-
1
-
-
0034671638
-
Familial breast and ovarian cancer: A Swedish population-based register study
-
Anderson H, Bladström A, Olsson H, Möller TR. 2000. Familial breast and ovarian cancer: A Swedish population-based register study. Am J Epidemiol 152:1154-1163.
-
(2000)
Am J Epidemiol
, vol.152
, pp. 1154-1163
-
-
Anderson, H.1
Bladström, A.2
Olsson, H.3
Möller, T.R.4
-
2
-
-
0014831432
-
Acrocephalosyndactyly type III: Chotzen's syndrome
-
Bartsocas CS, Weber AL, Crawford JD. 1970. Acrocephalosyndactyly type III: Chotzen's syndrome. J Pediatr 77:267-272.
-
(1970)
J Pediatr
, vol.77
, pp. 267-272
-
-
Bartsocas, C.S.1
Weber, A.L.2
Crawford, J.D.3
-
3
-
-
0036788297
-
Craniosynostosis in Twist heterozygous mice: A model for Saethre-Chotzen syndrome
-
Carver EA, Oram KF, Gridley T. 2002. Craniosynostosis in Twist heterozygous mice: A model for Saethre-Chotzen syndrome. Anat Rec 268:90-92.
-
(2002)
Anat Rec
, vol.268
, pp. 90-92
-
-
Carver, E.A.1
Oram, K.F.2
Gridley, T.3
-
4
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
El Ghouzzi V, Le Merrer M, Perrin-Schmitt F, Lajeunie E, Benit P, Renier D, Bourgeois P, Bolcato-Bellemin AL, Munnich A, Bonaventure J. 1997. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat Genet 15:42-46.
-
(1997)
Nat Genet
, vol.15
, pp. 42-46
-
-
El Ghouzzi, V.1
Le Merrer, M.2
Perrin-Schmitt, F.3
Lajeunie, E.4
Benit, P.5
Renier, D.6
Bourgeois, P.7
Bolcato-Bellemin, A.L.8
Munnich, A.9
Bonaventure, J.10
-
5
-
-
0032953019
-
Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome
-
El Ghouzzi V, Lajeunie E, Le Merrer M, Cormier-Daire V, Renier D, Munnich A, Bonaventure J. 1999. Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome. Eur J Hum Genet 7:27-33.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 27-33
-
-
El Ghouzzi, V.1
Lajeunie, E.2
Le Merrer, M.3
Cormier-Daire, V.4
Renier, D.5
Munnich, A.6
Bonaventure, J.7
-
6
-
-
0034701320
-
Saethre-Chotzen mutations cause TWIST protein degradation or impaired nuclear location
-
El Ghouzzi V, Legeai-Mallet L, Aresta S, Benoist C, Munnich A, de Gunzburg J, Bonaventure J. 2000. Saethre-Chotzen mutations cause TWIST protein degradation or impaired nuclear location. Hum Mol Genet 9:813-819.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 813-819
-
-
El Ghouzzi, V.1
Legeai-Mallet, L.2
Aresta, S.3
Benoist, C.4
Munnich, A.5
de Gunzburg, J.6
Bonaventure, J.7
-
7
-
-
0035831060
-
Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome
-
El Ghouzzi V, Legeai-Mallet L, Benoist-Lasselin C, Lajeunie E, Renier D, Munnich A, Bonaventure J. 2001. Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome. FEBS Lett 492:112-118.
-
(2001)
FEBS Lett
, vol.492
, pp. 112-118
-
-
El Ghouzzi, V.1
Legeai-Mallet, L.2
Benoist-Lasselin, C.3
Lajeunie, E.4
Renier, D.5
Munnich, A.6
Bonaventure, J.7
-
8
-
-
16844376635
-
Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities
-
Firulli BA, Krawchuk D, Centonze VE, Vargesson N, Virshup DM, Conway SJ, Cserjesi P, Laufer E, Firulli AB. 2005. Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities. Nat Genet 37:373-381.
-
(2005)
Nat Genet
, vol.37
, pp. 373-381
-
-
Firulli, B.A.1
Krawchuk, D.2
Centonze, V.E.3
Vargesson, N.4
Virshup, D.M.5
Conway, S.J.6
Cserjesi, P.7
Laufer, E.8
Firulli, A.B.9
-
9
-
-
0017740086
-
Saethre-Chotzen syndrome: A broad and variable pattern of skeletal malformations
-
Friedman JM, Hanson JW, Graham CB, Smith DW. 1977. Saethre-Chotzen syndrome: A broad and variable pattern of skeletal malformations. J Pediatr 91:929-933.
-
(1977)
J Pediatr
, vol.91
, pp. 929-933
-
-
Friedman, J.M.1
Hanson, J.W.2
Graham, C.B.3
Smith, D.W.4
-
10
-
-
0028845726
-
Expression of M-twist during postimplantation development of the mouse
-
Fuchtbauer EM. 1995. Expression of M-twist during postimplantation development of the mouse. Dev Dyn 204:316-322.
-
(1995)
Dev Dyn
, vol.204
, pp. 316-322
-
-
Fuchtbauer, E.M.1
-
11
-
-
0034800314
-
Common regulation of growth arrest and differentiation of osteoblasts by helix-loop-helix factors
-
Funato N, Ohtani K, Ohyama K, Kuroda T, Nakamura M. 2001. Common regulation of growth arrest and differentiation of osteoblasts by helix-loop-helix factors. Mol Cell Biol 21:7416-7428.
-
(2001)
Mol Cell Biol
, vol.21
, pp. 7416-7428
-
-
Funato, N.1
Ohtani, K.2
Ohyama, K.3
Kuroda, T.4
Nakamura, M.5
-
12
-
-
15244340251
-
TGFbeta1, back to the future: Revisiting its role as a transforming growth factor
-
Glick AB. 2004. TGFbeta1, back to the future: Revisiting its role as a transforming growth factor. Cancer Biol Ther 3:276-283.
-
(2004)
Cancer Biol Ther
, vol.3
, pp. 276-283
-
-
Glick, A.B.1
-
14
-
-
0031021336
-
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
-
Howard TD, Paznekas WA, Green ED, Chiang LC, Ma N, Ortiz de Luna RI, Garcia Delgado C, Gonzalez-Ramos M, Kline AD, Jabs EW. 1997. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat Genet 15: 36-41.
-
(1997)
Nat Genet
, vol.15
, pp. 36-41
-
-
Howard, T.D.1
Paznekas, W.A.2
Green, E.D.3
Chiang, L.C.4
Ma, N.5
Ortiz de Luna, R.I.6
Garcia Delgado, C.7
Gonzalez-Ramos, M.8
Kline, A.D.9
Jabs, E.W.10
-
15
-
-
0345700653
-
Twist is up-regulated in response to Wnt1 and inhibits mouse mammary cell differentiation
-
Howe LR, Watanabe O, Leonard J, Brown AMC. 2003. Twist is up-regulated in response to Wnt1 and inhibits mouse mammary cell differentiation. Cancer Res 63:1906-1913.
-
(2003)
Cancer Res
, vol.63
, pp. 1906-1913
-
-
Howe, L.R.1
Watanabe, O.2
Leonard, J.3
Brown, A.M.C.4
-
16
-
-
0032231374
-
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
-
Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, Barrow M, Njolstad PR, Kunz J, Ashworth GJ, Wall SA, Kearney L, Wilkie AO. 1998. A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. Am J Hum Genet 63:1282-1293.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1282-1293
-
-
Johnson, D.1
Horsley, S.W.2
Moloney, D.M.3
Oldridge, M.4
Twigg, S.R.5
Walsh, S.6
Barrow, M.7
Njolstad, P.R.8
Kunz, J.9
Ashworth, G.J.10
Wall, S.A.11
Kearney, L.12
Wilkie, A.O.13
-
18
-
-
0033200349
-
Twist is a potential oncogene that inhibits apoptosis
-
Maestro R, Dei Tos AP, Hamamori Y, Krasnokutsky S, Sartorelli V, Kedes L, Doglioni C, Beach DH, Hannon GJ. 1999. Twist is a potential oncogene that inhibits apoptosis. Genes Dev 13:2207-2217.
-
(1999)
Genes Dev
, vol.13
, pp. 2207-2217
-
-
Maestro, R.1
Dei Tos, A.P.2
Hamamori, Y.3
Krasnokutsky, S.4
Sartorelli, V.5
Kedes, L.6
Doglioni, C.7
Beach, D.H.8
Hannon, G.J.9
-
19
-
-
28344444026
-
Twist overexpression induces in vivo angiogenesis and correlates with chromosomal instability in breast cancer
-
Mironchik Y, Winnard PT Jr., Vesuna F, Kato Y, Wildes F, Pathak AP, Kominsky S, Artemov D, Bhujwalla Z, Van Diest P, Burger H, Glackin C, Raman V. 2005. Twist overexpression induces in vivo angiogenesis and correlates with chromosomal instability in breast cancer. Cancer Res 65:10801-10809.
-
(2005)
Cancer Res
, vol.65
, pp. 10801-10809
-
-
Mironchik, Y.1
Winnard Jr., P.T.2
Vesuna, F.3
Kato, Y.4
Wildes, F.5
Pathak, A.P.6
Kominsky, S.7
Artemov, D.8
Bhujwalla, Z.9
Van Diest, P.10
Burger, H.11
Glackin, C.12
Raman, V.13
-
20
-
-
15544381256
-
Prevention and management of hereditary breast cancer
-
Narod SA, Offit K. 2005. Prevention and management of hereditary breast cancer. J Clin Oncol 23:1656-1663.
-
(2005)
J Clin Oncol
, vol.23
, pp. 1656-1663
-
-
Narod, S.A.1
Offit, K.2
-
21
-
-
0035030368
-
Breast cancer genetics: What we know and what we need
-
Nathanson KL, Wooster R, Weber BL. 2001. Breast cancer genetics: What we know and what we need. Nat Med 7:552-556.
-
(2001)
Nat Med
, vol.7
, pp. 552-556
-
-
Nathanson, K.L.1
Wooster, R.2
Weber, B.L.3
-
22
-
-
0037370310
-
Notch1 functions as a tumor suppressor in mouse skin
-
Nicolas M, Wolfer A, Raj K, Kummer JA, Mill P, van Noort M, Hui CC, Clevers H, Dotto GP, Radtke F. 2003. Notch1 functions as a tumor suppressor in mouse skin. Nat Genet 33:416-421.
-
(2003)
Nat Genet
, vol.33
, pp. 416-421
-
-
Nicolas, M.1
Wolfer, A.2
Raj, K.3
Kummer, J.A.4
Mill, P.5
van Noort, M.6
Hui, C.C.7
Clevers, H.8
Dotto, G.P.9
Radtke, F.10
-
23
-
-
0016838555
-
The Saethre-Chotzen syndrome
-
Pantke OA, Cohen MM, Witkop CJ, Feingold M, Schaumann B, Pantke HC, Gorlin RJ. 1975. The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser 11:190-225.
-
(1975)
Birth Defects Orig Artic Ser
, vol.11
, pp. 190-225
-
-
Pantke, O.A.1
Cohen, M.M.2
Witkop, C.J.3
Feingold, M.4
Schaumann, B.5
Pantke, H.C.6
Gorlin, R.J.7
-
24
-
-
17344363396
-
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations
-
Paznekas WA, Cunningham ML, Howard TD, Korf BR, Lipson MH, Grix AW, Feingold M, Goldberg R, Borochowitz Z, Aleck K, Mulliken J, Yin M, Jabs EW. 1998. Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations. Am J Hum Genet 62:1370-1380.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1370-1380
-
-
Paznekas, W.A.1
Cunningham, M.L.2
Howard, T.D.3
Korf, B.R.4
Lipson, M.H.5
Grix, A.W.6
Feingold, M.7
Goldberg, R.8
Borochowitz, Z.9
Aleck, K.10
Mulliken, J.11
Yin, M.12
Jabs, E.W.13
-
26
-
-
0028263955
-
Saethre-Chotzen syndrome
-
Reardon W, Winter RM. 1994. Saethre-Chotzen syndrome. J Med Genet 31:393-396.
-
(1994)
J Med Genet
, vol.31
, pp. 393-396
-
-
Reardon, W.1
Winter, R.M.2
-
27
-
-
0030753595
-
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
-
Rose CS, Patel P, Reardon W, Malcolm S, Winter RM. 1997. The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases. Hum Mol Genet 6:1369-1373.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1369-1373
-
-
Rose, C.S.1
Patel, P.2
Reardon, W.3
Malcolm, S.4
Winter, R.M.5
-
28
-
-
0036840363
-
Differential expression of the epithelial-mesenchymal transition regulators snail, SIP1, and twist in gastric cancer
-
Rosivatz E, Becker I, Specht K, Fricke E, Luber B, Busch R, Hofler H, Becker KF. 2002. Differential expression of the epithelial-mesenchymal transition regulators snail, SIP1, and twist in gastric cancer. Am J Pathol 161:1881-1891.
-
(2002)
Am J Pathol
, vol.161
, pp. 1881-1891
-
-
Rosivatz, E.1
Becker, I.2
Specht, K.3
Fricke, E.4
Luber, B.5
Busch, R.6
Hofler, H.7
Becker, K.F.8
-
29
-
-
7144228871
-
The Saethre-Chotzen syndrome
-
Ortiz Monasterio F, editor, Bologna: Monduzzi Editore, pp
-
Sahlin P, Lauritzen C, Jensen P. 1994. The Saethre-Chotzen syndrome. In: Ortiz Monasterio F, editor. Craniofacial Surgery 5. Bologna: Monduzzi Editore, pp.153-156.
-
(1994)
Craniofacial Surgery
, vol.5
, pp. 153-156
-
-
Sahlin, P.1
Lauritzen, C.2
Jensen, P.3
-
30
-
-
0024042026
-
Sequence of the twist gene and nuclear localization of its protein in endomesodermal cells of early Drosophila embryos
-
Thisse B, Stoetzel C, Gorostiza-Thisse C, Perrin-Schmitt F. 1988. Sequence of the twist gene and nuclear localization of its protein in endomesodermal cells of early Drosophila embryos. EMBO J 7:2175-2183.
-
(1988)
EMBO J
, vol.7
, pp. 2175-2183
-
-
Thisse, B.1
Stoetzel, C.2
Gorostiza-Thisse, C.3
Perrin-Schmitt, F.4
-
31
-
-
10944221249
-
Oncogenic cooperation between H-Twist and N-Myc overrides failsafe programs in cancer cells
-
Valsesia-Wittmann S, Magdeleine M, Dupasquier S, Garin E, Jallas AC, Combaret V, Krause A, Leissner P, Puisieux A. 2004. Oncogenic cooperation between H-Twist and N-Myc overrides failsafe programs in cancer cells. Cancer Cell 6:625-630.
-
(2004)
Cancer Cell
, vol.6
, pp. 625-630
-
-
Valsesia-Wittmann, S.1
Magdeleine, M.2
Dupasquier, S.3
Garin, E.4
Jallas, A.C.5
Combaret, V.6
Krause, A.7
Leissner, P.8
Puisieux, A.9
-
32
-
-
0036734148
-
Activation of Notch-1 signaling maintains the neoplastic phenotype in human Ras-transformed cells
-
Weijzen S, Rizzo P, Braid M, Vaishnav R, Jonkheer SM, Zlobin A, Osborne BA, Gottipati S, Aster JC, Hahn WC, Rudolf M, Siziopikou K, Kast WM, Miele L. 2002. Activation of Notch-1 signaling maintains the neoplastic phenotype in human Ras-transformed cells. Nat Med 8:979-986.
-
(2002)
Nat Med
, vol.8
, pp. 979-986
-
-
Weijzen, S.1
Rizzo, P.2
Braid, M.3
Vaishnav, R.4
Jonkheer, S.M.5
Zlobin, A.6
Osborne, B.A.7
Gottipati, S.8
Aster, J.C.9
Hahn, W.C.10
Rudolf, M.11
Siziopikou, K.12
Kast, W.M.13
Miele, L.14
-
33
-
-
2942707848
-
Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis
-
Yang J, Mani SA, Donaher JL, Ramaswamy S, Itzykson RA, Come C, Savagner P, Gitelman I, Richardson A, Weinberg RA. 2004. Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell 117:927-939.
-
(2004)
Cell
, vol.117
, pp. 927-939
-
-
Yang, J.1
Mani, S.A.2
Donaher, J.L.3
Ramaswamy, S.4
Itzykson, R.A.5
Come, C.6
Savagner, P.7
Gitelman, I.8
Richardson, A.9
Weinberg, R.A.10
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