-
1
-
-
0029953941
-
An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene
-
Banerjee, C., Hiebert, S.W., Stein, J.L., Lian, J.B., and Stein, G.S. (1996). An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene. Proc. Natl. Acad. Sci. USA 93, 4968-4973.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 4968-4973
-
-
Banerjee, C.1
Hiebert, S.W.2
Stein, J.L.3
Lian, J.B.4
Stein, G.S.5
-
2
-
-
0024356535
-
An in situ transgenic enzyme marker for the midgestation mouse embryo and the visualization of inner cell mass clones during early organogenesis
-
Beddington, R.S.P., Morgernstern, J., Land, H., and Hogan, A. (1989). An in situ transgenic enzyme marker for the midgestation mouse embryo and the visualization of inner cell mass clones during early organogenesis. Development 106, 37-46.
-
(1989)
Development
, vol.106
, pp. 37-46
-
-
Beddington, R.S.P.1
Morgernstern, J.2
Land, H.3
Hogan, A.4
-
3
-
-
0028927556
-
Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene
-
Ducy, P., and Karsenty, G. (1995). Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene. Mol. Cell. Biol. 15, 1858-1869.
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 1858-1869
-
-
Ducy, P.1
Karsenty, G.2
-
4
-
-
0028836022
-
Toward a molecular understanding of skeletal development
-
Erlebacher, A., Filvaroff, E.H., Gitelman, S.E., and Derynck, R. (1995). Toward a molecular understanding of skeletal development. Cell 80, 371-378.
-
(1995)
Cell
, vol.80
, pp. 371-378
-
-
Erlebacher, A.1
Filvaroff, E.H.2
Gitelman, S.E.3
Derynck, R.4
-
5
-
-
0029417351
-
A PEBP2 alpha/AML-1 related factor increases osteocalcin promoter activity through its binding to an osteoblast-specific cis-acting element
-
Geoffroy, V., Ducy, P., and Karsenty, G. (1995). A PEBP2 alpha/AML-1 related factor increases osteocalcin promoter activity through its binding to an osteoblast-specific cis-acting element. J. Biol. Chem. 270, 30973-30979.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 30973-30979
-
-
Geoffroy, V.1
Ducy, P.2
Karsenty, G.3
-
6
-
-
0029686289
-
Encyclopedia of the mouse genome V. Mouse chromosome 17
-
Hamvas, R., Trachtulec, Z., Forejt, J., Williams, R.W., Arzt, K., Fischer-Lindahl, K., and Silver, L.M. (1996). Encyclopedia of the mouse genome V. Mouse chromosome 17. Mammalian Genome 6, S281-S299.
-
(1996)
Mammalian Genome
, vol.6
-
-
Hamvas, R.1
Trachtulec, Z.2
Forejt, J.3
Williams, R.W.4
Arzt, K.5
Fischer-Lindahl, K.6
Silver, L.M.7
-
7
-
-
0029866537
-
Structural alterations in the transcription factors PEBP2/CBF linked to four different types of leukemia
-
Ito, Y. (1996). Structural alterations in the transcription factors PEBP2/CBF linked to four different types of leukemia. J. Cancer Res. Clin. Oncol. 122, 266-274.
-
(1996)
J. Cancer Res. Clin. Oncol.
, vol.122
, pp. 266-274
-
-
Ito, Y.1
-
8
-
-
0003844593
-
-
San Diego, California: Academic Press
-
Kaufman, M.H., ed. (1992). The Atlas of Mouse Development (San Diego, California: Academic Press), pp. 495-506.
-
(1992)
The Atlas of Mouse Development
, pp. 495-506
-
-
Kaufman, M.H.1
-
9
-
-
0028136578
-
AML1, AML2 and AML3, the human members of the runt domain gene-family: CDNA structure, expression, and chromosomal localization
-
Levanon, D., Negreanu, V., Bernstein, Y., Bar-Am, I., Avivi, L., and Groner, Y. (1994). AML1, AML2 and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization. Genomics 23, 425-432.
-
(1994)
Genomics
, vol.23
, pp. 425-432
-
-
Levanon, D.1
Negreanu, V.2
Bernstein, Y.3
Bar-Am, I.4
Avivi, L.5
Groner, Y.6
-
10
-
-
0020384068
-
Development of alkaline phosphatase to give a less soluble red end-product
-
Malik, D.Y., and Damon, M.E. (1982). Development of alkaline phosphatase to give a less soluble red end-product. J. Clin. Pathol. 35, 1092-1094.
-
(1982)
J. Clin. Pathol.
, vol.35
, pp. 1092-1094
-
-
Malik, D.Y.1
Damon, M.E.2
-
11
-
-
0028891018
-
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family
-
Mundlos, S., Mulliken, J.B., Abramson, D.L., Warman, M.L., Knoll, J.H., and Olsen, B.R. (1995). Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family. Hum. Mol. Genet. 4, 71-75.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 71-75
-
-
Mundlos, S.1
Mulliken, J.B.2
Abramson, D.L.3
Warman, M.L.4
Knoll, J.H.5
Olsen, B.R.6
-
12
-
-
0030061554
-
AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis
-
Okuda, T., van Deursen, J., Hiebert, S.W., Grosveld, G., and Downing, J.R. (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, S.W.3
Grosveld, G.4
Downing, J.R.5
-
13
-
-
0030012454
-
Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity
-
Ramesar, R.S., Greenberg, J., Martin, R., Goliath, R., Bardien, S., Mundlos, S., and Beighton, P. (1996). Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity. J. Med. Genet. 33, 511-514.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 511-514
-
-
Ramesar, R.S.1
Greenberg, J.2
Martin, R.3
Goliath, R.4
Bardien, S.5
Mundlos, S.6
Beighton, P.7
-
14
-
-
0029973591
-
Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor β
-
Sasaki, K., Yagi, H., Bronson, R.T., Tominaga, K., Matsunashi, T., Deguchi, K., Tani, Y., Kishimoto, T., and Komori, T. (1996). Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor β. Proc. Natl. Acad. Sci. USA 93, 12359-12363.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 12359-12363
-
-
Sasaki, K.1
Yagi, H.2
Bronson, R.T.3
Tominaga, K.4
Matsunashi, T.5
Deguchi, K.6
Tani, Y.7
Kishimoto, T.8
Komori, T.9
-
15
-
-
0017895980
-
Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice: II. Description of proved mutations
-
Selby, P.B., and Selby, P.R. (1978). Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice: II. Description of proved mutations. Mut. Res. 51, 199-236.
-
(1978)
Mut. Res.
, vol.51
, pp. 199-236
-
-
Selby, P.B.1
Selby, P.R.2
-
16
-
-
0023181094
-
Animal model: Skeletal anomalies in mice with cleidocranial dysplasia
-
Sillence, D.O., Ritchie, H.E., and Selby, P.B. (1987). Animal model: skeletal anomalies in mice with cleidocranial dysplasia. Am. J. Med. Genet. 27, 75-85.
-
(1987)
Am. J. Med. Genet.
, vol.27
, pp. 75-85
-
-
Sillence, D.O.1
Ritchie, H.E.2
Selby, P.B.3
-
17
-
-
0029583960
-
A new transcription factor family associated with human leukemias
-
Speck, N.A., and Terryl, S. (1995). A new transcription factor family associated with human leukemias. Crit. Rev. Eukaryot. Gene Expr. 5, 337-364.
-
(1995)
Crit. Rev. Eukaryot. Gene Expr.
, vol.5
, pp. 337-364
-
-
Speck, N.A.1
Terryl, S.2
-
18
-
-
0029918597
-
Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis
-
Wang, Q., Stacy, T., Binder, M., Marin-Padilla, M., Sharpe, A.H., and Speck, N.A. (1996a). Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis. Proc. Natl. Acad. Sci. USA 93, 3444-3449.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 3444-3449
-
-
Wang, Q.1
Stacy, T.2
Binder, M.3
Marin-Padilla, M.4
Sharpe, A.H.5
Speck, N.A.6
-
19
-
-
0030588487
-
The CBFβ subunit is essential for CBFα2 (AML1) function in vivo
-
Wang, Q., Stacy, T., Miller, J.D., Lewis, A.F., Gu, T.-L., Huang, X., Bushweller, J.H., Bories, J.-C., Alt, F.W., Ryan, G., et al. (1996b). The CBFβ subunit is essential for CBFα2 (AML1) function in vivo. Cell 87, 697-708.
-
(1996)
Cell
, vol.87
, pp. 697-708
-
-
Wang, Q.1
Stacy, T.2
Miller, J.D.3
Lewis, A.F.4
Gu, T.-L.5
Huang, X.6
Bushweller, J.H.7
Bories, J.-C.8
Alt, F.W.9
Ryan, G.10
|