-
1
-
-
0029776032
-
A molecular mechanism for the effect of lithium on development
-
1 Klein PS, Melton DA. A molecular mechanism for the effect of lithium on development. Proc Natl Acad Sci USA 1996; 93: 8455-8459.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8455-8459
-
-
Klein, P.S.1
Melton, D.A.2
-
2
-
-
0024341795
-
Neural and developmental actions of lithium: A unifying hypothesis
-
2 Berridge MJ, Downes CP, Hanley MR. Neural and developmental actions of lithium: a unifying hypothesis. Cell 1989; 59: 411-419.
-
(1989)
Cell
, vol.59
, pp. 411-419
-
-
Berridge, M.J.1
Downes, C.P.2
Hanley, M.R.3
-
3
-
-
0028568147
-
Signaling by wingless in Drosphila
-
3 Klingensmith J, Nusse R. Signaling by wingless in Drosphila. Dev Biol 1994; 166: 396-414.
-
(1994)
Dev Biol
, vol.166
, pp. 396-414
-
-
Klingensmith, J.1
Nusse, R.2
-
4
-
-
0026772731
-
Wnt genes
-
4 Nusse R, Varmus HE. Wnt genes. Cell 1992; 69: 1073-1087.
-
(1992)
Cell
, vol.69
, pp. 1073-1087
-
-
Nusse, R.1
Varmus, H.E.2
-
5
-
-
0025188130
-
The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain
-
5 McMahon AP, Bradley A. The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain. Cell 1990; 62: 1073-1085.
-
(1990)
Cell
, vol.62
, pp. 1073-1085
-
-
McMahon, A.P.1
Bradley, A.2
-
6
-
-
0020216124
-
Many tumors induced by the mouse mammary tumor viruses contain a provirus integrated in the same region of the host genome
-
6 Nusse R, Varmus HE. Many tumors induced by the mouse mammary tumor viruses contain a provirus integrated in the same region of the host genome. Cell 1982; 31: 99-109.
-
(1982)
Cell
, vol.31
, pp. 99-109
-
-
Nusse, R.1
Varmus, H.E.2
-
7
-
-
0030068938
-
A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled
-
7 Wang Y, Macke JP, Abella BS, Andreasson K, Worley P, Gilbert DJ et al. A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled. J Biol Chem 1996; 271: 4468-4776.
-
(1996)
J Biol Chem
, vol.271
, pp. 4468-4776
-
-
Wang, Y.1
Macke, J.P.2
Abella, B.S.3
Andreasson, K.4
Worley, P.5
Gilbert, D.J.6
-
8
-
-
0030265570
-
A frizzled homolog functions in a vertebrate Wnt signaling pathway
-
8 Yang-Synder J, Miller JR, Brown JD, Lai CJ, Moon RT. A frizzled homolog functions in a vertebrate Wnt signaling pathway. Curr Biol 1996; 6: 1302-1306.
-
(1996)
Curr Biol
, vol.6
, pp. 1302-1306
-
-
Yang-Synder, J.1
Miller, J.R.2
Brown, J.D.3
Lai, C.J.4
Moon, R.T.5
-
9
-
-
0030905162
-
Family of secreted proteins contains homology to the cysteine-rich ligand-binding domain of frizzled receptors
-
9 Kattner A, Hsieh J-C, Smallwood PM, Gilbert DJ, Copeland NG, Jenkins NA at al. Family of secreted proteins contains homology to the cysteine-rich ligand-binding domain of frizzled receptors. Proc Natl Acad Sci USA 1997; 94: 2859-2863.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2859-2863
-
-
Kattner, A.1
Hsieh, J.-C.2
Smallwood, P.M.3
Gilbert, D.J.4
Copeland, N.G.5
Jenkins, N.A.6
-
10
-
-
0031459893
-
SARPS: A family of secreted apoposisrelated proteins
-
10 Melkanyan HS, Chang WC, Shapiro JP, Mahadevappa M, Fitzpatrick PA, Kiefer MC et al. SARPS: a family of secreted apoposisrelated proteins. Proc Natl Acad Sci 1997; 94: 13636-13641.
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 13636-13641
-
-
Melkanyan, H.S.1
Chang, W.C.2
Shapiro, J.P.3
Mahadevappa, M.4
Fitzpatrick, P.A.5
Kiefer, M.C.6
-
11
-
-
0030844356
-
Negative regulation of Armadillo, a wingless effector in Drosophila
-
11 Pai LM, Oursulic S, Bejsovec A, Peifer MK. Negative regulation of Armadillo, a wingless effector in Drosophila. Development 1997; 124: 2255-2266.
-
(1997)
Development
, vol.124
, pp. 2255-2266
-
-
Pai, L.M.1
Oursulic, S.2
Bejsovec, A.3
Peifer, M.K.4
-
13
-
-
0030900696
-
Stabilization of β-catenin by genetic defects in melanoma cell lines
-
13 Rubinfeld B, Robbins P, El-Gamil M, Albert I, Potfiri E, Polakis P. Stabilization of β-catenin by genetic defects in melanoma cell lines. Science 1997; 275: 1790-1792.
-
(1997)
Science
, vol.275
, pp. 1790-1792
-
-
Rubinfeld, B.1
Robbins, P.2
El-Gamil, M.3
Albert, I.4
Potfiri, E.5
Polakis, P.6
-
14
-
-
0032079884
-
Axin, a negative regulator of the Wnt signaling pathway, directly interacts with adenomatous polyposis coli and regulates the stabilization of β-catenin
-
14 Kishida S, Yamamoto H, Ikeda S, Kishida M, Sakamoto I, Koyama S et al. Axin, a negative regulator of the Wnt signaling pathway, directly interacts with adenomatous polyposis coli and regulates the stabilization of β-catenin. J Biol Chem 1998; 273: 10823-10826.
-
(1998)
J Biol Chem
, vol.273
, pp. 10823-10826
-
-
Kishida, S.1
Yamamoto, H.2
Ikeda, S.3
Kishida, M.4
Sakamoto, I.5
Koyama, S.6
-
15
-
-
0032493042
-
Axis determination in Xenopus involves biochemical interactions of axin, glycogen synthase kinase 3 and beta-catenin
-
15 Itoh K, Krupnik VE, Sokol SY. Axis determination in Xenopus involves biochemical interactions of axin, glycogen synthase kinase 3 and beta-catenin. Curr Biol 1998; 8: 591-594.
-
(1998)
Curr Biol
, vol.8
, pp. 591-594
-
-
Itoh, K.1
Krupnik, V.E.2
Sokol, S.Y.3
-
16
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
16 Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science 1996; 273; 1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
17
-
-
0029996490
-
Affected-sih-pair interval mapping and exclusion for complex genetic traits: Sampling considerations
-
17 Hauser ER, Boehnke M, Guo S-W, Risch N. Affected-sih-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genetic Epidemiol 1996; 13: 117-137.
-
(1996)
Genetic Epidemiol
, vol.13
, pp. 117-137
-
-
Hauser, E.R.1
Boehnke, M.2
Guo, S.-W.3
Risch, N.4
-
18
-
-
0028090414
-
Genetic dissection of complex traits
-
18 Lander ES, Schork NJ. Genetic dissection of complex traits. Science 1994; 265: 2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
19
-
-
0031423325
-
An integrated physical map of 18p11.2: A susceptibility region for bipolar disorder
-
19 Esterling LE, Cox Matise T, Sanders AR, Yoshikawa T, Overhauser I, Gershon ES et al. An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder. Mol Psychiatry 1997; 2: 501-504.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 501-504
-
-
Esterling, L.E.1
Cox Matise, T.2
Sanders, A.R.3
Yoshikawa, T.4
Overhauser, I.5
Gershon, E.S.6
-
20
-
-
0026321407
-
Statistical methods for multipoint radiation hybrid mapping
-
20 Boehnke M, Lange K, Cox DR. Statistical methods for multipoint radiation hybrid mapping. Am J Hum Gunet 1991; 49: 1174-1188.
-
(1991)
Am J Hum Gunet
, vol.49
, pp. 1174-1188
-
-
Boehnke, M.1
Lange, K.2
Cox, D.R.3
-
21
-
-
0025131820
-
Radiation hybrid mapping: A somatic cell genetic method for constructing high resolution maps for mammalian chromosomes
-
21 Cox DR, Burmeister M, Price ER, Kim S, Myers RM. Radiation hybrid mapping: a somatic cell genetic method for constructing high resolution maps for mammalian chromosomes. Science 1990; 250: 245-250.
-
(1990)
Science
, vol.250
, pp. 245-250
-
-
Cox, D.R.1
Burmeister, M.2
Price, E.R.3
Kim, S.4
Myers, R.M.5
-
22
-
-
0029835716
-
Isolation, characterization and chromosomal assignment of the human WNT7A gene
-
22 Ikegawa S, Kumano Y, Okui K, Fujiwara T, Takahashi E, Nakamura Y. Isolation, characterization and chromosomal assignment of the human WNT7A gene. Cytogenet Cell Genet 1996; 74: 149-152.
-
(1996)
Cytogenet Cell Genet
, vol.74
, pp. 149-152
-
-
Ikegawa, S.1
Kumano, Y.2
Okui, K.3
Fujiwara, T.4
Takahashi, E.5
Nakamura, Y.6
-
23
-
-
4243251133
-
Identification and characterization of fprHE, a novel stromal protein of the Frizzled gene family modulated during the endometrial cycle and malignant transformation
-
23 Abu-Jawdeh G, Comella N, Tomita Y, Brown L, Tognazzi K, Kocher O. Identification and characterization of fprHE, a novel stromal protein of the frizzled gene family modulated during the endometrial cycle and malignant transformation. FASEB J 1998; 12: 944.
-
(1998)
FASEB J
, vol.12
, pp. 944
-
-
Abu-Jawdeh, G.1
Comella, N.2
Tomita, Y.3
Brown, L.4
Tognazzi, K.5
Kocher, O.6
-
24
-
-
8944229701
-
cDNA characterization and chromosomal mapping of two human homologues of the Drosphila dishevelled polarity gene
-
24 Pizzuti A, Amati F, Calabrese G, Mari A, Golosimo A, Silani V et al. cDNA characterization and chromosomal mapping of two human homologues of the Drosphila dishevelled polarity gene. Hum Mol Genet 1996; 5: 953-958.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 953-958
-
-
Pizzuti, A.1
Amati, F.2
Calabrese, G.3
Mari, A.4
Golosimo, A.5
Silani, V.6
-
25
-
-
0030155254
-
Dishevelled-2 maps to human chromosome 17 and distal to Wnt3A and vestigial tail(vt) on mouse chromosome 11
-
25 Greco TL, Sussman DJ, Camper SA. Dishevelled-2 maps to human chromosome 17 and distal to Wnt3A and vestigial tail(vt) on mouse chromosome 11. Mammalian Genome 1996; 7: 475-476.
-
(1996)
Mammalian Genome
, vol.7
, pp. 475-476
-
-
Greco, T.L.1
Sussman, D.J.2
Camper, S.A.3
-
26
-
-
0031581105
-
cDNA cloning of a human dishevelled DVL-3 gene, mapping to 3q27, and expression in human breast and colon carcinomas
-
26 Bui TD, Beirer DR, Jonssen M, Smith K, Dorrington SM, Kaklamanis L et al. cDNA cloning of a human dishevelled DVL-3 gene, mapping to 3q27, and expression in human breast and colon carcinomas. Biochem Biophys Res Commun 1997; 239: 510-516.
-
(1997)
Biochem Biophys Res Commun
, vol.239
, pp. 510-516
-
-
Bui, T.D.1
Beirer, D.R.2
Jonssen, M.3
Smith, K.4
Dorrington, S.M.5
Kaklamanis, L.6
-
27
-
-
0030875687
-
Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3α and β isoforms in patients with NIDDM
-
27 Hansen L, Arden KC, Rasmussen SB, Viars CS, Vestergaard H, Hansen T et al. Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3α and β isoforms in patients with NIDDM. Diabetologia 1997; 40: 940-946.
-
(1997)
Diabetologia
, vol.40
, pp. 940-946
-
-
Hansen, L.1
Arden, K.C.2
Rasmussen, S.B.3
Viars, C.S.4
Vestergaard, H.5
Hansen, T.6
-
28
-
-
0030978030
-
Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22
-
28 Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C et al. Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. Am J Med Genet 1997; 74: 238-246.
-
(1997)
Am J Med Genet
, vol.74
, pp. 238-246
-
-
Edenberg, H.J.1
Foroud, T.2
Conneally, P.M.3
Sorbel, J.J.4
Carr, K.5
Crose, C.6
-
29
-
-
0031469645
-
WNT-7a induces axonal remodeling and increases synapsin I levels in cerebellar neurons
-
29 Lucas FR, Salinas PC. WNT-7a induces axonal remodeling and increases synapsin I levels in cerebellar neurons. Dev Biol 1997; 192: 31-44.
-
(1997)
Dev Biol
, vol.192
, pp. 31-44
-
-
Lucas, F.R.1
Salinas, P.C.2
-
30
-
-
0031043863
-
A novel human homologue of the Drosphila frizzled Wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23
-
30 Wang YK, Samos CH, Peoples R, Perez-Jurado LA, Nusse R, Francke U. A novel human homologue of the Drosphila frizzled Wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23. Hum Mol Genet 1997; 6: 465-472.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 465-472
-
-
Wang, Y.K.1
Samos, C.H.2
Peoples, R.3
Perez-Jurado, L.A.4
Nusse, R.5
Francke, U.6
-
31
-
-
0031811718
-
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin
-
31 Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR et al. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin. Am J Med Genet 1998; 78: 82-89.
-
(1998)
Am J Med Genet
, vol.78
, pp. 82-89
-
-
Wu, Y.Q.1
Sutton, V.R.2
Nickerson, E.3
Lupski, J.R.4
Potocki, L.5
Korenberg, J.R.6
-
32
-
-
0029891886
-
Delineation of 7q11.2 deletions associated with Williams-Beuren Syndrome and mapping of a repetitive sequence to within and to either side of the common deletion
-
32 Robinson WP, Waslynka J, Bernasconi F, Wang M, Clark S, Kotzot D et al. Delineation of 7q11.2 deletions associated with Williams-Beuren Syndrome and mapping of a repetitive sequence to within and to either side of the common deletion. Genomics 1996; 34: 17-23.
-
(1996)
Genomics
, vol.34
, pp. 17-23
-
-
Robinson, W.P.1
Waslynka, J.2
Bernasconi, F.3
Wang, M.4
Clark, S.5
Kotzot, D.6
-
33
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
33 Blouin J-L, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G et al. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nature 1998; 20: 70-73.
-
(1998)
Nature
, vol.20
, 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
-
34
-
-
12644293808
-
Searching for susceptibility genes in schizophrenia by genetic linkage analysis
-
34 Wildenauer DB, Hallmayer J, Schwab SG, Albus M, Eckstein GN, Zill P et al. Searching for susceptibility genes in schizophrenia by genetic linkage analysis. Cold Spring Harb Symp Quant Biol 1996; 61: 845-850.
-
(1996)
Cold Spring Harb Symp Quant Biol
, vol.61
, pp. 845-850
-
-
Wildenauer, D.B.1
Hallmayer, J.2
Schwab, S.G.3
Albus, M.4
Eckstein, G.N.5
Zill, P.6
-
35
-
-
0030951901
-
Initial genome scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 1,6,8,10 and 12
-
35 Rice JP, Goate A, Williams JT, Bierut L, Door D, Wu W et al. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1,6,8,10 and 12. Am J Med Genet 1997; 74: 247-253.
-
(1997)
Am J Med Genet
, vol.74
, pp. 247-253
-
-
Rice, J.P.1
Goate, A.2
Williams, J.T.3
Bierut, L.4
Door, D.5
Wu, W.6
-
36
-
-
17444448778
-
Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium
-
36 Faraone SV, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B et al. Genome scan of European-American schizophrenia pedigrees: results of the NIMH genetics initiative and millennium consortium. Am J Med Genet 1998; 81: 290-295.
-
(1998)
Am J Med Genet
, vol.81
, pp. 290-295
-
-
Faraone, S.V.1
Matise, T.2
Svrakic, D.3
Pepple, J.4
Malaspina, D.5
Suarez, B.6
-
37
-
-
13044281675
-
A high density genome scan detects evidence for a bipolar disorder susceptibility locus on 13q32, and other potential loci on 1q32 and 18p11.2
-
in press
-
37 Detera-Wadleigh SD, Badner JA, Berrettini WH, Yoshikawa T, Coldin LR, Turner G et al. A high density genome scan detects evidence for a bipolar disorder susceptibility locus on 13q32, and other potential loci on 1q32 and 18p11.2. Proc Natl Acad Sci USA 1999; (in press).
-
(1999)
Proc Natl Acad Sci USA
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Berrettini, W.H.3
Yoshikawa, T.4
Coldin, L.R.5
Turner, G.6
-
38
-
-
0029823845
-
Possible locus for bipolar disorder near the dopamine transporter on chromosome 5
-
38 Kelsoe JR, Sadovnick AD, Kristbjarnarson H, Bergesch P, Mroczkowski-Parder Z, Drennan M et al. Possible locus for bipolar disorder near the dopamine transporter on chromosome 5. Am J Med Genet 1996; 67: 533-540.
-
(1996)
Am J Med Genet
, vol.67
, pp. 533-540
-
-
Kelsoe, J.R.1
Sadovnick, A.D.2
Kristbjarnarson, H.3
Bergesch, P.4
Mroczkowski-Parder, Z.5
Drennan, M.6
-
39
-
-
0028941443
-
Five novel genes from the Cri-Du-Chat critical region isolated by direct selection
-
39 Simmons AD, Gondart SA, Gallardo TD. Overhauser J, Lovett M. Five novel genes from the Cri-Du-Chat critical region isolated by direct selection. Hum Mol Genet 1995; 4: 295-302.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 295-302
-
-
Simmons, A.D.1
Gondart, S.A.2
Gallardo, T.D.3
Overhauser, J.4
Lovett, M.5
-
40
-
-
0028938044
-
Isolation and characterization of a human pseudogene (CTNNAP2) and alpha E-catenin (CTNNA1): Assignment of the pseudogene to 5q22 and the alpha E-catenin gene to 5q31
-
40 Nollet F, van Hengel J, Berx G, Molemans F, van Roy F. Isolation and characterization of a human pseudogene (CTNNAP1) and alpha E-catenin (CTNNA1): assignment of the pseudogene to 5q22 and the alpha E-catenin gene to 5q31. Genomics 1995; 26: 410-413.
-
(1995)
Genomics
, vol.26
, pp. 410-413
-
-
Nollet, F.1
Van Hengel, J.2
Berx, G.3
Molemans, F.4
Van Roy, F.5
-
41
-
-
8244226000
-
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis
-
41 Schwab SG, Eckstein GN, Hallmayer J, Lerer B, Albus M, Borrmann M et al. Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis. Mol Psychiatry 1997; 2: 156-160.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 156-160
-
-
Schwab, S.G.1
Eckstein, G.N.2
Hallmayer, J.3
Lerer, B.4
Albus, M.5
Borrmann, M.6
-
42
-
-
0030980118
-
Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families
-
42 Straub RE, MacLean CJ, O'Neill FA, Walsh H, Kendler KS. Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families. Mol Psychiatry 1997; 2: 148-155.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 148-155
-
-
Straub, R.E.1
Maclean, C.J.2
O'Neill, F.A.3
Walsh, H.4
Kendler, K.S.5
-
43
-
-
0031149476
-
Activation of the Wnt signaling pathway: A molecular mechanism for lithium action
-
43 Hedgepeth CM, Conrad LJ, Zhang J, Huang H-C, Lee VMY, Klein PS. Activation of the Wnt signaling pathway: a molecular mechanism for lithium action. Dev Biol 1997; 185: 82-91.
-
(1997)
Dev Biol
, vol.185
, pp. 82-91
-
-
Hedgepeth, C.M.1
Conrad, L.J.2
Zhang, J.3
Huang, H.-C.4
Lee, V.M.Y.5
Klein, P.S.6
-
44
-
-
0030748390
-
Insulin and insulin-like growth factor-1 regulate lau phnsphorylation in cultured human neurons
-
44 Hong M, Lee VM. Insulin and insulin-like growth factor-1 regulate lau phnsphorylation in cultured human neurons. J Biol Chem 1997; 272; 19547-19553.
-
(1997)
J Biol Chem
, vol.272
, pp. 19547-19553
-
-
Hong, M.1
Lee, V.M.2
-
45
-
-
0031567583
-
Lithium inhibits Alzheimer's disease-like tau protein phosphorylation in neurons
-
45 Munoz-Montano FR, Moreno FJ, Avila J, Diaz-Nido J. Lithium inhibits Alzheimer's disease-like tau protein phosphorylation in neurons. FEBS Lett 1997; 411: 183-188.
-
(1997)
FEBS Lett
, vol.411
, pp. 183-188
-
-
Munoz-Montano, F.R.1
Moreno, F.J.2
Avila, J.3
Diaz-Nido, J.4
-
46
-
-
0031128131
-
Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome
-
46 Sirotkin H, O'Donnell H, DasGupta R, Halford S, Jore BS, Puech A et al. Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome. Genomics 1997; 41: 75-83.
-
(1997)
Genomics
, vol.41
, pp. 75-83
-
-
Sirotkin, H.1
O'Donnell, H.2
DasGupta, R.3
Halford, S.4
Jore, B.S.5
Puech, A.6
-
47
-
-
0030898042
-
Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22
-
47 Lachman HM, Kelsoe JR, Remick RA, Sadovnick AD, Rapaport MH, Lin M et al. Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22. Am J Med Genet 1997; 74: 121-128.
-
(1997)
Am J Med Genet
, vol.74
, pp. 121-128
-
-
Lachman, H.M.1
Kelsoe, J.R.2
Remick, R.A.3
Sadovnick, A.D.4
Rapaport, M.H.5
Lin, M.6
-
48
-
-
0032503887
-
22q11 deletion syndrome in adults with schizophrenia
-
48 Bassett AS, Hodgkinson K, Chow EWC, Correia S, Scutt LE, Weksberg R. 22q11 Deletion syndrome in adults with schizophrenia. Am J Med Genet 1998; 81: 328-337.
-
(1998)
Am J Med Genet
, vol.81
, pp. 328-337
-
-
Bassett, A.S.1
Hodgkinson, K.2
Chow, E.W.C.3
Correia, S.4
Scutt, L.E.5
Weksberg, R.6
-
49
-
-
0029874880
-
A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22)
-
40 Gill M, Vallada H, Collier D, Sham P, Holmans P, Murray R et al. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). Am J Med Genet 1996; 67: 40-45.
-
(1996)
Am J Med Genet
, vol.67
, pp. 40-45
-
-
Gill, M.1
Vallada, H.2
Collier, D.3
Sham, P.4
Holmans, P.5
Murray, R.6
-
50
-
-
0032507631
-
Abnormalities of wnt signalling in schizophrenia - Evidence for neurodevelopmental abnormality
-
50 Cotter D, Kerwin R, al-Sarraji S, Brion JP, Chadwich A, Lovestone S et al. Abnormalities of Wnt signalling in schizophrenia - evidence for neurodevelopmental abnormality. Neuroreport 1998; 9: 1379-1383.
-
(1998)
Neuroreport
, vol.9
, pp. 1379-1383
-
-
Cotter, D.1
Kerwin, R.2
Al-Sarraji, S.3
Brion, J.P.4
Chadwich, A.5
Lovestone, S.6
-
51
-
-
0029163012
-
A possible locus for manic depressive illness on chromosome 16p13
-
51 Ewald H, Mors O, Flint T, Koed K, Eiberg H, Kruse TA. A possible locus for manic depressive illness on chromosome 16p13. Psychiatr Genet 1995; 5: 71-81.
-
(1995)
Psychiatr Genet
, vol.5
, pp. 71-81
-
-
Ewald, H.1
Mors, O.2
Flint, T.3
Koed, K.4
Eiberg, H.5
Kruse, T.A.6
|