Bamforth SD, Braganca J, Eloranta JJ, Murdoch JN, Marques FI, Kranc KR, Farza H, Henderson DJ, Hurst HC, Bhattacharya S: Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator. Nat Genet. 2001, 29: 469-474. 10.1038/ng768.
Article
CAS
PubMed
Google Scholar
Barbera JP, Rodriguez TA, Greene ND, Weninger WJ, Simeone A, Copp AJ, Beddington RS, Dunwoodie S: Folic acid prevents exencephaly in Cited2 deficient mice. Hum Mol Genet. 2002, 11: 283-293. 10.1093/hmg/11.3.283.
Article
CAS
PubMed
Google Scholar
Bhattacherjee V, Horn KH, Singh S, Webb CL, Pisano MM, Greene RM: CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development. Int J Dev Biol. 2009, 53: 1097-1104. 10.1387/ijdb.072489vb.
Article
CAS
PubMed
PubMed Central
Google Scholar
Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RC, Masuno M, Tommerup N, van Ommen GJ, Goodman RH, Peters DJ, et al: Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature. 1995, 376: 348-351. 10.1038/376348a0.
Article
CAS
PubMed
Google Scholar
Tanaka Y, Naruse I, Hongo T, Xu M, Nakahata T, Maekawa T, Ishii S: Extensive brain hemorrhage and embryonic lethality in a mouse null mutant of CREB-binding protein. Mech Dev. 2000, 95: 133-145. 10.1016/S0925-4773(00)00360-9.
Article
CAS
PubMed
Google Scholar
Weninger WJ, Lopes Floro K, Bennett MB, Withington SL, Preis JI, Barbera JP, Mohun TJ, Dunwoodie SL: Cited2 is required both for heart morphogenesis and establishment of the left-right axis in mouse development. Development. 2005, 132: 1337-1348. 10.1242/dev.01696.
Article
CAS
PubMed
Google Scholar
Yadav N, Lee J, Kim J, Shen J, Hu MC, Aldaz CM, Bedford MT: Specific protein methylation defects and gene expression perturbations in coactivator-associated arginine methyltransferase 1-deficient mice. Proc Natl Acad Sci USA. 2003, 100: 6464-6468. 10.1073/pnas.1232272100.
Article
CAS
PubMed
PubMed Central
Google Scholar
Yao TP, Oh SP, Fuchs M, Zhou ND, Ch'ng LE, Newsome D, Bronson RT, Li E, Livingston DM, Eckner R: Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300. Cell. 1998, 93: 361-372. 10.1016/S0092-8674(00)81165-4.
Article
CAS
PubMed
Google Scholar
Zhao Q, Behringer RR, de Crombrugghe B: Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nat Genet. 1996, 13: 275-283. 10.1038/ng0796-275.
Article
CAS
PubMed
Google Scholar
Kitabayashi I, Aikawa Y, Nguyen LA, Yokoyama A, Ohki M: Activation of AML1-mediated transcription by MOZ and inhibition by the MOZ-CBP fusion protein. EMBO J. 2001, 20: 7184-7196. 10.1093/emboj/20.24.7184.
Article
CAS
PubMed
PubMed Central
Google Scholar
Xu W, Chen H, Du K, Asahara H, Tini M, Emerson BM, Montminy M, Evans RM: A transcriptional switch mediated by cofactor methylation. Science. 2001, 294: 2507-2511. 10.1126/science.1065961.
Article
CAS
PubMed
Google Scholar
Jayne S, Rothgiesser KM, Hottiger MO: CARM1 but not its enzymatic activity is required for transcriptional coactivation of NF-kappaB-dependent gene expression. J Mol Biol. 2009, 394: 485-495. 10.1016/j.jmb.2009.09.032.
Article
CAS
PubMed
Google Scholar
Chen SL, Loffler KA, Chen D, Stallcup MR, Muscat GE: The coactivator-associated arginine methyltransferase is necessary for muscle differentiation: CARM1 coactivates myocyte enhancer factor-2. J Biol Chem. 2002, 277: 4324-4333. 10.1074/jbc.M109835200.
Article
CAS
PubMed
Google Scholar
Volcik KA, Zhu H, Finnell RH, Shaw GM, Canfield M, Lammer EJ: Evaluation of the Cited2 gene and risk for spina bifida and congenital heart defects. Am J Med Genet A. 2004, 126A: 324-325. 10.1002/ajmg.a.20578.
Article
PubMed
Google Scholar
Yin Z, Haynie J, Yang X, Han B, Kiatchoosakun S, Restivo J, Yuan S, Prabhakar NR, Herrup K, Conlon RA, et al: The essential role of Cited2, a negative regulator for HIF-1alpha, in heart development and neurulation. Proc Natl Acad Sci USA. 2002, 99: 10488-10493. 10.1073/pnas.162371799.
Article
CAS
PubMed
PubMed Central
Google Scholar
Braganca J, Eloranta JJ, Bamforth SD, Ibbitt JC, Hurst HC, Bhattacharya S: Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2. J Biol Chem. 2003, 278: 16021-16029. 10.1074/jbc.M208144200.
Article
CAS
PubMed
Google Scholar
Zhang J, Hagopian-Donaldson S, Serbedzija G, Elsemore J, Plehn-Dujowich D, McMahon AP, Flavell RA, Williams T: Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2. Nature. 1996, 381: 238-241. 10.1038/381238a0.
Article
CAS
PubMed
Google Scholar
Schorle H, Meier P, Buchert M, Jaenisch R, Mitchell PJ: Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature. 1996, 381: 235-238. 10.1038/381235a0.
Article
CAS
PubMed
Google Scholar
Nottoli T, Hagopian-Donaldson S, Zhang J, Perkins A, Williams T: AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice. Proc Natl Acad Sci USA. 1998, 95: 13714-13719. 10.1073/pnas.95.23.13714.
Article
CAS
PubMed
PubMed Central
Google Scholar
Iioka T, Furukawa K, Yamaguchi A, Shindo H, Yamashita S, Tsukazaki T: P300/CBP acts as a coactivator to cartilage homeoprotein-1 (Cart1), paired-like homeoprotein, through acetylation of the conserved lysine residue adjacent to the homeodomain. J Bone Miner Res. 2003, 18: 1419-1429. 10.1359/jbmr.2003.18.8.1419.
Article
CAS
PubMed
Google Scholar
Zhao GQ, Zhou X, Eberspaecher H, Solursh M, de Crombrugghe B: Cartilage homeoprotein 1, a homeoprotein selectively expressed in chondrocytes. Proc Natl Acad Sci USA. 1993, 90: 8633-8637. 10.1073/pnas.90.18.8633.
Article
CAS
PubMed
PubMed Central
Google Scholar
Zhao GQ, Eberspaecher H, Seldin MF, de Crombrugghe B: The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development. Mech Dev. 1994, 48: 245-254. 10.1016/0925-4773(94)90063-9.
Article
CAS
PubMed
Google Scholar
Harris MJ: Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants. Birth Defects Res A Clin Mol Teratol. 2009, 85: 331-339. 10.1002/bdra.20552.
Article
CAS
PubMed
Google Scholar
Croen LA, Shaw GM, Jensvold NG, Harris JA: Birth defects monitoring in California: a resource for epidemiological research. Paediatr Perinat Epidemiol. 1991, 5: 423-427. 10.1111/j.1365-3016.1991.tb00728.x.
Article
CAS
PubMed
Google Scholar
De La Vega FM, Isaac HI, Scafe CR: A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns. Pac Symp Biocomput. 2006, 487-498. full_text.
Google Scholar
Baluja KF, Park J, Myers D: Inclusion of immigrant status in smoking prevalence statistics. Am J Public Health. 2003, 93: 642-646. 10.2105/AJPH.93.4.642.
Article
PubMed
PubMed Central
Google Scholar
Curry CJ, Lammer EJ, Nelson V, Shaw GM: Schizencephaly: heterogeneous etiologies in a population of 4 million California births. Am J Med Genet A. 2005, 137: 181-189.
Article
PubMed
Google Scholar
Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. Journal of the Royal Statistical Society Series B, Statistical methodology. 1995, 57: 289-
Google Scholar