-
1
-
-
0037321711
-
The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications
-
Asou N (2003) The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications. Crit Rev Oncol Hematol 45: 129-150
-
(2003)
Crit Rev Oncol Hematol
, vol.45
, pp. 129-150
-
-
Asou, N.1
-
2
-
-
7344248552
-
Expression of AML1-d, a short human AML1 isoform, in embryonic stem cells suppresses in vivo tumor growth and differentiation
-
Aziz-Aloya RB, Levanon D, Karn H, Kidron D, Goldenberg D, Lotem J, Polak-Chaklon S, Groner Y (1998) Expression of AML1-d, a short human AML1 isoform, in embryonic stem cells suppresses in vivo tumor growth and differentiation. Cell Death Differ 5: 765-773
-
(1998)
Cell Death Differ
, vol.5
, pp. 765-773
-
-
Aziz-Aloya, R.B.1
Levanon, D.2
Karn, H.3
Kidron, D.4
Goldenberg, D.5
Lotem, J.6
Polak-Chaklon, S.7
Groner, Y.8
-
3
-
-
0030665054
-
The Ets transcription factors interact with each other and with the c-Fos/c-Jun complex via distinct protein domains in a DNA-dependent and -independent manner
-
Basuyaux JP, Ferreira E, Stehelin D, Buttice G (1997) The Ets transcription factors interact with each other and with the c-Fos/c-Jun complex via distinct protein domains in a DNA-dependent and -independent manner. J Biol Chem 272: 26188-26195
-
(1997)
J Biol Chem
, vol.272
, pp. 26188-26195
-
-
Basuyaux, J.P.1
Ferreira, E.2
Stehelin, D.3
Buttice, G.4
-
4
-
-
85047696566
-
AML1 stimulates G1 to S progression via its transactivation domain
-
Bernardin F, Friedman AD (2002) AML1 stimulates G1 to S progression via its transactivation domain. Oncogene 21: 3247-3252
-
(2002)
Oncogene
, vol.21
, pp. 3247-3252
-
-
Bernardin, F.1
Friedman, A.D.2
-
5
-
-
0033579464
-
Sequence and structure-based prediction of eukaryotic protein phosphorylation sites
-
Blom N, Gammeltoft S, Brunak S (1999) Sequence and structure-based prediction of eukaryotic protein phosphorylation sites. J Mol Biol 294: 1351-1362
-
(1999)
J Mol Biol
, vol.294
, pp. 1351-1362
-
-
Blom, N.1
Gammeltoft, S.2
Brunak, S.3
-
7
-
-
0037355919
-
Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: Challenging the gene dosage effect hypothesis, part II
-
Cheon MS, Bajo M, Kim SH, Claudio JO, Stewart AK, Patterson D, Kruger WD, Kondoh H, Lubec G (2003) Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis, part II. Amino Acids 24: 119-125
-
(2003)
Amino Acids
, vol.24
, pp. 119-125
-
-
Cheon, M.S.1
Bajo, M.2
Kim, S.H.3
Claudio, J.O.4
Stewart, A.K.5
Patterson, D.6
Kruger, W.D.7
Kondoh, H.8
Lubec, G.9
-
8
-
-
0037356252
-
Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: Challenging the gene dosage effect hypothesis, part III
-
Cheon MS, Kim SH, Ovod V, Kopitar Jerala N, Morgan JI, Hatefi Y, Ijuin T, Takenawa T, Lubec G (2003) Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis, part III. Amino Acids 24: 127-134
-
(2003)
Amino Acids
, vol.24
, pp. 127-134
-
-
Cheon, M.S.1
Kim, S.H.2
Ovod, V.3
Kopitar Jerala, N.4
Morgan, J.I.5
Hatefi, Y.6
Ijuin, T.7
Takenawa, T.8
Lubec, G.9
-
9
-
-
0037354541
-
Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: Challenging the gene dosage effect hypothesis, part I
-
Cheon MS, Kim SH, Yaspo ML, Blasi F, Aoki Y, Melen K, Lubec G (2003) Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis, part I. Amino Acids 24: 111-117
-
(2003)
Amino Acids
, vol.24
, pp. 111-117
-
-
Cheon, M.S.1
Kim, S.H.2
Yaspo, M.L.3
Blasi, F.4
Aoki, Y.5
Melen, K.6
Lubec, G.7
-
10
-
-
0042268004
-
Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: Challenging the gene dosage effect hypothesis, part IV
-
Cheon MS, Shim KS, Kim SH, Hara A, Lubec G (2003) Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis, part IV. Amino Acids 25: 41-47
-
(2003)
Amino Acids
, vol.25
, pp. 41-47
-
-
Cheon, M.S.1
Shim, K.S.2
Kim, S.H.3
Hara, A.4
Lubec, G.5
-
11
-
-
0033852958
-
Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome
-
Chrast R, Scott HS, Madani R, Huber L, Wolfer DP, Prinz M, Aguzzi A, Lipp HP, Antonarakis SE (2000) Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome. Hum Mol Genet 9: 1853-1864
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1853-1864
-
-
Chrast, R.1
Scott, H.S.2
Madani, R.3
Huber, L.4
Wolfer, D.P.5
Prinz, M.6
Aguzzi, A.7
Lipp, H.P.8
Antonarakis, S.E.9
-
12
-
-
0032837516
-
Mild impairment of learning and memory in mice overexpressing the mSim2 gene located on chromosome 16: An animal model of Down's syndrome
-
Ema M, Ikegami S, Hosoya T, Mimura J, Ohtani H, Nakao K, Inokuchi K, Katsuki M, Fujii-Kuriyama Y (1999) Mild impairment of learning and memory in mice overexpressing the mSim2 gene located on chromosome 16: an animal model of Down's syndrome. Hum Mol Genet 8: 1409-1415
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1409-1415
-
-
Ema, M.1
Ikegami, S.2
Hosoya, T.3
Mimura, J.4
Ohtani, H.5
Nakao, K.6
Inokuchi, K.7
Katsuki, M.8
Fujii-Kuriyama, Y.9
-
13
-
-
0037339732
-
Molecular changes in fetal Down syndrome brain
-
Engidawork E, Lubec G (2003) Molecular changes in fetal Down syndrome brain. J Neurochem 84: 895-904
-
(2003)
J Neurochem
, vol.84
, pp. 895-904
-
-
Engidawork, E.1
Lubec, G.2
-
14
-
-
0035226136
-
Beta-amyloid precursor protein, ETS-2 and collagen alpha 1 (VI) chain precursor, encoded on chromosome 21, are not overexpressed in fetal Down syndrome: Further evidence against gene dosage effect
-
Engidawork E, Balic N, Fountoulakis M, Dierssen M, Greber-Platzer S, Lubec G (2001) Beta-amyloid precursor protein, ETS-2 and collagen alpha 1 (VI) chain precursor, encoded on chromosome 21, are not overexpressed in fetal Down syndrome: further evidence against gene dosage effect. J Neural Transm [Suppl] 61: 335-346
-
(2001)
J Neural Transm [Suppl]
, vol.61
, pp. 335-346
-
-
Engidawork, E.1
Balic, N.2
Fountoulakis, M.3
Dierssen, M.4
Greber-Platzer, S.5
Lubec, G.6
-
15
-
-
0000521855
-
Down syndrome
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds) McGraw Hill, New York
-
th edn, vol I. McGraw Hill, New York, pp 749-794
-
(1995)
th Edn
, vol.1
, pp. 749-794
-
-
Epstein, C.J.1
-
16
-
-
0029968399
-
Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome
-
Fan CM, Kuwana E, Bulfone A, Fletcher CF, Copeland NG, Jenkins NA, Crews S, Martinez S, Puelles L, Rubenstein LR, Tessier-Lavigne M (1996) Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome. Mol Cell Neurosci 7: 1-16
-
(1996)
Mol Cell Neurosci
, vol.7
, pp. 1-16
-
-
Fan, C.M.1
Kuwana, E.2
Bulfone, A.3
Fletcher, C.F.4
Copeland, N.G.5
Jenkins, N.A.6
Crews, S.7
Martinez, S.8
Puelles, L.9
Rubenstein, L.R.10
Tessier-Lavigne, M.11
-
17
-
-
0033605904
-
Increased steady state mRNA levels of DNA-repair genes XRCC1, ERCC2 and ERCC3 in brain of patients with Down syndrome
-
Fang-Kircher SG, Labudova O, Kitzmueller E, Rink H, Cairns N, Lubec G (1999) Increased steady state mRNA levels of DNA-repair genes XRCC1, ERCC2 and ERCC3 in brain of patients with Down syndrome. Life Sci 64: 1689-1699
-
(1999)
Life Sci
, vol.64
, pp. 1689-1699
-
-
Fang-Kircher, S.G.1
Labudova, O.2
Kitzmueller, E.3
Rink, H.4
Cairns, N.5
Lubec, G.6
-
18
-
-
1542614439
-
Overexpression of transciption factor BACH1 in fetal Down syndrome brain
-
Ferrando-Miguel R, Lubec G (2003) Overexpression of transciption factor BACH1 in fetal Down syndrome brain. J Neural Transm [Suppl] 67 (this volume)
-
(2003)
J Neural Transm [Suppl]
, vol.67 THIS VOLUME
-
-
Ferrando-Miguel, R.1
Lubec, G.2
-
19
-
-
0035232099
-
Deterioration of the transcriptional, splicing and elongation machinery in brain of fetal Down syndrome
-
Freidl M, Gulesserian T, Lubec G, Fountoulakis M, Lubec B (2001) Deterioration of the transcriptional, splicing and elongation machinery in brain of fetal Down syndrome. J Neural Transm [Suppl] 61: 47-57
-
(2001)
J Neural Transm [Suppl]
, vol.61
, pp. 47-57
-
-
Freidl, M.1
Gulesserian, T.2
Lubec, G.3
Fountoulakis, M.4
Lubec, B.5
-
21
-
-
0342602072
-
Down-regulation of actin genes precedes microfilament network disruption and actin cleavage during p53-mediated apoptosis
-
Guenal I, Risler Y, Mignotte B (1997) Down-regulation of actin genes precedes microfilament network disruption and actin cleavage during p53-mediated apoptosis. J Cell Sci 110: 489-495
-
(1997)
J Cell Sci
, vol.110
, pp. 489-495
-
-
Guenal, I.1
Risler, Y.2
Mignotte, B.3
-
22
-
-
0035233607
-
Antioxidant proteins in fetal brain: Superoxide dismutase-1 (SOD-1) protein is not overexpressed in fetal Down syndrome
-
Gulesserian T, Engidawork E, Fountoulakis M, Lubec G (2001) Antioxidant proteins in fetal brain: superoxide dismutase-1 (SOD-1) protein is not overexpressed in fetal Down syndrome. J Neural Transm [Suppl] 61: 71-84
-
(2001)
J Neural Transm [Suppl]
, vol.61
, pp. 71-84
-
-
Gulesserian, T.1
Engidawork, E.2
Fountoulakis, M.3
Lubec, G.4
-
23
-
-
0025861903
-
Mechanisms of complex transcriptional regulation: Implications for brain development
-
He X, Rosenfeld MG (1991) Mechanisms of complex transcriptional regulation: implications for brain development. Neuron 7: 183-196
-
(1991)
Neuron
, vol.7
, pp. 183-196
-
-
He, X.1
Rosenfeld, M.G.2
-
25
-
-
0037313210
-
Small Maf compound mutants display central nervous system neuronal degeneration, aberrant transcription, and Bach protein mislocalization coincident with myoclonus and abnormal startle response
-
Katsuoka F, Motohashi H, Tamagawa Y, Kure S, Igarashi K, Engel JD, Yamamoto M (2003) Small Maf compound mutants display central nervous system neuronal degeneration, aberrant transcription, and Bach protein mislocalization coincident with myoclonus and abnormal startle response. Mol Cell Biol 23: 1163-1174
-
(2003)
Mol Cell Biol
, vol.23
, pp. 1163-1174
-
-
Katsuoka, F.1
Motohashi, H.2
Tamagawa, Y.3
Kure, S.4
Igarashi, K.5
Engel, J.D.6
Yamamoto, M.7
-
26
-
-
0038526243
-
Bach1 functions as a hypoxia-inducible repressor for the heme oxygenase-1 gene in human cells
-
Kitamuro T, Takahashi K, Ogawa K, Udono-Fujimori R, Takeda K, Furuyama K, Nakayama M, Sun J, Fujita H, Hida W, Hattori T, Shirato K, Igarashi K, Shibahara S (2003) Bach1 functions as a hypoxia-inducible repressor for the heme oxygenase-1 gene in human cells. J Biol Chem 278: 9125-9133
-
(2003)
J Biol Chem
, vol.278
, pp. 9125-9133
-
-
Kitamuro, T.1
Takahashi, K.2
Ogawa, K.3
Udono-Fujimori, R.4
Takeda, K.5
Furuyama, K.6
Nakayama, M.7
Sun, J.8
Fujita, H.9
Hida, W.10
Hattori, T.11
Shirato, K.12
Igarashi, K.13
Shibahara, S.14
-
27
-
-
0032555414
-
Decreased transcription factor junD in brains of patients with Down syndrome
-
Labudova O, Krapfenbauer K, Moenkemann H, Rink H, Kitzmuller E, Cairns N, Lubec G (1998) Decreased transcription factor junD in brains of patients with Down syndrome. Neurosci Lett 252: 159-162
-
(1998)
Neurosci Lett
, vol.252
, pp. 159-162
-
-
Labudova, O.1
Krapfenbauer, K.2
Moenkemann, H.3
Rink, H.4
Kitzmuller, E.5
Cairns, N.6
Lubec, G.7
-
28
-
-
0032585813
-
Gene expression in fetal Down syndrome brain as revealed by subtractive hybridization
-
Labudova O, Kitzmueller E, Rink H, Cairns N, Lubec G (1999) Gene expression in fetal Down syndrome brain as revealed by subtractive hybridization. J Neural Transm [Suppl] 57: 125-136
-
(1999)
J Neural Transm [Suppl]
, vol.57
, pp. 125-136
-
-
Labudova, O.1
Kitzmueller, E.2
Rink, H.3
Cairns, N.4
Lubec, G.5
-
29
-
-
0031992848
-
Detection of actin cleavage in Alzheimer's disease
-
LeBlanc A (1998) Detection of actin cleavage in Alzheimer's disease. Am J Pathol 152: 329-332
-
(1998)
Am J Pathol
, vol.152
, pp. 329-332
-
-
LeBlanc, A.1
-
30
-
-
0035193558
-
Spatial and temporal expression pattern of Runx3 (Aml2) and Runx1 (Aml1) indicates non-redundant functions during mouse embryogenesis
-
Levanon D, Brenner O, Negreanu V, Bettoun D, Woolf E, Eilam R, Lotem J, Gat U, Otto F, Speck N, Groner Y (2001) Spatial and temporal expression pattern of Runx3 (Aml2) and Runx1 (Aml1) indicates non-redundant functions during mouse embryogenesis. Mech Dev 109: 413-411
-
(2001)
Mech Dev
, vol.109
, pp. 413-1411
-
-
Levanon, D.1
Brenner, O.2
Negreanu, V.3
Bettoun, D.4
Woolf, E.5
Eilam, R.6
Lotem, J.7
Gat, U.8
Otto, F.9
Speck, N.10
Groner, Y.11
-
31
-
-
0036406902
-
The brain in Down syndrome (TRISOMY 21)
-
Lubec G, Engidawork E (2002) The brain in Down syndrome (TRISOMY 21). J Neurol 249: 1347-1356
-
(2002)
J Neurol
, vol.249
, pp. 1347-1356
-
-
Lubec, G.1
Engidawork, E.2
-
32
-
-
0034684616
-
Expression and function of Ets transcription factors in mammalian development: A regulatory network
-
Maroulakou IG, Bowe DB (2000) Expression and function of Ets transcription factors in mammalian development: a regulatory network. Oncogene 19: 6432-6442
-
(2000)
Oncogene
, vol.19
, pp. 6432-6442
-
-
Maroulakou, I.G.1
Bowe, D.B.2
-
33
-
-
0036778378
-
Alteration of intracellular structure and function of glyceraldehyde-3-phosphate dehydrogenase: A common phenotype of neurodegenerative disorders
-
Mazzola JL, Sirover MA (2002) Alteration of intracellular structure and function of glyceraldehyde-3-phosphate dehydrogenase: a common phenotype of neurodegenerative disorders. Neurotoxicology 23: 603-609
-
(2002)
Neurotoxicology
, vol.23
, pp. 603-609
-
-
Mazzola, J.L.1
Sirover, M.A.2
-
34
-
-
0025908356
-
The Consortium to Establish a Registry for Alzheimer's Disease (CERAD) Part 2 Standardization of the neuropathologic assessment of Alzheimer's disease
-
Mirra SS, Heyman A, McKeel D, Sumi SM, Crain BJ, Brownlee LM, Vogel FS, Hughes JP, van Belle G, Berg L (1991) The Consortium to Establish a Registry for Alzheimer's Disease (CERAD) Part 2 Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology 41: 479-486
-
(1991)
Neurology
, vol.41
, pp. 479-486
-
-
Mirra, S.S.1
Heyman, A.2
McKeel, D.3
Sumi, S.M.4
Crain, B.J.5
Brownlee, L.M.6
Vogel, F.S.7
Hughes, J.P.8
Van Belle, G.9
Berg, L.10
-
35
-
-
0030200971
-
Characterization of msim, a murine homologue of the Drosophila sim transcription factor
-
Moffett P, Dayo M, Reece M, McCormick MK, Pelletier J (1996) Characterization of msim, a murine homologue of the Drosophila sim transcription factor. Genomics 35: 144-155
-
(1996)
Genomics
, vol.35
, pp. 144-155
-
-
Moffett, P.1
Dayo, M.2
Reece, M.3
McCormick, M.K.4
Pelletier, J.5
-
36
-
-
0028787577
-
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
-
Muenke M, Bone LJ, Mitchell HF, Hart I, Walton K, Hall-Johnson K, Ippel EF, Dietz-Band J, Kvaloy K, Fan CM (1995) Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome. Am J Hum Genet 57: 1074-1079
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1074-1079
-
-
Muenke, M.1
Bone, L.J.2
Mitchell, H.F.3
Hart, I.4
Walton, K.5
Hall-Johnson, K.6
Ippel, E.F.7
Dietz-Band, J.8
Kvaloy, K.9
Fan, C.M.10
-
37
-
-
1542405142
-
Spectrum of cognitive, behavioural and emotional problems in children and young adults with Down syndrome
-
Nicham R, Weitzdörfer R, Hauser E, Freidl M, Schubert M, Wurst E, Lubec G, Seidl R (2003) Spectrum of cognitive, behavioural and emotional problems in children and young adults with Down syndrome. J Neural Transm [Suppl 67] (this volume)
-
(2003)
J Neural Transm
, vol.THIS VOLUME
, Issue.67 SUPPL.
-
-
Nicham, R.1
Weitzdörfer, R.2
Hauser, E.3
Freidl, M.4
Schubert, M.5
Wurst, E.6
Lubec, G.7
Seidl, R.8
-
38
-
-
17944372665
-
Heme mediates derepression of Maf recognition element through direct binding to transcription repressor Bach1
-
Ogawa K, Sun J, Taketani S, Nakajima O, Nishitani C, Sassa S, Hayashi N, Yamamoto M, Shibahara S, Fujita H, Igarashi K (2001) Heme mediates derepression of Maf recognition element through direct binding to transcription repressor Bach1. EMBO J 20: 2835-2843
-
(2001)
EMBO J
, vol.20
, pp. 2835-2843
-
-
Ogawa, K.1
Sun, J.2
Taketani, S.3
Nakajima, O.4
Nishitani, C.5
Sassa, S.6
Hayashi, N.7
Yamamoto, M.8
Shibahara, S.9
Fujita, H.10
Igarashi, K.11
-
39
-
-
0030061554
-
AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis
-
Okuda T, van Deursen J, Hiebert JW, Grosveld G, Downing JR (1996) AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis. Cell 84: 321-330
-
(1996)
Cell
, vol.84
, pp. 321-330
-
-
Okuda, T.1
Van Deursen, J.2
Hiebert, J.W.3
Grosveld, G.4
Downing, J.R.5
-
40
-
-
0029805130
-
Bach proteins belong to a novel family of BTB-basic leucine zipper transcription factors that interact with MafK and regulate transcription through the NF-E2 site
-
Oyake T, Itoh K, Motohashi H, Hayashi N, Hoshino H, Nishizawa M, Yamamoto M, Igarashi K (1996) Bach proteins belong to a novel family of BTB-basic leucine zipper transcription factors that interact with MafK and regulate transcription through the NF-E2 site. Mol Cell Biol 16: 6083-6095
-
(1996)
Mol Cell Biol
, vol.16
, pp. 6083-6095
-
-
Oyake, T.1
Itoh, K.2
Motohashi, H.3
Hayashi, N.4
Hoshino, H.5
Nishizawa, M.6
Yamamoto, M.7
Igarashi, K.8
-
41
-
-
0036137654
-
Runx1/AML1 in leukemia: Disrupted association with diverse protein partners
-
Perry C, Eldor A, Soreq H (2002) Runx1/AML1 in leukemia: disrupted association with diverse protein partners. Leuk Res 26: 221-228
-
(2002)
Leuk Res
, vol.26
, pp. 221-228
-
-
Perry, C.1
Eldor, A.2
Soreq, H.3
-
42
-
-
0037028246
-
Complex regulation of acetylcholinesterase gene expression in human brain tumors
-
Perry C, Sklan EH, Birikh K, Shapira M, Trejo L, Eldor A, Soreq H (2002) Complex regulation of acetylcholinesterase gene expression in human brain tumors. Oncogene 21: 8428-8441
-
(2002)
Oncogene
, vol.21
, pp. 8428-8441
-
-
Perry, C.1
Sklan, E.H.2
Birikh, K.3
Shapira, M.4
Trejo, L.5
Eldor, A.6
Soreq, H.7
-
43
-
-
0032585811
-
Neuronal cell death in Down's syndrome
-
Sawa A (1999) Neuronal cell death in Down's syndrome. J Neurol Transm [Suppl] 57: 87-97
-
(1999)
J Neurol Transm [Suppl]
, vol.57
, pp. 87-97
-
-
Sawa, A.1
-
44
-
-
0033793044
-
Heme oxygenase-1: Role in brain aging and neurodegeneration
-
Schipper HM (2000) Heme oxygenase-1: role in brain aging and neurodegeneration. Exp Gerontol 35: 821-830
-
(2000)
Exp Gerontol
, vol.35
, pp. 821-830
-
-
Schipper, H.M.1
-
45
-
-
18644378321
-
Hemoprotein Bach1 regulates enhancer availability of heme oxygenase-1 gene
-
Sun J, Hoshino H, Takaku K, Nakajima O, Muto A, Suzuki H, Tashiro S, Takahashi S, Shibahara S, Alam J, Taketo MM, Yamamoto M, Igarashi K (2002) Hemoprotein Bach1 regulates enhancer availability of heme oxygenase-1 gene. EMBO J 21: 5216-5224
-
(2002)
EMBO J
, vol.21
, pp. 5216-5224
-
-
Sun, J.1
Hoshino, H.2
Takaku, K.3
Nakajima, O.4
Muto, A.5
Suzuki, H.6
Tashiro, S.7
Takahashi, S.8
Shibahara, S.9
Alam, J.10
Taketo, M.M.11
Yamamoto, M.12
Igarashi, K.13
-
46
-
-
0023833603
-
The NINCDS-ADRDA Work Group criteria for the clinical diagnosis of probable Alzheimer's disease: A clinicopathologic study of 57 cases
-
Tierney MC, Fisher RH, Lewis AJ, Zorzitto ML, Snow WG, Reid DW, Nieuwstraten P (1998) The NINCDS-ADRDA Work Group criteria for the clinical diagnosis of probable Alzheimer's disease: a clinicopathologic study of 57 cases. Neurology 38: 359-364
-
(1998)
Neurology
, vol.38
, pp. 359-364
-
-
Tierney, M.C.1
Fisher, R.H.2
Lewis, A.J.3
Zorzitto, M.L.4
Snow, W.G.5
Reid, D.W.6
Nieuwstraten, P.7
-
47
-
-
0034684614
-
Ets factors and regulation of the extracellular matrix
-
Trojanowska M (2000) Ets factors and regulation of the extracellular matrix. Oncogene 19: 6464-6471
-
(2000)
Oncogene
, vol.19
, pp. 6464-6471
-
-
Trojanowska, M.1
-
48
-
-
0033931515
-
Identification and expression of a novel 3′-exon of mouse Runx1/Pebp2 alphaB/Cbfa2/AML1 gene
-
Tsuji K, Noda M (2000) Identification and expression of a novel 3′-exon of mouse Runx1/Pebp2 alphaB/Cbfa2/AML1 gene. Biochem Biophys Res Commun 274: 171-176
-
(2000)
Biochem Biophys Res Commun
, vol.274
, pp. 171-176
-
-
Tsuji, K.1
Noda, M.2
-
49
-
-
0035907282
-
Identification of amino acid residues in the ETS transcription factor Erg that mediate Erg-Jun/Fos-DNA ternary complex formation
-
Verger A, Buisine E, Carrere S, Wintjens R, Flourens A, Coll J, Stehelin D, Duterque-Coquillaud M (2000) Identification of amino acid residues in the ETS transcription factor Erg that mediate Erg-Jun/Fos-DNA ternary complex formation. J Biol Chem 276: 17181-17189
-
(2000)
J Biol Chem
, vol.276
, pp. 17181-17189
-
-
Verger, A.1
Buisine, E.2
Carrere, S.3
Wintjens, R.4
Flourens, A.5
Coll, J.6
Stehelin, D.7
Duterque-Coquillaud, M.8
-
50
-
-
0034636503
-
Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: A novel whole-mount based RNA hybridization study
-
Vialard F, Toyama K, Vernoux S, Carlson EJ, Epstein CJ, Sinet PM, Rahmani Z (2000) Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study. Brain Res Dev Brain Res 121: 73-78
-
(2000)
Brain Res Dev Brain Res
, vol.121
, pp. 73-78
-
-
Vialard, F.1
Toyama, K.2
Vernoux, S.3
Carlson, E.J.4
Epstein, C.J.5
Sinet, P.M.6
Rahmani, Z.7
-
51
-
-
0033256932
-
Mammalian runt-domain proteins and their roles in hematopoiesis, osteogenesis, and leukaemia
-
Westendorf JJ, Hiebert SW (1999) Mammalian runt-domain proteins and their roles in hematopoiesis, osteogenesis, and leukaemia. J Cell Biochem [Suppl] 32: 51-58
-
(1999)
J Cell Biochem [Suppl]
, vol.32
, pp. 51-58
-
-
Westendorf, J.J.1
Hiebert, S.W.2
-
52
-
-
0037012042
-
Molecular cloning of ESET, a novel histone H3-specific methyltransferase that interacts with ERG transcription factor
-
Yang L, Xia L, Wu DY, Wang H, Chansky HA, Schubach WH, Hickstein DD, Zhang Y (2002) Molecular cloning of ESET, a novel histone H3-specific methyltransferase that interacts with ERG transcription factor. Oncogene 21: 148-152
-
(2002)
Oncogene
, vol.21
, pp. 148-152
-
-
Yang, L.1
Xia, L.2
Wu, D.Y.3
Wang, H.4
Chansky, H.A.5
Schubach, W.H.6
Hickstein, D.D.7
Zhang, Y.8
-
53
-
-
0032585821
-
Downregulation of the transcription factor scleraxis in brain of patients with Down syndrome
-
Yeghiazaryan K, Turhani-Schatzmann D, Labudova O, Schuller E, Olson EN, Cairns N, Lubec G (1999) Downregulation of the transcription factor scleraxis in brain of patients with Down syndrome. J Neural Transm [Suppl] 57: 305-314
-
(1999)
J Neural Transm [Suppl]
, vol.57
, pp. 305-314
-
-
Yeghiazaryan, K.1
Turhani-Schatzmann, D.2
Labudova, O.3
Schuller, E.4
Olson, E.N.5
Cairns, N.6
Lubec, G.7
-
54
-
-
0030894642
-
Inhibition of apoptosis by normal and aberrant Fli-1 and erg proteins involved in human solid tumors and leukemias
-
Yi H, Fujimura Y, Ouchida M, Prasad DD, Rao VN, Reddy ES (1997) Inhibition of apoptosis by normal and aberrant Fli-1 and erg proteins involved in human solid tumors and leukemias. Oncogene 14: 1259-1268
-
(1997)
Oncogene
, vol.14
, pp. 1259-1268
-
-
Yi, H.1
Fujimura, Y.2
Ouchida, M.3
Prasad, D.D.4
Rao, V.N.5
Reddy, E.S.6
|