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Results: 1 to 20 of 38

1.

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.

Sugathan A, Biagioli M, Golzio C, Erdin S, Blumenthal I, Manavalan P, Ragavendran A, Brand H, Lucente D, Miles J, Sheridan SD, Stortchevoi A, Kellis M, Haggarty SJ, Katsanis N, Gusella JF, Talkowski ME.

Proc Natl Acad Sci U S A. 2014 Oct 7. pii: 201405266. [Epub ahead of print]

PMID:
25294932
[PubMed - as supplied by publisher]
2.

Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly.

Prontera P, Ottaviani V, Toccaceli D, Rogaia D, Ardisia C, Romani R, Stangoni G, Pierini A, Donti E.

Am J Med Genet A. 2014 Sep 24. doi: 10.1002/ajmg.a.36741. [Epub ahead of print]

PMID:
25257502
[PubMed - as supplied by publisher]
3.

The BRAF Oncoprotein Functions through the Transcriptional Repressor MAFG to Mediate the CpG Island Methylator Phenotype.

Fang M, Ou J, Hutchinson L, Green MR.

Mol Cell. 2014 Sep 18;55(6):904-15. doi: 10.1016/j.molcel.2014.08.010. Epub 2014 Sep 11.

PMID:
25219500
[PubMed - in process]
4.

[Progress in autism: de novo mutation and CHD8 functions].

Xiong XX, He M, Chen XQ.

Sheng Li Ke Xue Jin Zhan. 2014 Jun;45(3):185-9. Chinese.

PMID:
25219269
[PubMed - in process]
5.

Pathogenesis of CpG island methylator phenotype-positive colorectal cancers: role of genetic alteration and colonic flora.

Tahara T, Arisawa T.

Epigenomics. 2014 Jun;6(3):249-51. doi: 10.2217/epi.14.25. No abstract available.

PMID:
25111477
[PubMed - in process]
6.

Disruptive CHD8 mutations define a subtype of autism early in development.

Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, Schuurs-Hoeijmakers JH, Fichera M, Bosco P, Buono S, Alberti A, Failla P, Peeters H, Steyaert J, Vissers LE, Francescatto L, Mefford HC, Rosenfeld JA, Bakken T, O'Roak BJ, Pawlus M, Moon R, Shendure J, Amaral DG, Lein E, Rankin J, Romano C, de Vries BB, Katsanis N, Eichler EE.

Cell. 2014 Jul 17;158(2):263-76. doi: 10.1016/j.cell.2014.06.017. Epub 2014 Jul 3.

PMID:
24998929
[PubMed - in process]
7.

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.

Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ, Ernst C, Roeder K, Devlin B, Gusella JF, Talkowski ME.

Am J Hum Genet. 2014 Jun 5;94(6):870-83. doi: 10.1016/j.ajhg.2014.05.004.

PMID:
24906019
[PubMed - indexed for MEDLINE]
8.

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.

McCarthy SE, Gillis J, Kramer M, Lihm J, Yoon S, Berstein Y, Mistry M, Pavlidis P, Solomon R, Ghiban E, Antoniou E, Kelleher E, O'Brien C, Donohoe G, Gill M, Morris DW, McCombie WR, Corvin A.

Mol Psychiatry. 2014 Jun;19(6):652-8. doi: 10.1038/mp.2014.29. Epub 2014 Apr 29.

PMID:
24776741
[PubMed - in process]
9.

A de novo convergence of autism genetics and molecular neuroscience.

Krumm N, O'Roak BJ, Shendure J, Eichler EE.

Trends Neurosci. 2014 Feb;37(2):95-105. doi: 10.1016/j.tins.2013.11.005. Epub 2013 Dec 30. Review.

PMID:
24387789
[PubMed - indexed for MEDLINE]
10.

Fusobacterium in colonic flora and molecular features of colorectal carcinoma.

Tahara T, Yamamoto E, Suzuki H, Maruyama R, Chung W, Garriga J, Jelinek J, Yamano HO, Sugai T, An B, Shureiqi I, Toyota M, Kondo Y, Estécio MR, Issa JP.

Cancer Res. 2014 Mar 1;74(5):1311-8. doi: 10.1158/0008-5472.CAN-13-1865. Epub 2014 Jan 2.

PMID:
24385213
[PubMed - indexed for MEDLINE]
11.

The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes.

Subtil-Rodríguez A, Vázquez-Chávez E, Ceballos-Chávez M, Rodríguez-Paredes M, Martín-Subero JI, Esteller M, Reyes JC.

Nucleic Acids Res. 2014 Feb;42(4):2185-96. doi: 10.1093/nar/gkt1161. Epub 2013 Nov 21.

PMID:
24265227
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome.

Terrone G, Cappuccio G, Genesio R, Esposito A, Fiorentino V, Riccitelli M, Nitsch L, Brunetti-Pierri N, Del Giudice E.

Am J Med Genet A. 2014 Jan;164A(1):190-3. doi: 10.1002/ajmg.a.36200. Epub 2013 Nov 15.

PMID:
24243641
[PubMed - in process]
13.

Colorectal carcinomas with CpG island methylator phenotype 1 frequently contain mutations in chromatin regulators.

Tahara T, Yamamoto E, Madireddi P, Suzuki H, Maruyama R, Chung W, Garriga J, Jelinek J, Yamano HO, Sugai T, Kondo Y, Toyota M, Issa JP, Estécio MR.

Gastroenterology. 2014 Feb;146(2):530-38.e5. doi: 10.1053/j.gastro.2013.10.060. Epub 2013 Nov 6.

PMID:
24211491
[PubMed - indexed for MEDLINE]
14.

A new small supernumerary marker chromosome involving 14pter → q12 in a child with severe neurodevelopmental retardation: case report and literature review.

Qi M, Zhao Y, Wang Y, Li T.

Gene. 2013 Dec 1;531(2):457-61. doi: 10.1016/j.gene.2013.08.084. Epub 2013 Sep 5. Review.

PMID:
24013083
[PubMed - indexed for MEDLINE]
15.

CHD8 is an independent prognostic indicator that regulates Wnt/β-catenin signaling and the cell cycle in gastric cancer.

Sawada G, Ueo H, Matsumura T, Uchi R, Ishibashi M, Mima K, Kurashige J, Takahashi Y, Akiyoshi S, Sudo T, Sugimachi K, Doki Y, Mori M, Mimori K.

Oncol Rep. 2013 Sep;30(3):1137-42. doi: 10.3892/or.2013.2597. Epub 2013 Jul 8.

PMID:
23835524
[PubMed - indexed for MEDLINE]
16.

Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disorders.

Griesi-Oliveira K, Sunaga DY, Alvizi L, Vadasz E, Passos-Bueno MR.

Autism Res. 2013 Oct;6(5):354-61. doi: 10.1002/aur.1296. Epub 2013 Jun 25.

PMID:
23801657
[PubMed - indexed for MEDLINE]
Free Article
17.

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.

PMID:
23568486
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Identification and characterization of FAM124B as a novel component of a CHD7 and CHD8 containing complex.

Batsukh T, Schulz Y, Wolf S, Rabe TI, Oellerich T, Urlaub H, Schaefer IM, Pauli S.

PLoS One. 2012;7(12):e52640. doi: 10.1371/journal.pone.0052640. Epub 2012 Dec 21.

PMID:
23285124
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

O'Roak BJ, Vives L, Fu W, Egertson JD, Stanaway IB, Phelps IG, Carvill G, Kumar A, Lee C, Ankenman K, Munson J, Hiatt JB, Turner EH, Levy R, O'Day DR, Krumm N, Coe BP, Martin BK, Borenstein E, Nickerson DA, Mefford HC, Doherty D, Akey JM, Bernier R, Eichler EE, Shendure J.

Science. 2012 Dec 21;338(6114):1619-22. doi: 10.1126/science.1227764. Epub 2012 Nov 15.

PMID:
23160955
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Chromodomain helicase binding protein 8 (Chd8) is a novel A-kinase anchoring protein expressed during rat cardiac development.

Shanks MO, Lund LM, Manni S, Russell M, Mauban JR, Bond M.

PLoS One. 2012;7(10):e46316. doi: 10.1371/journal.pone.0046316. Epub 2012 Oct 10.

PMID:
23071553
[PubMed - indexed for MEDLINE]
Free PMC Article

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