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Items: 1 to 20 of 82

1.

Silencing of G0/G1 switch gene 2 in cutaneous squamous cell carcinoma.

Nobeyama Y, Watanabe Y, Nakagawa H.

PLoS One. 2017 Oct 26;12(10):e0187047. doi: 10.1371/journal.pone.0187047. eCollection 2017.

2.

Genomic variants link to hepatitis C racial disparities.

Yeh MM, Boukhar S, Roberts B, Dasgupta N, Daoud SS.

Oncotarget. 2017 Aug 1;8(35):59455-59475. doi: 10.18632/oncotarget.19755. eCollection 2017 Aug 29.

3.

The non-canonical poly(A) polymerase FAM46C acts as an onco-suppressor in multiple myeloma.

Mroczek S, Chlebowska J, Kuliński TM, Gewartowska O, Gruchota J, Cysewski D, Liudkovska V, Borsuk E, Nowis D, Dziembowski A.

Nat Commun. 2017 Sep 20;8(1):619. doi: 10.1038/s41467-017-00578-5.

4.

Silencing of interferon regulatory factor gene 6 in melanoma.

Nobeyama Y, Nakagawa H.

PLoS One. 2017 Sep 6;12(9):e0184444. doi: 10.1371/journal.pone.0184444. eCollection 2017.

5.

MSDB: A Comprehensive Database of Simple Sequence Repeats.

Avvaru AK, Saxena S, Sowpati DT, Mishra RK.

Genome Biol Evol. 2017 Jun 1;9(6):1797-1802. doi: 10.1093/gbe/evx132.

6.

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.

7.

Regulation of type 1 iodothyronine deiodinase by LXRα.

Sakane Y, Kanamoto N, Yamauchi I, Tagami T, Morita Y, Miura M, Sone M, Yasoda A, Kimura T, Nakao K, Inagaki N.

PLoS One. 2017 Jun 15;12(6):e0179213. doi: 10.1371/journal.pone.0179213. eCollection 2017.

8.

Genomic structure, expression pattern, and functional characterization of transcription factor E2F-2 from black tiger shrimp (Penaeus monodon).

Xie B, Wang P, Zhao C, Qiu L.

PLoS One. 2017 May 30;12(5):e0177420. doi: 10.1371/journal.pone.0177420. eCollection 2017.

9.

Fatty Acids of CLA-Enriched Egg Yolks Can Induce Transcriptional Activation of Peroxisome Proliferator-Activated Receptors in MCF-7 Breast Cancer Cells.

Koronowicz AA, Banks P, Master A, Domagała D, Piasna-Słupecka E, Drozdowska M, Sikora E, Laidler P.

PPAR Res. 2017;2017:2865283. doi: 10.1155/2017/2865283. Epub 2017 Mar 26.

10.

On the Molecular Evolution of Leptin, Leptin Receptor, and Endospanin.

Londraville RL, Prokop JW, Duff RJ, Liu Q, Tuttle M.

Front Endocrinol (Lausanne). 2017 Apr 10;8:58. doi: 10.3389/fendo.2017.00058. eCollection 2017.

11.

Efficacy and Safety of Immuno-Magnetically Sorted Smooth Muscle Progenitor Cells Derived from Human-Induced Pluripotent Stem Cells for Restoring Urethral Sphincter Function.

Li Y, Green M, Wen Y, Wei Y, Wani P, Wang Z, Reijo Pera R, Chen B.

Stem Cells Transl Med. 2017 Apr;6(4):1158-1167. doi: 10.1002/sctm.16-0160. Epub 2017 Feb 18.

12.

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.

13.

Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma.

Brečević L, Rinčić M, Krsnik Ž, Sedmak G, Hamid AB, Kosyakova N, Galić I, Liehr T, Borovečki F.

Transl Neurosci. 2015 Mar 2;6(1):59-86. doi: 10.1515/tnsci-2015-0007. eCollection 2015. Review.

14.

Sherpas share genetic variations with Tibetans for high-altitude adaptation.

Bhandari S, Zhang X, Cui C, Yangla, Liu L, Ouzhuluobu, Baimakangzhuo, Gonggalanzi, Bai C, Bianba, Peng Y, Zhang H, Xiang K, Shi H, Liu S, Gengdeng, Wu T, Qi X, Su B.

Mol Genet Genomic Med. 2016 Nov 23;5(1):76-84. doi: 10.1002/mgg3.264. eCollection 2017 Jan.

15.

Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing.

Lardelli RM, Schaffer AE, Eggens VR, Zaki MS, Grainger S, Sathe S, Van Nostrand EL, Schlachetzki Z, Rosti B, Akizu N, Scott E, Silhavy JL, Heckman LD, Rosti RO, Dikoglu E, Gregor A, Guemez-Gamboa A, Musaev D, Mande R, Widjaja A, Shaw TL, Markmiller S, Marin-Valencia I, Davies JH, de Meirleir L, Kayserili H, Altunoglu U, Freckmann ML, Warwick L, Chitayat D, Blaser S, Çağlayan AO, Bilguvar K, Per H, Fagerberg C, Christesen HT, Kibaek M, Aldinger KA, Manchester D, Matsumoto N, Muramatsu K, Saitsu H, Shiina M, Ogata K, Foulds N, Dobyns WB, Chi NC, Traver D, Spaccini L, Bova SM, Gabriel SB, Gunel M, Valente EM, Nassogne MC, Bennett EJ, Yeo GW, Baas F, Lykke-Andersen J, Gleeson JG.

Nat Genet. 2017 Mar;49(3):457-464. doi: 10.1038/ng.3762. Epub 2017 Jan 16.

16.

Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients.

Besbas N, Gulhan B, Soylemezoglu O, Ozcakar ZB, Korkmaz E, Hayran M, Ozaltin F.

BMC Nephrol. 2017 Jan 5;18(1):6. doi: 10.1186/s12882-016-0420-6.

17.

CYP1A1, CYP2E1 and EPHX1 polymorphisms in sporadic colorectal neoplasms.

Fernandes GM, Russo A, Proença MA, Gazola NF, Rodrigues GH, Biselli-Chicote PM, Silva AE, Netinho JG, Pavarino ÉC, Goloni-Bertollo EM.

World J Gastroenterol. 2016 Dec 7;22(45):9974-9983. doi: 10.3748/wjg.v22.i45.9974.

18.

Genetic Analysis of Human Chymotrypsin-Like Elastases 3A and 3B (CELA3A and CELA3B) to Assess the Role of Complex Formation between Proelastases and Procarboxypeptidases in Chronic Pancreatitis.

Párniczky A, Hegyi E, Tóth AZ, Szücs Á, Szentesi A, Vincze Á, Izbéki F, Németh BC, Hegyi P, Sahin-Tóth M.

Int J Mol Sci. 2016 Dec 20;17(12). pii: E2148. doi: 10.3390/ijms17122148.

19.

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.

20.

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.

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