-
1
-
-
0042829294
-
Msx1 is required for dorsal diencephalon patterning
-
Bach A, Lallemand Y, Nicola MA, Ramos C, Mathis L, Maufras M, Robert B. 2003. Msx1 is required for dorsal diencephalon patterning. Development 130:4025-4036.
-
(2003)
Development
, vol.130
, pp. 4025-4036
-
-
Bach, A.1
Lallemand, Y.2
Nicola, M.A.3
Ramos, C.4
Mathis, L.5
Maufras, M.6
Robert, B.7
-
2
-
-
0034682072
-
Roles for Msx and DIx homeoproteins in vertebrate development
-
Bendall AJ, Abate-Shen C. 2000. Roles for Msx and DIx homeoproteins in vertebrate development. Gene 247:17-31.
-
(2000)
Gene
, vol.247
, pp. 17-31
-
-
Bendall, A.J.1
Abate-Shen, C.2
-
3
-
-
0029164842
-
The function and evolution of Msx genes: Pointers and paradoxes
-
Davidson D. 1995. The function and evolution of Msx genes: Pointers and paradoxes. Trends Genet 11:405-411.
-
(1995)
Trends Genet
, vol.11
, pp. 405-411
-
-
Davidson, D.1
-
4
-
-
0025787003
-
Position-dependent expression of two related homeobox genes in developing vertebrate limbs
-
Davidson DR, Crawley A, Hill RE, Tickle C. 1991. Position-dependent expression of two related homeobox genes in developing vertebrate limbs. Nature 352:429-431.
-
(1991)
Nature
, vol.352
, pp. 429-431
-
-
Davidson, D.R.1
Crawley, A.2
Hill, R.E.3
Tickle, C.4
-
5
-
-
35348916693
-
Conditional alleles of Msx1 and Msx2
-
Fu H, Ishii M, Gu Y, Maxson R. 2007. Conditional alleles of Msx1 and Msx2. Genesis 45:477-481.
-
(2007)
Genesis
, vol.45
, pp. 477-481
-
-
Fu, H.1
Ishii, M.2
Gu, Y.3
Maxson, R.4
-
6
-
-
34548529914
-
Concerted action of Msxl and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development
-
Han J, Ishii M, Bringas P Jr, Maas RL, Maxson RE Jr, Chai Y. 2007. Concerted action of Msxl and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development. Mech Dev 124:729-745.
-
(2007)
Mech Dev
, vol.124
, pp. 729-745
-
-
Han, J.1
Ishii, M.2
Bringas Jr, P.3
Maas, R.L.4
Maxson Jr, R.E.5
Chai, Y.6
-
7
-
-
0024574583
-
A new family of mouse homeobox-containing genes: Molecular structure, chromosomal location, and developmental expression of Hox-7.1
-
Hill RE, Jones PF, Rees AR, Sime CM, Justice MJ, Copeland NG, Jenkins NA, Graham E, Davidson DR. 1989. A new family of mouse homeobox-containing genes: Molecular structure, chromosomal location, and developmental expression of Hox-7.1. Genes Dev 3:26-37.
-
(1989)
Genes Dev
, vol.3
, pp. 26-37
-
-
Hill, R.E.1
Jones, P.F.2
Rees, A.R.3
Sime, C.M.4
Justice, M.J.5
Copeland, N.G.6
Jenkins, N.A.7
Graham, E.8
Davidson, D.R.9
-
8
-
-
0031193368
-
Insertional mutation of the mouse Msx1 homeobox gene by an nLacZ reporter gene
-
Houzelstein D, Cohen A, Buckingham ME, Robert B. 1997. Insertional mutation of the mouse Msx1 homeobox gene by an nLacZ reporter gene. Mech Dev 65:123-133.
-
(1997)
Mech Dev
, vol.65
, pp. 123-133
-
-
Houzelstein, D.1
Cohen, A.2
Buckingham, M.E.3
Robert, B.4
-
9
-
-
28844480515
-
Combined deficiencies of Msx1 and Msx2 cause impaired patterning and survival of the cranial neural crest
-
Ishii M, Han J, Yen HY, Sucov HM, Chai Y, Maxson RE Jr. 2005. Combined deficiencies of Msx1 and Msx2 cause impaired patterning and survival of the cranial neural crest. Development 132:4937-4950.
-
(2005)
Development
, vol.132
, pp. 4937-4950
-
-
Ishii, M.1
Han, J.2
Yen, H.Y.3
Sucov, H.M.4
Chai, Y.5
Maxson Jr., R.E.6
-
10
-
-
0346252654
-
Msx2 and Twist cooperatively control the development of the neural crest derived skeletogenic mesenchyme of the murine skull vault
-
Ishii M, Merrill AE, Chan YS, Gitelman I, Rice DP, Sucov HM, Maxson RE Jr. 2003. Msx2 and Twist cooperatively control the development of the neural crest derived skeletogenic mesenchyme of the murine skull vault. Development 130:6131-6142.
-
(2003)
Development
, vol.130
, pp. 6131-6142
-
-
Ishii, M.1
Merrill, A.E.2
Chan, Y.S.3
Gitelman, I.4
Rice, D.P.5
Sucov, H.M.6
Maxson Jr., R.E.7
-
11
-
-
0034969492
-
A nonsense mutation in MSX1 causes Witkop syndrome
-
Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. 2001. A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet 69:67-74.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 67-74
-
-
Jumlongras, D.1
Bei, M.2
Stimson, J.M.3
Wang, W.F.4
DePalma, S.R.5
Seidman, C.E.6
Felbor, U.7
Maas, R.8
Seidman, J.G.9
Olsen, B.R.10
-
12
-
-
0023665902
-
An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs
-
Kozak M. 1987. An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res 15:8125-8148.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 8125-8148
-
-
Kozak, M.1
-
14
-
-
0032030846
-
Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase
-
Lallemand Y, Luria V, Haffner-Krausz R, Lonai P. 1998. Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase. Transgenic Res 7:105-112.
-
(1998)
Transgenic Res
, vol.7
, pp. 105-112
-
-
Lallemand, Y.1
Luria, V.2
Haffner-Krausz, R.3
Lonai, P.4
-
15
-
-
23144435172
-
Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development
-
Lallemand Y, Nicola MA, Ramos C, Bach A, Saint Cloment C, Robert B. 2005. Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development. Development 132:3003-3014.
-
(2005)
Development
, vol.132
, pp. 3003-3014
-
-
Lallemand, Y.1
Nicola, M.A.2
Ramos, C.3
Bach, A.4
Saint Cloment, C.5
Robert, B.6
-
16
-
-
20944449214
-
Ventral abdominal wall dysmorphogenesis of Msx1/Msx2 double-mutant mice. Anat Rec A Discov Mol Cell
-
Ogi H, Suzuki K, Ogino Y, Kamimura M, Miyado M, Ying X, Zhang Z, Shinohara M, Chen Y, Yamada G. 2005. Ventral abdominal wall dysmorphogenesis of Msx1/Msx2 double-mutant mice. Anat Rec A Discov Mol Cell Evol Biol 284:424-430.
-
(2005)
Evol Biol
, vol.284
, pp. 424-430
-
-
Ogi, H.1
Suzuki, K.2
Ogino, Y.3
Kamimura, M.4
Miyado, M.5
Ying, X.6
Zhang, Z.7
Shinohara, M.8
Chen, Y.9
Yamada, G.10
-
17
-
-
0026267740
-
The apical ectodermal ridge regulates Hox-7 and Hox-8 gene expression in developing chick limb buds
-
Robert B, Lyons G, Simandl BK, Kuroiwa A, Buckingham M. 1991. The apical ectodermal ridge regulates Hox-7 and Hox-8 gene expression in developing chick limb buds. Genes Dev 5:2363-2374.
-
(1991)
Genes Dev
, vol.5
, pp. 2363-2374
-
-
Robert, B.1
Lyons, G.2
Simandl, B.K.3
Kuroiwa, A.4
Buckingham, M.5
-
18
-
-
0024452548
-
Hox-7s, a mouse homeobox gene with a novel pattern of expression during embryogenesls
-
Robert B, Sassoon D, Jacq B, Gehring W, Buckingham M. 1989. Hox-7s, a mouse homeobox gene with a novel pattern of expression during embryogenesls. EMBO J 8:91-100.
-
(1989)
EMBO J
, vol.8
, pp. 91-100
-
-
Robert, B.1
Sassoon, D.2
Jacq, B.3
Gehring, W.4
Buckingham, M.5
-
19
-
-
0034041160
-
High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP
-
Rodriguez CI, Buchholz F, Galloway J, Sequerra R, Kasper J, Ayala R, Stewart AF, Dymecki SM. 2000. High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP. Nat Genet 25:139-140.
-
(2000)
Nat Genet
, vol.25
, pp. 139-140
-
-
Rodriguez, C.I.1
Buchholz, F.2
Galloway, J.3
Sequerra, R.4
Kasper, J.5
Ayala, R.6
Stewart, A.F.7
Dymecki, S.M.8
-
20
-
-
0034029571
-
Msx2s deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
-
Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R. 2000. Msx2s deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 24:391-395.
-
(2000)
Nat Genet
, vol.24
, pp. 391-395
-
-
Satokata, I.1
Ma, L.2
Ohshima, H.3
Bei, M.4
Woo, I.5
Nishizawa, K.6
Maeda, T.7
Takano, Y.8
Uchiyama, M.9
Heaney, S.10
Peters, H.11
Tang, Z.12
Maxson, R.13
Maas, R.14
-
21
-
-
0028292605
-
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
-
Satokata I, Maas R. 1994. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet 6:348-356.
-
(1994)
Nat Genet
, vol.6
, pp. 348-356
-
-
Satokata, I.1
Maas, R.2
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