Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 79

1.

Plasticity of Functional MAOA Gene Methylation in Acrophobia.

Schiele MA, Ziegler C, Kollert L, Katzorke A, Schartner C, Busch Y, Gromer D, Reif A, Pauli P, Deckert J, Herrmann MJ, Domschke K.

Int J Neuropsychopharmacol. 2018 Sep 1;21(9):822-827. doi: 10.1093/ijnp/pyy050.

2.

A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case report.

Buena-Atienza E, Nasser F, Kohl S, Wissinger B.

BMC Med Genet. 2018 Jun 26;19(1):107. doi: 10.1186/s12881-018-0623-8.

3.

HEV ORF3 downregulates TLR7 to inhibit the generation of type I interferon via impairment of multiple signaling pathways.

Lei Q, Li L, Zhang S, Li T, Zhang X, Ding X, Qin B.

Sci Rep. 2018 Jun 5;8(1):8585. doi: 10.1038/s41598-018-26975-4.

4.

Preleukemic and second-hit mutational events in an acute myeloid leukemia patient with a novel germline RUNX1 mutation.

Ng IK, Lee J, Ng C, Kosmo B, Chiu L, Seah E, Mok MMH, Tan K, Osato M, Chng WJ, Yan B, Tan LK.

Biomark Res. 2018 May 11;6:16. doi: 10.1186/s40364-018-0130-2. eCollection 2018.

5.

High Percentage of Isomeric Human MicroRNA and Their Analytical Challenges.

Mwangi JN, Chiu NHL.

Noncoding RNA. 2016 Dec 2;2(4). pii: E13. doi: 10.3390/ncrna2040013.

6.

An intronic mutation c.6430-3C>G in the F8 gene causes splicing efficiency and premature termination in hemophilia A.

Xia Z, Lin J, Lu L, Kim C, Yu P, Qi M.

Blood Coagul Fibrinolysis. 2018 Jun;29(4):381-386. doi: 10.1097/MBC.0000000000000730.

7.

Detection of fusion gene in cell-free DNA of a gastric synovial sarcoma.

Ogino S, Konishi H, Ichikawa D, Hamada J, Shoda K, Arita T, Komatsu S, Shiozaki A, Okamoto K, Yamazaki S, Yasukawa S, Konishi E, Otsuji E.

World J Gastroenterol. 2018 Feb 28;24(8):949-956. doi: 10.3748/wjg.v24.i8.949.

8.

Two novel variants of the PHEX gene in patients with X‑linked dominant hypophosphatemic rickets and prenatal diagnosis for fetuses in these families.

Liao H, Zhu HM, Liu HQ, Li LP, Liu SL, Wang H.

Int J Mol Med. 2018 Apr;41(4):2012-2020. doi: 10.3892/ijmm.2018.3402. Epub 2018 Jan 18.

9.

Monoamine Oxidase A Gene Methylation and Its Role in Posttraumatic Stress Disorder: First Evidence from the South Eastern Europe (SEE)-PTSD Study.

Ziegler C, Wolf C, Schiele MA, Feric Bojic E, Kucukalic S, Sabic Dzananovic E, Goci Uka A, Hoxha B, Haxhibeqiri V, Haxhibeqiri S, Kravic N, Muminovic Umihanic M, Cima Franc A, Jaksic N, Babic R, Pavlovic M, Warrings B, Bravo Mehmedbasic A, Rudan D, Aukst-Margetic B, Kucukalic A, Marjanovic D, Babic D, Bozina N, Jakovljevic M, Sinanovic O, Avdibegovic E, Agani F, Dzubur-Kulenovic A, Deckert J, Domschke K.

Int J Neuropsychopharmacol. 2018 May 1;21(5):423-432. doi: 10.1093/ijnp/pyx111.

10.

X-derived marker chromosome in patient with mosaic Turner syndrome and Dandy-Walker syndrome: a case report.

Telepova AS, Romanenko SA, Lemskaya NA, Maksimova YV, Shorina AR, Yudkin DV.

Mol Cytogenet. 2017 Nov 17;10:43. doi: 10.1186/s13039-017-0344-2. eCollection 2017.

11.

Integrity of the corpus callosum in patients with periventricular nodular heterotopia related epilepsy by FLNA mutation.

Liu W, An D, Niu R, Gong Q, Zhou D.

Neuroimage Clin. 2017 Oct 13;17:109-114. doi: 10.1016/j.nicl.2017.10.002. eCollection 2018.

12.

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.

13.

Coexistence of EZH2, NOTCH1, IL7R, and PHF6 Mutations in Adult T-cell Acute Lymphoblastic Leukemia.

Zhou X, Gu Y, Han Q, Soliman M, Song C, Ge Z.

Turk J Haematol. 2017 Dec 1;34(4):366-368. doi: 10.4274/tjh.2017.0194. Epub 2017 Jul 27. No abstract available.

14.

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.

15.

Androgen inhibits key atherosclerotic processes by directly activating ADTRP transcription.

Luo C, Pook E, Tang B, Zhang W, Li S, Leineweber K, Cheung SH, Chen Q, Bechem M, Hu JS, Laux V, Wang QK.

Biochim Biophys Acta Mol Basis Dis. 2017 Sep;1863(9):2319-2332. doi: 10.1016/j.bbadis.2017.06.015. Epub 2017 Jun 20.

16.

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability.

Zahir FR, Mwenifumbo JC, Chun HE, Lim EL, Van Karnebeek CDM, Couse M, Mungall KL, Lee L, Makela N, Armstrong L, Boerkoel CF, Langlois SL, McGillivray BM, Jones SJM, Friedman JM, Marra MA.

BMC Genomics. 2017 May 24;18(1):403. doi: 10.1186/s12864-017-3671-0.

17.

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.

18.

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.

19.

MicroRNA Modulation during the In vitro Culture of Hematopoietic Stem Cells Prior to Transplantation.

Shahrabi S, Kaviani S, Soleimani M, Pourfathollah AA, Bakhshandeh B, Hajizamani S, Saki N.

Iran J Med Sci. 2017 Jan;42(1):40-47.

20.

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.

Supplemental Content

Support Center