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Items: 1 to 20 of 67

1.

Genetic Approaches to Understanding Psychiatric Disease.

Michaelson JJ.

Neurotherapeutics. 2017 Jul;14(3):564-581. doi: 10.1007/s13311-017-0551-x. Review.

PMID:
28608171
2.

E3 Ubiquitin Ligases Neurobiological Mechanisms: Development to Degeneration.

Upadhyay A, Joshi V, Amanullah A, Mishra R, Arora N, Prasad A, Mishra A.

Front Mol Neurosci. 2017 May 19;10:151. doi: 10.3389/fnmol.2017.00151. eCollection 2017. Review.

3.

Maternal Factors that Induce Epigenetic Changes Contribute to Neurological Disorders in Offspring.

Banik A, Kandilya D, Ramya S, Stünkel W, Chong YS, Dheen ST.

Genes (Basel). 2017 May 24;8(6). pii: E150. doi: 10.3390/genes8060150. Review.

4.

Modulation of trinucleotide repeat instability by DNA polymerase β polymorphic variant R137Q.

Ren Y, Lai Y, Laverde EE, Lei R, Rein HL, Liu Y.

PLoS One. 2017 May 5;12(5):e0177299. doi: 10.1371/journal.pone.0177299. eCollection 2017.

5.

The tandem Agenet domain of fragile X mental retardation protein interacts with FUS.

He Q, Ge W.

Sci Rep. 2017 Apr 19;7(1):962. doi: 10.1038/s41598-017-01175-8.

6.

A Drosophila model of Fragile X syndrome exhibits defects in phagocytosis by innate immune cells.

O'Connor RM, Stone EF, Wayne CR, Marcinkevicius EV, Ulgherait M, Delventhal R, Pantalia MM, Hill VM, Zhou CG, McAllister S, Chen A, Ziegenfuss JS, Grueber WB, Canman JC, Shirasu-Hiza MM.

J Cell Biol. 2017 Mar 6;216(3):595-605. doi: 10.1083/jcb.201607093. Epub 2017 Feb 21.

PMID:
28223318
7.

APP Causes Hyperexcitability in Fragile X Mice.

Westmark CJ, Chuang SC, Hays SA, Filon MJ, Ray BC, Westmark PR, Gibson JR, Huber KM, Wong RK.

Front Mol Neurosci. 2016 Dec 15;9:147. doi: 10.3389/fnmol.2016.00147. eCollection 2016.

8.

ATXN2 trinucleotide repeat length correlates with risk of ALS.

Sproviero W, Shatunov A, Stahl D, Shoai M, van Rheenen W, Jones AR, Al-Sarraj S, Andersen PM, Bonini NM, Conforti FL, Van Damme P, Daoud H, Del Mar Amador M, Fogh I, Forzan M, Gaastra B, Gellera C, Gitler AD, Hardy J, Fratta P, La Bella V, Le Ber I, Van Langenhove T, Lattante S, Lee YC, Malaspina A, Meininger V, Millecamps S, Orrell R, Rademakers R, Robberecht W, Rouleau G, Ross OA, Salachas F, Sidle K, Smith BN, Soong BW, Sorarù G, Stevanin G, Kabashi E, Troakes C, van Broeckhoven C, Veldink JH, van den Berg LH, Shaw CE, Powell JF, Al-Chalabi A.

Neurobiol Aging. 2017 Mar;51:178.e1-178.e9. doi: 10.1016/j.neurobiolaging.2016.11.010. Epub 2016 Nov 24.

9.

RNA G-quadruplexes: emerging mechanisms in disease.

Cammas A, Millevoi S.

Nucleic Acids Res. 2017 Feb 28;45(4):1584-1595. doi: 10.1093/nar/gkw1280.

10.

Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.

Hoyos LR, Thakur M.

J Assist Reprod Genet. 2017 Mar;34(3):315-323. doi: 10.1007/s10815-016-0854-6. Epub 2016 Dec 19. Review.

PMID:
27995424
11.
12.

Pathogenesis of Börjeson-Forssman-Lehmann syndrome: Insights from PHF6 function.

Jahani-Asl A, Cheng C, Zhang C, Bonni A.

Neurobiol Dis. 2016 Dec;96:227-235. doi: 10.1016/j.nbd.2016.09.011. Epub 2016 Sep 12. Review.

PMID:
27633282
13.
14.

New X-chromosomal interactors of dFMRP regulate axonal and synaptic morphology of brain neurons in Drosophila melanogaster.

Georgieva D, Dimitrov R, Kitanova M, Genova G.

Biotechnol Biotechnol Equip. 2014 Jul 4;28(4):697-709. Epub 2014 Oct 23.

15.

PacBio Sequencing and Its Applications.

Rhoads A, Au KF.

Genomics Proteomics Bioinformatics. 2015 Oct;13(5):278-89. doi: 10.1016/j.gpb.2015.08.002. Epub 2015 Nov 2. Review.

16.

Chromatin deregulation in disease.

Mirabella AC, Foster BM, Bartke T.

Chromosoma. 2016 Mar;125(1):75-93. doi: 10.1007/s00412-015-0530-0. Epub 2015 Jul 19. Review.

17.

FMRP interacts with G-quadruplex structures in the 3'-UTR of its dendritic target Shank1 mRNA.

Zhang Y, Gaetano CM, Williams KR, Bassell GJ, Mihailescu MR.

RNA Biol. 2014;11(11):1364-74. doi: 10.1080/15476286.2014.996464.

18.

iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth.

Doers ME, Musser MT, Nichol R, Berndt ER, Baker M, Gomez TM, Zhang SC, Abbeduto L, Bhattacharyya A.

Stem Cells Dev. 2014 Aug 1;23(15):1777-87. doi: 10.1089/scd.2014.0030. Epub 2014 Apr 30.

19.
20.

Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome.

Yao B, Lin L, Street RC, Zalewski ZA, Galloway JN, Wu H, Nelson DL, Jin P.

Hum Mol Genet. 2014 Feb 15;23(4):1095-107. doi: 10.1093/hmg/ddt504. Epub 2013 Oct 9.

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