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Items: 1 to 20 of 78

1.

The first case report of a large deletion of the BRCA1 gene in Croatia: A case report.

Musani V, Sušac I, Ozretić P, Eljuga D, Levanat S.

Medicine (Baltimore). 2017 Dec;96(48):e8667. doi: 10.1097/MD.0000000000008667.

2.

First-decade patient with colorectal cancer carrying both germline and somatic mutations in APC gene.

Yeh YS, Chang YT, Ma CJ, Huang CW, Tsai HL, Chen YT, Wang JY.

BMC Cancer. 2017 Dec 14;17(1):849. doi: 10.1186/s12885-017-3878-0.

3.

Association of miR-21, miR-126 and miR-605 gene polymorphisms with ischemic stroke risk.

Xiang Y, Guo J, Peng YF, Tan T, Huang HT, Luo HC, Wei YS.

Oncotarget. 2017 Sep 28;8(56):95755-95763. doi: 10.18632/oncotarget.21316. eCollection 2017 Nov 10.

4.

HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions.

Brechka H, Bhanvadia RR, VanOpstall C, Vander Griend DJ.

Genes Dis. 2017 Jun;4(2):75-87. doi: 10.1016/j.gendis.2017.01.003. Epub 2017 Feb 16.

5.

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.

6.

Genome-wide TOP2A DNA cleavage is biased toward translocated and highly transcribed loci.

Yu X, Davenport JW, Urtishak KA, Carillo ML, Gosai SJ, Kolaris CP, Byl JAW, Rappaport EF, Osheroff N, Gregory BD, Felix CA.

Genome Res. 2017 Jul;27(7):1238-1249. doi: 10.1101/gr.211615.116. Epub 2017 Apr 6.

7.

Diagnostic exome sequencing in 266 Dutch patients with visual impairment.

Haer-Wigman L, van Zelst-Stams WA, Pfundt R, van den Born LI, Klaver CC, Verheij JB, Hoyng CB, Breuning MH, Boon CJ, Kievit AJ, Verhoeven VJ, Pott JW, Sallevelt SC, van Hagen JM, Plomp AS, Kroes HY, Lelieveld SH, Hehir-Kwa JY, Castelein S, Nelen M, Scheffer H, Lugtenberg D, Cremers FP, Hoefsloot L, Yntema HG.

Eur J Hum Genet. 2017 May;25(5):591-599. doi: 10.1038/ejhg.2017.9. Epub 2017 Feb 22.

8.

Detection of aberrant methylated SEPT9 and NTRK3 genes in sporadic colorectal cancer patients as a potential diagnostic biomarker.

Behrouz Sharif S, Hashemzadeh S, Mousavi Ardehaie R, Eftekharsadat A, Ghojazadeh M, Mehrtash AH, Estiar MA, Teimoori-Toolabi L, Sakhinia E.

Oncol Lett. 2016 Dec;12(6):5335-5343. doi: 10.3892/ol.2016.5327. Epub 2016 Oct 31.

9.

Clonal evolution in therapy-related neoplasms.

Fabiani E, Falconi G, Fianchi L, Criscuolo M, Ottone T, Cicconi L, Hohaus S, Sica S, Postorino M, Neri A, Lionetti M, Leone G, Lo-Coco F, Voso MT.

Oncotarget. 2017 Feb 14;8(7):12031-12040. doi: 10.18632/oncotarget.14509.

10.

Identification of ITGA2B and ITGB3 Single-Nucleotide Polymorphisms and Their Influences on the Platelet Function.

Xiang Q, Ji SD, Zhang Z, Zhao X, Cui YM.

Biomed Res Int. 2016;2016:5675084. Epub 2016 Nov 14.

11.

Usher syndrome in Denmark: mutation spectrum and some clinical observations.

Dad S, Rendtorff ND, Tranebjærg L, Grønskov K, Karstensen HG, Brox V, Nilssen Ø, Roux AF, Rosenberg T, Jensen H, Møller LB.

Mol Genet Genomic Med. 2016 Jun 28;4(5):527-539. eCollection 2016 Sep.

12.

Anisakis pegreffii (Nematoda: Anisakidae) products modulate oxidative stress and apoptosis-related biomarkers in human cell lines.

Messina CM, Pizzo F, Santulli A, Bušelić I, Boban M, Orhanović S, Mladineo I.

Parasit Vectors. 2016 Nov 25;9(1):607.

13.

HOXB4 Gene Expression Is Regulated by CDX2 in Intestinal Epithelial Cells.

Jørgensen S, Coskun M, Homburg KM, Pedersen OB, Troelsen JT.

PLoS One. 2016 Oct 18;11(10):e0164555. doi: 10.1371/journal.pone.0164555. eCollection 2016.

14.

Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.

Geard A, Pule GD, Chelo D, Bitoungui VJ, Wonkam A.

OMICS. 2016 Oct;20(10):581-592. Review.

15.

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.

16.

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.

Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, Petit C.

PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016.

17.

Telomere status in chronic lymphocytic leukemia with TP53 disruption.

Guièze R, Pages M, Véronèse L, Combes P, Lemal R, Gay-Bellile M, Chauvet M, Callanan M, Kwiatkowski F, Pereira B, Vago P, Bay JO, Tournilhac O, Tchirkov A.

Oncotarget. 2016 Aug 30;7(35):56976-56985. doi: 10.18632/oncotarget.10927.

18.

The Expression Levels of XLF and Mutant P53 Are Inversely Correlated in Head and Neck Cancer Cells.

Feng S, Rabii R, Liang G, Song C, Chen W, Guo M, Wei X, Messadi D, Hu S.

J Cancer. 2016 Jun 30;7(11):1374-82. doi: 10.7150/jca.14669. eCollection 2016.

19.

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.

Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C.

Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27.

20.

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.

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