-
1
-
-
0001045827
-
Sur la motificationsponta-nee de la queue chez la souris nouveau-nee et sur l'existence d'un caractere hereditaire 'non viable'
-
Dobrovolskaia-Zavadskaia N (1927) Sur la motificationsponta-nee de la queue chez la souris nouveau-nee et sur l'existence d'un caractere hereditaire 'non viable'. cr hebd Soc Biol 97: 3.
-
(1927)
Cr Hebd Soc Biol
, vol.97
, pp. 3
-
-
Dobrovolskaia-Zavadskaia, N.1
-
2
-
-
84982064361
-
Development of the short-tailed mutant in the house mouse
-
Chesley P (1935) Development of the short-tailed mutant in the house mouse. The Journal of Experimental Zoology 70: 7.
-
(1935)
The Journal of Experimental Zoology
, vol.70
, pp. 7
-
-
Chesley, P.1
-
3
-
-
0000000459
-
The Development of Two Tailless Mutants in the House Mouse
-
Gluecksohn-Schoenheimer S (1938) The Development of Two Tailless Mutants in the House Mouse. Genetics 23: 573-584.
-
(1938)
Genetics
, vol.23
, pp. 573-584
-
-
Gluecksohn-Schoenheimer, S.1
-
4
-
-
0027282961
-
The Brachyury gene encodes a novel DNA binding protein
-
Kispert A, Herrmann BG (1993) The Brachyury gene encodes a novel DNA binding protein. EMBO J 12: 3211-3220. (Pubitemid 23232752)
-
(1993)
EMBO Journal
, vol.12
, Issue.8
, pp. 3211-3220
-
-
Kispert, A.1
Herrmann, B.G.2
-
5
-
-
0342658137
-
Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development
-
DOI 10.1002/(SICI)1097-0177(199608)206:4<379::AID
-
Chapman DL, Garvey N, Hancock S, Alexiou M, Agulnik SI, et al. (1996) Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development. Dev Dyn 206: 379-390. (Pubitemid 26260172)
-
(1996)
Developmental Dynamics
, vol.206
, Issue.4
, pp. 379-390
-
-
Chapman, D.L.1
Garvey, N.2
Hancock, S.3
Alexiou, M.4
Agulnik, S.I.5
Gibson-Brown, J.J.6
Cebra-Thomas, J.7
Bollag, R.J.8
Silver, L.M.9
Papaioannou, V.E.10
-
6
-
-
0028241951
-
An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus
-
DOI 10.1038/ng0794-383
-
Bollag RJ, Siegfried Z, Cebra-Thomas JA, Garvey N, Davison EM, et al. (1994) An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus. Nat Genet 7: 383-389. (Pubitemid 24204414)
-
(1994)
Nature Genetics
, vol.7
, Issue.3
, pp. 383-389
-
-
Bollag, R.J.1
Siegfried, Z.2
Cebra-Thomas, J.A.3
Garvey, N.4
Davison, E.M.5
Silver, L.M.6
-
7
-
-
0029743355
-
Evolution of mouse T-box genes by tandem duplication and cluster dispersion
-
Agulnik SI, Garvey N, Hancock S, Ruvinsky I, Chapman DL, et al. (1996) Evolution of mouse T-box genes by tandem duplication and cluster dispersion. Genetics 144: 249-254. (Pubitemid 26291934)
-
(1996)
Genetics
, vol.144
, Issue.1
, pp. 249-254
-
-
Agulnik, S.I.1
Garvey, N.2
Hancock, S.3
Ruvinsky, I.4
Chapman, D.L.5
Agulnik, I.6
Bollag, R.7
Papaioannou, V.8
Silver, L.M.9
-
9
-
-
0030986873
-
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
-
DOI 10.1038/ng0797-311
-
Bamshad M, Lin RC, Law DJ, Watkins WC, Krakowiak PA, et al. (1997) Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nat Genet 16: 311-315. (Pubitemid 27280219)
-
(1997)
Nature Genetics
, vol.16
, Issue.3
, pp. 311-315
-
-
Bamshad, M.1
Lin, R.C.2
Law, D.J.3
Watkins, W.S.4
Krakowiak, P.A.5
Moore, M.E.6
Franceschini, P.7
Lala, R.8
Holmes, L.B.9
Gebuhr, T.C.10
Bruneau, B.G.11
Schinzel, A.12
Seidman, J.G.13
Seidman, C.E.14
Jorde, L.B.15
-
10
-
-
0033621059
-
Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome
-
DOI 10.1073/pnas.96.18.10212
-
He M, Wen L, Campbell CE, Wu JY, Rao Y (1999) Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome. Proc Natl Acad Sci U S A 96: 10212-10217. (Pubitemid 29422538)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.18
, pp. 10212-10217
-
-
He, M.-L.1
Wen, L.2
Campbell, C.E.3
Wu, J.Y.4
Rao, Y.5
-
12
-
-
0034722673
-
Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2
-
Sinha S, Abraham S, Gronostajski RM, Campbell CE (2000) Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2. Gene 258: 15-29.
-
(2000)
Gene
, vol.258
, pp. 15-29
-
-
Sinha, S.1
Abraham, S.2
Gronostajski, R.M.3
Campbell, C.E.4
-
14
-
-
0035445835
-
Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome
-
Ghosh TK, Packham EA, Bonser AJ, Robinson TE, Cross SJ, et al. (2001) Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome. Hum Mol Genet 10: 1983-1994. (Pubitemid 32910543)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.18
, pp. 1983-1994
-
-
Ghosh, T.K.1
Packham, E.A.2
Bonser, A.J.3
Robinson, T.E.4
Cross, S.J.5
Brook, J.D.6
-
15
-
-
23244457575
-
DII1 is a downstream target of Tbx6 in the paraxial mesoderm
-
DOI 10.1002/gene.20140
-
White PH, Chapman DL (2005) Dll1 is a downstream target of Tbx6 in the paraxial mesoderm. Genesis 42: 193-202. (Pubitemid 41099678)
-
(2005)
Genesis
, vol.42
, Issue.3
, pp. 193-202
-
-
White, P.H.1
Chapman, D.L.2
-
16
-
-
34548477406
-
Transcriptional repression by the T-box proteins Tbx18 and Tbx15 depends on groucho corepressors
-
DOI 10.1074/jbc.M703724200
-
Farin HF, Bussen M, Schmidt MK, Singh MK, Schuster-Gossler K, et al. (2007) Transcriptional repression by the T-box proteins Tbx18 and Tbx15 depends on Groucho corepressors. J Biol Chem 282: 25748-25759. (Pubitemid 47372830)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.35
, pp. 25748-25759
-
-
Farin, H.F.1
Bussen, M.2
Schmidt, M.K.3
Singh, M.K.4
Schuster-Gossler, K.5
Kispert, A.6
-
17
-
-
0034778407
-
Determinants of T box protein specificity
-
Conlon FL, Fairclough L, Price BM, Casey ES, Smith JC (2001) Determinants of T box protein specificity. Development 128: 3749-3758. (Pubitemid 32998924)
-
(2001)
Development
, vol.128
, Issue.19
, pp. 3749-3758
-
-
Conlon, F.L.1
Fairclough, L.2
Price, B.M.J.3
Casey, E.S.4
Smith, J.C.5
-
18
-
-
0029165111
-
The T protein encoded by Brachyury is a tissue-specific transcription factor
-
Kispert A, Koschorz B, Herrmann BG (1995) The T protein encoded by Brachyury is a tissue-specific transcription factor. EMBO J 14: 4763-4772.
-
(1995)
EMBO J
, vol.14
, pp. 4763-4772
-
-
Kispert, A.1
Koschorz, B.2
Herrmann, B.G.3
-
19
-
-
17344369067
-
Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation
-
DOI 10.1093/hmg/ddi081
-
Stoller JZ, Epstein JA (2005) Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation. Hum Mol Genet 14: 885-892. (Pubitemid 40533099)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.7
, pp. 885-892
-
-
Stoller, J.Z.1
Epstein, J.A.2
-
20
-
-
10744223651
-
Role of TBX1 in human del22q11.2 syndrome
-
DOI 10.1016/S0140-6736(03)14632-6
-
Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, et al. (2003) Role of TBX1 in human del22q11.2 syndrome. Lancet 362: 1366-1373. (Pubitemid 37338337)
-
(2003)
Lancet
, vol.362
, Issue.9393
, pp. 1366-1373
-
-
Yagi, H.1
Furutani, Y.2
Hamada, H.3
Sasaki, T.4
Asakawa, S.5
Minoshima, S.6
Ichida, F.7
Joo, K.8
Kimura, M.9
Imamura, S.-I.10
Kamatani, N.11
Momma, K.12
Takao, A.13
Nakazawa, M.14
Shimizu, N.15
Matsuoka, R.16
-
21
-
-
33847196100
-
Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions
-
Zweier C, Sticht H, Aydin-Yaylagul I, Campbell CE, Rauch A (2007) Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions. Am J Hum Genet 80: 510-517.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 510-517
-
-
Zweier, C.1
Sticht, H.2
Aydin-Yaylagul, I.3
Campbell, C.E.4
Rauch, A.5
-
22
-
-
17744395906
-
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/ DiGeorge syndrome
-
DOI 10.1016/S0092-8674(01)00247-1
-
Merscher S, Funke B, Epstein JA, Heyer J, Puech A, et al. (2001) TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell 104: 619-629. (Pubitemid 32201955)
-
(2001)
Cell
, vol.104
, Issue.4
, pp. 619-629
-
-
Merscher, S.1
Funke, B.2
Epstein, J.A.3
Heyer, J.4
Puech, A.5
Lu, M.M.6
Xavier, R.J.7
Demay, M.B.8
Russell, R.G.9
Factor, S.10
Tokooya, K.11
Jore, B.St.12
Lopez, M.13
Pandita, R.K.14
Lia, M.15
Carrion, D.16
Xu, H.17
Schorle, H.18
Kobler, J.B.19
Scambler, P.20
Wynshaw-Boris, A.21
Skoultchi, A.I.22
Morrow, B.E.23
Kucherlapati, R.24
more..
-
23
-
-
0035098557
-
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
-
DOI 10.1038/85845
-
Jerome LA, Papaioannou VE (2001) DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1. Nat Genet 27: 286-291. (Pubitemid 32201849)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 286-291
-
-
Jerome, L.A.1
Papaioannou, V.E.2
-
24
-
-
0035263599
-
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
-
DOI 10.1038/35065105
-
Lindsay EA, Vitelli F, Su H, Morishima M, Huynh T, et al. (2001) Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 410: 97-101. (Pubitemid 32225843)
-
(2001)
Nature
, vol.410
, Issue.6824
, pp. 97-101
-
-
Lindsay, E.A.1
Vitelli, F.2
Su, H.3
Morishima, M.4
Huynh, T.5
Pramparo, T.6
Jurecic, V.7
Ogunrinu, G.8
Sutherland, H.F.9
Scambler, P.J.10
Bradley, A.11
Baldini, A.12
-
25
-
-
25844503071
-
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1
-
DOI 10.1016/j.ydbio.2005.06.026, PII S0012160605004458
-
Ivins S, Lammerts van Beuren K, Roberts C, James C, Lindsay E, et al. (2005) Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. Dev Biol 285: 554-569. (Pubitemid 41394039)
-
(2005)
Developmental Biology
, vol.285
, Issue.2
, pp. 554-569
-
-
Ivins, S.1
Van Beuren, K.L.2
Roberts, C.3
James, C.4
Lindsay, E.5
Baldini, A.6
Ataliotis, P.7
Scambler, P.J.8
-
26
-
-
41149107746
-
Identification of downstream genetic pathways of Tbx1 in the second heart field
-
Liao J, Aggarwal VS, Nowotschin S, Bondarev A, Lipner S, et al. (2008) Identification of downstream genetic pathways of Tbx1 in the second heart field. Dev Biol 316: 524-537.
-
(2008)
Dev Biol
, vol.316
, pp. 524-537
-
-
Liao, J.1
Aggarwal, V.S.2
Nowotschin, S.3
Bondarev, A.4
Lipner, S.5
-
27
-
-
77951203831
-
Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome
-
van Bueren KL, Papangeli I, Rochais F, Pearce K, Roberts C, et al. (2010) Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome. Dev Biol 340: 369-380.
-
(2010)
Dev Biol
, vol.340
, pp. 369-380
-
-
Van Bueren, K.L.1
Papangeli, I.2
Rochais, F.3
Pearce, K.4
Roberts, C.5
-
28
-
-
84857039820
-
Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development
-
Monks DC, Morrow BE (2012) Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development. Dev Dyn 241: 563-573.
-
(2012)
Dev Dyn
, vol.241
, pp. 563-573
-
-
Monks, D.C.1
Morrow, B.E.2
-
29
-
-
0036797067
-
A genetic link between Tbx1 and fibroblast growth factor signaling
-
Vitelli F, Taddei I, Morishima M, Meyers EN, Lindsay EA, et al. (2002) A genetic link between Tbx1 and fibroblast growth factor signaling. Development 129: 4605-4611. (Pubitemid 35203741)
-
(2002)
Development
, vol.129
, Issue.19
, pp. 4605-4611
-
-
Vitelli, F.1
Taddei, I.2
Morishima, M.3
Meyers, E.N.4
Lindsay, E.A.5
Baldini, A.6
-
30
-
-
0036800025
-
Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse
-
Abu-Issa R, Smyth G, Smoak I, Yamamura K, Meyers EN (2002) Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. Development 129: 4613-4625. (Pubitemid 35203742)
-
(2002)
Development
, vol.129
, Issue.19
, pp. 4613-4625
-
-
Abu-Issa, R.1
Smyth, G.2
Smoak, I.3
Yamamura, K.-I.4
Meyers, E.N.5
-
31
-
-
33646706385
-
Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field
-
DOI 10.1242/dev.02309
-
Nowotschin S, Liao J, Gage PJ, Epstein JA, Campione M, et al. (2006) Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development 133: 1565-1573. (Pubitemid 43732969)
-
(2006)
Development
, vol.133
, Issue.8
, pp. 1565-1573
-
-
Nowotschin, S.1
Liao, J.2
Gage, P.J.3
Epstein, J.A.4
Campione, M.5
Morrow, B.E.6
-
32
-
-
70449360736
-
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice
-
Randall V, McCue K, Roberts C, Kyriakopoulou V, Beddow S, et al. (2009) Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. J Clin Invest 119: 3301-3310.
-
(2009)
J Clin Invest
, vol.119
, pp. 3301-3310
-
-
Randall, V.1
McCue, K.2
Roberts, C.3
Kyriakopoulou, V.4
Beddow, S.5
-
33
-
-
77951833399
-
Tbx1 regulates Vegfr3 and is required for lymphatic vessel development
-
Chen L, Mupo A, Huynh T, Cioffi S, Woods M, et al. (2010) Tbx1 regulates Vegfr3 and is required for lymphatic vessel development. J Cell Biol 189: 417-424.
-
(2010)
J Cell Biol
, vol.189
, pp. 417-424
-
-
Chen, L.1
Mupo, A.2
Huynh, T.3
Cioffi, S.4
Woods, M.5
-
34
-
-
79953328073
-
A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis
-
Guo C, Sun Y, Zhou B, Adam RM, Li X, et al. (2011) A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. J Clin Invest 121: 1585-1595.
-
(2011)
J Clin Invest
, vol.121
, pp. 1585-1595
-
-
Guo, C.1
Sun, Y.2
Zhou, B.3
Adam, R.M.4
Li, X.5
-
35
-
-
84866025303
-
MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome
-
Voss AK, Vanyai HK, Collin C, Dixon MP, McLennan TJ, et al. (2012) MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome. Dev Cell 23: 652-663.
-
(2012)
Dev Cell
, vol.23
, pp. 652-663
-
-
Voss, A.K.1
Vanyai, H.K.2
Collin, C.3
Dixon, M.P.4
McLennan, T.J.5
-
36
-
-
84859244178
-
Transcriptional control in cardiac progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a
-
Chen L, Fulcoli FG, Ferrentino R, Martucciello S, Illingworth EA, et al. (2012) Transcriptional control in cardiac progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a. PLoS Genet 8: e1002571.
-
(2012)
PLoS Genet
, vol.8
-
-
Chen, L.1
Fulcoli, F.G.2
Ferrentino, R.3
Martucciello, S.4
Illingworth, E.A.5
-
37
-
-
45549083841
-
Determination and functional analysis of the consensus binding site for TFII-I family member BEN, implicated in Williams-Beuren syndrome
-
Lazebnik MB, Tussie-Luna MI, Roy AL (2008) Determination and functional analysis of the consensus binding site for TFII-I family member BEN, implicated in Williams-Beuren syndrome. J Biol Chem 283: 11078-11082.
-
(2008)
J Biol Chem
, vol.283
, pp. 11078-11082
-
-
Lazebnik, M.B.1
Tussie-Luna, M.I.2
Roy, A.L.3
-
38
-
-
46049106746
-
Novel flanking DNA sequences enhance FOXO1a DNA binding affinity but do not alter DNA bending
-
DOI 10.1021/bi702495m
-
Sidhu A, Miller PJ, Johanson KE, Hollenbach AD (2008) Novel flanking DNA sequences enhance FOXO1a DNA binding affinity but do not alter DNA bending. Biochemistry 47: 6809-6818. (Pubitemid 351898936)
-
(2008)
Biochemistry
, vol.47
, Issue.26
, pp. 6809-6818
-
-
Sidhu, A.1
Miller, P.J.2
Johanson, K.E.3
Hollenbach, A.D.4
-
39
-
-
79956328426
-
Genomic selection identifies vertebrate transcription factor Fezf2 binding sites and target genes
-
Chen L, Zheng J, Yang N, Li H, Guo S (2011) Genomic selection identifies vertebrate transcription factor Fezf2 binding sites and target genes. J Biol Chem 286: 18641-18649.
-
(2011)
J Biol Chem
, vol.286
, pp. 18641-18649
-
-
Chen, L.1
Zheng, J.2
Yang, N.3
Li, H.4
Guo, S.5
-
40
-
-
34248515435
-
SELEX experiments: New prospects, applications and data analysis in inferring regulatory pathways
-
Djordjevic M (2007) SELEX experiments: new prospects, applications and data analysis in inferring regulatory pathways. Biomol Eng 24: 179-189.
-
(2007)
Biomol Eng
, vol.24
, pp. 179-189
-
-
Djordjevic, M.1
-
41
-
-
83355166954
-
The orchestration of mammalian tissue morphogenesis through a series of coherent feed-forward loops
-
Xie Q, Cvekl A (2011) The orchestration of mammalian tissue morphogenesis through a series of coherent feed-forward loops. J Biol Chem 286: 43259-43271.
-
(2011)
J Biol Chem
, vol.286
, pp. 43259-43271
-
-
Xie, Q.1
Cvekl, A.2
-
42
-
-
0033889169
-
Regulation of human myocilin/TIGR gene transcription in trabecular meshwork cells and astrocytes: Role of upstream stimulatory factor
-
DOI 10.1046/j.1365-2443.2000.00355.x
-
Kirstein L, Cvekl A, Chauhan BK, Tamm ER (2000) Regulation of human myocilin/TIGR gene transcription in trabecular meshwork cells and astrocytes: role of upstream stimulatory factor. Genes Cells 5: 661-676. (Pubitemid 30641958)
-
(2000)
Genes to Cells
, vol.5
, Issue.8
, pp. 661-676
-
-
Kirstein, L.1
Cvekl, A.2
Chauhan, B.K.3
Tamm, E.R.4
-
43
-
-
3042680569
-
Functional interactions between alternatively spliced forms of Pax6 in crystallin gene regulation and in haploinsufficiency
-
DOI 10.1093/nar/gkh334
-
Chauhan BK, Yang Y, Cveklova K, Cvekl A (2004) Functional interactions between alternatively spliced forms of Pax6 in crystallin gene regulation and in haploinsufficiency. Nucleic Acids Res 32: 1696-1709. (Pubitemid 38832714)
-
(2004)
Nucleic Acids Research
, vol.32
, Issue.5
, pp. 1696-1709
-
-
Chauhan, B.K.1
Yang, Y.2
Cveklova, K.3
Cvekl, A.4
-
44
-
-
23744458086
-
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
-
DOI 10.1101/gr.3715005
-
Siepel A, Bejerano G, Pedersen JS, Hinrichs AS, Hou M, et al. (2005) Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res 15: 1034-1050. (Pubitemid 41126859)
-
(2005)
Genome Research
, vol.15
, Issue.8
, pp. 1034-1050
-
-
Siepel, A.1
Bejerano, G.2
Pedersen, J.S.3
Hinrichs, A.S.4
Hou, M.5
Rosenbloom, K.6
Clawson, H.7
Spieth, J.8
Hillier, L.W.9
Richards, S.10
Weinstock, G.M.11
Wilson, R.K.12
Gibbs, R.A.13
Kent, W.J.14
Miller, W.15
Haussler, D.16
-
45
-
-
33750211988
-
Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy
-
DOI 10.1093/hmg/ddl399
-
Aggarwal VS, Liao J, Bondarev A, Schimmang T, Lewandoski M, et al. (2006) Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy. Hum Mol Genet 15: 3219-3228. (Pubitemid 44605501)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.21
, pp. 3219-3228
-
-
Aggarwal, V.S.1
Liao, J.2
Bondarev, A.3
Schimmang, T.4
Lewandoski, M.5
Locker, J.6
Shanske, A.7
Campione, M.8
Morrow, B.E.9
-
46
-
-
58549112996
-
Bioinformatics enrichment tools: Paths toward the comprehensive functional analysis of large gene lists
-
Huang da W, Sherman BT, Lempicki RA (2009) Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res 37: 1-13.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 1-13
-
-
Huang Da, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
47
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
Huang da W, Sherman BT, Lempicki RA (2009) Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 4: 44-57.
-
(2009)
Nat Protoc
, vol.4
, pp. 44-57
-
-
Huang Da, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
48
-
-
32344438935
-
Identification of evolutionary conserved regulatory elements in the mouse Fgf8 locus
-
DOI 10.1002/gene.20177
-
Beermann F, Kaloulis K, Hofmann D, Murisier F, Bucher P, et al. (2006) Identification of evolutionarily conserved regulatory elements in the mouse Fgf8 locus. Genesis 44: 1-6. (Pubitemid 43222204)
-
(2006)
Genesis
, vol.44
, Issue.1
, pp. 1-6
-
-
Beermann, F.1
Kaloulis, K.2
Hofmann, D.3
Murisier, F.4
Bucher, P.5
Trumpp, A.6
-
49
-
-
41149150649
-
Transcription of fgf8 is regulated by activating and repressive cis-elements at the midbrain-hindbrain boundary in zebrafish embryos
-
Inoue F, Parvin MS, Yamasu K (2008) Transcription of fgf8 is regulated by activating and repressive cis-elements at the midbrain-hindbrain boundary in zebrafish embryos. Dev Biol 316: 471-486.
-
(2008)
Dev Biol
, vol.316
, pp. 471-486
-
-
Inoue, F.1
Parvin, M.S.2
Yamasu, K.3
-
50
-
-
9444265974
-
Tbx1 regulates fibroblast growth factors in the anterior heart field through reinforcing autoregulatory loop involving forkhead transcription factors
-
DOI 10.1242/dev.01399
-
Hu T, Yamagishi H, Maeda J, McAnally J, Yamagishi C, et al. (2004) Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors. Development 131: 5491-5502. (Pubitemid 39562191)
-
(2004)
Development
, vol.131
, Issue.21
, pp. 5491-5502
-
-
Hu, T.1
Yamagishi, H.2
Maeda, J.3
McAnally, J.4
Yamagishi, C.5
Srivastava, D.6
-
51
-
-
0033951215
-
Targeted disruption of Otog results in deafness and severe imbalance
-
DOI 10.1038/72793
-
Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, et al. (2000) Targeted disruption of otog results in deafness and severe imbalance. Nat Genet 24: 139-143. (Pubitemid 30094713)
-
(2000)
Nature Genetics
, vol.24
, Issue.2
, pp. 139-143
-
-
Simmler, M.-C.1
Cohen-Salmon, M.2
El-Amraoui, A.3
Guillaud, L.4
Benichou, J.-C.5
Petit, C.6
Panthier, J.-J.7
-
52
-
-
9444242167
-
The del22q11.2 candidate gene Tbx1 regulates branchiometric myogenesis
-
DOI 10.1093/hmg/ddh304
-
Kelly RG, Jerome-Majewska LA, Papaioannou VE (2004) The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis. Hum Mol Genet 13: 2829-2840. (Pubitemid 39562547)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.22
, pp. 2829-2840
-
-
Kelly, R.G.1
Jerome-Majewska, L.A.2
Papaioannou, V.E.3
-
53
-
-
0039706410
-
Crystallographic structure of the T domain-DNA complex of the Brachyury transcription factor
-
DOI 10.1038/39929
-
Muller CW, Herrmann BG (1997) Crystallographic structure of the T domain-DNA complex of the Brachyury transcription factor. Nature 389: 884-888. (Pubitemid 27462986)
-
(1997)
Nature
, vol.389
, Issue.6653
, pp. 884-888
-
-
Muller, C.W.1
Herrmann, B.G.2
-
54
-
-
84887050388
-
Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome
-
El Omari K, De Mesmaeker J, Karia D, Ginn H, Bhattacharya S, et al. (2011) Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome. Proteins.
-
(2011)
Proteins
-
-
El Omari, K.1
De Mesmaeker, J.2
Karia, D.3
Ginn, H.4
Bhattacharya, S.5
-
55
-
-
84878572579
-
Interactions between the R2R3-MYB transcription factor, AtMYB61, and target DNA binding sites
-
Prouse MB, Campbell MM (2013) Interactions between the R2R3-MYB transcription factor, AtMYB61, and target DNA binding sites. PLoS One 8: e65132.
-
(2013)
PLoS One
, vol.8
-
-
Prouse, M.B.1
Campbell, M.M.2
-
56
-
-
0032580207
-
Allosteric effects of DNA on transcriptional regulators
-
DOI 10.1038/31860
-
Lefstin JA, Yamamoto KR (1998) Allosteric effects of DNA on transcriptional regulators. Nature 392: 885-888. (Pubitemid 28232051)
-
(1998)
Nature
, vol.392
, Issue.6679
, pp. 885-888
-
-
Lefstin, J.A.1
Yamamoto, K.R.2
-
57
-
-
65249167505
-
DNA binding site sequence directs glucocorticoid receptor structure and activity
-
Meijsing SH, Pufall MA, So AY, Bates DL, Chen L, et al. (2009) DNA binding site sequence directs glucocorticoid receptor structure and activity. Science 324: 407-410.
-
(2009)
Science
, vol.324
, pp. 407-410
-
-
Meijsing, S.H.1
Pufall, M.A.2
So, A.Y.3
Bates, D.L.4
Chen, L.5
-
58
-
-
0035514706
-
Chromosomal microdeletions: Dissecting del22q11 syndrome
-
Lindsay EA (2001) Chromosomal microdeletions: dissecting del22q11 syndrome. Nat Rev Genet 2: 858-868.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 858-868
-
-
Lindsay, E.A.1
-
59
-
-
2442710327
-
The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments
-
DOI 10.1101/gad.300104
-
Bussen M, Petry M, Schuster-Gossler K, Leitges M, Gossler A, et al. (2004) The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments. Genes Dev 18: 1209-1221. (Pubitemid 38669041)
-
(2004)
Genes and Development
, vol.18
, Issue.10
, pp. 1209-1221
-
-
Bussen, M.1
Petry, M.2
Schuster-Gossler, K.3
Leitges, M.4
Gossler, A.5
Kispert, A.6
-
60
-
-
33644866845
-
Tbx6-mediated Notch signaling controls somite-specific Mesp2 expression
-
DOI 10.1073/pnas.0508238103
-
Yasuhiko Y, Haraguchi S, Kitajima S, Takahashi Y, Kanno J, et al. (2006) Tbx6-mediated Notch signaling controls somite-specific Mesp2 expression. Proc Natl Acad Sci U S A 103: 3651-3656. (Pubitemid 43376610)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.10
, pp. 3651-3656
-
-
Yasuhiko, Y.1
Haraguchi, S.2
Kitajima, S.3
Takahashi, Y.4
Kanno, J.5
Saga, Y.6
-
62
-
-
77956641239
-
ChIP-Seq identification of weakly conserved heart enhancers
-
Blow MJ, McCulley DJ, Li Z, Zhang T, Akiyama JA, et al. (2010) ChIP-Seq identification of weakly conserved heart enhancers. Nat Genet 42: 806-810.
-
(2010)
Nat Genet
, vol.42
, pp. 806-810
-
-
Blow, M.J.1
McCulley, D.J.2
Li, Z.3
Zhang, T.4
Akiyama, J.A.5
-
63
-
-
59449089844
-
Asymmetrical distribution of non-conserved regulatory sequences at PHOX2B is reflected at the ENCODE loci and illuminates a possible genome-wide trend
-
McGaughey DM, Stine ZE, Huynh JL, Vinton RM, McCallion AS (2009) Asymmetrical distribution of non-conserved regulatory sequences at PHOX2B is reflected at the ENCODE loci and illuminates a possible genome-wide trend. BMC Genomics 10: 8.
-
(2009)
BMC Genomics
, vol.10
, pp. 8
-
-
McGaughey, D.M.1
Stine, Z.E.2
Huynh, J.L.3
Vinton, R.M.4
McCallion, A.S.5
-
64
-
-
77953062527
-
Five-vertebrate ChIP-seq reveals the evolutionary dynamics of transcription factor binding
-
Schmidt D, Wilson MD, Ballester B, Schwalie PC, Brown GD, et al. (2010) Five-vertebrate ChIP-seq reveals the evolutionary dynamics of transcription factor binding. Science 328: 1036-1040.
-
(2010)
Science
, vol.328
, pp. 1036-1040
-
-
Schmidt, D.1
Wilson, M.D.2
Ballester, B.3
Schwalie, P.C.4
Brown, G.D.5
-
65
-
-
80054109588
-
Conserved and non-conserved enhancers direct tissue specific transcription in ancient germ layer specific developmental control genes
-
Chatterjee S, Bourque G, Lufkin T (2011) Conserved and non-conserved enhancers direct tissue specific transcription in ancient germ layer specific developmental control genes. BMC Dev Biol 11: 63.
-
(2011)
BMC Dev Biol
, vol.11
, pp. 63
-
-
Chatterjee, S.1
Bourque, G.2
Lufkin, T.3
-
66
-
-
84878652408
-
Natural selection drives rapid evolution of mouse embryonic heart enhancers
-
Liao BY, Weng MP (2012) Natural selection drives rapid evolution of mouse embryonic heart enhancers. BMC Syst Biol 6 Suppl 2: S1.
-
(2012)
BMC Syst Biol
, vol.6
, Issue.SUPPL. 2
-
-
Liao, B.Y.1
Weng, M.P.2
-
67
-
-
0033789235
-
Crossveinless 2 contains cysteine-rich domains and is required for high levels of BMP-like activity during the formation of the cross veins in Drosophila
-
Conley CA, Silburn R, Singer MA, Ralston A, Rohwer-Nutter D, et al. (2000) Crossveinless 2 contains cysteine-rich domains and is required for high levels of BMP-like activity during the formation of the cross veins in Drosophila. Development 127: 3947-3959.
-
(2000)
Development
, vol.127
, pp. 3947-3959
-
-
Conley, C.A.1
Silburn, R.2
Singer, M.A.3
Ralston, A.4
Rohwer-Nutter, D.5
-
68
-
-
17644378679
-
Kielin/chordin-like protein, a novel enhancer of BMP signaling, attenuates renal fibrotic disease
-
DOI 10.1038/nm1217
-
Lin J, Patel SR, Cheng X, Cho EA, Levitan I, et al. (2005) Kielin/chordin-like protein, a novel enhancer of BMP signaling, attenuates renal fibrotic disease. Nat Med 11: 387-393. (Pubitemid 40562328)
-
(2005)
Nature Medicine
, vol.11
, Issue.4
, pp. 387-393
-
-
Lin, J.1
Patel, S.R.2
Cheng, X.3
Cho, E.A.4
Levitan, I.5
Ullenbruch, M.6
Phan, S.H.7
Park, J.M.8
Dressler, G.R.9
-
69
-
-
10744233059
-
Human Crossveinless-2 is a novel inhibitor of bone morphogenetic proteins
-
DOI 10.1016/j.bbrc.2004.01.048
-
Binnerts ME, Wen X, Cante-Barrett K, Bright J, Chen HT, et al. (2004) Human Crossveinless-2 is a novel inhibitor of bone morphogenetic proteins. Biochem Biophys Res Commun 315: 272-280. (Pubitemid 38183104)
-
(2004)
Biochemical and Biophysical Research Communications
, vol.315
, Issue.2
, pp. 272-280
-
-
Binnerts, M.E.1
Wen, X.2
Cante-Barrett, K.3
Bright, J.4
Chen, H.-T.5
Asundi, V.6
Sattari, P.7
Tang, T.8
Boyle, B.9
Funk, W.10
Rupp, F.11
-
70
-
-
24344491888
-
MyoD and the transcriptional control of myogenesis
-
DOI 10.1016/j.semcdb.2005.07.006, PII S108495210500087X, Biology of Hypoxia and Myogenesis and Muscle Disease
-
Berkes CA, Tapscott SJ (2005) MyoD and the transcriptional control of myogenesis. Semin Cell Dev Biol 16: 585-595. (Pubitemid 41247882)
-
(2005)
Seminars in Cell and Developmental Biology
, vol.16
, Issue.4-5
, pp. 585-595
-
-
Berkes, C.A.1
Tapscott, S.J.2
-
71
-
-
0031260577
-
Muscle determination: Another key player in myogenesis?
-
Borycki AG, Emerson CP (1997) Muscle determination: another key player in myogenesis? Curr Biol 7: R620-623.
-
(1997)
Curr Biol
, vol.7
-
-
Borycki, A.G.1
Emerson, C.P.2
-
72
-
-
54549124624
-
Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos
-
Grifone R, Jarry T, Dandonneau M, Grenier J, Duprez D, et al. (2008) Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos. Dev Dyn 237: 3071-3078.
-
(2008)
Dev Dyn
, vol.237
, pp. 3071-3078
-
-
Grifone, R.1
Jarry, T.2
Dandonneau, M.3
Grenier, J.4
Duprez, D.5
-
73
-
-
0034897601
-
Spatiotemporal expression of otogelin in the developing and adult mouse inner ear
-
DOI 10.1016/S0378-5955(01)00312-4, PII S0378595501003124
-
El-Amraoui A, Cohen-Salmon M, Petit C, Simmler MC (2001) Spatiotemporal expression of otogelin in the developing and adult mouse inner ear. Hear Res 158: 151-159. (Pubitemid 32739287)
-
(2001)
Hearing Research
, vol.158
, Issue.1-2
, pp. 151-159
-
-
El-Amraoui, A.1
Cohen-Salmon, M.2
Petit, C.3
Simmler, M.-C.4
-
74
-
-
84868364276
-
Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment
-
Schraders M, Ruiz-Palmero L, Kalay E, Oostrik J, del Castillo FJ, et al. (2012) Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment. Am J Hum Genet 91: 883-889.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 883-889
-
-
Schraders, M.1
Ruiz-Palmero, L.2
Kalay, E.3
Oostrik, J.4
Del Castillo, F.J.5
-
75
-
-
84868126624
-
Functional characterization of tissue-specific enhancers in the DLX5/6 locus
-
Birnbaum RY, Everman DB, Murphy KK, Gurrieri F, Schwartz CE, et al. (2012) Functional characterization of tissue-specific enhancers in the DLX5/6 locus. Hum Mol Genet 21: 4930-4938.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4930-4938
-
-
Birnbaum, R.Y.1
Everman, D.B.2
Murphy, K.K.3
Gurrieri, F.4
Schwartz, C.E.5
|