Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 59


Brain size regulations by cbp haploinsufficiency evaluated by in-vivo MRI based volumetry.

Ateca-Cabarga JC, Cosa A, Pallarés V, López-Atalaya JP, Barco Á, Canals S, Moratal D.

Sci Rep. 2015 Nov 6;5:16256. doi: 10.1038/srep16256.


FGFR2 mutation in 46,XY sex reversal with craniosynostosis.

Bagheri-Fam S, Ono M, Li L, Zhao L, Ryan J, Lai R, Katsura Y, Rossello FJ, Koopman P, Scherer G, Bartsch O, Eswarakumar JV, Harley VR.

Hum Mol Genet. 2015 Dec 1;24(23):6699-710. doi: 10.1093/hmg/ddv374. Epub 2015 Sep 11.


Exome Sequencing Identification of EP300 Mutation in a Proband with Coloboma and Imperforate Anus: Possible Expansion of the Phenotypic Spectrum of Rubinstein-Taybi Syndrome.

Masuda K, Akiyama K, Arakawa M, Nishi E, Kitazawa N, Higuchi T, Katou Y, Shirahige K, Izumi K.

Mol Syndromol. 2015 Jul;6(2):99-103. doi: 10.1159/000375542. Epub 2015 Mar 3.


Face scanning and spontaneous emotion preference in Cornelia de Lange syndrome and Rubinstein-Taybi syndrome.

Crawford H, Moss J, McCleery JP, Anderson GM, Oliver C.

J Neurodev Disord. 2015;7(1):22. doi: 10.1186/s11689-015-9119-4. Epub 2015 Jul 30.


Mutation burden of rare variants in schizophrenia candidate genes.

Girard SL, Dion PA, Bourassa CV, Geoffroy S, Lachance-Touchette P, Barhdadi A, Langlois M, Joober R, Krebs MO, Dubé MP, Rouleau GA.

PLoS One. 2015 Jun 3;10(6):e0128988. doi: 10.1371/journal.pone.0128988. eCollection 2015.


Whole exome sequencing for a patient with Rubinstein-Taybi syndrome reveals de novo variants besides an overt CREBBP mutation.

Yoo HJ, Kim K, Kim IH, Rho SH, Park JE, Lee KY, Kim SA, Choi BY, Kim N.

Int J Mol Sci. 2015 Mar 11;16(3):5697-713. doi: 10.3390/ijms16035697.


The roles of post-translational modifications in the context of protein interaction networks.

Duan G, Walther D.

PLoS Comput Biol. 2015 Feb 18;11(2):e1004049. doi: 10.1371/journal.pcbi.1004049. eCollection 2015 Feb.


Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management.

Milani D, Manzoni FM, Pezzani L, Ajmone P, Gervasini C, Menni F, Esposito S.

Ital J Pediatr. 2015 Jan 20;41:4. doi: 10.1186/s13052-015-0110-1.


Deficiency of the chromatin regulator BRPF1 causes abnormal brain development.

You L, Zou J, Zhao H, Bertos NR, Park M, Wang E, Yang XJ.

J Biol Chem. 2015 Mar 13;290(11):7114-29. doi: 10.1074/jbc.M114.635250. Epub 2015 Jan 7.


Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant Behavior.

Butler MG, Usrey K, Roberts JL, Schroeder SR, Manzardo AM.

Genet Res Int. 2014;2014:408516. doi: 10.1155/2014/408516. Epub 2014 Oct 20.


Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin states.

Fahrner JA, Bjornsson HT.

Annu Rev Genomics Hum Genet. 2014;15:269-93. doi: 10.1146/annurev-genom-090613-094245. Review.


Insights into synaptic function from mouse models of human cognitive disorders.

Banko JL, Trotter J, Weeber EJ.

Future Neurol. 2011 Jan;6(1):113-125.


Histone acetyltransferases in plant development and plasticity.

Boycheva I, Vassileva V, Iantcheva A.

Curr Genomics. 2014 Feb;15(1):28-37. doi: 10.2174/138920291501140306112742.


METTL23, a transcriptional partner of GABPA, is essential for human cognition.

Reiff RE, Ali BR, Baron B, Yu TW, Ben-Salem S, Coulter ME, Schubert CR, Hill RS, Akawi NA, Al-Younes B, Kaya N, Evrony GD, Al-Saffar M, Felie JM, Partlow JN, Sunu CM, Schembri-Wismayer P, Alkuraya FS, Meyer BF, Walsh CA, Al-Gazali L, Mochida GH.

Hum Mol Genet. 2014 Jul 1;23(13):3456-66. doi: 10.1093/hmg/ddu054. Epub 2014 Feb 5.


Genetic interaction between mutations in c-Myb and the KIX domains of CBP and p300 affects multiple blood cell lineages and influences both gene activation and repression.

Kasper LH, Fukuyama T, Lerach S, Chang Y, Xu W, Wu S, Boyd KL, Brindle PK.

PLoS One. 2013 Dec 10;8(12):e82684. doi: 10.1371/journal.pone.0082684. eCollection 2013.


Acetyltransferases (HATs) as targets for neurological therapeutics.

Schneider A, Chatterjee S, Bousiges O, Selvi BR, Swaminathan A, Cassel R, Blanc F, Kundu TK, Boutillier AL.

Neurotherapeutics. 2013 Oct;10(4):568-88. doi: 10.1007/s13311-013-0204-7. Review.


Of mice and men: molecular genetics of congenital heart disease.

Andersen TA, Troelsen Kde L, Larsen LA.

Cell Mol Life Sci. 2014 Apr;71(8):1327-52. doi: 10.1007/s00018-013-1430-1. Epub 2013 Aug 10. Review.


Differences in specificity and selectivity between CBP and p300 acetylation of histone H3 and H3/H4.

Henry RA, Kuo YM, Andrews AJ.

Biochemistry. 2013 Aug 27;52(34):5746-59. doi: 10.1021/bi400684q. Epub 2013 Aug 12.


From neural development to cognition: unexpected roles for chromatin.

Ronan JL, Wu W, Crabtree GR.

Nat Rev Genet. 2013 May;14(5):347-59. doi: 10.1038/nrg3413. Epub 2013 Apr 9. Review. Erratum in: Nat Rev Genet. 2013 Jun;14(6):440.


Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders.

Valor LM, Viosca J, Lopez-Atalaya JP, Barco A.

Curr Pharm Des. 2013;19(28):5051-64. Review.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk