-
1
-
-
34248154652
-
Mechanism and Function of Formins in Control of Actin Assembly
-
Goode BL, Eck MJ. Mechanism and Function of Formins in Control of Actin Assembly. Annu Rev Biochem 2007;76:593-627.
-
(2007)
Annu Rev Biochem
, vol.76
, pp. 593-627
-
-
Goode, B.L.1
Eck, M.J.2
-
2
-
-
0041758426
-
The formins: Active scaffolds that remodel the cytoskeleton
-
Wallar BJ, Alberts AS. The formins: active scaffolds that remodel the cytoskeleton. Trends Cell Biol 2003;138:435-46.
-
(2003)
Trends Cell Biol
, vol.138
, pp. 435-446
-
-
Wallar, B.J.1
Alberts, A.S.2
-
3
-
-
0033160196
-
Cooperation between mDia1 and ROCK in Rho-induced actin reorganization
-
Watanabe N, Kato T, Fujita A, Ishizaki T, Narumiya S. Cooperation between mDia1 and ROCK in Rho-induced actin reorganization. Nat Cell Biol 1999;13:136-43.
-
(1999)
Nat Cell Biol
, vol.13
, pp. 136-143
-
-
Watanabe, N.1
Kato, T.2
Fujita, A.3
Ishizaki, T.4
Narumiya, S.5
-
4
-
-
0035951824
-
Identification of a carboxyl-terminal diaphanous-related formin homology protein autoregulatory domain
-
Alberts AS. Identification of a carboxyl-terminal diaphanous-related formin homology protein autoregulatory domain. J Biol Chem 2001;2764:2824-30.
-
(2001)
J Biol Chem
, vol.2764
, pp. 2824-2830
-
-
Alberts, A.S.1
-
5
-
-
0030707797
-
-
Lynch ED, Lee MK, Morrow JE, Welcsh PL, Leon PE, King MC. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous [see comments]. Science 1997;2785341:1315-8.
-
Lynch ED, Lee MK, Morrow JE, Welcsh PL, Leon PE, King MC. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous [see comments]. Science 1997;2785341:1315-8.
-
-
-
-
6
-
-
18844438774
-
Formin proteins: A domain-based approach
-
Higgs HN. Formin proteins: a domain-based approach. Trends Biochem Sci 2005;306:342-53.
-
(2005)
Trends Biochem Sci
, vol.306
, pp. 342-353
-
-
Higgs, H.N.1
-
7
-
-
17344369363
-
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: Evidence for conserved function in oogenesis and implications for human sterility
-
Bione S, Sala C, Manzini C, et al. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. Am J Hum Genet 1998;623:533-41.
-
(1998)
Am J Hum Genet
, vol.623
, pp. 533-541
-
-
Bione, S.1
Sala, C.2
Manzini, C.3
-
8
-
-
0037382160
-
Disruption of the Diaphanous-related formin Drf1 gene encoding mDia1 reveals a role for Drf3 as an effector for Cdc42
-
Peng J, Wallar BJ, Flanders A, Swiatek PJ, Alberts AS. Disruption of the Diaphanous-related formin Drf1 gene encoding mDia1 reveals a role for Drf3 as an effector for Cdc42. Curr Biol 2003;137:534-45.
-
(2003)
Curr Biol
, vol.137
, pp. 534-545
-
-
Peng, J.1
Wallar, B.J.2
Flanders, A.3
Swiatek, P.J.4
Alberts, A.S.5
-
9
-
-
0030911424
-
p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin
-
Watanabe N, Madaule P, Reid T, et al. p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin. EMBO J 1997;1611:3044-56.
-
(1997)
EMBO J
, vol.1611
, pp. 3044-3056
-
-
Watanabe, N.1
Madaule, P.2
Reid, T.3
-
10
-
-
0027484361
-
Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20
-
Swiatek PJ, Gridley T. Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20. Genes Dev 1993;711:2071-84.
-
(1993)
Genes Dev
, vol.711
, pp. 2071-2084
-
-
Swiatek, P.J.1
Gridley, T.2
-
11
-
-
33846515640
-
Myelodysplastic syndromes: The complexity of stem-cell diseases
-
Corey SJ, Minden MD, Barber DL, Kantarjian H, Wang JC, Schimmer AD. Myelodysplastic syndromes: the complexity of stem-cell diseases. Nat Rev Cancer 2007;72:118-29.
-
(2007)
Nat Rev Cancer
, vol.72
, pp. 118-129
-
-
Corey, S.J.1
Minden, M.D.2
Barber, D.L.3
Kantarjian, H.4
Wang, J.C.5
Schimmer, A.D.6
-
12
-
-
0142248933
-
Sweet's syndrome revisited: A review of disease concepts
-
Cohen PR, Kurzrock R. Sweet's syndrome revisited: a review of disease concepts. Int J Dermatol 2003;4210:761-78.
-
(2003)
Int J Dermatol
, vol.4210
, pp. 761-778
-
-
Cohen, P.R.1
Kurzrock, R.2
-
13
-
-
24344437303
-
-
Grisendi S, Bernardi R, Rossi M, et al. Role of nucleophosmin in embryonic development and tumorigenesis. Nature 2005;4377055:147-53.
-
Grisendi S, Bernardi R, Rossi M, et al. Role of nucleophosmin in embryonic development and tumorigenesis. Nature 2005;4377055:147-53.
-
-
-
-
14
-
-
33646196395
-
Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia
-
Royer-Pokora B, Trost D, Muller N, Hildebrandt B, Germing U, Beier M. Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia. Cancer Genet Cytogenet 2006;1671:66-9.
-
(2006)
Cancer Genet Cytogenet
, vol.1671
, pp. 66-69
-
-
Royer-Pokora, B.1
Trost, D.2
Muller, N.3
Hildebrandt, B.4
Germing, U.5
Beier, M.6
-
15
-
-
33846113924
-
Chromosome 5q deletion and epigenetic suppression of the gene encoding α-catenin (CTNNA1) in myeloid cell transformation
-
Liu TX, Becker MW, Jelinek J, et al. Chromosome 5q deletion and epigenetic suppression of the gene encoding α-catenin (CTNNA1) in myeloid cell transformation. Nat Med 2007;131:78-83.
-
(2007)
Nat Med
, vol.131
, pp. 78-83
-
-
Liu, T.X.1
Becker, M.W.2
Jelinek, J.3
-
16
-
-
0034177514
-
Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31
-
Horrigan SK, Arbieva ZH, Xie HY, et al. Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31. Blood 2000;957:2372-7.
-
(2000)
Blood
, vol.957
, pp. 2372-2377
-
-
Horrigan, S.K.1
Arbieva, Z.H.2
Xie, H.Y.3
-
17
-
-
34547092452
-
Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders
-
Joslin JM, Fernald AA, Tennant TR, et al. Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders. Blood 2007;110:719-26.
-
(2007)
Blood
, vol.110
, pp. 719-726
-
-
Joslin, J.M.1
Fernald, A.A.2
Tennant, T.R.3
-
18
-
-
0024416787
-
Structure, chromosome mapping and regulation of the mouse zinc-finger gene Krox-24; evidence for a common regulatory pathway for immediate-early serum-response genes
-
Janssen-Timmen U, Lemaire P, Mattei MG, Revelant O, Charnay P. Structure, chromosome mapping and regulation of the mouse zinc-finger gene Krox-24; evidence for a common regulatory pathway for immediate-early serum-response genes. Gene 1989;802:325-36.
-
(1989)
Gene
, vol.802
, pp. 325-336
-
-
Janssen-Timmen, U.1
Lemaire, P.2
Mattei, M.G.3
Revelant, O.4
Charnay, P.5
-
19
-
-
0035816691
-
Differential usage of signal transduction pathways defines two types of serum response factor target gene
-
27627
-
Gineitis D, Treisman R. Differential usage of signal transduction pathways defines two types of serum response factor target gene. J Biol Chem 2001;27627:24531-9.
-
(2001)
J Biol Chem
, pp. 24531-24539
-
-
Gineitis, D.1
Treisman, R.2
-
20
-
-
0012644537
-
Diaphanous-related formins bridge Rho GTPase and Src tyrosine kinase signaling
-
Tominaga T, Sahai E, Chardin P, McCormick F, Courtneidge SA, Alberts AS. Diaphanous-related formins bridge Rho GTPase and Src tyrosine kinase signaling. Molecular Cell 2000;51:13-25.
-
(2000)
Molecular Cell
, vol.51
, pp. 13-25
-
-
Tominaga, T.1
Sahai, E.2
Chardin, P.3
McCormick, F.4
Courtneidge, S.A.5
Alberts, A.S.6
|