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High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos.

White CR, Denomme MM, Tekpetey FR, Feyles V, Power SG, Mann MR.

Sci Rep. 2015 Dec 2;5:17311. doi: 10.1038/srep17311.


Variations in Antioxidant Genes and Male Infertility.

Yu B, Huang Z.

Biomed Res Int. 2015;2015:513196. doi: 10.1155/2015/513196. Epub 2015 Nov 5. Review.


Polymorphisms in mucin genes in the development of gastric cancer.

Wen R, Gao F, Zhou CJ, Jia YB.

World J Gastrointest Oncol. 2015 Nov 15;7(11):328-37. doi: 10.4251/wjgo.v7.i11.328. Review.


Contribution of BDNF and DRD2 genetic polymorphisms to continued opioid use in patients receiving methadone treatment for opioid use disorder: an observational study.

Bawor M, Dennis BB, Tan C, Pare G, Varenbut M, Daiter J, Plater C, Worster A, Marsh DC, Steiner M, Anglin R, Desai D, Thabane L, Samaan Z.

Addict Sci Clin Pract. 2015 Oct 6;10:19. doi: 10.1186/s13722-015-0040-7.


CRISPR/Cas9 System as an Agent for Eliminating Polyomavirus JC Infection.

Wollebo HS, Bellizzi A, Kaminski R, Hu W, White MK, Khalili K.

PLoS One. 2015 Sep 11;10(9):e0136046. doi: 10.1371/journal.pone.0136046. eCollection 2015.


The PI3K/AKT/mTOR pathway is a potential predictor of distinct invasive and migratory capacities in human ovarian cancer cell lines.

Bai H, Li H, Li W, Gui T, Yang J, Cao D, Shen K.

Oncotarget. 2015 Sep 22;6(28):25520-32. doi: 10.18632/oncotarget.4550.


Recombination of chl-fus gene (Plastid Origin) downstream of hop: a locus of chromosomal instability.

Salinas Castellanos LC, Chomilier J, Hernández-Torres J.

BMC Genomics. 2015 Aug 4;16:573. doi: 10.1186/s12864-015-1780-1.


Data supporting the design and evaluation of a universal primer pair for pseudogene-free amplification of HPRT1 in real-time PCR.

Valadan R, Hedayatizadeh-Omran A, Alhosseini-Abyazani MN, Amjadi O, Rafiei A, Tehrani M, Alizadeh-Navaei R.

Data Brief. 2015 Jul 6;4:384-9. doi: 10.1016/j.dib.2015.06.009. eCollection 2015 Sep.


The transcriptome and miRNome profiling of glioblastoma tissues and peritumoral regions highlights molecular pathways shared by tumors and surrounding areas and reveals differences between short-term and long-term survivors.

Fazi B, Felsani A, Grassi L, Moles A, D'Andrea D, Toschi N, Sicari D, De Bonis P, Anile C, Guerrisi MG, Luca E, Farace MG, Maira G, Ciafré SA, Mangiola A.

Oncotarget. 2015 Sep 8;6(26):22526-52.


An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population.

Zhang F, Liu X, Wang B, Cheng Z, Zhao X, Zhu J, Wang D, Wang Y, Dong A, Li P, Jin C.

Neuropsychiatr Dis Treat. 2015 Jun 12;11:1443-8. doi: 10.2147/NDT.S85370. eCollection 2015.


Do housekeeping genes exist?

Zhang Y, Li D, Sun B.

PLoS One. 2015 May 13;10(5):e0123691. doi: 10.1371/journal.pone.0123691. eCollection 2015.


Damaging the Integrated HIV Proviral DNA with TALENs.

Strong CL, Guerra HP, Mathew KR, Roy N, Simpson LR, Schiller MR.

PLoS One. 2015 May 6;10(5):e0125652. doi: 10.1371/journal.pone.0125652. eCollection 2015.


Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study.

Masemola ML, van der Merwe L, Lombard Z, Viljoen D, Ramsay M.

Front Genet. 2015 Mar 10;6:85. doi: 10.3389/fgene.2015.00085. eCollection 2015.


Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.

Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS.

Haematologica. 2015 May;100(5):e166-8. doi: 10.3324/haematol.2014.117408. Epub 2015 Feb 14. No abstract available.


Genetics of transfusion recipient alloimmunization: can clues from susceptibility to autoimmunity pave the way?

Tatari-Calderone Z, Luban NL, Vukmanovic S.

Transfus Med Hemother. 2014 Nov;41(6):436-45. doi: 10.1159/000369145. Epub 2014 Nov 17. Review.


Extending reference assembly models.

Church DM, Schneider VA, Steinberg KM, Schatz MC, Quinlan AR, Chin CS, Kitts PA, Aken B, Marth GT, Hoffman MM, Herrero J, Mendoza ML, Durbin R, Flicek P.

Genome Biol. 2015 Jan 24;16:13. doi: 10.1186/s13059-015-0587-3.


Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trio.

Bodian DL, Solomon BD, Khromykh A, Thach DC, Iyer RK, Link K, Baker RL, Baveja R, Vockley JG, Niederhuber JE.

Mol Genet Genomic Med. 2014 Nov;2(6):530-8. doi: 10.1002/mgg3.107. Epub 2014 Aug 26.


Transcriptional Profiles of Imprinted Genes in Human Embryonic Stem Cells During In vitro Differentiation.

Park SW, Do HS, Kim D, Ko JY, Lee SH, Han YM.

Int J Stem Cells. 2014 Nov;7(2):108-17. doi: 10.15283/ijsc.2014.7.2.108.


Can pharmacogenetics explain efficacy and safety of cisplatin pharmacotherapy?

Roco A, Cayún J, Contreras S, Stojanova J, Quiñones L.

Front Genet. 2014 Nov 14;5:391. doi: 10.3389/fgene.2014.00391. eCollection 2014. Review.

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