-
1
-
-
0032434102
-
Molecular timing of primate divergences as estimated by two non-primate calibration points
-
Arnason U, Gullberg A, Janke A (1998) Molecular timing of primate divergences as estimated by two non-primate calibration points. J Mol Evol 47:718-727
-
(1998)
J. Mol. Evol.
, vol.47
, pp. 718-727
-
-
Arnason, U.1
Gullberg, A.2
Janke, A.3
-
2
-
-
0030331236
-
The human H-twist gene is located at 7p21 and encodes a b-HLH protein which is 96% similar to its murine counterpart
-
Bourgeois P, Stoetzel C, Bolcato-Bellemin A-L, Mattéi M-G, Perrin-Schmitt F (1996) The human H-twist gene is located at 7p21 and encodes a b-HLH protein which is 96% similar to its murine counterpart. Mamm Genome 7:915-917
-
(1996)
Mamm. Genome.
, vol.7
, pp. 915-917
-
-
Bourgeois, P.1
Stoetzel, C.2
Bolcato-Bellemin, A.-L.3
Mattéi, M.-G.4
Perrin-Schmitt, F.5
-
3
-
-
0031832127
-
The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome
-
Bourgeois P, Bolcato-Bellemin A-L, Danse JM, Bloch-Zupan A, Yoshiba K, Stoetzel C, Perrin-Schmitt F (1998) The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome. Hum Mol Genet 7:945-957
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 945-957
-
-
Bourgeois, P.1
Bolcato-Bellemin, A.-L.2
Danse, J.M.3
Bloch-Zupan, A.4
Yoshiba, K.5
Stoetzel, C.6
Perrin-Schmitt, F.7
-
4
-
-
0028933142
-
Twist is required in head mesenchyme for cranial neural tube morphogenesis
-
Chen ZF, Behringer RR (1995) twist is required in head mesenchyme for cranial neural tube morphogenesis. Genes Dev 9:686-699
-
(1995)
Genes. Dev.
, vol.9
, pp. 686-699
-
-
Chen, Z.F.1
Behringer, R.R.2
-
5
-
-
0029364324
-
Hominoid phylogeny estimated by model selection using goodness of significance tests
-
Czelusniak J, Goodman M (1995) Hominoid phylogeny estimated by model selection using goodness of significance tests. Mol Phylogenet Evol 4:283-290
-
(1995)
Mol. Phylogenet. Evol.
, vol.4
, pp. 283-290
-
-
Czelusniak, J.1
Goodman, M.2
-
6
-
-
0033150184
-
Evolution of a HOXB6 intergenic region within the great apes and human
-
Deinard A, Kidd K (1999) Evolution of a HOXB6 intergenic region within the great apes and human. J Hum Evol 36:687-703
-
(1999)
J. Hum. Evol.
, vol.36
, pp. 687-703
-
-
Deinard, A.1
Kidd, K.2
-
7
-
-
0034945023
-
Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22
-
Dollfus H, Kumaramanickavel G, Biswas P, Stoetzel C, Quillet R, Denton M, Maw M, Perrin-Schmitt F (2001) Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22. J Med Genet 58:470-471
-
(2001)
J. Med. Genet.
, vol.58
, pp. 470-471
-
-
Dollfus, H.1
Kumaramanickavel, G.2
Biswas, P.3
Stoetzel, C.4
Quillet, R.5
Denton, M.6
Maw, M.7
Perrin-Schmitt, F.8
-
8
-
-
0036569364
-
Saethre-Chotzen syndrome: Notable intrafamilial phenotypic variability in a large family with a TWIST mutation
-
Dollfus H, Parthna B, Kumaramanickavel G, Stoetzel C, Quillet R, Lajeunie E, Renier D, Perrin-Schmitt F (2002) Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with a TWIST mutation. Am J Med Genet 109:218-225
-
(2002)
Am. J. Med. Genet.
, vol.109
, pp. 218-225
-
-
Dollfus, H.1
Parthna, B.2
Kumaramanickavel, G.3
Stoetzel, C.4
Quillet, R.5
Lajeunie, E.6
Renier, D.7
Perrin-Schmitt, F.8
-
9
-
-
0035213012
-
A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals
-
Elanko N, Sibbring JS, Metcalfe KA, Clayton-Smith J, Donnai D, Temple IK, Wall SA, Wilkie AO (2001) A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals. Hum Mutat 18:535-541
-
(2001)
Hum. Mutat.
, vol.18
, pp. 535-541
-
-
Elanko, N.1
Sibbring, J.S.2
Metcalfe, K.A.3
Clayton-Smith, J.4
Donnai, D.5
Temple, I.K.6
Wall, S.A.7
Wilkie, A.O.8
-
10
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
El Ghouzzi V, Le Meffer M, Peffin-Schmitt F, Lajeunie E, Benit P, Renier D, Bourgeois P, Bolcato-Bellemin A-L, 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 Meffer, M.2
Peffin-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
-
11
-
-
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 Med Genet 7:27-33
-
(1999)
Eur. J. Med. 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
-
13
-
-
0033525094
-
Regulation of histone acetyltransferases p300 and PCAF by the bHLH protein TWIST and adenoviral oncoprotein E1A
-
Hamamori Y, Sartorelli V, Ogryzko V, Purl PL, Wu H-Y, Wang JYJ, Nakatani Y, Kedes L (1999) Regulation of histone acetyltransferases p300 and PCAF by the bHLH protein TWIST and adenoviral oncoprotein E1A. Cell 96:405-413
-
(1999)
Cell
, vol.96
, pp. 405-413
-
-
Hamamori, Y.1
Sartorelli, V.2
Ogryzko, V.3
Purl, P.L.4
Wu, H.-Y.5
Wang, J.Y.J.6
Nakatani, Y.7
Kedes, L.8
-
14
-
-
12244280552
-
Phylogénie et classification: L'exemple des primates
-
Hoffstetter R (1978) Phylogénie et classification: l'exemple des primates. Bull Soc Zool Fr 103:183-188
-
(1978)
Bull Soc. Zool. Fr.
, vol.103
, pp. 183-188
-
-
Hoffstetter, R.1
-
15
-
-
0024781157
-
A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest
-
Hopwood ND, Pluck A, Gurdon JB (1989) A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest. Cell 59:893-903
-
(1989)
Cell
, vol.59
, pp. 893-903
-
-
Hopwood, N.D.1
Pluck, A.2
Gurdon, J.B.3
-
16
-
-
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, Delgado CG, 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
Delgado, C.G.7
Gonzalez-Ramos, M.8
Kline, A.D.9
Jabs, E.W.10
-
17
-
-
0024766891
-
A molecular view of primate phylogeny and important systematic and evolutionary questions
-
Koop BE Tagle DA, Goodman M, Slighton JL (1989) A molecular view of primate phylogeny and important systematic and evolutionary questions. Mol Biol Evol 6:580-612
-
(1989)
Mol. Biol. Evol.
, vol.6
, pp. 580-612
-
-
Koop, B.E.1
Tagle, D.A.2
Goodman, M.3
Slighton, J.L.4
-
18
-
-
0027357085
-
The B-HLH protein encoding M-twist gene is located by in situ hybridization on murine chromosome 12
-
Mattei MG, Stoetzel C, Perrin-Schmitt F (1993) The B-HLH protein encoding M-twist gene is located by in situ hybridization on murine chromosome 12. Mamm Genome 4:127-128
-
(1993)
Mamm. Genome.
, vol.4
, pp. 127-128
-
-
Mattei, M.G.1
Stoetzel, C.2
Perrin-Schmitt, F.3
-
19
-
-
0024554495
-
A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins
-
Murre C, McCaw PS, Baltimore D (1989) A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins. Cell 56:767-773
-
(1989)
Cell
, vol.56
, pp. 767-773
-
-
Murre, C.1
McCaw, P.S.2
Baltimore, D.3
-
20
-
-
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
-
21
-
-
0031059627
-
The locations of the H-twist and H-dermo-1 genes are distinct on the human genome
-
1360
-
Perrin-Schmitt F, Bolcato-Bellemin A-L, Bourgeois P, Stoetzel C, Danse J-M (1997) The locations of the H-twist and H-dermo-1 genes are distinct on the human genome. Biochim Biophys Acta 1360:1-2
-
(1997)
Biochim. Biophys. Acta.
, pp. 1-2
-
-
Perrin-Schmitt, F.1
Bolcato-Bellemin, A.-L.2
Bourgeois, P.3
Stoetzel, C.4
Danse, J.-M.5
-
22
-
-
0031592950
-
Sequence of the primate E-globin gene: Implications for systematics of the marmosets and other New World primates
-
Porter CA, Czelusniak J, Schneider H, Schneider MPC, Sampaio I, Goodman M (1997) Sequence of the primate E-globin gene: implications for systematics of the marmosets and other New World primates. Gene 205:59-71
-
(1997)
Gene
, vol.205
, pp. 59-71
-
-
Porter, C.A.1
Czelusniak, J.2
Schneider, H.3
Schneider, M.P.C.4
Sampaio, I.5
Goodman, M.6
-
24
-
-
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 CSP, 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 8:1369-1373
-
(1997)
Hum. Mol. Genet.
, vol.8
, pp. 1369-1373
-
-
Rose, C.S.P.1
Reardon, W.2
Malcolm, S.3
Winter, R.M.4
-
25
-
-
0032172097
-
Phylogenetic analysis of anthropoid relationships
-
Ross C, Williams B, Kay R (1998) Phylogenetic analysis of anthropoid relationships. J Hum Evol 35:221-306
-
(1998)
J. Hum. Evol.
, vol.35
, pp. 221-306
-
-
Ross, C.1
Williams, B.2
Kay, R.3
-
26
-
-
0031049003
-
Molecular phylogeny of the hominoids: Interferences from multiple independent DNA sequence data sets
-
Ruvolo M (1997) Molecular phylogeny of the hominoids: interferences from multiple independent DNA sequence data sets. Mol Biol Evol 14:248-265
-
(1997)
Mol. Biol. Evol.
, vol.14
, pp. 248-265
-
-
Ruvolo, M.1
-
27
-
-
0028556805
-
Gene trees and hominoid phylogeny
-
Ruvolo M, Pan D, Zehr S, Goldberg T, Disotell T, Von Dornum M (1994) Gene trees and hominoid phylogeny. Proc Natl Acad Sci USA 91:8900-8904
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 8900-8904
-
-
Ruvolo, M.1
Pan, D.2
Zehr, S.3
Goldberg, T.4
Disotell, T.5
Von Dornum, M.6
-
28
-
-
0025232016
-
DNA hybridisation evidence of hominoid phylogeny: A reanalysis of the data
-
Sibley CG, Comstock JA, Ahlquist JE (1990) DNA hybridisation evidence of hominoid phylogeny: a reanalysis of the data. J Mol Evol 30:202-236
-
(1990)
J. Mol. Evol.
, vol.30
, pp. 202-236
-
-
Sibley, C.G.1
Comstock, J.A.2
Ahlquist, J.E.3
-
29
-
-
0031046540
-
Cloning of the human twist gene: Its expression is retained in adult mesodermally-derived tissues
-
Wang SM, Colje VW, Pignolo RJ, Rotenberg MO, Cristofalo VJ, Sierra F (1997) Cloning of the human twist gene: its expression is retained in adult mesodermally-derived tissues. Gene 187:83-92
-
(1997)
Gene
, vol.187
, pp. 83-92
-
-
Wang, S.M.1
Colje, V.W.2
Pignolo, R.J.3
Rotenberg, M.O.4
Cristofalo, V.J.5
Sierra, F.6
-
30
-
-
0025963454
-
The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and Drosophila twist genes
-
Wolf C, Thisse C, Stoetzel C, Thisse B, Gerlinger P, Perrin-Schmitt F (1991) The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and Drosophila twist genes. Dev Biol 143:363-373
-
(1991)
Dev. Biol.
, vol.143
, pp. 363-373
-
-
Wolf, C.1
Thisse, C.2
Stoetzel, C.3
Thisse, B.4
Gerlinger, P.5
Perrin-Schmitt, F.6
-
31
-
-
0020027910
-
The origin of man: A chromosomal pictorial legacy
-
Yunis J, Prakash O (1982) The origin of man: a chromosomal pictorial legacy. Science 215:1525-1530
-
(1982)
Science
, vol.215
, pp. 1525-1530
-
-
Yunis, J.1
Prakash, O.2
|