-
1
-
-
26644456963
-
Mammary serine protease inhibitor (Maspin) binds directly to interferon regulatory factor 6: identification of a novel serpin partnership
-
Bailey CM, Khalkhali-Ellis Z, Kondo S, Margaryan NV, Seftor RE, Wheaton WW, Amir S, Pins MR, Schutte BC, Hendrix MJ. 2005. Mammary serine protease inhibitor (Maspin) binds directly to interferon regulatory factor 6: identification of a novel serpin partnership. J Biol Chem 280: 34210-34217.
-
(2005)
J Biol Chem
, vol.280
, pp. 34210-34217
-
-
Bailey, C.M.1
Khalkhali-Ellis, Z.2
Kondo, S.3
Margaryan, N.V.4
Seftor, R.E.5
Wheaton, W.W.6
Amir, S.7
Pins, M.R.8
Schutte, B.C.9
Hendrix, M.J.10
-
2
-
-
77952886672
-
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
-
Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinski I, Hetmanski JB, Liang KY, Wu T, Murray T, Fallin MD, Redett RA, Raymond G, Schwender H, Jin SC, Cooper ME, Dunnwald M, Mansilla MA, Leslie E, Bullard S, Lidral AC, Moreno LM, Menezes R, Vieira AR, Petrin A, Wilcox AJ, Lie RT, Jabs EW, Wu-Chou YH, Chen PK, Wang H, Ye X, Huang S, Yeow V, Chong SS, Jee SH, Shi B, Christensen K, Melbye M, Doheny KF, Pugh EW, Ling H, Castilla EE, Czeizel AE, Ma L, Field LL, Brody L, Pangilinan F, Mills JL, Molloy AM, Kirke PN, Scott JM, Arcos-Burgos M, Scott AF. 2010. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet 42: 525-529.
-
(2010)
Nat Genet
, vol.42
, pp. 525-529
-
-
Beaty, T.H.1
Murray, J.C.2
Marazita, M.L.3
Munger, R.G.4
Ruczinski, I.5
Hetmanski, J.B.6
Liang, K.Y.7
Wu, T.8
Murray, T.9
Fallin, M.D.10
Redett, R.A.11
Raymond, G.12
Schwender, H.13
Jin, S.C.14
Cooper, M.E.15
Dunnwald, M.16
Mansilla, M.A.17
Leslie, E.18
Bullard, S.19
Lidral, A.C.20
Moreno, L.M.21
Menezes, R.22
Vieira, A.R.23
Petrin, A.24
Wilcox, A.J.25
Lie, R.T.26
Jabs, E.W.27
Wu-Chou, Y.H.28
Chen, P.K.29
Wang, H.30
Ye, X.31
Huang, S.32
Yeow, V.33
Chong, S.S.34
Jee, S.H.35
Shi, B.36
Christensen, K.37
Melbye, M.38
Doheny, K.F.39
Pugh, E.W.40
Ling, H.41
Castilla, E.E.42
Czeizel, A.E.43
Ma, L.44
Field, L.L.45
Brody, L.46
Pangilinan, F.47
Mills, J.L.48
Molloy, A.M.49
Kirke, P.N.50
Scott, J.M.51
Arcos-Burgos, M.52
Scott, A.F.53
more..
-
3
-
-
84856090335
-
Interferon regulatory factor 6 is necessary but not sufficient for keratinocyte differentiation
-
Epub ahead of print].
-
Biggs LC, Rhea L, Schutte BC, Dunnwald M. 2011. Interferon regulatory factor 6 is necessary but not sufficient for keratinocyte differentiation. J Invest Derm [Epub ahead of print].
-
(2011)
J Invest Derm
-
-
Biggs, L.C.1
Rhea, L.2
Schutte, B.C.3
Dunnwald, M.4
-
4
-
-
73149092971
-
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate
-
Birnbaum S, Ludwig KU, Reutter H, Herms S, de Assis NA, Diaz-Lacava A, Barth S, Lauster C, Schmidt G, Scheer M, Saffar M, Martini M, Reich RH, Schiefke F, Hemprich A, Potzsch S, Potzsch B, Wienker TF, Hoffmann P, Knapp M, Kramer FJ, Nothen MM, Mangold E. 2009. IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci 117: 766-769.
-
(2009)
Eur J Oral Sci
, vol.117
, pp. 766-769
-
-
Birnbaum, S.1
Ludwig, K.U.2
Reutter, H.3
Herms, S.4
de Assis, N.A.5
Diaz-Lacava, A.6
Barth, S.7
Lauster, C.8
Schmidt, G.9
Scheer, M.10
Saffar, M.11
Martini, M.12
Reich, R.H.13
Schiefke, F.14
Hemprich, A.15
Potzsch, S.16
Potzsch, B.17
Wienker, T.F.18
Hoffmann, P.19
Knapp, M.20
Kramer, F.J.21
Nothen, M.M.22
Mangold, E.23
more..
-
6
-
-
0028025616
-
Programming gene expression in developing epidermis
-
Byrne C, Tainsky M, Fuchs E. 1994. Programming gene expression in developing epidermis. Development 120: 2369-2383.
-
(1994)
Development
, vol.120
, pp. 2369-2383
-
-
Byrne, C.1
Tainsky, M.2
Fuchs, E.3
-
7
-
-
1242263325
-
Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology
-
Cox TC. 2004. Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology. Clin Genet 65: 163-176.
-
(2004)
Clin Genet
, vol.65
, pp. 163-176
-
-
Cox, T.C.1
-
8
-
-
70349131331
-
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome
-
de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S, Katz L, Marazita ML, Compton J, Bale S, Hehr U, Dixon MJ, Daack-Hirsch S, Boute O, Bayet B, Revencu N, Verellen-Dumoulin C, Vikkula M, Richieri-Costa A, Moretti-Ferreira D, Murray JC, Schutte BC. 2009. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genet Med 11: 241-247.
-
(2009)
Genet Med
, vol.11
, pp. 241-247
-
-
de Lima, R.L.1
Hoper, S.A.2
Ghassibe, M.3
Cooper, M.E.4
Rorick, N.K.5
Kondo, S.6
Katz, L.7
Marazita, M.L.8
Compton, J.9
Bale, S.10
Hehr, U.11
Dixon, M.J.12
Daack-Hirsch, S.13
Boute, O.14
Bayet, B.15
Revencu, N.16
Verellen-Dumoulin, C.17
Vikkula, M.18
Richieri-Costa, A.19
Moretti-Ferreira, D.20
Murray, J.C.21
Schutte, B.C.22
more..
-
9
-
-
79851473886
-
A high-resolution anatomical atlas of the transcriptome in the mouse embryo
-
Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D, Magen A, Canidio E, Pagani M, Peluso I, Lin-Marq N, Koch M, Bilio M, Cantiello I, Verde R, De Masi C, Bianchi SA, Cicchini J, Perroud E, Mehmeti S, Dagand E, Schrinner S, Nurnberger A, Schmidt K, Metz K, Zwingmann C, Brieske N, Springer C, Hernandez AM, Herzog S, Grabbe F, Sieverding C, Fischer B, Schrader K, Brockmeyer M, Dettmer S, Helbig C, Alunni V, Battaini MA, Mura C, Henrichsen CN, Garcia-Lopez R, Echevarria D, Puelles E, Garcia-Calero E, Kruse S, Uhr M, Kauck C, Feng G, Milyaev N, Ong CK, Kumar L, Lam M, Semple CA, Gyenesei A, Mundlos S, Radelof U, Lehrach H, Sarmientos P, Reymond A, Davidson DR, Dolle P, Antonarakis SE, Yaspo ML, Martinez S, Baldock RA, Eichele G, Ballabio A. 2011. A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol 9: e1000582.
-
(2011)
PLoS Biol
, vol.9
-
-
Diez-Roux, G.1
Banfi, S.2
Sultan, M.3
Geffers, L.4
Anand, S.5
Rozado, D.6
Magen, A.7
Canidio, E.8
Pagani, M.9
Peluso, I.10
Lin-Marq, N.11
Koch, M.12
Bilio, M.13
Cantiello, I.14
Verde, R.15
De Masi, C.16
Bianchi, S.A.17
Cicchini, J.18
Perroud, E.19
Mehmeti, S.20
Dagand, E.21
Schrinner, S.22
Nurnberger, A.23
Schmidt, K.24
Metz, K.25
Zwingmann, C.26
Brieske, N.27
Springer, C.28
Hernandez, A.M.29
Herzog, S.30
Grabbe, F.31
Sieverding, C.32
Fischer, B.33
Schrader, K.34
Brockmeyer, M.35
Dettmer, S.36
Helbig, C.37
Alunni, V.38
Battaini, M.A.39
Mura, C.40
Henrichsen, C.N.41
Garcia-Lopez, R.42
Echevarria, D.43
Puelles, E.44
Garcia-Calero, E.45
Kruse, S.46
Uhr, M.47
Kauck, C.48
Feng, G.49
Milyaev, N.50
Ong, C.K.51
Kumar, L.52
Lam, M.53
Semple, C.A.54
Gyenesei, A.55
Mundlos, S.56
Radelof, U.57
Lehrach, H.58
Sarmientos, P.59
Reymond, A.60
Davidson, D.R.61
Dolle, P.62
Antonarakis, S.E.63
Yaspo, M.L.64
Martinez, S.65
Baldock, R.A.66
Eichele, G.67
Ballabio, A.68
more..
-
10
-
-
33846669882
-
Palatal fusion - where do the midline cells go? A review on cleft palate, a major human birth defect
-
Dudas M, Li WY, Kim J, Yang A, Kaartinen V. 2007. Palatal fusion - where do the midline cells go? A review on cleft palate, a major human birth defect. Acta Histochem 109: 1-14.
-
(2007)
Acta Histochem
, vol.109
, pp. 1-14
-
-
Dudas, M.1
Li, W.Y.2
Kim, J.3
Yang, A.4
Kaartinen, V.5
-
11
-
-
46849098205
-
Multiple loci with different cancer specificities within the 8q24 gene desert
-
Ghoussaini M, Song H, Koessler T, Al Olama AA, Kote-Jarai Z, Driver KE, Pooley KA, Ramus SJ, Kjaer SK, Hogdall E, DiCioccio RA, Whittemore AS, Gayther SA, Giles GG, Guy M, Edwards SM, Morrison J, Donovan JL, Hamdy FC, Dearnaley DP, Ardern-Jones AT, Hall AL, O'Brien LT, Gehr-Swain BN, Wilkinson RA, Brown PM, Hopper JL, Neal DE, Pharoah PD, Ponder BA, Eeles RA, Easton DF, Dunning AM. 2008. Multiple loci with different cancer specificities within the 8q24 gene desert. J Natl Cancer Inst 100: 962-966.
-
(2008)
J Natl Cancer Inst
, vol.100
, pp. 962-966
-
-
Ghoussaini, M.1
Song, H.2
Koessler, T.3
Al Olama, A.A.4
Kote-Jarai, Z.5
Driver, K.E.6
Pooley, K.A.7
Ramus, S.J.8
Kjaer, S.K.9
Hogdall, E.10
DiCioccio, R.A.11
Whittemore, A.S.12
Gayther, S.A.13
Giles, G.G.14
Guy, M.15
Edwards, S.M.16
Morrison, J.17
Donovan, J.L.18
Hamdy, F.C.19
Dearnaley, D.P.20
Ardern-Jones, A.T.21
Hall, A.L.22
O'Brien, L.T.23
Gehr-Swain, B.N.24
Wilkinson, R.A.25
Brown, P.M.26
Hopper, J.L.27
Neal, D.E.28
Pharoah, P.D.29
Ponder, B.A.30
Eeles, R.A.31
Easton, D.F.32
Dunning, A.M.33
more..
-
12
-
-
33750452339
-
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)
-
Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, Murray JC, Schutte BC. 2006. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nat Genet 38: 1335-1340.
-
(2006)
Nat Genet
, vol.38
, pp. 1335-1340
-
-
Ingraham, C.R.1
Kinoshita, A.2
Kondo, S.3
Yang, B.4
Sajan, S.5
Trout, K.J.6
Malik, M.I.7
Dunnwald, M.8
Goudy, S.L.9
Lovett, M.10
Murray, J.C.11
Schutte, B.C.12
-
13
-
-
84856225501
-
A novel mutation in IRF6 underlies hearing loss, pulp stones, large craniofacial sinuses, and limb anomalies in Van der Woude Syndrome patients
-
Kantaputra PN, Limwongse C, Assawamakin A, Praditsap O, Kemaleelakul U, Kondo S, Schutte BC. 2004. A novel mutation in IRF6 underlies hearing loss, pulp stones, large craniofacial sinuses, and limb anomalies in Van der Woude Syndrome patients. Oral Biosci Med 4: 277-282.
-
(2004)
Oral Biosci Med
, vol.4
, pp. 277-282
-
-
Kantaputra, P.N.1
Limwongse, C.2
Assawamakin, A.3
Praditsap, O.4
Kemaleelakul, U.5
Kondo, S.6
Schutte, B.C.7
-
14
-
-
33744922620
-
Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome
-
Knight AS, Schutte BC, Jiang R, Dixon MJ. 2006. Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome. Dev Dyn 235: 1441-1447.
-
(2006)
Dev Dyn
, vol.235
, pp. 1441-1447
-
-
Knight, A.S.1
Schutte, B.C.2
Jiang, R.3
Dixon, M.J.4
-
15
-
-
18644374446
-
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
-
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. 2002. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet 32: 285-289.
-
(2002)
Nat Genet
, vol.32
, pp. 285-289
-
-
Kondo, S.1
Schutte, B.C.2
Richardson, R.J.3
Bjork, B.C.4
Knight, A.S.5
Watanabe, Y.6
Howard, E.7
de Lima, R.L.8
Daack-Hirsch, S.9
Sander, A.10
McDonald-McGinn, D.M.11
Zackai, E.H.12
Lammer, E.J.13
Aylsworth, A.S.14
Ardinger, H.H.15
Lidral, A.C.16
Pober, B.R.17
Moreno, L.18
Arcos-Burgos, M.19
Valencia, C.20
Houdayer, C.21
Bahuau, M.22
Moretti-Ferreira, D.23
Richieri-Costa, A.24
Dixon, M.J.25
Murray, J.C.26
more..
-
16
-
-
77951865156
-
A regulatory feedback loop involving p63 and IRF6 links the pathogenesis of 2 genetically different human ectodermal dysplasias
-
Moretti F, Marinari B, Lo Iacono N, Botti E, Giunta A, Spallone G, Garaffo G, Vernersson-Lindahl E, Merlo G, Mills AA, Ballaro C, Alema S, Chimenti S, Guerrini L, Costanzo A. 2010. A regulatory feedback loop involving p63 and IRF6 links the pathogenesis of 2 genetically different human ectodermal dysplasias. J Clin Invest 120: 1570-1577.
-
(2010)
J Clin Invest
, vol.120
, pp. 1570-1577
-
-
Moretti, F.1
Marinari, B.2
Lo Iacono, N.3
Botti, E.4
Giunta, A.5
Spallone, G.6
Garaffo, G.7
Vernersson-Lindahl, E.8
Merlo, G.9
Mills, A.A.10
Ballaro, C.11
Alema, S.12
Chimenti, S.13
Guerrini, L.14
Costanzo, A.15
-
17
-
-
34547820974
-
Abnormal brain structure in children with isolated clefts of the lip or palate
-
Nopoulos P, Langbehn DR, Canady J, Magnotta V, Richman L. 2007a. Abnormal brain structure in children with isolated clefts of the lip or palate. Arch Pediatr Adolesc Med 161: 753-758.
-
(2007)
Arch Pediatr Adolesc Med
, vol.161
, pp. 753-758
-
-
Nopoulos, P.1
Langbehn, D.R.2
Canady, J.3
Magnotta, V.4
Richman, L.5
-
18
-
-
34247219779
-
Cognitive dysfunction in adults with Van der Woude syndrome
-
Nopoulos P, Richman L, Andreasen N, Murray JC, Schutte B. 2007b. Cognitive dysfunction in adults with Van der Woude syndrome. Genet Med 9: 213-218.
-
(2007)
Genet Med
, vol.9
, pp. 213-218
-
-
Nopoulos, P.1
Richman, L.2
Andreasen, N.3
Murray, J.C.4
Schutte, B.5
-
19
-
-
0035174489
-
An enhancer sequence directs LacZ expression to developing pharyngeal endoderm in transgenic mice
-
Parmar H, Coletta PL, Faruque N, Sharpe PT. 2001. An enhancer sequence directs LacZ expression to developing pharyngeal endoderm in transgenic mice. Genesis 31: 57-63.
-
(2001)
Genesis
, vol.31
, pp. 57-63
-
-
Parmar, H.1
Coletta, P.L.2
Faruque, N.3
Sharpe, P.T.4
-
20
-
-
55049105999
-
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip
-
Rahimov F, Marazita ML, Visel A, Cooper ME, Hitchler MJ, Rubini M, Domann FE, Govil M, Christensen K, Bille C, Melbye M, Jugessur A, Lie RT, Wilcox AJ, Fitzpatrick DR, Green ED, Mossey PA, Little J, Steegers-Theunissen RP, Pennacchio LA, Schutte BC, Murray JC. 2008. Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Nat Genet 40: 1341-1347.
-
(2008)
Nat Genet
, vol.40
, pp. 1341-1347
-
-
Rahimov, F.1
Marazita, M.L.2
Visel, A.3
Cooper, M.E.4
Hitchler, M.J.5
Rubini, M.6
Domann, F.E.7
Govil, M.8
Christensen, K.9
Bille, C.10
Melbye, M.11
Jugessur, A.12
Lie, R.T.13
Wilcox, A.J.14
Fitzpatrick, D.R.15
Green, E.D.16
Mossey, P.A.17
Little, J.18
Steegers-Theunissen, R.P.19
Pennacchio, L.A.20
Schutte, B.C.21
Murray, J.C.22
more..
-
21
-
-
33750441851
-
Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch
-
Richardson RJ, Dixon J, Malhotra S, Hardman MJ, Knowles L, Boot-Handford RP, Shore P, Whitmarsh A, Dixon MJ. 2006. Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch. Nat Genet 38: 1329-1334.
-
(2006)
Nat Genet
, vol.38
, pp. 1329-1334
-
-
Richardson, R.J.1
Dixon, J.2
Malhotra, S.3
Hardman, M.J.4
Knowles, L.5
Boot-Handford, R.P.6
Shore, P.7
Whitmarsh, A.8
Dixon, M.J.9
-
22
-
-
67649862248
-
Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence
-
Richardson RJ, Dixon J, Jiang R, Dixon MJ. 2009a. Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence. Hum Mol Genet 18: 2632-2642.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 2632-2642
-
-
Richardson, R.J.1
Dixon, J.2
Jiang, R.3
Dixon, M.J.4
-
23
-
-
75549087628
-
EMAGE mouse embryo spatial gene expression database: 2010 update
-
doi:10.1093/nar/gkp763.
-
Richardson L, Venkataraman S, Stevenson P, Yang Y, Burton N, Rao J, Fisher M. Baldock RA, Davidson DR, Christiansen JH. 2009b. EMAGE mouse embryo spatial gene expression database: 2010 update. Nucleic Acids Res doi:10.1093/nar/gkp763.
-
(2009)
Nucleic Acids Res
-
-
Richardson, L.1
Venkataraman, S.2
Stevenson, P.3
Yang, Y.4
Burton, N.5
Rao, J.6
Fisher, M.7
Baldock, R.A.8
Davidson, D.R.9
Christiansen, J.H.10
-
24
-
-
0037134008
-
Optical projection tomography as a tool for 3D microscopy and gene expression studies
-
Sharpe J, Ahlgren U, Perry P, Hill B, Ross A, Hecksher-Sorensen J, Baldock R, Davidson D. 2002. Optical projection tomography as a tool for 3D microscopy and gene expression studies. Science 296: 541-545.
-
(2002)
Science
, vol.296
, pp. 541-545
-
-
Sharpe, J.1
Ahlgren, U.2
Perry, P.3
Hill, B.4
Ross, A.5
Hecksher-Sorensen, J.6
Baldock, R.7
Davidson, D.8
-
25
-
-
77951849894
-
Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice
-
Thomason HA, Zhou H, Kouwenhoven EN, Dotto GP, Restivo G, Nguyen BC, Little H, Dixon MJ, van Bokhoven H, Dixon J. 2010. Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice. J Clin Invest 120: 1561-1569.
-
(2010)
J Clin Invest
, vol.120
, pp. 1561-1569
-
-
Thomason, H.A.1
Zhou, H.2
Kouwenhoven, E.N.3
Dotto, G.P.4
Restivo, G.5
Nguyen, B.C.6
Little, H.7
Dixon, M.J.8
van Bokhoven, H.9
Dixon, J.10
-
26
-
-
68149170044
-
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling
-
Tuupanen S, Turunen M, Lehtonen R, Hallikas O, Vanharanta S, Kivioja T, Bjorklund M, Wei G, Yan J, Niittymaki I, Mecklin JP, Jarvinen H, Ristimaki A, Di-Bernardo M, East P, Carvajal-Carmona L, Houlston RS, Tomlinson I, Palin K, Ukkonen E, Karhu A, Taipale J, Aaltonen LA. 2009. The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. Nat Genet 41: 885-890.
-
(2009)
Nat Genet
, vol.41
, pp. 885-890
-
-
Tuupanen, S.1
Turunen, M.2
Lehtonen, R.3
Hallikas, O.4
Vanharanta, S.5
Kivioja, T.6
Bjorklund, M.7
Wei, G.8
Yan, J.9
Niittymaki, I.10
Mecklin, J.P.11
Jarvinen, H.12
Ristimaki, A.13
Di-Bernardo, M.14
East, P.15
Carvajal-Carmona, L.16
Houlston, R.S.17
Tomlinson, I.18
Palin, K.19
Ukkonen, E.20
Karhu, A.21
Taipale, J.22
Aaltonen, L.A.23
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-
-
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Cell autonomous requirement for Tgfbr2 in the disappearance of medial edge epithelium during palatal fusion
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Xu X, Han J, Ito Y, Bringas P Jr, Urata MM, Chai Y. 2006. Cell autonomous requirement for Tgfbr2 in the disappearance of medial edge epithelium during palatal fusion. Dev Biol 297: 238-248.
-
(2006)
Dev Biol
, vol.297
, pp. 238-248
-
-
Xu, X.1
Han, J.2
Ito, Y.3
Bringas Jr., P.4
Urata, M.M.5
Chai, Y.6
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