-
1
-
-
0038682002
-
Mechanisms of TGF-β signaling from cell membrane to the nucleus
-
Shi, Y., and Massagué, J. (2003) Mechanisms of TGF-β signaling from cell membrane to the nucleus. Cell 113, 685-700
-
(2003)
Cell
, vol.113
, pp. 685-700
-
-
Shi, Y.1
Massagué, J.2
-
2
-
-
35148883003
-
TGF-βa signaling in development
-
Kitisin, K., Saha, T., Blake, T., Golestaneh, N., Deng, M., Kim, C., Tang, Y., Shetty, K., Mishra, B., and Mishra, L. (2007) TGF-βa signaling in development. Sci. STKE 2007, cm1
-
(2007)
Sci. STKE
, vol.2007
-
-
Kitisin, K.1
Saha, T.2
Blake, T.3
Golestaneh, N.4
Deng, M.5
Kim, C.6
Tang, Y.7
Shetty, K.8
Mishra, B.9
Mishra, L.10
-
3
-
-
61749097816
-
TGF-β superfamily signaling in embryonic development and homeostasis
-
Wu, M. Y., and Hill, C. S. (2009) TGF-β superfamily signaling in embryonic development and homeostasis. Dev. Cell 16, 329-343
-
(2009)
Dev. Cell
, vol.16
, pp. 329-343
-
-
Wu, M.Y.1
Hill, C.S.2
-
4
-
-
0028170226
-
Mechanism of activation of the TGF-β receptor
-
Wrana, J. L., Attisano, L., Wieser, R., Ventura, F., and Massagué, J. (1994) Mechanism of activation of the TGF-β receptor. Nature 370, 341-347
-
(1994)
Nature
, vol.370
, pp. 341-347
-
-
Wrana, J.L.1
Attisano, L.2
Wieser, R.3
Ventura, F.4
Massagué, J.5
-
5
-
-
0031438047
-
TGF-β signaling from cell membrane to nucleus through SMAD proteins
-
Heldin, C. H., Miyazono, K., and ten Dijke, P. (1997) TGF-β signaling from cell membrane to nucleus through SMAD proteins. Nature 390, 465-471
-
(1997)
Nature
, vol.390
, pp. 465-471
-
-
Heldin, C.H.1
Miyazono, K.2
Ten Dijke, P.3
-
6
-
-
0142104985
-
Smad-dependent and Smad-independent pathways in TGF-β family signaling
-
Derynck, R., and Zhang, Y. E. (2003) Smad-dependent and Smad-independent pathways in TGF-β family signaling. Nature 425, 577-584
-
(2003)
Nature
, vol.425
, pp. 577-584
-
-
Derynck, R.1
Zhang, Y.E.2
-
7
-
-
0030576525
-
The immunophilin FKBP12 functions as a common inhibitor of the TGF-β family type i receptors
-
Wang, T., Li, B. Y., Danielson, P. D., Shah, P. C., Rockwell, S., Lechleider, R. J., Martin, J., Manganaro, T., and Donahoe, P. K. (1996) The immunophilin FKBP12 functions as a common inhibitor of the TGF-β family type I receptors. Cell 86, 435-444
-
(1996)
Cell
, vol.86
, pp. 435-444
-
-
Wang, T.1
Li, B.Y.2
Danielson, P.D.3
Shah, P.C.4
Rockwell, S.5
Lechleider, R.J.6
Martin, J.7
Manganaro, T.8
Donahoe, P.K.9
-
8
-
-
0033524943
-
Crystal structure of the cytoplasmic domain of the type i TGFβ receptor in complex with FKBP12
-
Huse, M., Chen, Y. G., Massagué, J., and Kuriyan, J. (1999) Crystal structure of the cytoplasmic domain of the type I TGFβ receptor in complex with FKBP12. Cell 96, 425-436
-
(1999)
Cell
, vol.96
, pp. 425-436
-
-
Huse, M.1
Chen, Y.G.2
Massagué, J.3
Kuriyan, J.4
-
9
-
-
0034796457
-
The TGFβ receptor activation process. An inhibitor-to substratebinding switch
-
Huse, M., Muir, T. W., Xu, L., Chen, Y. G., Kuriyan, J., and Massagué, J. (2001) The TGFβ receptor activation process. An inhibitor-to substratebinding switch. Mol. Cell 8, 671-682
-
(2001)
Mol. Cell
, vol.8
, pp. 671-682
-
-
Huse, M.1
Muir, T.W.2
Xu, L.3
Chen, Y.G.4
Kuriyan, J.5
Massagué, J.6
-
10
-
-
0035695116
-
Structural basis of Smad1 activation by receptor kinase phosphorylation
-
Qin, B. Y., Chacko, B. M., Lam, S. S., de Caestecker, M. P., Correia, J. J., and Lin, K. (2001) Structural basis of Smad1 activation by receptor kinase phosphorylation. Mol. Cell 8, 1303-1312
-
(2001)
Mol. Cell
, vol.8
, pp. 1303-1312
-
-
Qin, B.Y.1
Chacko, B.M.2
Lam, S.S.3
De Caestecker, M.P.4
Correia, J.J.5
Lin, K.6
-
11
-
-
18244362844
-
Crystal structure of a phosphorylated Smad2. Recognition of phosphoserine by theMH2domain and insights on Smad function in TGF-β signaling
-
Wu, J. W., Hu, M., Chai, J., Seoane, J., Huse, M., Li, C., Rigotti, D. J., Kyin, S., Muir, T. W., Fairman, R., Massagué, J., and Shi, Y. (2001) Crystal structure of a phosphorylated Smad2. Recognition of phosphoserine by theMH2domain and insights on Smad function in TGF-β signaling. Mol. Cell 8, 1277-1289
-
(2001)
Mol. Cell
, vol.8
, pp. 1277-1289
-
-
Wu, J.W.1
Hu, M.2
Chai, J.3
Seoane, J.4
Huse, M.5
Li, C.6
Rigotti, D.J.7
Kyin, S.8
Muir, T.W.9
Fairman, R.10
Massagué, J.11
Shi, Y.12
-
12
-
-
33744773190
-
Dysregulation of the BMP-4 signaling pathway in fibrodysplasia ossificans progressiva
-
Kaplan, F. S., Fiori, J., de la Peña, L. S., Ahn, J., Billings, P. C., and Shore, E. M. (2006) Dysregulation of the BMP-4 signaling pathway in fibrodysplasia ossificans progressiva. Ann. N.Y. Acad. Sci. 1068, 54-65
-
(2006)
Ann. N.Y. Acad. Sci.
, vol.1068
, pp. 54-65
-
-
Kaplan, F.S.1
Fiori, J.2
De La Peña, L.S.3
Ahn, J.4
Billings, P.C.5
Shore, E.M.6
-
13
-
-
77956275161
-
Inherited human diseases of heterotopic bone formation
-
Shore, E. M., and Kaplan, F. S. (2010) Inherited human diseases of heterotopic bone formation. Nat. Rev. Rheumatol. 6, 518-527
-
(2010)
Nat. Rev. Rheumatol.
, vol.6
, pp. 518-527
-
-
Shore, E.M.1
Kaplan, F.S.2
-
14
-
-
33646348736
-
A recurrent mutation in the BMP type i receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
-
Shore, E. M., Xu, M., Feldman, G. J., Fenstermacher, D. A., Cho, T. J., Choi, I. H., Connor, J. M., Delai, P., Glaser, D. L., LeMerrer, M., Morhart, R., Rogers, J. G., Smith, R., Triffitt, J. T., Urtizberea, J. A., Zasloff, M., Brown, M. A., and Kaplan, F. S. (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat. Genet. 38, 525-527
-
(2006)
Nat. Genet.
, vol.38
, pp. 525-527
-
-
Shore, E.M.1
Xu, M.2
Feldman, G.J.3
Fenstermacher, D.A.4
Cho, T.J.5
Choi, I.H.6
Connor, J.M.7
Delai, P.8
Glaser, D.L.9
Lemerrer, M.10
Morhart, R.11
Rogers, J.G.12
Smith, R.13
Triffitt, J.T.14
Urtizberea, J.A.15
Zasloff, M.16
Brown, M.A.17
Kaplan, F.S.18
-
15
-
-
38849093307
-
A unique case of fibrodysplasia ossificans progressiva with an ACVR1 mutation, G356D, other than the common mutation (R206H)
-
Furuya, H., Ikezoe, K., Wang, L., Ohyagi, Y., Motomura, K., Fujii, N., Kira, J., and Fukumaki, Y. (2008) A unique case of fibrodysplasia ossificans progressiva with an ACVR1 mutation, G356D, other than the common mutation (R206H). Am. J. Med. Genet. 146, 459-463
-
(2008)
Am. J. Med. Genet.
, vol.146
, pp. 459-463
-
-
Furuya, H.1
Ikezoe, K.2
Wang, L.3
Ohyagi, Y.4
Motomura, K.5
Fujii, N.6
Kira, J.7
Fukumaki, Y.8
-
16
-
-
61649084689
-
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type i receptor ACVR1
-
Kaplan, F. S., Xu, M., Seemann, P., Connor, J. M., Glaser, D. L., Carroll, L., Delai, P., Fastnacht-Urban, E., Forman, S. J., Gillessen-Kaesbach, G., Hoover-Fong, J., Köster, B., Pauli, R. M., Reardon, W., Zaidi, S. A., Zasloff, M., Morhart, R., Mundlos, S., Groppe, J., and Shore, E. M. (2009) Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1. Hum. Mutat. 30, 379-390
-
(2009)
Hum. Mutat.
, vol.30
, pp. 379-390
-
-
Kaplan, F.S.1
Xu, M.2
Seemann, P.3
Connor, J.M.4
Glaser, D.L.5
Carroll, L.6
Delai, P.7
Fastnacht-Urban, E.8
Forman, S.J.9
Gillessen-Kaesbach, G.10
Hoover-Fong, J.11
Köster, B.12
Pauli, R.M.13
Reardon, W.14
Zaidi, S.A.15
Zasloff, M.16
Morhart, R.17
Mundlos, S.18
Groppe, J.19
Shore, E.M.20
more..
-
17
-
-
63749106137
-
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients
-
Petrie, K. A., Lee, W. H., Bullock, A. N., Pointon, J. J., Smith, R., Russell, R. G., Brown, M. A., Wordsworth, B. P., and Triffitt, J. T. (2009) Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients. PloS ONE 4, e5005
-
(2009)
PloS ONE
, vol.4
-
-
Petrie, K.A.1
Lee, W.H.2
Bullock, A.N.3
Pointon, J.J.4
Smith, R.5
Russell, R.G.6
Brown, M.A.7
Wordsworth, B.P.8
Triffitt, J.T.9
-
18
-
-
79751537956
-
A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date
-
Gregson,C.L.,Hollingworth,P.,Williams,M.,Petrie,K.A.,Bullock,A.N.,Brown, M. A., Tobias, J. H., and Triffitt, J. T. (2011) A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date. Bone 48, 654-658
-
(2011)
Bone
, vol.48
, pp. 654-658
-
-
Tobias, J.H.1
Triffitt, J.T.2
-
19
-
-
60749137428
-
Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva. Confirmations and advancements
-
Bocciardi, R., Bordo, D., Di Duca, M., Di Rocco, M., and Ravazzolo, R. (2009) Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva. Confirmations and advancements. Eur. J. Hum. Genet. 17, 311-318
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 311-318
-
-
Bocciardi, R.1
Bordo, D.2
Di Duca, M.3
Di Rocco, M.4
Ravazzolo, R.5
-
20
-
-
84857283030
-
Fibrodysplasia ossificans progressiva. Middle-age onset of heterotopic ossification from a unique missense mutation (c.974G3C, p.G325A) in ACVR1
-
Whyte, M. P., Wenkert, D., Demertzis, J. L., DiCarlo, E. F., Westenberg, E., and Mumm, S. (2012) Fibrodysplasia ossificans progressiva. Middle-age onset of heterotopic ossification from a unique missense mutation (c.974G3C, p.G325A) in ACVR1. J. Bone Miner. Res. 27, 729-737
-
(2012)
J. Bone Miner. Res.
, vol.27
, pp. 729-737
-
-
Whyte, M.P.1
Wenkert, D.2
Demertzis, J.L.3
Dicarlo, E.F.4
Westenberg, E.5
Mumm, S.6
-
21
-
-
4644264945
-
Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype
-
Kan, L., Hu, M., Gomes, W. A., and Kessler, J. A. (2004) Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype. Am. J. Pathol. 165, 1107-1115
-
(2004)
Am. J. Pathol.
, vol.165
, pp. 1107-1115
-
-
Kan, L.1
Hu, M.2
Gomes, W.A.3
Kessler, J.A.4
-
22
-
-
57349171954
-
BMP type i receptor inhibition reduces heterotopic (corrected) ossification
-
Yu, P. B., Deng, D. Y., Lai, C. S., Hong, C. C., Cuny, G. D., Bouxsein, M. L., Hong, D. W., McManus, P. M., Katagiri, T., Sachidanandan, C., Kamiya, N., Fukuda, T., Mishina, Y., Peterson, R. T., and Bloch, K. D. (2008) BMP type I receptor inhibition reduces heterotopic (corrected) ossification. Nat. Med. 14, 1363-1369
-
(2008)
Nat. Med.
, vol.14
, pp. 1363-1369
-
-
Yu, P.B.1
Deng, D.Y.2
Lai, C.S.3
Hong, C.C.4
Cuny, G.D.5
Bouxsein, M.L.6
Hong, D.W.7
McManus, P.M.8
Katagiri, T.9
Sachidanandan, C.10
Kamiya, N.11
Fukuda, T.12
Mishina, Y.13
Peterson, R.T.14
Bloch, K.D.15
-
23
-
-
0029022221
-
GS domain mutations that constitutively activate TβR-I, the downstream signaling component in the TGF-β receptor complex
-
Wieser, R., Wrana, J. L., and Massagué, J. (1995) GS domain mutations that constitutively activate TβR-I, the downstream signaling component in the TGF-β receptor complex. EMBO J. 14, 2199-2208
-
(1995)
EMBO J.
, vol.14
, pp. 2199-2208
-
-
Wieser, R.1
Wrana, J.L.2
Massagué, J.3
-
24
-
-
78650018824
-
Conversion of vascular endothelial cells into multipotent stem-like cells
-
Medici, D., Shore, E. M., Lounev, V. Y., Kaplan, F. S., Kalluri, R., and Olsen, B. R. (2010) Conversion of vascular endothelial cells into multipotent stem-like cells. Nat. Med. 16, 1400-1406
-
(2010)
Nat. Med.
, vol.16
, pp. 1400-1406
-
-
Medici, D.1
Shore, E.M.2
Lounev, V.Y.3
Kaplan, F.S.4
Kalluri, R.5
Olsen, B.R.6
-
25
-
-
56049098488
-
A unique mutation of ALK2, G356D, found in a patient with fibrodysplasia ossificans progressiva is a moderately activated BMP type i receptor
-
Fukuda, T., Kanomata, K., Nojima, J., Kokabu, S., Akita, M., Ikebuchi, K., Jimi, E., Komori, T., Maruki, Y., Matsuoka, M., Miyazono, K., Nakayama, K., Nanba, A., Tomoda, H., Okazaki, Y., Ohtake, A., Oda, H., Owan, I., Yoda, T., Haga, N., Furuya, H., and Katagiri, T. (2008) A unique mutation of ALK2, G356D, found in a patient with fibrodysplasia ossificans progressiva is a moderately activated BMP type I receptor. Biochem. Biophys. Res. Commun. 377, 905-909
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.377
, pp. 905-909
-
-
Fukuda, T.1
Kanomata, K.2
Nojima, J.3
Kokabu, S.4
Akita, M.5
Ikebuchi, K.6
Jimi, E.7
Komori, T.8
Maruki, Y.9
Matsuoka, M.10
Miyazono, K.11
Nakayama, K.12
Nanba, A.13
Tomoda, H.14
Okazaki, Y.15
Ohtake, A.16
Oda, H.17
Owan, I.18
Yoda, T.19
Haga, N.20
Furuya, H.21
Katagiri, T.22
more..
-
26
-
-
65449139561
-
Constitutively activated ALK2 and increased SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva
-
Fukuda, T., Kohda, M., Kanomata, K., Nojima, J., Nakamura, A., Kamizono, J., Noguchi, Y., Iwakiri, K., Kondo, T., Kurose, J., Endo, K., Awakura, T., Fukushi, J., Nakashima, Y., Chiyonobu, T., Kawara, A., Nishida, Y., Wada, I., Akita, M., Komori, T., Nakayama, K., Nanba, A., Maruki, Y., Yoda, T., Tomoda, H., Yu, P. B., Shore, E. M., Kaplan, F. S., Miyazono, K., and Matsuoka, M., Ikebuchi, K., Ohtake, A., Oda, H., Jimi, E., Owan, I., Okazaki, Y., and Katagiri, T. (2009) Constitutively activated ALK2 and increased SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva. J. Biol. Chem. 284, 7149-7156
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 7149-7156
-
-
Fukuda, T.1
Kohda, M.2
Kanomata, K.3
Nojima, J.4
Nakamura, A.5
Kamizono, J.6
Noguchi, Y.7
Iwakiri, K.8
Kondo, T.9
Kurose, J.10
Endo, K.11
Awakura, T.12
Fukushi, J.13
Nakashima, Y.14
Chiyonobu, T.15
Kawara, A.16
Nishida, Y.17
Wada, I.18
Akita, M.19
Komori, T.20
Nakayama, K.21
Nanba, A.22
Maruki, Y.23
Yoda, T.24
Tomoda, H.25
Yu, P.B.26
Shore, E.M.27
Kaplan, F.S.28
Miyazono, K.29
Matsuoka, M.30
Ikebuchi, K.31
Ohtake, A.32
Oda, H.33
Jimi, E.34
Owan, I.35
Okazaki, Y.36
Katagiri, T.37
more..
-
27
-
-
70449366408
-
The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization
-
Shen, Q., Little, S. C., Xu, M., Haupt, J., Ast, C., Katagiri, T., Mundlos, S., Seemann, P., Kaplan, F. S., Mullins, M. C., and Shore, E. M. (2009) The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization. J. Clin. Invest. 119, 3462-3472
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 3462-3472
-
-
Shen, Q.1
Little, S.C.2
Xu, M.3
Haupt, J.4
Ast, C.5
Katagiri, T.6
Mundlos, S.7
Seemann, P.8
Kaplan, F.S.9
Mullins, M.C.10
Shore, E.M.11
-
28
-
-
77954588190
-
Molecular consequences of the ACVR1(R206H) mutation of fibrodysplasia ossificans progressiva
-
Song, G. A., Kim, H. J., Woo, K. M., Baek, J. H., Kim, G. S., Choi, J. Y., and Ryoo, H. M. (2010) Molecular consequences of the ACVR1(R206H) mutation of fibrodysplasia ossificans progressiva. J. Biol. Chem. 285, 22542-22553
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 22542-22553
-
-
Song, G.A.1
Kim, H.J.2
Woo, K.M.3
Baek, J.H.4
Kim, G.S.5
Choi, J.Y.6
Ryoo, H.M.7
-
29
-
-
77953497987
-
ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type i receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation
-
van Dinther, M., Visser, N., de Gorter, D. J., Doorn, J., Goumans, M. J., de Boer, J., and ten Dijke, P. (2010) ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation. J. Bone Miner. Res. 25, 1208-1215
-
(2010)
J. Bone Miner. Res.
, vol.25
, pp. 1208-1215
-
-
Van Dinther, M.1
Visser, N.2
De Gorter, D.J.3
Doorn, J.4
Goumans, M.J.5
De Boer, J.6
Ten Dijke, P.7
-
30
-
-
79953163208
-
A novel mutation of ALK2, L196P, found in the most benign case of fibrodysplasia ossificans progressiva activates BMP-specific intracellular signaling equivalent to a typical mutation, R206H
-
Ohte, S., Shin, M., Sasanuma, H., Yoneyama, K., Akita, M., Ikebuchi, K., Jimi, E., Maruki, Y., Matsuoka, M., Namba, A., Tomoda, H., Okazaki, Y., Ohtake, A., Oda, H.,Owan,I.,Yoda,T.,Furuya,H.,Kamizono,J.,Kitoh,H.,Nakashima,Y.,Susami, T., Haga, N., Komori, T., and Katagiri, T. (2011) A novel mutation of ALK2, L196P, found in the most benign case of fibrodysplasia ossificans progressiva activates BMP-specific intracellular signaling equivalent to a typical mutation, R206H. Biochem. Biophys. Res. Commun. 407, 213-218
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.407
, pp. 213-218
-
-
Ohte, S.1
Shin, M.2
Sasanuma, H.3
Yoneyama, K.4
Akita, M.5
Ikebuchi, K.6
Jimi, E.7
Maruki, Y.8
Matsuoka, M.9
Namba, A.10
Tomoda, H.11
Okazaki, Y.12
Ohtake, A.13
Oda, H.14
Owan, I.15
Yoda, T.16
Furuya, H.17
Kamizono, J.18
Kitoh, H.19
Nakashima, Y.20
Susami, T.21
Haga, N.22
Komori, T.23
Katagiri, T.24
more..
-
31
-
-
37249010753
-
Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism
-
Yu, P. B., Hong, C. C., Sachidanandan, C., Babitt, J. L., Deng, D. Y., Hoyng, S. A., Lin, H. Y., Bloch, K. D., and Peterson, R. T. (2008) Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat. Chem. Biol. 4, 33-41
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 33-41
-
-
Yu, P.B.1
Hong, C.C.2
Sachidanandan, C.3
Babitt, J.L.4
Deng, D.Y.5
Hoyng, S.A.6
Lin, H.Y.7
Bloch, K.D.8
Peterson, R.T.9
-
32
-
-
33644874235
-
The integration of macromolecular diffraction data
-
Leslie, A. G. (2006) The integration of macromolecular diffraction data. Acta Crystallogr. D Biol. Crystallogr. 62, 48-57
-
(2006)
Acta Crystallogr. D Biol. Crystallogr.
, vol.62
, pp. 48-57
-
-
Leslie, A.G.1
-
34
-
-
34447508216
-
Phaser crystallographic software
-
McCoy, A. J., Grosse-Kunstleve, R. W., Adams, P. D., Winn, M. D., Storoni, L. C., and Read, R. J. (2007) Phaser crystallographic software. J. Appl. Crystallogr. 40, 658-674
-
(2007)
J. Appl. Crystallogr.
, vol.40
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
Read, R.J.6
-
36
-
-
0035788112
-
ARP/ wARP and molecular replacement
-
Perrakis, A., Harkiolaki, M., Wilson, K. S., and Lamzin, V. S. (2001) ARP/ wARP and molecular replacement. Acta Crystallogr. D Biol. Crystallogr. 57, 1445-1450
-
(2001)
Acta Crystallogr. D Biol. Crystallogr.
, vol.57
, pp. 1445-1450
-
-
Perrakis, A.1
Harkiolaki, M.2
Wilson, K.S.3
Lamzin, V.S.4
-
37
-
-
33748337934
-
The Buccaneer software for automated model building. 1. Tracing protein chains
-
Cowtan, K. (2006) The Buccaneer software for automated model building. 1. Tracing protein chains. Acta Crystallogr.DBiol. Crystallogr. 62, 1002-1011
-
(2006)
Acta Crystallogr.DBiol. Crystallogr.
, vol.62
, pp. 1002-1011
-
-
Cowtan, K.1
-
38
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G. N., Vagin, A. A., and Dodson, E. J. (1997) Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. D Biol. Crystallogr. 53, 240-255
-
(1997)
Acta Crystallogr. D Biol. Crystallogr.
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
40
-
-
33646260450
-
Optimal description of a protein structure in terms of multiple groups undergoing TLS motion
-
Painter, J., and Merritt, E. A. (2006) Optimal description of a protein structure in terms of multiple groups undergoing TLS motion. Acta Crystallogr. D Biol. Crystallogr. 62, 439-450
-
(2006)
Acta Crystallogr. D Biol. Crystallogr.
, vol.62
, pp. 439-450
-
-
Painter, J.1
Merritt, E.A.2
-
41
-
-
34547592557
-
MolProbity. All-atom contacts and structure validation for proteins and nucleic acids
-
Davis, I. W., Leaver-Fay, A., Chen, V. B., Block, J. N., Kapral, G. J., Wang, X., Murray,L.W.,Arendall,W.B.,3rd,Snoeyink,J.,Richardson,J.S., andRichardson, D. C. (2007) MolProbity. All-atom contacts and structure validation for proteins and nucleic acids. Nucleic Acids Res. 35, W375-W383
-
(2007)
Nucleic Acids Res.
, vol.35
-
-
Davis, I.W.1
Leaver-Fay, A.2
Chen, V.B.3
Block, J.N.4
Kapral, G.J.5
Wang, X.6
Murray, L.W.7
Arendall III, W.B.8
Snoeyink, J.9
Richardson, J.S.10
Richardson, D.C.11
-
42
-
-
84862762318
-
Promiscuity and specificity in BMP receptor activation
-
Mueller, T. D., and Nickel, J. (2012) Promiscuity and specificity in BMP receptor activation. FEBS Lett. 586, 1846-1859
-
(2012)
FEBS Lett.
, vol.586
, pp. 1846-1859
-
-
Mueller, T.D.1
Nickel, J.2
-
43
-
-
51049098368
-
BMP-2/4 and BMP-6/7 differentially utilize cell surface receptors to induce osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells
-
Lavery, K., Swain, P., Falb, D., and Alaoui-Ismaili, M. H. (2008) BMP-2/4 and BMP-6/7 differentially utilize cell surface receptors to induce osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells. J. Biol. Chem. 283, 20948-20958
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 20948-20958
-
-
Lavery, K.1
Swain, P.2
Falb, D.3
Alaoui-Ismaili, M.H.4
-
44
-
-
0028108801
-
Specific interaction of type i receptors of the TGF-β family with the immunophilin FKBP-12
-
Wang, T., Donahoe, P. K., and Zervos, A. S. (1994) Specific interaction of type I receptors of the TGF-β family with the immunophilin FKBP-12. Science 265, 674-676
-
(1994)
Science
, vol.265
, pp. 674-676
-
-
Wang, T.1
Donahoe, P.K.2
Zervos, A.S.3
-
45
-
-
34748887926
-
Crystal structure of activin receptor type IIB kinase domain from human at 2.0 Angstrom resolution
-
Han, S., Loulakis, P., Griffor, M., and Xie, Z. (2007) Crystal structure of activin receptor type IIB kinase domain from human at 2.0 Angstrom resolution. Protein Sci. 16, 2272-2277
-
(2007)
Protein Sci.
, vol.16
, pp. 2272-2277
-
-
Han, S.1
Loulakis, P.2
Griffor, M.3
Xie, Z.4
-
46
-
-
73949158814
-
Structure and functional characterization of the atypical human kinase haspin
-
Eswaran, J., Patnaik, D., Filippakopoulos, P., Wang, F., Stein, R. L., Murray, J. W., Higgins, J. M., and Knapp, S. (2009) Structure and functional characterization of the atypical human kinase haspin. Proc. Natl. Acad. Sci. U.S.A. 106, 20198-20203
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 20198-20203
-
-
Eswaran, J.1
Patnaik, D.2
Filippakopoulos, P.3
Wang, F.4
Stein, R.L.5
Murray, J.W.6
Higgins, J.M.7
Knapp, S.8
-
47
-
-
80051799654
-
In vitro analyses of the dysregulated R206H ALK2 kinase-FKBP12 interaction associated with heterotopic ossification in FOP
-
Groppe, J. C., Wu, J., Shore, E. M., and Kaplan, F. S. (2011) In vitro analyses of the dysregulated R206H ALK2 kinase-FKBP12 interaction associated with heterotopic ossification in FOP. Cells Tissues Organs 194, 291-295
-
(2011)
Cells Tissues Organs
, vol.194
, pp. 291-295
-
-
Groppe, J.C.1
Wu, J.2
Shore, E.M.3
Kaplan, F.S.4
-
48
-
-
70849128432
-
Applications of small molecule BMP inhibitors in physiology and disease
-
Hong, C. C., and Yu, P. B. (2009) Applications of small molecule BMP inhibitors in physiology and disease. Cytokine Growth Factor Rev. 20, 409-418
-
(2009)
Cytokine Growth Factor Rev.
, vol.20
, pp. 409-418
-
-
Hong, C.C.1
Yu, P.B.2
-
49
-
-
34249777526
-
Eris. An automated estimator of protein stability
-
Yin, S., Ding, F., and Dokholyan, N. V. (2007) Eris. An automated estimator of protein stability. Nat. Methods 4, 466-467
-
(2007)
Nat. Methods
, vol.4
, pp. 466-467
-
-
Yin, S.1
Ding, F.2
Dokholyan, N.V.3
-
50
-
-
83655203094
-
Hyperactive BMP signaling induced by ALK2(R206H) requires type II receptor function in a Drosophila model for classic fibrodysplasia ossificans progressiva
-
Le, V. Q., and Wharton, K. A. (2012) Hyperactive BMP signaling induced by ALK2(R206H) requires type II receptor function in a Drosophila model for classic fibrodysplasia ossificans progressiva. Dev. Dyn. 241, 200-214
-
(2012)
Dev. Dyn.
, vol.241
, pp. 200-214
-
-
Le, V.Q.1
Wharton, K.A.2
-
51
-
-
0037085441
-
Identification and functional characterization of distinct critically important bone morphogenetic protein-specific response elements in the Id1 promoter
-
Korchynskyi, O., and ten Dijke, P. (2002) Identification and functional characterization of distinct critically important bone morphogenetic protein-specific response elements in the Id1 promoter. J. Biol. Chem. 277, 4883-4891
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 4883-4891
-
-
Korchynskyi, O.1
Ten Dijke, P.2
|