Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 90


A complex microsatellite at chromosome 7q33 as a new prognostic marker of colorectal cancer.

Ye X, Deng H, Su M, Liao Q, Huang D, Liao DF, Xiao ZQ, Cao D.

Oncotarget. 2017 Sep 16;8(51):88760-88769. doi: 10.18632/oncotarget.21077. eCollection 2017 Oct 24.


Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes (PPROM).

Modi BP, Teves ME, Pearson LN, Parikh HI, Haymond-Thornburg H, Tucker JL, Chaemsaithong P, Gomez-Lopez N, York TP, Romero R, Strauss JF 3rd.

Mol Genet Genomic Med. 2017 Nov;5(6):720-729. doi: 10.1002/mgg3.330. Epub 2017 Aug 23.


Association study of IGFBP1 and IGFBP3 polymorphisms with hypertension and cardio-cerebral vascular diseases in a Chinese Han population.

Fang Z, Yang S, Zhu L, Li Y, Chen Y, Jin Y, Zhao X, Zhao H, Chen X, Zhao Y, Shen C, Yao Y.

Oncotarget. 2017 Sep 12;8(44):77836-77845. doi: 10.18632/oncotarget.20839. eCollection 2017 Sep 29.


Association between plasminogen activator inhibitor gene polymorphisms and osteonecrosis of the femoral head susceptibility: A case-control study.

Li Y, Liu FX, Yuan C, Meng L.

Medicine (Baltimore). 2017 Oct;96(42):e7047. doi: 10.1097/MD.0000000000007047.


Structure, organization and tissue expression of the pig SLC13A1 and SLC13A4 sulfate transporter genes.

Barnes SK, Eiby YA, Lee S, Lingwood BE, Dawson PA.

Biochem Biophys Rep. 2017 Apr 13;10:215-223. doi: 10.1016/j.bbrep.2017.04.005. eCollection 2017 Jul.


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.


Validation of optimal reference genes for quantitative real time PCR in muscle and adipose tissue for obesity and diabetes research.

Perez LJ, Rios L, Trivedi P, D'Souza K, Cowie A, Nzirorera C, Webster D, Brunt K, Legare JF, Hassan A, Kienesberger PC, Pulinilkunnil T.

Sci Rep. 2017 Jun 15;7(1):3612. doi: 10.1038/s41598-017-03730-9.


eNOS S-nitrosylates β-actin on Cys374 and regulates PKC-θ at the immune synapse by impairing actin binding to profilin-1.

García-Ortiz A, Martín-Cofreces NB, Ibiza S, Ortega Á, Izquierdo-Álvarez A, Trullo A, Victor VM, Calvo E, Sot B, Martínez-Ruiz A, Vázquez J, Sánchez-Madrid F, Serrador JM.

PLoS Biol. 2017 Apr 10;15(4):e2000653. doi: 10.1371/journal.pbio.2000653. eCollection 2017 Apr.


Diagnosis of a mild peroxisomal phenotype with next-generation sequencing.

Ventura MJ, Wheaton D, Xu M, Birch D, Bowne SJ, Sullivan LS, Daiger SP, Whitney AE, Jones RO, Moser AB, Chen R, Wangler MF.

Mol Genet Metab Rep. 2016 Nov 11;9:75-78. eCollection 2016 Dec.


The use of targeted genomic capture and massively parallel sequencing in diagnosis of Chinese Leukoencephalopathies.

Wang X, He F, Yin F, Chen C, Wu L, Yang L, Peng J.

Sci Rep. 2016 Oct 25;6:35936. doi: 10.1038/srep35936.


Homology Requirements for Efficient, Footprintless Gene Editing at the CFTR Locus in Human iPSCs with Helper-dependent Adenoviral Vectors.

Palmer DJ, Grove NC, Ing J, Crane AM, Venken K, Davis BR, Ng P.

Mol Ther Nucleic Acids. 2016 Oct 11;5(10):e372. doi: 10.1038/mtna.2016.83.


Association and regulation of protein factors of field effect in prostate tissues.

Gabriel KN, Jones AC, Nguyen JP, Antillon KS, Janos SN, Overton HN, Jenkins SM, Frisch EH, Trujillo KA, Bisoffi M.

Int J Oncol. 2016 Oct;49(4):1541-1552. doi: 10.3892/ijo.2016.3666. Epub 2016 Aug 22.


Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes.

Wills ES, Cnossen WR, Veltman JA, Woestenenk R, Steehouwer M, Salomon J, Te Morsche RH, Huch M, Hehir-Kwa JY, Banning MJ, Pfundt R, Roepman R, Hoischen A, Drenth JP.

Eur J Hum Genet. 2016 Dec;24(12):1707-1714. doi: 10.1038/ejhg.2016.97. Epub 2016 Aug 24.


PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1.

Vogt J, Wernstedt A, Ripperger T, Pabst B, Zschocke J, Kratz C, Wimmer K.

Eur J Hum Genet. 2016 Nov;24(11):1598-1604. doi: 10.1038/ejhg.2016.75. Epub 2016 Jun 22.


Spectrum of PEX1 and PEX6 variants in Heimler syndrome.

Smith CE, Poulter JA, Levin AV, Capasso JE, Price S, Ben-Yosef T, Sharony R, Newman WG, Shore RC, Brookes SJ, Mighell AJ, Inglehearn CF.

Eur J Hum Genet. 2016 Nov;24(11):1565-1571. doi: 10.1038/ejhg.2016.62. Epub 2016 Jun 15.


Associations of ChREBP and Global DNA Methylation with Genetic and Environmental Factors in Chinese Healthy Adults.

Gao J, Qiu X, Wang X, Peng C, Zheng F.

PLoS One. 2016 Jun 9;11(6):e0157128. doi: 10.1371/journal.pone.0157128. eCollection 2016.


Illegitimate RAG-mediated recombination events are involved in IKZF1 Δ3-6 deletion in BCR-ABL1 lymphoblastic leukaemia.

Dong Y, Liu F, Wu C, Li S, Zhao X, Zhang P, Jiao J, Yu X, Ji Y, Zhang M.

Clin Exp Immunol. 2016 Sep;185(3):320-31. doi: 10.1111/cei.12812. Epub 2016 Jul 28.


Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.

Yu LW, Wang F, Yang XY, Sun SN, Zheng YF, Li BB, Gui YH, Wang HY.

Sci Rep. 2016 Apr 1;6:23662. doi: 10.1038/srep23662.


Discovery and characterization of Isofistularin-3, a marine brominated alkaloid, as a new DNA demethylating agent inducing cell cycle arrest and sensitization to TRAIL in cancer cells.

Florean C, Schnekenburger M, Lee JY, Kim KR, Mazumder A, Song S, Kim JM, Grandjenette C, Kim JG, Yoon AY, Dicato M, Kim KW, Christov C, Han BW, Proksch P, Diederich M.

Oncotarget. 2016 Apr 26;7(17):24027-49. doi: 10.18632/oncotarget.8210.

Supplemental Content

Support Center