerebral cortex
-
Mochida GH, Walsh CA. Genetic basis of developmental malformations of the cerebral cortex. Arch Neurol. 2004;61(5):637-640.
-
(2004)
Arch Neurol
, vol.61
, Issue.5
, pp. 637-640
-
-
Mochida, G.H.1
Walsh, C.A.2
-
18
-
-
0037191046
-
Assembly of centrosomal proteins and microtubule organization depends on PCM-1
-
Dammermann A, Merdes A. Assembly of centrosomal proteins and microtubule organization depends on PCM-1. J Cell Biol. 2002;159(2):255-266.
-
(2002)
J Cell Biol
, vol.159
, Issue.2
, pp. 255-266
-
-
Dammermann, A.1
Merdes, A.2
-
19
-
-
0037348834
-
Non-membranous granular organelle consisting of PCM-1: Subcellular distribution and cell-cycle-dependent assembly/disassembly
-
Kubo A, Tsukita S. Non-membranous granular organelle consisting of PCM-1: subcellular distribution and cell-cycle-dependent assembly/disassembly. J Cell Sci. 2003;116(pt5):919-928.
-
(2003)
J Cell Sci
, vol.116
, Issue.PT5
, pp. 919-928
-
-
Kubo, A.1
Tsukita, S.2
-
20
-
-
0033615982
-
Centriolar satellites: Molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis
-
Kubo A, Sasaki H, Yuba-Kubo A, Tsukita S, Shiina N. Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis. J Cell Biol. 1999;147(5):969-980.
-
(1999)
J Cell Biol
, vol.147
, Issue.5
, pp. 969-980
-
-
Kubo, A.1
Sasaki, H.2
Yuba-Kubo, A.3
Tsukita, S.4
Shiina, N.5
-
21
-
-
20244381625
-
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression
-
Kim JC, Badano JL, Sibold S, Esmail MA, Hill J, Hoskins BE, Leitch CC, Venner K, AnsleySJ, Ross AJ, Leroux MR, Katsanis N, Beales PL. The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nat Genet. 2004:36(5):462-470.
-
(2004)
Nat Genet
, vol.36
, Issue.5
, pp. 462-470
-
-
Kim, J.C.1
Badano, J.L.2
Sibold, S.3
Esmail, M.A.4
Hill, J.5
Hoskins, B.E.6
Leitch, C.C.7
Venner, K.8
Ansley, S.J.9
Ross, A.J.10
Leroux, M.R.11
Katsanis, N.12
Beales, P.L.13
-
22
-
-
19944431708
-
Clinical and geneticepidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study
-
Moore SJ, Green JS, Fan Y, Bhogal AK, Dicks E, Fernandez BA, Stefanelli M, Murphy C, Cramer BC, Dean JC, Beales PL, Katsanis N, Bassett AS, Davidson WS, Parfrey PS. Clinical and geneticepidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study. Am J Med Genet A. 2005;132(4):352-360.
-
(2005)
Am J Med Genet A
, vol.132
, Issue.4
, pp. 352-360
-
-
Moore, S.J.1
Green, J.S.2
Fan, Y.3
Bhogal, A.K.4
Dicks, E.5
Fernandez, B.A.6
Stefanelli, M.7
Murphy, C.8
Cramer, B.C.9
Dean, J.C.10
Beales, P.L.11
Katsanis, N.12
Bassett, A.S.13
Davidson, W.S.14
Parfrey, P.S.15
-
23
-
-
0033062278
-
New criteria for improved diagnosis of Bardet-Biedl syndrome: Results of a population survey
-
Beales PL, Elcioglu N, Woolf AS, Parker D, Flinter FA. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey. J Med Genet. 1999;36(6):437-446.
-
(1999)
J Med Genet
, vol.36
, Issue.6
, pp. 437-446
-
-
Beales, P.L.1
Elcioglu, N.2
Woolf, A.S.3
Parker, D.4
Flinter, F.A.5
-
24
-
-
1842579395
-
-
Katsanis N. The oligogenic properties of Bardet-Biedl syndrome. Hum Mol Genet. 2004;13(spec no 1):R65-R71.
-
Katsanis N. The oligogenic properties of Bardet-Biedl syndrome. Hum Mol Genet. 2004;13(spec no 1):R65-R71.
-
-
-
-
25
-
-
0142104970
-
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
-
Ansley SJ, Badano JL, Blacque OE, Hill J, Hoskins BE, Leitch CC, Kim JC, Ross AJ, Eichers ER, Teslovich TM, Mah AK, Johnsen RC, Cavender JC, Lewis RA, Leroux MR, Beales PL, Katsanis N. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Nature. 2003;425(6958):628-633.
-
(2003)
Nature
, vol.425
, Issue.6958
, pp. 628-633
-
-
Ansley, S.J.1
Badano, J.L.2
Blacque, O.E.3
Hill, J.4
Hoskins, B.E.5
Leitch, C.C.6
Kim, J.C.7
Ross, A.J.8
Eichers, E.R.9
Teslovich, T.M.10
Mah, A.K.11
Johnsen, R.C.12
Cavender, J.C.13
Lewis, R.A.14
Leroux, M.R.15
Beales, P.L.16
Katsanis, N.17
-
26
-
-
27144460671
-
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates
-
Ross AJ, May-Simera H, Eichers ER, Kai M, Hill J, Jagger DJ, Leitch CC, Chappie JP, Munro PM, Fisher S, Tan PL, Phillips HM, Leroux MR, Henderson DJ, Murdoch JN, Copp AJ, Eliot MM, Lupski JR, Kemp DT, Dollfus H, Tada M, Katsanis N, Forge A, Beales PL. Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat Genet. 2005;37(10):1135-1140.
-
(2005)
Nat Genet
, vol.37
, Issue.10
, pp. 1135-1140
-
-
Ross, A.J.1
May-Simera, H.2
Eichers, E.R.3
Kai, M.4
Hill, J.5
Jagger, D.J.6
Leitch, C.C.7
Chappie, J.P.8
Munro, P.M.9
Fisher, S.10
Tan, P.L.11
Phillips, H.M.12
Leroux, M.R.13
Henderson, D.J.14
Murdoch, J.N.15
Copp, A.J.16
Eliot, M.M.17
Lupski, J.R.18
Kemp, D.T.19
Dollfus, H.20
Tada, M.21
Katsanis, N.22
Forge, A.23
Beales, P.L.24
more..
-
27
-
-
3042738924
-
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
-
Blacque OE, Reardon MJ, Li C, McCarthy J, Mahjoub MR, Ansley SJ, Badano JL, Mah AK, Beales PL, Davidson WS, Johnsen RCAudeh M, Plasterk RH, Baillie DL, Katsanis N, Quarmby LM, Wicks SR, Leroux MR. Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport. Genes Dev. 2004;18(13):1630-1642.
-
(2004)
Genes Dev
, vol.18
, Issue.13
, pp. 1630-1642
-
-
Blacque, O.E.1
Reardon, M.J.2
Li, C.3
McCarthy, J.4
Mahjoub, M.R.5
Ansley, S.J.6
Badano, J.L.7
Mah, A.K.8
Beales, P.L.9
Davidson, W.S.10
Johnsen RCAudeh, M.11
Plasterk, R.H.12
Baillie, D.L.13
Katsanis, N.14
Quarmby, L.M.15
Wicks, S.R.16
Leroux, M.R.17
-
28
-
-
4444254983
-
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse
-
Kulaga HM, Leitch CC, Eichers ER, Badano JL, Lesemann A, Hoskins BE, Lupski JR, Beales PL, Reed RR, Katsanis N. Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nat Genet. 2004:36(9):994-998.
-
(2004)
Nat Genet
, vol.36
, Issue.9
, pp. 994-998
-
-
Kulaga, H.M.1
Leitch, C.C.2
Eichers, E.R.3
Badano, J.L.4
Lesemann, A.5
Hoskins, B.E.6
Lupski, J.R.7
Beales, P.L.8
Reed, R.R.9
Katsanis, N.10
-
29
-
-
33144456230
-
Bardet- Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function
-
Yen HJ, Tayeh MK, Mullins RF, Stone EM, Sheffield VC, Slusarski DC. Bardet- Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function. Hum Mol Genet. 2006;15(5):667-677.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.5
, pp. 667-677
-
-
Yen, H.J.1
Tayeh, M.K.2
Mullins, R.F.3
Stone, E.M.4
Sheffield, V.C.5
Slusarski, D.C.6
-
30
-
-
34250012834
-
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
-
Nachury MV, Loktev AV, Zhang Q, Westlake CJ, Peranen J, Merdes A, Slusarski DC, Scheller RH, Bazan JF, Sheffield VC, Jackson PK. A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Cell. 2007;129(6)1201-1213.
-
(2007)
Cell
, vol.129
, Issue.6
, pp. 1201-1213
-
-
Nachury, M.V.1
Loktev, A.V.2
Zhang, Q.3
Westlake, C.J.4
Peranen, J.5
Merdes, A.6
Slusarski, D.C.7
Scheller, R.H.8
Bazan, J.F.9
Sheffield, V.C.10
Jackson, P.K.11
-
31
-
-
28544453286
-
A schizophrenia- associated mutation of DISC1 perturbs cerebral cortexdevelopment
-
Kamiya A, Kubo K,Tomoda T, Takaki M, Youn R, Ozeki Y, Sawamura N, Park U, Kudo C, Okawa M, Ross CA, Hatten ME, Nakajima K, Sawa A. A schizophrenia- associated mutation of DISC1 perturbs cerebral cortexdevelopment. Nat Cell Biol. 2005;7(12)1167-1178.
-
(2005)
Nat Cell Biol
, vol.7
, Issue.12
, pp. 1167-1178
-
-
Kamiya, A.1
Kubo, K.2
Tomoda, T.3
Takaki, M.4
Youn, R.5
Ozeki, Y.6
Sawamura, N.7
Park, U.8
Kudo, C.9
Okawa, M.10
Ross, C.A.11
Hatten, M.E.12
Nakajima, K.13
Sawa, A.14
-
32
-
-
33750388150
-
DISC1-NDEL1/ NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1
-
Kamiya A, TomodaT, Chang J, Takaki M, Zhan C, Morita M, Cascio MB, Elashvili S, Koizumi H, Jakanezawa Y, Dickerson F,Yolken R, Arai H, Sawa A. DISC1-NDEL1/ NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1. Hum Mol Genet. 2006;15(22):3313-3323.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.22
, pp. 3313-3323
-
-
Kamiya, A.1
Tomoda, T.2
Chang, J.3
Takaki, M.4
Zhan, C.5
Morita, M.6
Cascio, M.B.7
Elashvili, S.8
Koizumi, H.9
Jakanezawa, Y.10
Dickerson, F.11
Yolken, R.12
Arai, H.13
Sawa, A.14
-
33
-
-
1942504197
-
DISC1 localizes to the centrosome by binding to kendrin
-
Miyoshi K, Asanuma M, Miyazaki I, Diaz-Corrales FJ, Katayama T, Tohyama M, Ogawa N. DISC1 localizes to the centrosome by binding to kendrin. Biochem Biophys Res Commun. 2004;317(4) 1195-1199.
-
(2004)
Biochem Biophys Res Commun
, vol.317
, Issue.4
, pp. 1195-1199
-
-
Miyoshi, K.1
Asanuma, M.2
Miyazaki, I.3
Diaz-Corrales, F.J.4
Katayama, T.5
Tohyama, M.6
Ogawa, N.7
-
34
-
-
0024520745
-
Site-directed mutagenesis by overlap extension using the polymerase chain reaction
-
HoSN, Hunt HD, Horton RM, Pullen JK, Pease LR. Site-directed mutagenesis by overlap extension using the polymerase chain reaction. Gene. 1989;77(1 ):51-59.
-
(1989)
Gene
, vol.77
, Issue.1
, pp. 51-59
-
-
Ho, S.N.1
Hunt, H.D.2
Horton, R.M.3
Pullen, J.K.4
Pease, L.R.5
-
35
-
-
18344396250
-
Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia
-
Ishikawa H. Kubo A, Tsukita S, Tsukita S. Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia. Nat Cell Biol. 2005;7(5):517-524.
-
(2005)
Nat Cell Biol
, vol.7
, Issue.5
, pp. 517-524
-
-
Ishikawa, H.1
Kubo, A.2
Tsukita, S.3
Tsukita, S.4
-
36
-
-
0037197914
-
RN A interference by expression of short-interfering RNAs and hairpin RNAs in mammalian cells
-
Yu JY, DeRuiter SL, Turner DL. RN A interference by expression of short-interfering RNAs and hairpin RNAs in mammalian cells. Proc Natl Acad Sci U S A. 2002: 99(9):6047-6052.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, Issue.9
, pp. 6047-6052
-
-
Yu, J.Y.1
DeRuiter, S.L.2
Turner, D.L.3
-
37
-
-
0030868934
-
Glyceraldehyde-3-phosphate dehydrogenase: Nucleartranslocation participates in neuronal and nonneuronal cell death
-
Sawa A, Khan AA, Hester LD, Snyder SH. Glyceraldehyde-3-phosphate dehydrogenase: nucleartranslocation participates in neuronal and nonneuronal cell death. Proc Natl Acad Sci US A. 1997;94(21):11669-11674.
-
(1997)
Proc Natl Acad Sci US A
, vol.94
, Issue.21
, pp. 11669-11674
-
-
Sawa, A.1
Khan, A.A.2
Hester, L.D.3
Snyder, S.H.4
-
38
-
-
0035804770
-
Efficient in utero gene transfer system to the developing mouse brain using electroporation: Visualization of neuronal migration in the developing cortex
-
Tabata H, Nakajima K. Efficient in utero gene transfer system to the developing mouse brain using electroporation: visualization of neuronal migration in the developing cortex. Neuroscience. 2001;103(4):865-872.
-
(2001)
Neuroscience
, vol.103
, Issue.4
, pp. 865-872
-
-
Tabata, H.1
Nakajima, K.2
-
39
-
-
33847759937
-
Schizophrenia: A common disease caused by multiple rare alleles
-
McClellan JM, Susser E, King MC. Schizophrenia: a common disease caused by multiple rare alleles. Br J Psychiatry. 2007;190:194-199.
-
(2007)
Br J Psychiatry
, vol.190
, pp. 194-199
-
-
McClellan, J.M.1
Susser, E.2
King, M.C.3
-
40
-
-
0033525169
-
A perfect message: RNA surveillance and nonsense-mediated decay
-
Hentze MW, Kulozik AE. A perfect message: RNA surveillance and nonsense-mediated decay. Cell. 1999;96(3):307-310.
-
(1999)
Cell
, vol.96
, Issue.3
, pp. 307-310
-
-
Hentze, M.W.1
Kulozik, A.E.2
-
42
-
-
0034100029
-
Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p,and 10p in the Irish Study of High-Density Schizophrenia Families
-
Kendler KS, Myers JM, O'Neill FA, Martin R, Murphy B, MacLean CJ, Walsh D, Straub RE. Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p,and 10p in the Irish Study of High-Density Schizophrenia Families. Am J Psychiatry. 2000;157(3):402-408.
-
(2000)
Am J Psychiatry
, vol.157
, Issue.3
, pp. 402-408
-
-
Kendler, K.S.1
Myers, J.M.2
O'Neill, F.A.3
Martin, R.4
Murphy, B.5
MacLean, C.J.6
Walsh, D.7
Straub, R.E.8
-
43
-
-
0023883767
-
Deficit and nondeficit forms of schizophrenia: The concept
-
Carpenter WT Jr, Heinrichs DW. Wagman AM. Deficit and nondeficit forms of schizophrenia: the concept. Am J Psychiatry. 1988;145(5):578-583.
-
(1988)
Am J Psychiatry
, vol.145
, Issue.5
, pp. 578-583
-
-
Carpenter Jr, W.T.1
Heinrichs, D.W.2
Wagman, A.M.3
-
44
-
-
0031907791
-
The clinical stigmata of aberrant neurodevelopment in schizophrenia
-
Buckley PF. The clinical stigmata of aberrant neurodevelopment in schizophrenia. J Nerv Ment Dis. 1998;186(2):79-86.
-
(1998)
J Nerv Ment Dis
, vol.186
, Issue.2
, pp. 79-86
-
-
Buckley, P.F.1
-
45
-
-
12944329900
-
Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 gene
-
lannaccone A, Mykytyn K, Persico AM, Searby CC, Baldi A, Jablonski MM, Sheffield VC. Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 gene. Am J Med Genet A. 2005;132(4):343-346.
-
(2005)
Am J Med Genet A
, vol.132
, Issue.4
, pp. 343-346
-
-
lannaccone, A.1
Mykytyn, K.2
Persico, A.M.3
Searby, C.C.4
Baldi, A.5
Jablonski, M.M.6
Sheffield, V.C.7
-
46
-
-
3342901698
-
Physical health monitoring of patients with schizophrenia
-
Marder SR, Essock SM, Miller AL, Buchanan RW, Casey DE, Davis JM, Kane JM, Lieberman JA, Schooler NR, Covell N, Stroup S, Weissman EM, Wirshing DA, Hall CS, Pogach L, Pi-SunyerX, Bigger JT Jr, Friedman A, Kleinberg D, Yevich SJ, Davis B, Shon S. Physical health monitoring of patients with schizophrenia. Am J Psychiatry. 2004;161(8)1334-1349.
-
(2004)
Am J Psychiatry
, vol.161
, Issue.8
, pp. 1334-1349
-
-
Marder, S.R.1
Essock, S.M.2
Miller, A.L.3
Buchanan, R.W.4
Casey, D.E.5
Davis, J.M.6
Kane, J.M.7
Lieberman, J.A.8
Schooler, N.R.9
Covell, N.10
Stroup, S.11
Weissman, E.M.12
Wirshing, D.A.13
Hall, C.S.14
Pogach, L.15
SunyerX, P.16
Bigger Jr, J.T.17
Friedman, A.18
Kleinberg, D.19
Yevich, S.J.20
Davis, B.21
Shon, S.22
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