-
1
-
-
0842286647
-
Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands
-
Als T.D., Dahl H.A., Flint T.J., Wang A.G., Vang M., Mors O., Kruse T.A., and Ewald H. Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands. Mol. Psychiatry 9 (2004) 93-98
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 93-98
-
-
Als, T.D.1
Dahl, H.A.2
Flint, T.J.3
Wang, A.G.4
Vang, M.5
Mors, O.6
Kruse, T.A.7
Ewald, H.8
-
2
-
-
34447293761
-
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome
-
Cano A., Rouzier C., Monnot S., Chabrol B., Conrath J., Lecomte P., Delobel B., Boileau P., Valero R., Procaccio V., Paquis-Flucklinger V., and Vialettes B. Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome. Am. J. Med. Genet. A 143 (2007) 1605-1612
-
(2007)
Am. J. Med. Genet. A
, vol.143
, pp. 1605-1612
-
-
Cano, A.1
Rouzier, C.2
Monnot, S.3
Chabrol, B.4
Conrath, J.5
Lecomte, P.6
Delobel, B.7
Boileau, P.8
Valero, R.9
Procaccio, V.10
Paquis-Flucklinger, V.11
Vialettes, B.12
-
3
-
-
33644622470
-
Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder
-
Cheng R., Juo S.H., Loth J.E., Nee J., Iossifov I., Blumenthal R., Sharpe L., Kanyas K., Lerer B., Lilliston B., Smith M., Trautman K., Gilliam T.C., Endicott J., and Baron M. Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder. Mol. Psychiatry 11 (2006) 252-260
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 252-260
-
-
Cheng, R.1
Juo, S.H.2
Loth, J.E.3
Nee, J.4
Iossifov, I.5
Blumenthal, R.6
Sharpe, L.7
Kanyas, K.8
Lerer, B.9
Lilliston, B.10
Smith, M.11
Trautman, K.12
Gilliam, T.C.13
Endicott, J.14
Baron, M.15
-
4
-
-
0037041306
-
Is there a relationship between Wolfram syndrome carrier status and suicide?
-
Crawford J., Zielinski M.A., Fisher L.J., Sutherland G.R., and Goldney R.D. Is there a relationship between Wolfram syndrome carrier status and suicide?. Am. J. Med. Genet. 114 (2002) 343-346
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 343-346
-
-
Crawford, J.1
Zielinski, M.A.2
Fisher, L.J.3
Sutherland, G.R.4
Goldney, R.D.5
-
6
-
-
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
-
Detera-Wadleigh S.D., Badner J.A., Berrettini W.H., Yoshikawa T., Goldin L.R., Turner G., Rollins D.Y., Moses T., Sanders A.R., Karkera J.D., Esterling L.E., Zeng J., Ferraro T.N., Guroff J.J., Kazuba D., Maxwell M.E., Nurnberger Jr. J.I., and Gershon E.S. 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. U.S.A. 96 (1999) 5604-5609
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 5604-5609
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Berrettini, W.H.3
Yoshikawa, T.4
Goldin, L.R.5
Turner, G.6
Rollins, D.Y.7
Moses, T.8
Sanders, A.R.9
Karkera, J.D.10
Esterling, L.E.11
Zeng, J.12
Ferraro, T.N.13
Guroff, J.J.14
Kazuba, D.15
Maxwell, M.E.16
Nurnberger Jr., J.I.17
Gershon, E.S.18
-
7
-
-
34548337050
-
Sequence variation in DOCK9 and heterogeneity in bipolar disorder
-
Detera-Wadleigh S.D., Liu C.Y., Maheshwari M., Cardona I., Corona W., Akula N., Steele C.J., Badner J.A., Kundu M., Kassem L., Potash J.B., Gibbs R., Gershon E.S., and Mcmahon F.J. Sequence variation in DOCK9 and heterogeneity in bipolar disorder. Psychiatry Genet. 17 (2007) 274-286
-
(2007)
Psychiatry Genet.
, vol.17
, pp. 274-286
-
-
Detera-Wadleigh, S.D.1
Liu, C.Y.2
Maheshwari, M.3
Cardona, I.4
Corona, W.5
Akula, N.6
Steele, C.J.7
Badner, J.A.8
Kundu, M.9
Kassem, L.10
Potash, J.B.11
Gibbs, R.12
Gershon, E.S.13
Mcmahon, F.J.14
-
8
-
-
33645395576
-
Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease
-
Domenech E., Gomez-Zaera M., and Nunes V. Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease. Pediatr. Endocrinol. Rev. 3 (2006) 249-257
-
(2006)
Pediatr. Endocrinol. Rev.
, vol.3
, pp. 249-257
-
-
Domenech, E.1
Gomez-Zaera, M.2
Nunes, V.3
-
9
-
-
0034599864
-
Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder
-
Evans K.L., Lawson D., Meitinger T., Blackwood D.H., and Porteous D.J. Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder. Am. J. Med. Genet. 96 (2000) 158-160
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 158-160
-
-
Evans, K.L.1
Lawson, D.2
Meitinger, T.3
Blackwood, D.H.4
Porteous, D.J.5
-
10
-
-
0031718092
-
Support for the possible locus on chromosome 4p16 for bipolar affective disorder
-
Ewald H., Degn B., Mors O., and Kruse T.A. Support for the possible locus on chromosome 4p16 for bipolar affective disorder. Mol. Psychiatry 3 (1998) 442-448
-
(1998)
Mol. Psychiatry
, vol.3
, pp. 442-448
-
-
Ewald, H.1
Degn, B.2
Mors, O.3
Kruse, T.A.4
-
11
-
-
0036373344
-
A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13. 3
-
Ewald H., Flint T., Kruse T.A., and Mors O. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13. 3. Mol. Psychiatry 7 (2002) 734-744
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 734-744
-
-
Ewald, H.1
Flint, T.2
Kruse, T.A.3
Mors, O.4
-
12
-
-
0037470195
-
A review of 25 years of the social interaction test
-
File S.E., and Seth P. A review of 25 years of the social interaction test. Eur. J. Pharmacol. 463 (2003) 35-53
-
(2003)
Eur. J. Pharmacol.
, vol.463
, pp. 35-53
-
-
File, S.E.1
Seth, P.2
-
13
-
-
28244435870
-
WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic beta-cells
-
Fonseca S.G., Fukuma M., Lipson K.L., Nguyen L.X., Allen J.R., Oka Y., and Urano F. WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic beta-cells. J. Biol. Chem. 280 (2005) 39609-39615
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 39609-39615
-
-
Fonseca, S.G.1
Fukuma, M.2
Lipson, K.L.3
Nguyen, L.X.4
Allen, J.R.5
Oka, Y.6
Urano, F.7
-
14
-
-
0036788036
-
The Wnt signaling pathway in bipolar disorder
-
Gould T.D., and Manji H.K. The Wnt signaling pathway in bipolar disorder. Neuroscientist 8 (2002) 497-511
-
(2002)
Neuroscientist
, vol.8
, pp. 497-511
-
-
Gould, T.D.1
Manji, H.K.2
-
15
-
-
17344362695
-
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)
-
Inoue H., Tanizawa Y., Wasson J., Behn P., Kalidas K., Bernal-Mizrachi E., Mueckler M., Marshall H., Donis-Keller H., Crock P., Rogers D., Mikuni M., Kumashiro H., Higashi K., Sobue G., Oka Y., and Permutt M.A. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat. Genet. 20 (1998) 143-148
-
(1998)
Nat. Genet.
, vol.20
, pp. 143-148
-
-
Inoue, H.1
Tanizawa, Y.2
Wasson, J.3
Behn, P.4
Kalidas, K.5
Bernal-Mizrachi, E.6
Mueckler, M.7
Marshall, H.8
Donis-Keller, H.9
Crock, P.10
Rogers, D.11
Mikuni, M.12
Kumashiro, H.13
Higashi, K.14
Sobue, G.15
Oka, Y.16
Permutt, M.A.17
-
16
-
-
2942731683
-
Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion
-
Ishihara H., Takeda S., Tamura A., Takahashi R., Yamaguchi S., Takei D., Yamada T., Inoue H., Soga H., Katagiri H., Tanizawa Y., and Oka Y. Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion. Hum. Mol. Genet. 13 (2004) 1159-1170
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1159-1170
-
-
Ishihara, H.1
Takeda, S.2
Tamura, A.3
Takahashi, R.4
Yamaguchi, S.5
Takei, D.6
Yamada, T.7
Inoue, H.8
Soga, H.9
Katagiri, H.10
Tanizawa, Y.11
Oka, Y.12
-
17
-
-
33646252263
-
Small GTPase Rnd1 is involved in neuronal activity-dependent dendritic development in hippocampal neurons
-
Ishikawa Y., Katoh H., and Negishi M. Small GTPase Rnd1 is involved in neuronal activity-dependent dendritic development in hippocampal neurons. Neurosci. Lett. 400 (2006) 218-223
-
(2006)
Neurosci. Lett.
, vol.400
, pp. 218-223
-
-
Ishikawa, Y.1
Katoh, H.2
Negishi, M.3
-
18
-
-
0032851813
-
The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins
-
Joberty G., Perlungher R.R., and Macara I.G. The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins. Mol. Cell Biol. 19 (1999) 6585-6597
-
(1999)
Mol. Cell Biol.
, vol.19
, pp. 6585-6597
-
-
Joberty, G.1
Perlungher, R.R.2
Macara, I.G.3
-
19
-
-
33645280897
-
XBP1 induces WFS1 through an endoplasmic reticulum stress response element-like motif in SH-SY5Y cells
-
Kakiuchi C., Ishiwata M., Hayashi A., and Kato T. XBP1 induces WFS1 through an endoplasmic reticulum stress response element-like motif in SH-SY5Y cells. J. Neurochem. 97 (2006) 545-555
-
(2006)
J. Neurochem.
, vol.97
, pp. 545-555
-
-
Kakiuchi, C.1
Ishiwata, M.2
Hayashi, A.3
Kato, T.4
-
20
-
-
33745712834
-
Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes
-
523
-
Kasahara T., Kubota M., Miyauchi T., Noda Y., Mouri A., Nabeshima T., and Kato T. Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes. Mol. Psychiatry 11 (2006) 577-593 523
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 577-593
-
-
Kasahara, T.1
Kubota, M.2
Miyauchi, T.3
Noda, Y.4
Mouri, A.5
Nabeshima, T.6
Kato, T.7
-
21
-
-
0034280096
-
Mitochondrial dysfunction in bipolar disorder
-
Kato T., and Kato N. Mitochondrial dysfunction in bipolar disorder. Bipolar Disord. 2 (2000) 180-190
-
(2000)
Bipolar Disord.
, vol.2
, pp. 180-190
-
-
Kato, T.1
Kato, N.2
-
22
-
-
0037336382
-
The WFS1 (Wolfram syndrome 1) is not a major susceptibility gene for the development of psychiatric disorders
-
Martorell L., Zaera M.G., Valero J., Serrano D., Figuera L., Joven J., Labad A., Vilella E., and Nunes V. The WFS1 (Wolfram syndrome 1) is not a major susceptibility gene for the development of psychiatric disorders. Psychiatry Genet. 13 (2003) 29-32
-
(2003)
Psychiatry Genet.
, vol.13
, pp. 29-32
-
-
Martorell, L.1
Zaera, M.G.2
Valero, J.3
Serrano, D.4
Figuera, L.5
Joven, J.6
Labad, A.7
Vilella, E.8
Nunes, V.9
-
23
-
-
34548297658
-
Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signalling pathway
-
Matigian N., Windus L., Smith H., Filippich C., Pantelis C., Mcgrath J., Mowry B., and Hayward N. Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signalling pathway. Mol. Psychiatry 12 (2007) 815-825
-
(2007)
Mol. Psychiatry
, vol.12
, pp. 815-825
-
-
Matigian, N.1
Windus, L.2
Smith, H.3
Filippich, C.4
Pantelis, C.5
Mcgrath, J.6
Mowry, B.7
Hayward, N.8
-
24
-
-
0042202625
-
Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia
-
Miyakawa T., Leiter L.M., Gerber D.J., Gainetdinov R.R., Sotnikova T.D., Zeng H., Caron M.G., and Tonegawa S. Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia. Proc. Natl. Acad. Sci. U.S.A. 100 (2003) 8987-8992
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 8987-8992
-
-
Miyakawa, T.1
Leiter, L.M.2
Gerber, D.J.3
Gainetdinov, R.R.4
Sotnikova, T.D.5
Zeng, H.6
Caron, M.G.7
Tonegawa, S.8
-
25
-
-
0034176621
-
WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder
-
Ohtsuki T., Ishiguro H., Yoshikawa T., and Arinami T. WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder. J. Affect Disord. 58 (2000) 11-17
-
(2000)
J. Affect Disord.
, vol.58
, pp. 11-17
-
-
Ohtsuki, T.1
Ishiguro, H.2
Yoshikawa, T.3
Arinami, T.4
-
26
-
-
0347362797
-
Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium
-
Osman A.A., Saito M., Makepeace C., Permutt M.A., Schlesinger P., and Mueckler M. Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium. J. Biol. Chem. 278 (2003) 52755-52762
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 52755-52762
-
-
Osman, A.A.1
Saito, M.2
Makepeace, C.3
Permutt, M.A.4
Schlesinger, P.5
Mueckler, M.6
-
27
-
-
0038210268
-
Involvement of 5-HT1A receptors in animal tests of anxiety and depression: evidence from genetic models
-
Overstreet D.H., Commissaris R.C., De La Garza II R., File S.E., Knapp D.J., and Seiden L.S. Involvement of 5-HT1A receptors in animal tests of anxiety and depression: evidence from genetic models. Stress 6 (2003) 101-110
-
(2003)
Stress
, vol.6
, pp. 101-110
-
-
Overstreet, D.H.1
Commissaris, R.C.2
De La Garza II, R.3
File, S.E.4
Knapp, D.J.5
Seiden, L.S.6
-
28
-
-
0348142662
-
Learned immobility is also involved in the forced swimming test in mice
-
Parra A., Vinader-Caerols C., Monleon S., and Simon V.M. Learned immobility is also involved in the forced swimming test in mice. Psicothema 11 (1999) 239-246
-
(1999)
Psicothema
, vol.11
, pp. 239-246
-
-
Parra, A.1
Vinader-Caerols, C.2
Monleon, S.3
Simon, V.M.4
-
29
-
-
24644480656
-
Expressional and functional studies of Wolframin, the gene function deficient in Wolfram syndrome, in mice and patient cells
-
Philbrook C., Fritz E., and Weiher H. Expressional and functional studies of Wolframin, the gene function deficient in Wolfram syndrome, in mice and patient cells. Exp. Gerontol. 40 (2005) 671-678
-
(2005)
Exp. Gerontol.
, vol.40
, pp. 671-678
-
-
Philbrook, C.1
Fritz, E.2
Weiher, H.3
-
30
-
-
27744523525
-
Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis
-
Riggs A.C., Bernal-Mizrachi E., Ohsugi M., Wasson J., Fatrai S., Welling C., Murray J., Schmidt R.E., Herrera P.L., and Permutt M.A. Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis. Diabetologia 48 (2005) 2313-2321
-
(2005)
Diabetologia
, vol.48
, pp. 2313-2321
-
-
Riggs, A.C.1
Bernal-Mizrachi, E.2
Ohsugi, M.3
Wasson, J.4
Fatrai, S.5
Welling, C.6
Murray, J.7
Schmidt, R.E.8
Herrera, P.L.9
Permutt, M.A.10
-
31
-
-
0027337386
-
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome)
-
Rotig A., Cormier V., Chatelain P., Francois R., Saudubray J.M., Rustin P., and Munnich A. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). J. Inherit. Metab. Dis. 16 (1993) 527-530
-
(1993)
J. Inherit. Metab. Dis.
, vol.16
, pp. 527-530
-
-
Rotig, A.1
Cormier, V.2
Chatelain, P.3
Francois, R.4
Saudubray, J.M.5
Rustin, P.6
Munnich, A.7
-
32
-
-
0031761895
-
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein
-
Strom T.M., Hortnagel K., Hofmann S., Gekeler F., Scharfe C., Rabl W., Gerbitz K.D., and Meitinger T. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum. Mol. Genet. 7 (1998) 2021-2028
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 2021-2028
-
-
Strom, T.M.1
Hortnagel, K.2
Hofmann, S.3
Gekeler, F.4
Scharfe, C.5
Rabl, W.6
Gerbitz, K.D.7
Meitinger, T.8
-
33
-
-
0342369343
-
Psychiatric disorders and mutations at the Wolfram syndrome locus
-
Swift M., and Swift R.G. Psychiatric disorders and mutations at the Wolfram syndrome locus. Biol. Psychiatry 47 (2000) 787-793
-
(2000)
Biol. Psychiatry
, vol.47
, pp. 787-793
-
-
Swift, M.1
Swift, R.G.2
-
34
-
-
0025081836
-
Psychiatric findings in Wolfram syndrome homozygotes
-
Swift R.G., Sadler D.B., and Swift M. Psychiatric findings in Wolfram syndrome homozygotes. Lancet 336 (1990) 667-669
-
(1990)
Lancet
, vol.336
, pp. 667-669
-
-
Swift, R.G.1
Sadler, D.B.2
Swift, M.3
-
35
-
-
0035283066
-
WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain
-
Takeda K., Inoue H., Tanizawa Y., Matsuzaki Y., Oba J., Watanabe Y., Shinoda K., and Oka Y. WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain. Hum. Mol. Genet. 10 (2001) 477-484
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 477-484
-
-
Takeda, K.1
Inoue, H.2
Tanizawa, Y.3
Matsuzaki, Y.4
Oba, J.5
Watanabe, Y.6
Shinoda, K.7
Oka, Y.8
-
36
-
-
33749342602
-
WFS1 protein modulates the free Ca(2+) concentration in the endoplasmic reticulum
-
Takei D., Ishihara H., Yamaguchi S., Yamada T., Tamura A., Katagiri H., Maruyama Y., and Oka Y. WFS1 protein modulates the free Ca(2+) concentration in the endoplasmic reticulum. FEBS Lett. 580 (2006) 5635-5640
-
(2006)
FEBS Lett.
, vol.580
, pp. 5635-5640
-
-
Takei, D.1
Ishihara, H.2
Yamaguchi, S.3
Yamada, T.4
Tamura, A.5
Katagiri, H.6
Maruyama, Y.7
Oka, Y.8
-
37
-
-
0030982564
-
Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42
-
Threadgill R., Bobb K., and Ghosh A. Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42. Neuron 19 (1997) 625-634
-
(1997)
Neuron
, vol.19
, pp. 625-634
-
-
Threadgill, R.1
Bobb, K.2
Ghosh, A.3
-
38
-
-
17744377382
-
Mutation screening of the Wolfram syndrome gene in psychiatric patients
-
Torres R., Leroy E., Hu X., Katrivanou A., Gourzis P., Papachatzopoulou A., Athanassiadou A., Beratis S., Collier D., and Polymeropoulos M.H. Mutation screening of the Wolfram syndrome gene in psychiatric patients. Mol. Psychiatry 6 (2001) 39-43
-
(2001)
Mol. Psychiatry
, vol.6
, pp. 39-43
-
-
Torres, R.1
Leroy, E.2
Hu, X.3
Katrivanou, A.4
Gourzis, P.5
Papachatzopoulou, A.6
Athanassiadou, A.7
Beratis, S.8
Collier, D.9
Polymeropoulos, M.H.10
-
39
-
-
33745202552
-
WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells
-
Yamada T., Ishihara H., Tamura A., Takahashi R., Yamaguchi S., Takei D., Tokita A., Satake C., Tashiro F., Katagiri H., Aburatani H., Miyazaki J., and Oka Y. WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells. Hum. Mol. Genet. 15 (2006) 1600-1609
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1600-1609
-
-
Yamada, T.1
Ishihara, H.2
Tamura, A.3
Takahashi, R.4
Yamaguchi, S.5
Takei, D.6
Tokita, A.7
Satake, C.8
Tashiro, F.9
Katagiri, H.10
Aburatani, H.11
Miyazaki, J.12
Oka, Y.13
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