-
2
-
-
33845246849
-
PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations
-
DOI 10.1002/ajmg.a.31367
-
Avila JR, Jezewski PA, Vieira AR, Orioli IM, Castilla EE, Christensen K, Daack-Hirsch S, Romitti PA, Murray JC. PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. Am J Med Genet A. 2006;140:2562-2570. (Pubitemid 44865084)
-
(2006)
American Journal of Medical Genetics, Part A
, vol.140
, Issue.23
, pp. 2562-2570
-
-
Avila, J.R.1
Jezewski, P.A.2
Vieira, A.R.3
Orioli, I.M.4
Castilla, E.E.5
Christensen, K.6
Daack-Hirsch, S.7
Romitti, P.A.8
Murray, J.C.9
-
3
-
-
77952886672
-
A genome wide association study of cleft lip with/without cleft palate using case-parent trios of European and Asian ancestry identifies MAFB and ABCA4 as novel candidate genes
-
Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinski I, Hetmanski JB, Liang KY, Wu T, Murray T, Fallin MD, et al. A genome wide association study of cleft lip with/without cleft palate using case-parent trios of European and Asian ancestry identifies MAFB and ABCA4 as novel candidate genes. Nat Genet. 2010;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
-
4
-
-
63449105241
-
Key susceptibilty locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
-
Birnbaum S, Ludwig KU, Reutter H, Herms S, Steffens M, Rubini M, Baluardo C, Ferrian M, Almeida de Assis N, Alblas MA, et al. Key susceptibilty locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nat Genet. 2009;41:473-477.
-
(2009)
Nat Genet
, vol.41
, pp. 473-477
-
-
Birnbaum, S.1
Ludwig, K.U.2
Reutter, H.3
Herms, S.4
Steffens, M.5
Rubini, M.6
Baluardo, C.7
Ferrian, M.8
Almeida De Assis, N.9
Alblas, M.A.10
-
5
-
-
79954416964
-
Epidemiology of orofacial clefts in Africa: Methodological challenges in ascertainment
-
Butali A, Mossey PA. Epidemiology of orofacial clefts in Africa: methodological challenges in ascertainment. Pan Afr Med J. 2009; 2:2-5.
-
(2009)
Pan Afr Med J
, vol.2
, pp. 2-5
-
-
Butali, A.1
Mossey, P.A.2
-
6
-
-
0028831127
-
Transcriptional repression by Msx-1 does not require homeodomain DNA-binding sites
-
Catron KM, Zhang H, Marshall SC, Inostroza JA, Wilson JM, Abate C. Transcriptional repression by Msx-1 does not require homeodomain DNA-binding sites. Mol Cell Biol. 1995;15:861-871.
-
(1995)
Mol Cell Biol
, vol.15
, pp. 861-871
-
-
Catron, K.M.1
Zhang, H.2
Marshall, S.C.3
Inostroza, J.A.4
Wilson, J.M.5
Abate, C.6
-
7
-
-
33749064639
-
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
-
DOI 10.1007/s10038-006-0037-x
-
Chishti MS, Muhammad D, Haider M, Ahmad W. A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families. J Hum Genet. 2006;51:872-878. (Pubitemid 44465697)
-
(2006)
Journal of Human Genetics
, vol.51
, Issue.10
, pp. 872-878
-
-
Chishti, M.S.1
Muhammad, D.2
Haider, M.3
Ahmad, W.4
-
8
-
-
3343015549
-
A novel MSX1 mutation in hypodontia
-
De Muynck S, Schollen E, Matthijs G, Verdonck A, Devriendt K, Carels C. A novel MSX1 mutation in hypodontia. Am J Med Genet. 2004;128:401-403. (Pubitemid 38988642)
-
(2004)
American Journal of Medical Genetics
, vol.128 A
, Issue.4
, pp. 401-403
-
-
De Muynck, S.1
Schollen, E.2
Matthijs, G.3
Verdonck, A.4
Devriendt, K.5
Carels, C.6
-
9
-
-
62449313460
-
Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers
-
Finnerty JR, Mazza ME, Jezewski PA. Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers. BMC Evol Biol. 2009;9:18.
-
(2009)
BMC Evol Biol
, vol.9
, pp. 18
-
-
Finnerty, J.R.1
Mazza, M.E.2
Jezewski, P.A.3
-
10
-
-
73949148687
-
A genome - Wide association study identifies a locus for non-syndromic cleft lip with or without cleft palate on 8q24
-
Grant SF, Wang K, Zhang H, Glaberson W, Annaiah K, Kim CE, Bradfield PJ, Glessner JT, Thomas KA, Garris M, et al. A genome - wide association study identifies a locus for non-syndromic cleft lip with or without cleft palate on 8q24. J Pediatr. 2009;155:909-913.
-
(2009)
J Pediatr
, vol.155
, pp. 909-913
-
-
Grant, S.F.1
Wang, K.2
Zhang, H.3
Glaberson, W.4
Annaiah, K.5
Kim, C.E.6
Bradfield, P.J.7
Glessner, J.T.8
Thomas, K.A.9
Garris, M.10
-
11
-
-
0031930052
-
Incidence of cleft lip and palate and risks of additional malformations
-
DOI 10.1597/1545-1569(1998)035<0040:IOCLAP>2.3.CO;2
-
Hagberg C, Larson O, Milerad J. Incidence of cleft lip and palate and risks of additional malformations. Cleft Palate Craniofac J. 1998; 35:40-45. (Pubitemid 28095996)
-
(1998)
Cleft Palate-Craniofacial Journal
, vol.35
, Issue.1
, pp. 40-45
-
-
Hagberg, C.1
Larson, O.2
Milerad, J.3
-
12
-
-
0019954428
-
The incidence of cleft lip and cleft palate in Nigeria
-
Iregbulem IM. The incidence of cleft lip and cleft palate in Nigeria. Cleft Palate J. 1982;19:201-205.
-
(1982)
Cleft Palate J
, vol.19
, pp. 201-205
-
-
Iregbulem, I.M.1
-
13
-
-
0038545785
-
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
-
Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE. Complete sequencing shows a role for MSX1 in nonsyndromic cleft lip and palate. J Med Genet. 2003;40:399-407. (Pubitemid 36760656)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.6
, pp. 399-407
-
-
Jezewski, P.A.1
Vieira, A.R.2
Nishimura, C.3
Ludwig, B.4
Johnson, M.5
O'Brien, S.E.6
Daack-Hirsch, S.7
Schultz, R.E.8
Weber, A.9
Nepomucena, B.10
Romitti, P.A.11
Christensen, K.12
Orioli, I.M.13
Castilla, E.E.14
Machida, J.15
Natsume, N.16
Murray, J.C.17
-
14
-
-
70349097584
-
The genetics of isolated orofacial clefts: From genotypes to subphenotypes
-
Jugessur A, Farlie PG, Kilpatrick N. The genetics of isolated orofacial clefts: from genotypes to subphenotypes. Oral Dis. 2009;15:437-453.
-
(2009)
Oral Dis
, vol.15
, pp. 437-453
-
-
Jugessur, A.1
Farlie, P.G.2
Kilpatrick, N.3
-
15
-
-
10744223971
-
Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains
-
DOI 10.1093/hmg/ddg329
-
Lavoie H, Debeane F, Trinh QD, Turcotte JF, Corbeil-Girard LP, Dicaire MJ, Saint- Denis A, Pagé M, Rouleau GA, Brais B. Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains. Hum Mol Genet. 2003;12:2967-2979. (Pubitemid 37442025)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.22
, pp. 2967-2979
-
-
Lavoie, H.1
Debeane, F.2
Trinh, Q.-D.3
Turcotte, J.-F.4
Corbeil-Girard, L.-P.5
Dicaire, M.-J.6
Saint-Denis, A.7
Page, M.8
Rouleau, G.A.9
Brais, B.10
-
17
-
-
0032231873
-
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
-
DOI 10.1086/301956
-
Lidral AC, Romiti PA, Basart AM, Doetschman T, Leysens NJ, Daack- Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, et al. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet. 1998;63:557-568. (Pubitemid 30418638)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.2
, pp. 557-568
-
-
Lidral, A.C.1
Romitti, P.A.2
Basart, A.M.3
Doetschman, T.4
Leysens, N.J.5
Daack-Hirsch, S.6
Semina, E.V.7
Johnson, L.R.8
Machida, J.9
Burds, A.10
Parnell, T.J.11
Rubenstein, J.L.R.12
Murray, J.C.13
-
18
-
-
73349086542
-
Susceptibility loci for non-syndromic cleft lip with or without cleft palate on chromosome 17q22 and 10q25.3
-
Mangold E, Ludwig KU, Birnbaum S, Baluardo C, Ferrian M, Herms S, Reutter H, Almeida de Assis N, Al Chawa T, Mattheisen M, et al. Susceptibility loci for non-syndromic cleft lip with or without cleft palate on chromosome 17q22 and 10q25.3. Nat Genet. 2010;42: 24-26.
-
(2010)
Nat Genet
, vol.42
, pp. 24-26
-
-
Mangold, E.1
Ludwig, K.U.2
Birnbaum, S.3
Baluardo, C.4
Ferrian, M.5
Herms, S.6
Reutter, H.7
Almeida De Assis, N.8
Al Chawa, T.9
Mattheisen, M.10
-
19
-
-
3242672318
-
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
-
DOI 10.1086/422475
-
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein TH, Maher BS, Daack-Hirsch S, Shultz S, Mansilla MA, et al. Meta-analysis of 13 gene scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet. 2004;75: 161-173. (Pubitemid 38943861)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.2
, pp. 161-173
-
-
Marazita, M.L.1
Murray, J.C.2
Lidral, A.C.3
Arcos-Burgos, M.4
Cooper, M.E.5
Goldstein, T.6
Maher, B.S.7
Daack-Hirsch, S.8
Schultz, R.9
Mansilla, M.A.10
Field, L.L.11
Liu, Y.-E.12
Prescott, N.13
Malcolm, S.14
Winter, R.15
Ray, A.16
Moreno, L.17
Valencia, C.18
Neiswanger, K.19
Wyszynski, D.F.20
Bailey-Wilson, J.E.21
Albacha-Hejazi, H.22
Beaty, T.H.23
McIntosh, I.24
Hetmanski, J.B.25
Tuncbilek, G.26
Edwards, M.27
Harkin, L.28
Scott, R.29
Roddick, L.G.30
more..
-
20
-
-
67349104211
-
Molecular mechanisms underlying polyalanine diseases
-
Messaed C, Rouleau GA. Molecular mechanisms underlying polyalanine diseases. Neurobiol Dis. 2009;34:397-405.
-
(2009)
Neurobiol Dis
, vol.34
, pp. 397-405
-
-
Messaed, C.1
Rouleau, G.A.2
-
21
-
-
33745369332
-
MSX1 and orofacial clefting with and without tooth agenes
-
DOI 10.1177/154405910608500612
-
Modesto A, Moreno LM, Krahn K, King S, Lidral AC. MSX1 and orofacial clefting with and without tooth agenesis. J Dent Res. 2006;85:542-546. (Pubitemid 43945493)
-
(2006)
Journal of Dental Research
, vol.85
, Issue.6
, pp. 542-546
-
-
Modesto, A.1
Moreno, L.M.2
Krahn, K.3
King, S.4
Lidral, A.C.5
-
22
-
-
70450191205
-
FOXE1 association with isolated cleft lip with or without cleft palate, and isolated cleft palate
-
Moreno LM, Mansilla MA, Bullard SA, Cooper ME, Busch TD, Machida J, Johnson MK, Brauer D, Krahn K, Daack-Hirsch S, et al. FOXE1 association with isolated cleft lip with or without cleft palate, and isolated cleft palate. Hum Mol Genet. 2009;18:4879-4896.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4879-4896
-
-
Moreno, L.M.1
Mansilla, M.A.2
Bullard, S.A.3
Cooper, M.E.4
Busch, T.D.5
Machida, J.6
Johnson, M.K.7
Brauer, D.8
Krahn, K.9
Daack-Hirsch, S.10
-
23
-
-
0242670655
-
Epidemiology of oral clefts: An international perspective
-
Wyszynski DF, ed. New York: Oxford University Press
-
Mossey PA, Little J. Epidemiology of oral clefts: an international perspective. In: Wyszynski DF, ed. Cleft Lip and Palate: From Origin to Treatment. New York: Oxford University Press; 2002.
-
(2002)
Cleft Lip and Palate: From Origin to Treatment
-
-
Mossey, P.A.1
Little, J.2
-
24
-
-
70449629175
-
Cleft lip and palate
-
Mossey PA, Little J, Munger RG, Dixon M, Shaw WC. Cleft lip and palate. Lancet. 2009;374:1773-1785.
-
(2009)
Lancet
, vol.374
, pp. 1773-1785
-
-
Mossey, P.A.1
Little, J.2
Munger, R.G.3
Dixon, M.4
Shaw, W.C.5
-
25
-
-
77954263310
-
Knowledge and cultural beliefs about the etiology and management of orofacial clefts in Nigeria's major ethnic groups
-
Oginni F, Asuku M, Oladele A, Obuekwe O, Nnabuko R. Knowledge and cultural beliefs about the etiology and management of orofacial clefts in Nigeria's major ethnic groups. Cleft Palate Craniofac J. 2010;47: 327-334.
-
(2010)
Cleft Palate Craniofac J
, vol.47
, pp. 327-334
-
-
Oginni, F.1
Asuku, M.2
Oladele, A.3
Obuekwe, O.4
Nnabuko, R.5
-
26
-
-
0027566907
-
Incidence of cleft lip and palate in a newborn Zairian sample
-
Ogle OE. Incidence of cleft lip and palate in a newborn Zairian sample. Cleft Palate Craniofac J. 1993;30:250-251.
-
(1993)
Cleft Palate Craniofac J
, vol.30
, pp. 250-251
-
-
Ogle, O.E.1
-
29
-
-
55049105999
-
Disruption of an AP-2a binding site in am IRF6 enhancer is strongly associated with cleft lip
-
Rahimov F, Marazita ML, Visel A, Cooper ME, Hitchler MJ, Rubini M, Domann FE, Govil M, Christensen K, Bille C, et al. Disruption of an AP-2a binding site in am IRF6 enhancer is strongly associated with cleft lip. Nat Genet. 2008;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
-
30
-
-
34248347081
-
Impaired FGF signaling contributes to cleft lip and palate
-
DOI 10.1073/pnas.0607956104
-
Riley BM, Mansilla MA, Ma J, Daack-Hirsch S, Maher BS, Raffensperger LM, Russo ET, Vieira AR, Dodé C, Mohammadi M, et al. Impaired FGF signaling contributes to cleft lip and palate. Proc Natl Acad Sci U S A. 2007;104:4512-4517. (Pubitemid 47186256)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.11
, pp. 4512-4517
-
-
Riley, B.M.1
Mansilla, M.A.2
Ma, J.3
Daack-Hirsch, S.4
Maher, B.S.5
Raffensperger, L.M.6
Russo, E.T.7
Vieira, A.R.8
Dode, C.9
Mohammad, M.10
Marazita, M.L.11
Murray, J.C.12
-
31
-
-
0028292605
-
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
-
DOI 10.1038/ng0494-348
-
Satokata I, Maas R. MSX1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet. 1994;6:348-356. (Pubitemid 24190017)
-
(1994)
Nature Genetics
, vol.6
, Issue.4
, pp. 348-356
-
-
Satokata, I.1
Maas, R.2
-
32
-
-
56749097071
-
Genes causing clefting syndromes as candidates for nonsyndromic cleft lip with or without cleft palate: A family-based association study
-
Scapoli L, Martinelli M, Arlotti M, Palmieri A, Masiero E, Pezzetti F, Carinci F. Genes causing clefting syndromes as candidates for nonsyndromic cleft lip with or without cleft palate: a family-based association study. Eur J Oral Sci. 2008;116:507-511.
-
(2008)
Eur J Oral Sci
, vol.116
, pp. 507-511
-
-
Scapoli, L.1
Martinelli, M.2
Arlotti, M.3
Palmieri, A.4
Masiero, E.5
Pezzetti, F.6
Carinci, F.7
-
33
-
-
0021967526
-
Culture, rehabilitation, and facial birth defects: International case studies
-
Strauss RP. Culture, rehabilitation, and facial birth defects: international case studies. Cleft Palate J. 1985;22:56-62. (Pubitemid 15171790)
-
(1985)
Cleft Palate Journal
, vol.22
, Issue.1
, pp. 56-62
-
-
Strauss, R.P.1
-
34
-
-
61849147400
-
Mutations in BMP4 are associated with sub-epithelial, microform, and overt cleft lip
-
Suzuki S, Marazita ML, Cooper ME, Miwa N, Hing A, Jugessur A, Natsume N, Shimozato K, Ohbayashi N, Suzuki Y, et al. Mutations in BMP4 are associated with sub-epithelial, microform, and overt cleft lip. Am J Hum Genet. 2009;84:406-411.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 406-411
-
-
Suzuki, S.1
Marazita, M.L.2
Cooper, M.E.3
Miwa, N.4
Hing, A.5
Jugessur, A.6
Natsume, N.7
Shimozato, K.8
Ohbayashi, N.9
Suzuki, Y.10
-
35
-
-
2642522952
-
In a Vietnamese population, MSX1 variants contribute to cleft lip and palate
-
DOI 10.1097/01.GIM.0000127275.52925.05
-
Suzuki Y, Jezewski P, Machida J, Watanabe Y, Min Shi MS, Cooper ME, Viet LT, Nguyen TDT, Hai H, Natsume N, et al. In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genet Med. 2004;6:117-125. (Pubitemid 38715502)
-
(2004)
Genetics in Medicine
, vol.6
, Issue.3
, pp. 117-125
-
-
Suzuki, Y.1
Jezewski, P.A.2
Machida, J.3
Watanabe, Y.4
Shi, M.5
Cooper, M.E.6
Viet, L.T.7
Tin, N.T.D.8
Hai, H.9
Natsume, N.10
Shimozato, K.11
Marazita, M.L.12
Murray, J.C.13
-
36
-
-
84904517258
-
Classification and birth prevalence of orofacial clefts
-
Tolarova MM, Cervenka J. Classification and birth prevalence of orofacial clefts. Nat Genet. 1995;11:415-421.
-
(1995)
Nat Genet
, vol.11
, pp. 415-421
-
-
Tolarova, M.M.1
Cervenka, J.2
-
37
-
-
77952880032
-
MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population
-
DOI 10.1007/s10038-006-0006-4
-
Tongkobpetch S, Siriwan P, Shotelersuk V. MSX1 mutation contribute to nonsyndromic cleft lip in Thai population. J Human Genet. 2006;51:671-676. (Pubitemid 44354678)
-
(2006)
Journal of Human Genetics
, vol.51
, Issue.8
, pp. 671-676
-
-
Tongkobpetch, S.1
Siriwan, P.2
Shotelersuk, V.3
-
38
-
-
24644469155
-
Mutation analysis of CLPTM 1 and PVRL 1 genes in patients with non-syndromic clefts of lip, alveolus and palate
-
DOI 10.1016/j.jcms.2005.04.004, PII S1010518205000880
-
Turhani D, Item CB, Watzinger E, Sinko K, Watzinger F, Lauer G, Ewers R. Mutation analysis of CLPTM 1 and PVRL 1 genes in patients with non-syndromic clefts of lip, alveolus and palate. J Craniomaxillofac Surg. 2005;33:301-306. (Pubitemid 41283246)
-
(2005)
Journal of Cranio-Maxillofacial Surgery
, vol.33
, Issue.5
, pp. 301-306
-
-
Turhani, D.1
Item, C.B.2
Watzinger, E.3
Sinko, K.4
Watzinger, F.5
Lauer, G.6
Ewers, R.7
-
39
-
-
57049154545
-
The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts
-
van den Boogaard MJ, de Costa D, Krapels IP, Liu F, van Duijn C, Sinke RJ, Lindhout D, Steegers-Theunissen RP. The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts. Hum Genet. 2008;124:525-534.
-
(2008)
Hum Genet
, vol.124
, pp. 525-534
-
-
Van Den Boogaard, M.J.1
De Costa, D.2
Krapels, I.P.3
Liu, F.4
Van Duijn, C.5
Sinke, R.J.6
Lindhout, D.7
Steegers-Theunissen, R.P.8
-
40
-
-
0030017452
-
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
-
DOI 10.1038/ng0896-417
-
Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet. 1996;13:417-421. (Pubitemid 26256614)
-
(1996)
Nature Genetics
, vol.13
, Issue.4
, pp. 417-421
-
-
Vastardis, H.1
Karimbux, N.2
Guthua, S.W.3
Seidman, J.G.4
Seidman, C.E.5
-
41
-
-
34547516140
-
Medical sequencing of candidate genes for nonsyndromic cleftlip and palate
-
Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Felix TM, Rahimov F, Harrington J, Schultz RR, Watanabe Y, Johnson M, et al. Medical sequencing of candidate genes for nonsyndromic cleftlip and palate. PLoS Genet. 2005;1:e64.
-
(2005)
PLoS Genet
, vol.1
-
-
Vieira, A.R.1
Avila, J.R.2
Daack-Hirsch, S.3
Dragan, E.4
Felix, T.M.5
Rahimov, F.6
Harrington, J.7
Schultz, R.R.8
Watanabe, Y.9
Johnson, M.10
-
42
-
-
12344300197
-
Análisis mutacional del gen homeobox de segmento muscular 1 (MSX1) en chilenos con fisuras orales
-
Vieira AR, Castillo Taucher S, Aravena T, Astete C, Sanz P, Tastets ME, Monasterio L, Murray JC. Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate. Rev Med Chil. 2004;132:816-822. (Pubitemid 40137685)
-
(2004)
Revista Medica de Chile
, vol.132
, Issue.7
, pp. 816-822
-
-
Vieira, A.R.1
Taucher, S.C.2
Aravena, T.3
Astete, C.4
Sanz, P.5
Tastets, M.E.6
Monasterio, L.7
Murray, J.C.8
-
46
-
-
45049086606
-
Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia
-
Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia. Arch Oral Biol. 2008;53:773-779.
-
(2008)
Arch Oral Biol
, vol.53
, pp. 773-779
-
-
Xuan, K.1
Jin, F.2
Liu, Y.L.3
Yuan, L.T.4
Wen, L.Y.5
Yang, F.S.6
Wang, X.J.7
Wang, G.H.8
Jin, Y.9
-
47
-
-
0029944653
-
A role for the Msx-1 homeodomain in transcriptional regulation: Residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression
-
DOI 10.1073/pnas.93.5.1764
-
Zhang H, Catron KM, Abate-Shen C. A role for the Msx-1 homeodomain in transcriptional regulation: residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression. Proc Natl Acad Sci U S A. 1996;93:1764-1769. (Pubitemid 26079831)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.5
, pp. 1764-1769
-
-
Zhang, H.1
Catron, K.M.2
Abate-Shen, C.3
-
48
-
-
4143115809
-
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
-
DOI 10.1056/NEJMoa032909
-
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribiero L, Caprau D, Christensen K, Suzuki Y, Machida J, et al. Interferon regulatory factor 6 (IRF6) gene variants and the risks of isolated cleft lip or palate. N Engl J Med. 2004;351:769-780. (Pubitemid 39095312)
-
(2004)
New England Journal of Medicine
, vol.351
, Issue.8
, pp. 769-780
-
-
Zucchero, T.M.1
Cooper, M.E.2
Maher, B.S.3
Daack-Hirsch, S.4
Nepomuceno, B.5
Ribeiro, L.6
Caprau, D.7
Christensen, K.8
Suzuki, Y.9
Machida, J.10
Natsume, N.11
Yoshiura, K.-I.12
Vieira, A.R.13
Orioli, I.M.14
Castilla, E.E.15
Moreno, L.16
Arcos-Burgos, M.17
Lidral, A.C.18
Field, L.L.19
Liu, Y.-E.20
Ray, A.21
Goldstein, T.H.22
Schultz, R.E.23
Shi, M.24
Johnson, M.K.25
Kondo, S.26
Schutte, B.C.27
Marazita, M.L.28
Murray, J.C.29
more..
|