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G9a regulates breast cancer growth by modulating iron homeostasis through the repression of ferroxidase hephaestin.

Wang YF, Zhang J, Su Y, Shen YY, Jiang DX, Hou YY, Geng MY, Ding J, Chen Y.

Nat Commun. 2017 Aug 17;8(1):274. doi: 10.1038/s41467-017-00350-9.


Cell sex affects extracellular matrix protein expression and proliferation of smooth muscle progenitor cells derived from human pluripotent stem cells.

Li Y, Wen Y, Green M, Cabral EK, Wani P, Zhang F, Wei Y, Baer TM, Chen B.

Stem Cell Res Ther. 2017 Jul 4;8(1):156. doi: 10.1186/s13287-017-0606-2.


Transcriptional regulation of FOXP3 requires integrated activation of both promoter and CNS regions in tumor-induced CD8+ Treg cells.

Chakraborty S, Panda AK, Bose S, Roy D, Kajal K, Guha D, Sa G.

Sci Rep. 2017 May 9;7(1):1628. doi: 10.1038/s41598-017-01788-z.


Factors affecting the loss of MED12-mutated leiomyoma cells during in vitro growth.

Bloch J, Holzmann C, Koczan D, Helmke BM, Bullerdiek J.

Oncotarget. 2017 May 23;8(21):34762-34772. doi: 10.18632/oncotarget.16711.


Ribosomal RNA Genes Contribute to the Formation of Pseudogenes and Junk DNA in the Human Genome.

Robicheau BM, Susko E, Harrigan AM, Snyder M.

Genome Biol Evol. 2017 Feb 1;9(2):380-397. doi: 10.1093/gbe/evw307.


LuCaP Prostate Cancer Patient-Derived Xenografts Reflect the Molecular Heterogeneity of Advanced Disease an--d Serve as Models for Evaluating Cancer Therapeutics.

Nguyen HM, Vessella RL, Morrissey C, Brown LG, Coleman IM, Higano CS, Mostaghel EA, Zhang X, True LD, Lam HM, Roudier M, Lange PH, Nelson PS, Corey E.

Prostate. 2017 May;77(6):654-671. doi: 10.1002/pros.23313. Epub 2017 Feb 3.


Evaluation of IL-12RB1, IL-12B, CXCR-3 and IL-17a expression in cases affected by a non-healing form of cutaneous leishmaniasis: an observational study design.

Moafi M, Rezvan H, Sherkat R, Taleban R, Asilian A, Zarkesh Esfahani SH, Nilforoushzadeh MA, Jaffary F, Feizi A.

BMJ Open. 2017 Jan 27;7(1):e013006. doi: 10.1136/bmjopen-2016-013006.


GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss.

Xing G, Yao J, Liu C, Wei Q, Qian X, Wu L, Lu Y, Cao X.

J Med Genet. 2017 Jun;54(6):426-430. doi: 10.1136/jmedgenet-2016-104320. Epub 2017 Jan 17.


Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets.

Li SS, Gu JM, Yu WJ, He JW, Fu WZ, Zhang ZL.

Int J Mol Med. 2016 Dec;38(6):1703-1714. doi: 10.3892/ijmm.2016.2796. Epub 2016 Nov 7.


A novel FGD1 mutation in a family with Aarskog-Scott syndrome and predominant features of congenital joint contractures.

Griffin LB, Farley FA, Antonellis A, Keegan CE.

Cold Spring Harb Mol Case Stud. 2016 Jul;2(4):a000943. doi: 10.1101/mcs.a000943.


Epigenetic features of FoxP3 in children with cow's milk allergy.

Paparo L, Nocerino R, Cosenza L, Aitoro R, D'Argenio V, Del Monaco V, Di Scala C, Amoroso A, Di Costanzo M, Salvatore F, Berni Canani R.

Clin Epigenetics. 2016 Aug 12;8:86. doi: 10.1186/s13148-016-0252-z. eCollection 2016.


Decreased Dp71 expression is associated with gastric adenocarcinoma prognosis.

Tan S, Tan J, Tan S, Zhao S, Cao X, Chen Z, Weng Q, Zhang H, Wang K, Zhou J, Xiao X.

Oncotarget. 2016 Aug 16;7(33):53702-53711. doi: 10.18632/oncotarget.10724.


An LTR Retrotransposon-Derived Gene Displays Lineage-Specific Structural and Putative Species-Specific Functional Variations in Eutherians.

Irie M, Koga A, Kaneko-Ishino T, Ishino F.

Front Chem. 2016 Jun 23;4:26. doi: 10.3389/fchem.2016.00026. eCollection 2016.


Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing Strategy.

Thomas CP, Mansilla MA, Sompallae R, Mason SO, Nishimura CJ, Kimble MJ, Campbell CA, Kwitek AE, Darbro BW, Stewart ZA, Smith RJ.

Am J Transplant. 2017 Feb;17(2):401-410. doi: 10.1111/ajt.13970. Epub 2016 Aug 24.


A genetic analysis of 23 Chinese patients with hemophilia B.

Wang QY, Hu B, Liu H, Tang L, Zeng W, Wu YY, Cheng ZP, Hu Y.

Sci Rep. 2016 Apr 25;6:25024. doi: 10.1038/srep25024.


Genetic Comparison of Stemness of Human Umbilical Cord and Dental Pulp.

Kang CM, Kim H, Song JS, Choi BJ, Kim SO, Jung HS, Moon SJ, Choi HJ.

Stem Cells Int. 2016;2016:3453890. doi: 10.1155/2016/3453890. Epub 2016 Mar 21.


A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.

Garagiola I, Seregni S, Mortarino M, Mancuso ME, Fasulo MR, Notarangelo LD, Peyvandi F.

Mol Genet Genomic Med. 2015 Dec 14;4(2):152-9. doi: 10.1002/mgg3.189. eCollection 2016 Mar.


MAOA gene hypomethylation in panic disorder-reversibility of an epigenetic risk pattern by psychotherapy.

Ziegler C, Richter J, Mahr M, Gajewska A, Schiele MA, Gehrmann A, Schmidt B, Lesch KP, Lang T, Helbig-Lang S, Pauli P, Kircher T, Reif A, Rief W, Vossbeck-Elsebusch AN, Arolt V, Wittchen HU, Hamm AO, Deckert J, Domschke K.

Transl Psychiatry. 2016 Apr 5;6:e773. doi: 10.1038/tp.2016.41.


Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype.

Limprasert P, Thanakitgosate J, Jaruthamsophon K, Sripo T.

Genet Res Int. 2016;2016:8319287. doi: 10.1155/2016/8319287. Epub 2016 Mar 2.

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