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Items: 1 to 20 of 101

1.

HDNetDB: A Molecular Interaction Database for Network-Oriented Investigations into Huntington's Disease.

Kalathur RKR, Pedro Pinto J, Sahoo B, Chaurasia G, Futschik ME.

Sci Rep. 2017 Jul 12;7(1):5216. doi: 10.1038/s41598-017-05224-0.

2.

Identification of differentially expressed genes and regulatory relationships in Huntington's disease by bioinformatics analysis.

Dong X, Cong S.

Mol Med Rep. 2018 Mar;17(3):4317-4326. doi: 10.3892/mmr.2018.8410. Epub 2018 Jan 9.

3.

Bioinformatic analysis of microRNA expression in Huntington's disease.

Dong X, Cong S.

Mol Med Rep. 2018 Sep;18(3):2857-2865. doi: 10.3892/mmr.2018.9238. Epub 2018 Jun 29.

4.

The dynamics of early-state transcriptional changes and aggregate formation in a Huntington's disease cell model.

van Hagen M, Piebes DGE, de Leeuw WC, Vuist IM, van Roon-Mom WMC, Moerland PD, Verschure PJ.

BMC Genomics. 2017 May 12;18(1):373. doi: 10.1186/s12864-017-3745-z.

5.

Huntington's Disease: Relationship Between Phenotype and Genotype.

Sun YM, Zhang YB, Wu ZY.

Mol Neurobiol. 2017 Jan;54(1):342-348. doi: 10.1007/s12035-015-9662-8. Epub 2016 Jan 7. Review.

PMID:
26742514
6.

Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.

Lin L, Park JW, Ramachandran S, Zhang Y, Tseng YT, Shen S, Waldvogel HJ, Curtis MA, Faull RL, Troncoso JC, Pletnikova O, Ross CA, Davidson BL, Xing Y.

Hum Mol Genet. 2016 Aug 15;25(16):3454-3466. doi: 10.1093/hmg/ddw187. Epub 2016 Jul 4.

7.

Epigenetics of Huntington's Disease.

Bassi S, Tripathi T, Monziani A, Di Leva F, Biagioli M.

Adv Exp Med Biol. 2017;978:277-299. doi: 10.1007/978-3-319-53889-1_15. Review.

PMID:
28523552
8.

Huntington's disease and its therapeutic target genes: a global functional profile based on the HD Research Crossroads database.

Kalathur RK, Hernández-Prieto MA, Futschik ME.

BMC Neurol. 2012 Jun 28;12:47. doi: 10.1186/1471-2377-12-47.

9.

The unfolded protein response and its potential role in Huntington's disease elucidated by a systems biology approach.

Kalathur RK, Giner-Lamia J, Machado S, Barata T, Ayasolla KR, Futschik ME.

Version 2. F1000Res. 2015 May 1 [revised 2016 Jan 1];4:103. doi: 10.12688/f1000research.6358.2. eCollection 2015.

10.

Systems Genetic Analyses Highlight a TGFβ-FOXO3 Dependent Striatal Astrocyte Network Conserved across Species and Associated with Stress, Sleep, and Huntington's Disease.

Scarpa JR, Jiang P, Losic B, Readhead B, Gao VD, Dudley JT, Vitaterna MH, Turek FW, Kasarskis A.

PLoS Genet. 2016 Jul 8;12(7):e1006137. doi: 10.1371/journal.pgen.1006137. eCollection 2016 Jul.

11.

Clinical Features of Huntington's Disease.

Ghosh R, Tabrizi SJ.

Adv Exp Med Biol. 2018;1049:1-28. doi: 10.1007/978-3-319-71779-1_1. Review.

PMID:
29427096
12.

Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington's Disease Knock-In Mice.

Neto JL, Lee JM, Afridi A, Gillis T, Guide JR, Dempsey S, Lager B, Alonso I, Wheeler VC, Pinto RM.

Genetics. 2017 Feb;205(2):503-516. doi: 10.1534/genetics.116.195578. Epub 2016 Dec 2.

13.

RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation.

Miller JR, Lo KK, Andre R, Hensman Moss DJ, Träger U, Stone TC, Jones L, Holmans P, Plagnol V, Tabrizi SJ.

Hum Mol Genet. 2016 Jul 15;25(14):2893-2904. Epub 2016 May 11.

14.

Chromosomal instability during neurogenesis in Huntington's disease.

Ruzo A, Croft GF, Metzger JJ, Galgoczi S, Gerber LJ, Pellegrini C, Wang H Jr, Fenner M, Tse S, Marks A, Nchako C, Brivanlou AH.

Development. 2018 Jan 29;145(2). pii: dev156844. doi: 10.1242/dev.156844.

15.

RNA toxicity induced by expanded CAG repeats in Huntington's disease.

Martí E.

Brain Pathol. 2016 Nov;26(6):779-786. doi: 10.1111/bpa.12427. Review.

PMID:
27529325
16.

High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds.

Ament SA, Pearl JR, Grindeland A, St Claire J, Earls JC, Kovalenko M, Gillis T, Mysore J, Gusella JF, Lee JM, Kwak S, Howland D, Lee MY, Baxter D, Scherler K, Wang K, Geman D, Carroll JB, MacDonald ME, Carlson G, Wheeler VC, Price ND, Hood LE.

Hum Mol Genet. 2017 Mar 1;26(5):913-922. doi: 10.1093/hmg/ddx006.

17.

The Complexity of Clinical Huntington's Disease: Developments in Molecular Genetics, Neuropathology and Neuroimaging Biomarkers.

Tippett LJ, Waldvogel HJ, Snell RG, Vonsattel JP, Young AB, Faull RLM.

Adv Neurobiol. 2017;15:129-161. doi: 10.1007/978-3-319-57193-5_5. Review.

PMID:
28674980
18.

Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.

Mariani LL, Tesson C, Charles P, Cazeneuve C, Hahn V, Youssov K, Freeman L, Grabli D, Roze E, Noël S, Peuvion JN, Bachoud-Levi AC, Brice A, Stevanin G, Durr A.

JAMA Neurol. 2016 Sep 1;73(9):1105-14. doi: 10.1001/jamaneurol.2016.2215.

PMID:
27400454
19.

HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes.

Galkina EI, Shin A, Coser KR, Shioda T, Kohane IS, Seong IS, Wheeler VC, Gusella JF, Macdonald ME, Lee JM.

PLoS One. 2014 Apr 21;9(4):e95556. doi: 10.1371/journal.pone.0095556. eCollection 2014.

20.

First preimplantation genetic testing case for monogenic disease in Latvia.

Perminov D, Voložonoka L, Korņejeva L, Jokste-Pțmane E, Blumberga A, Krasucka S, Seimuškina N, Kovaļova I, Fodina V.

Gynecol Endocrinol. 2017;33(sup1):47-49. doi: 10.1080/09513590.2017.1404239.

PMID:
29264979

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