-
1
-
-
0032858912
-
Incriminating gene suspects, Prader-Willi style
-
Nicholls R.D. Incriminating gene suspects, Prader-Willi style. Nat. Genet. 23 (1999) 132-134
-
(1999)
Nat. Genet.
, vol.23
, pp. 132-134
-
-
Nicholls, R.D.1
-
2
-
-
0030726998
-
Prader-Willi syndrome
-
Cassidy S.B. Prader-Willi syndrome. J. Med. Genet. 34 (1997) 917-923
-
(1997)
J. Med. Genet.
, vol.34
, pp. 917-923
-
-
Cassidy, S.B.1
-
3
-
-
0345062183
-
Disruption of the mouse necdin gene results in early post-natal lethality
-
Gerard M., Hernandez L., Wevrick R., and Stewart C.L. Disruption of the mouse necdin gene results in early post-natal lethality. Nat. Genet. 23 (1999) 199-202
-
(1999)
Nat. Genet.
, vol.23
, pp. 199-202
-
-
Gerard, M.1
Hernandez, L.2
Wevrick, R.3
Stewart, C.L.4
-
4
-
-
0034642301
-
Disruption of the mouse necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
-
Muscatelli F., Abrous D.N., Massacrier A., Boccaccio I., Moal M.L., Cau P., and Cremer H. Disruption of the mouse necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum. Mol. Genet. 9 (2000) 3101-3110
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 3101-3110
-
-
Muscatelli, F.1
Abrous, D.N.2
Massacrier, A.3
Boccaccio, I.4
Moal, M.L.5
Cau, P.6
Cremer, H.7
-
5
-
-
0036829043
-
Ectopic expression of Necdin induces differentiation of mouse neuroblastoma cells
-
Kobayashi M., Taniura H., and Yoshikawa K. Ectopic expression of Necdin induces differentiation of mouse neuroblastoma cells. J. Biol. Chem. 277 (2002) 42128-42135
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 42128-42135
-
-
Kobayashi, M.1
Taniura, H.2
Yoshikawa, K.3
-
6
-
-
0347087481
-
Necdin-related MAGE proteins differentially interact with E2F1 transcription factor and the p75 neurotrophin receptor
-
Kuwako K., Taniura H., and Yoshikawa K. Necdin-related MAGE proteins differentially interact with E2F1 transcription factor and the p75 neurotrophin receptor. J. Biol. Chem. 279 (2004) 1703-1712
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 1703-1712
-
-
Kuwako, K.1
Taniura, H.2
Yoshikawa, K.3
-
7
-
-
23044445639
-
Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival
-
Kuwako K., Hosokawa A., Nishimura I., Uetsuki T., Yamada M., Nada S., Okada M., and Yoshikawa K. Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J. Neurosci. 25 (2006) 7090-7099
-
(2006)
J. Neurosci.
, vol.25
, pp. 7090-7099
-
-
Kuwako, K.1
Hosokawa, A.2
Nishimura, I.3
Uetsuki, T.4
Yamada, M.5
Nada, S.6
Okada, M.7
Yoshikawa, K.8
-
8
-
-
0037335439
-
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
-
Ren J., Lee S., Pagliardini S., Gerard M., Stewart C.L., Greer J.J., and Wevrick R. Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. J. Neurosci. 23 (2003) 1569-1573
-
(2003)
J. Neurosci.
, vol.23
, pp. 1569-1573
-
-
Ren, J.1
Lee, S.2
Pagliardini, S.3
Gerard, M.4
Stewart, C.L.5
Greer, J.J.6
Wevrick, R.7
-
9
-
-
0037086294
-
The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease
-
Barker P.A., and Salehi A. The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease. J. Neurosci. Res. 67 (2002) 705-712
-
(2002)
J. Neurosci. Res.
, vol.67
, pp. 705-712
-
-
Barker, P.A.1
Salehi, A.2
-
10
-
-
0032532480
-
Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1
-
Michaud J.L., Rosenquist T., May N.R., and Fan C.M. Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1. Genes Dev. 12 (1998) 3264-3275
-
(1998)
Genes Dev.
, vol.12
, pp. 3264-3275
-
-
Michaud, J.L.1
Rosenquist, T.2
May, N.R.3
Fan, C.M.4
-
11
-
-
0034016043
-
Profound obesity associated with a balanced translocation that disrupts the SIM1 gene
-
Holder Jr. J.L., Butte N.F., and Zinn A.R. Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. Hum. Mol. Genet. 9 (2000) 101-108
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 101-108
-
-
Holder Jr., J.L.1
Butte, N.F.2
Zinn, A.R.3
-
12
-
-
18444412266
-
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
-
Faivre L., et al. Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. J. Med. Genet. 39 (2002) 594-596
-
(2002)
J. Med. Genet.
, vol.39
, pp. 594-596
-
-
Faivre, L.1
-
13
-
-
0035393437
-
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
-
Michaud J.L., Boucher F., Melnyk A., Gauthier F., Goshu E., Levy E., Mitchell G.A., Himms-Hagen J., and Fan C.M. Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Hum. Mol. Genet. 10 (2001) 1465-1473
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1465-1473
-
-
Michaud, J.L.1
Boucher, F.2
Melnyk, A.3
Gauthier, F.4
Goshu, E.5
Levy, E.6
Mitchell, G.A.7
Himms-Hagen, J.8
Fan, C.M.9
-
14
-
-
0033977276
-
Different transcriptional properties of mSim-1 and mSim-2
-
Moffett P., and Pelletier J. Different transcriptional properties of mSim-1 and mSim-2. FEBS Lett. 466 (2000) 80-86
-
(2000)
FEBS Lett.
, vol.466
, pp. 80-86
-
-
Moffett, P.1
Pelletier, J.2
-
15
-
-
0023124097
-
Firefly luciferase gene: structure and expression in mammalian cells
-
de Wet J.R., Wood K.V., DeLuca M., Helinski D.R., and Subramami S. Firefly luciferase gene: structure and expression in mammalian cells. Mol. Cell. Biol. 7 (1987) 725-737
-
(1987)
Mol. Cell. Biol.
, vol.7
, pp. 725-737
-
-
de Wet, J.R.1
Wood, K.V.2
DeLuca, M.3
Helinski, D.R.4
Subramami, S.5
-
16
-
-
0242497624
-
Identification of the downstream targets of SIM1 and ARNT2, a pair of transcription factors essential for neuroendocrine cell differentiation
-
Liu C., Goshu E., Wells A., and Fan C.M. Identification of the downstream targets of SIM1 and ARNT2, a pair of transcription factors essential for neuroendocrine cell differentiation. J. Biol. Chem. 278 (2003) 44857-44867
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 44857-44867
-
-
Liu, C.1
Goshu, E.2
Wells, A.3
Fan, C.M.4
-
17
-
-
21244488269
-
Negative regulation of hypoxia inducible factor-1α by necdin
-
Moon H.E., Ahn M.Y., Park J.A., Min K.J., Kwon Y.W., and Kim K.W. Negative regulation of hypoxia inducible factor-1α by necdin. FEBS Lett. 579 (2005) 3797-3801
-
(2005)
FEBS Lett.
, vol.579
, pp. 3797-3801
-
-
Moon, H.E.1
Ahn, M.Y.2
Park, J.A.3
Min, K.J.4
Kwon, Y.W.5
Kim, K.W.6
-
18
-
-
0031964697
-
Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1
-
Taniura H., Taniguchi N., Hara M., and Yoshikawa K. Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1. J. Biol. Chem. 273 (1998) 720-728
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 720-728
-
-
Taniura, H.1
Taniguchi, N.2
Hara, M.3
Yoshikawa, K.4
-
19
-
-
20444395224
-
Functional domains of necdin for protein-protein interaction, nuclear matrix targeting, and cell growth suppression
-
Taniura H., Kobayash M., and Yoshikawa K. Functional domains of necdin for protein-protein interaction, nuclear matrix targeting, and cell growth suppression. J. Cell. Biochem. 94 (2005) 804-815
-
(2005)
J. Cell. Biochem.
, vol.94
, pp. 804-815
-
-
Taniura, H.1
Kobayash, M.2
Yoshikawa, K.3
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