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Items: 1 to 20 of 104

1.

Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development.

Liu Z, Zhang N, Zhang Y, Du Y, Zhang T, Li Z, Wu J, Wang X.

Front Genet. 2018 Sep 18;9:349. doi: 10.3389/fgene.2018.00349. eCollection 2018.

2.

Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes.

Kasah S, Oddy C, Basson MA.

J Anat. 2018 Oct 2. doi: 10.1111/joa.12889. [Epub ahead of print]

PMID:
30277262
3.

Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer.

Wagner AH, Devarakonda S, Skidmore ZL, Krysiak K, Ramu A, Trani L, Kunisaki J, Masood A, Waqar SN, Spies NC, Morgensztern D, Waligorski J, Ponce J, Fulton RS, Maggi LB Jr, Weber JD, Watson MA, O'Conor CJ, Ritter JH, Olsen RR, Cheng H, Mukhopadhyay A, Can I, Cessna MH, Oliver TG, Mardis ER, Wilson RK, Griffith M, Griffith OL, Govindan R.

Nat Commun. 2018 Sep 17;9(1):3787. doi: 10.1038/s41467-018-06162-9.

4.

Regulatory genes and pathways disrupted in autism spectrum disorders.

Ayhan F, Konopka G.

Prog Neuropsychopharmacol Biol Psychiatry. 2018 Aug 28;89:57-64. doi: 10.1016/j.pnpbp.2018.08.017. [Epub ahead of print] Review.

PMID:
30165121
5.

Sex bias in autism: new insights from Chd8 mutant mice?

Andreae LC, Basson MA.

Nat Neurosci. 2018 Sep;21(9):1144-1146. doi: 10.1038/s41593-018-0217-y. No abstract available.

PMID:
30127425
6.

Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8.

Marie C, Clavairoly A, Frah M, Hmidan H, Yan J, Zhao C, Van Steenwinckel J, Daveau R, Zalc B, Hassan B, Thomas JL, Gressens P, Ravassard P, Moszer I, Martin DM, Lu QR, Parras C.

Proc Natl Acad Sci U S A. 2018 Aug 28;115(35):E8246-E8255. doi: 10.1073/pnas.1802620115. Epub 2018 Aug 14.

7.

The autism spectrum phenotype in ADNP syndrome.

Arnett AB, Rhoads CL, Hoekzema K, Turner TN, Gerdts J, Wallace AS, Bedrosian-Sermone S, Eichler EE, Bernier RA.

Autism Res. 2018 Aug 14. doi: 10.1002/aur.1980. [Epub ahead of print]

PMID:
30107084
8.

Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice.

Jung H, Park H, Choi Y, Kang H, Lee E, Kweon H, Roh JD, Ellegood J, Choi W, Kang J, Rhim I, Choi SY, Bae M, Kim SG, Lee J, Chung C, Yoo T, Park H, Kim Y, Ha S, Um SM, Mo S, Kwon Y, Mah W, Bae YC, Kim H, Lerch JP, Paik SB, Kim E.

Nat Neurosci. 2018 Sep;21(9):1218-1228. doi: 10.1038/s41593-018-0208-z. Epub 2018 Aug 13.

PMID:
30104731
9.

Identification of common differentially-expressed miRNAs in ovarian cancer cells and their exosomes compared with normal ovarian surface epithelial cell cells.

Zhang S, Zhang X, Fu X, Li W, Xing S, Yang Y.

Oncol Lett. 2018 Aug;16(2):2391-2401. doi: 10.3892/ol.2018.8954. Epub 2018 Jun 12.

10.

Chromatin Remodeling Proteins in Epilepsy: Lessons From CHD2-Associated Epilepsy.

Lamar KJ, Carvill GL.

Front Mol Neurosci. 2018 Jun 15;11:208. doi: 10.3389/fnmol.2018.00208. eCollection 2018. Review.

11.

Molecular Characterization and Putative Pathogenic Pathways of Tuberous Sclerosis Complex-Associated Renal Cell Carcinoma.

Park JH, Lee C, Chang MS, Kim K, Choi S, Lee H, Lee HS, Moon KC.

Transl Oncol. 2018 Aug;11(4):962-970. doi: 10.1016/j.tranon.2018.05.010. Epub 2018 Jun 18.

12.

Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and Repair.

Zhao C, Dong C, Frah M, Deng Y, Marie C, Zhang F, Xu L, Ma Z, Dong X, Lin Y, Koenig S, Nait-Oumesmar B, Martin DM, Wu LN, Xin M, Zhou W, Parras C, Lu QR.

Dev Cell. 2018 Jun 18;45(6):753-768.e8. doi: 10.1016/j.devcel.2018.05.022.

PMID:
29920279
13.

The Autism-Related Protein CHD8 Cooperates with C/EBPβ to Regulate Adipogenesis.

Kita Y, Katayama Y, Shiraishi T, Oka T, Sato T, Suyama M, Ohkawa Y, Miyata K, Oike Y, Shirane M, Nishiyama M, Nakayama KI.

Cell Rep. 2018 May 15;23(7):1988-2000. doi: 10.1016/j.celrep.2018.04.050.

14.

Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.

Suetterlin P, Hurley S, Mohan C, Riegman KLH, Pagani M, Caruso A, Ellegood J, Galbusera A, Crespo-Enriquez I, Michetti C, Yee Y, Ellingford R, Brock O, Delogu A, Francis-West P, Lerch JP, Scattoni ML, Gozzi A, Fernandes C, Basson MA.

Cereb Cortex. 2018 Jun 1;28(6):2192-2206. doi: 10.1093/cercor/bhy058.

15.

Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid.

Mao Q, Chin R, Xie W, Deng Y, Zhang W, Xu H, Zhang RY, Shi Q, Peters EE, Gulbahce N, Li Z, Chen F, Drmanac R, Peters BA.

Clin Chem. 2018 Apr;64(4):715-725. doi: 10.1373/clinchem.2017.281220. Epub 2018 Mar 15.

PMID:
29545257
16.

Loss of Chromatin-Remodeling Proteins and/or CDKN2A Associates With Metastasis of Pancreatic Neuroendocrine Tumors and Reduced Patient Survival Times.

Roy S, LaFramboise WA, Liu TC, Cao D, Luvison A, Miller C, Lyons MA, O'Sullivan RJ, Zureikat AH, Hogg ME, Tsung A, Lee KK, Bahary N, Brand RE, Chennat JS, Fasanella KE, McGrath K, Nikiforova MN, Papachristou GI, Slivka A, Zeh HJ, Singhi AD.

Gastroenterology. 2018 Jun;154(8):2060-2063.e8. doi: 10.1053/j.gastro.2018.02.026. Epub 2018 Mar 2.

17.

Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation.

Fueyo R, Iacobucci S, Pappa S, Estarás C, Lois S, Vicioso-Mantis M, Navarro C, Cruz-Molina S, Reyes JC, Rada-Iglesias Á, de la Cruz X, Martínez-Balbás MA.

Nucleic Acids Res. 2018 Apr 20;46(7):3351-3365. doi: 10.1093/nar/gky093.

18.

Enriched expression of genes associated with autism spectrum disorders in human inhibitory neurons.

Wang P, Zhao D, Lachman HM, Zheng D.

Transl Psychiatry. 2018 Jan 10;8(1):13. doi: 10.1038/s41398-017-0058-6.

19.

Exome Pool-Seq in neurodevelopmental disorders.

Popp B, Ekici AB, Thiel CT, Hoyer J, Wiesener A, Kraus C, Reis A, Zweier C.

Eur J Hum Genet. 2017 Dec;25(12):1364-1376. doi: 10.1038/s41431-017-0022-1. Epub 2017 Nov 20.

20.

Large-scale automated function prediction of protein sequences and an experimental case study validation on PTEN transcript variants.

Rifaioglu AS, Doğan T, Saraç ÖS, Ersahin T, Saidi R, Atalay MV, Martin MJ, Cetin-Atalay R.

Proteins. 2018 Feb;86(2):135-151. doi: 10.1002/prot.25416. Epub 2017 Nov 29.

PMID:
29098713

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