Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 105


Loss of Kdm5c Causes Spurious Transcription and Prevents the Fine-Tuning of Activity-Regulated Enhancers in Neurons.

Scandaglia M, Lopez-Atalaya JP, Medrano-Fernandez A, Lopez-Cascales MT, Del Blanco B, Lipinski M, Benito E, Olivares R, Iwase S, Shi Y, Barco A.

Cell Rep. 2017 Oct 3;21(1):47-59. doi: 10.1016/j.celrep.2017.09.014.


JARID1 Histone Demethylases: Emerging Targets in Cancer.

Harmeyer KM, Facompre ND, Herlyn M, Basu D.

Trends Cancer. 2017 Oct;3(10):713-725. doi: 10.1016/j.trecan.2017.08.004. Epub 2017 Sep 12. Review.


Histone Lysine Methylation and Neurodevelopmental Disorders.

Kim JH, Lee JH, Lee IS, Lee SB, Cho KS.

Int J Mol Sci. 2017 Jun 30;18(7). pii: E1404. doi: 10.3390/ijms18071404. Review.


Multifaceted Regulation of Gene Expression by the Apoptosis- and Splicing-Associated Protein Complex and Its Components.

Deka B, Singh KK.

Int J Biol Sci. 2017 Apr 10;13(5):545-560. doi: 10.7150/ijbs.18649. eCollection 2017. Review.


Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.

Grau C, Starkovich M, Azamian MS, Xia F, Cheung SW, Evans P, Henderson A, Lalani SR, Scott DA.

PLoS One. 2017 Apr 17;12(4):e0175962. doi: 10.1371/journal.pone.0175962. eCollection 2017.


The defining DNA methylation signature of Floating-Harbor Syndrome.

Hood RL, Schenkel LC, Nikkel SM, Ainsworth PJ, Pare G, Boycott KM, Bulman DE, Sadikovic B.

Sci Rep. 2016 Dec 9;6:38803. doi: 10.1038/srep38803.


The KDM5 family is required for activation of pro-proliferative cell cycle genes during adipocyte differentiation.

Brier AB, Loft A, Madsen JGS, Rosengren T, Nielsen R, Schmidt SF, Liu Z, Yan Q, Gronemeyer H, Mandrup S.

Nucleic Acids Res. 2017 Feb 28;45(4):1743-1759. doi: 10.1093/nar/gkw1156.


Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias.

Dunford A, Weinstock DM, Savova V, Schumacher SE, Cleary JP, Yoda A, Sullivan TJ, Hess JM, Gimelbrant AA, Beroukhim R, Lawrence MS, Getz G, Lane AA.

Nat Genet. 2017 Jan;49(1):10-16. doi: 10.1038/ng.3726. Epub 2016 Nov 21.


Cofactors-loaded quaternary structure of lysine-specific demethylase 5C (KDM5C) protein: Computational model.

Peng Y, Alexov E.

Proteins. 2016 Dec;84(12):1797-1809. doi: 10.1002/prot.25162. Epub 2016 Oct 1.


Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.

Genovese G, Fromer M, Stahl EA, Ruderfer DM, Chambert K, Landén M, Moran JL, Purcell SM, Sklar P, Sullivan PF, Hultman CM, McCarroll SA.

Nat Neurosci. 2016 Nov;19(11):1433-1441. doi: 10.1038/nn.4402. Epub 2016 Oct 3.


Enhancer deregulation in cancer and other diseases.

Herz HM.

Bioessays. 2016 Oct;38(10):1003-15. doi: 10.1002/bies.201600106. Epub 2016 Aug 29. Review.


Kdm5/Lid Regulates Chromosome Architecture in Meiotic Prophase I Independently of Its Histone Demethylase Activity.

Zhaunova L, Ohkura H, Breuer M.

PLoS Genet. 2016 Aug 5;12(8):e1006241. doi: 10.1371/journal.pgen.1006241. eCollection 2016 Aug.


Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.

Wei G, Deng X, Agarwal S, Iwase S, Disteche C, Xu J.

J Mol Neurosci. 2016 Sep;60(1):33-45. doi: 10.1007/s12031-016-0770-3. Epub 2016 Jul 16.


A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features.

Xie B, Fan X, Lei Y, Chen R, Wang J, Fu C, Yi S, Luo J, Zhang S, Yang Q, Chen S, Shen Y.

Mol Cytogenet. 2016 May 31;9:41. doi: 10.1186/s13039-016-0251-y. eCollection 2016.


New Insights Into Intellectual Disability Caused by Mutations in a Chromatin Regulator.

Brookes E.

EBioMedicine. 2016 Apr;6:2-3. doi: 10.1016/j.ebiom.2016.04.001. Epub 2016 Apr 4. No abstract available.


Deletion of JMJD2B in neurons leads to defective spine maturation, hyperactive behavior and memory deficits in mouse.

Fujiwara K, Fujita Y, Kasai A, Onaka Y, Hashimoto H, Okada H, Yamashita T.

Transl Psychiatry. 2016 Mar 29;6:e766. doi: 10.1038/tp.2016.31.


A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation.

Iwase S, Brookes E, Agarwal S, Badeaux AI, Ito H, Vallianatos CN, Tomassy GS, Kasza T, Lin G, Thompson A, Gu L, Kwan KY, Chen C, Sartor MA, Egan B, Xu J, Shi Y.

Cell Rep. 2016 Feb 9;14(5):1000-1009. doi: 10.1016/j.celrep.2015.12.091. Epub 2016 Jan 21.


Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family.

Kalscheuer VM, James VM, Himelright ML, Long P, Oegema R, Jensen C, Bienek M, Hu H, Haas SA, Topf M, Hoogeboom AJ, Harvey K, Walikonis R, Harvey RJ.

Front Mol Neurosci. 2016 Jan 11;8:85. doi: 10.3389/fnmol.2015.00085. eCollection 2015.


Landmarks in the Evolution of (t)-RNAs from the Origin of Life up to Their Present Role in Human Cognition.

Balke D, Kuss A, Müller S.

Life (Basel). 2015 Dec 23;6(1). pii: E1. doi: 10.3390/life6010001. Review.


Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.

Peng Y, Suryadi J, Yang Y, Kucukkal TG, Cao W, Alexov E.

Int J Mol Sci. 2015 Nov 13;16(11):27270-87. doi: 10.3390/ijms161126022.

Supplemental Content

Support Center