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Items: 1 to 20 of 133

1.

Mitophagy and mitochondrial biogenesis in atrial tissue of patients undergoing heart surgery with cardiopulmonary bypass.

Andres AM, Tucker KC, Thomas A, Taylor DJ, Sengstock D, Jahania SM, Dabir R, Pourpirali S, Brown JA, Westbrook DG, Ballinger SW, Mentzer RM Jr, Gottlieb RA.

JCI Insight. 2017 Feb 23;2(4):e89303. doi: 10.1172/jci.insight.89303.

2.

Paxillin: a crossroad in pathological cell migration.

López-Colomé AM, Lee-Rivera I, Benavides-Hidalgo R, López E.

J Hematol Oncol. 2017 Feb 18;10(1):50. doi: 10.1186/s13045-017-0418-y. Review.

3.

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 15. doi: 10.1093/gbe/evw307. [Epub ahead of print] No abstract available.

4.

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.

5.

Size-selective separation and overall-amplification of cell-free fetal DNA fragments using PCR-based enrichment.

Yang Q, Du Z, Song Y, Gao S, Yu S, Zhu H, Ren M, Zhang G.

Sci Rep. 2017 Jan 19;7:40936. doi: 10.1038/srep40936.

6.

Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology.

Ogden KK, Chen W, Swanger SA, McDaniel MJ, Fan LZ, Hu C, Tankovic A, Kusumoto H, Kosobucki GJ, Schulien AJ, Su Z, Pecha J, Bhattacharya S, Petrovski S, Cohen AE, Aizenman E, Traynelis SF, Yuan H.

PLoS Genet. 2017 Jan 17;13(1):e1006536. doi: 10.1371/journal.pgen.1006536. eCollection 2017 Jan.

7.

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

van der Zee J, Gijselinck I, Van Mossevelde S, Perrone F, Dillen L, Heeman B, Bäumer V, Engelborghs S, De Bleecker J, Baets J, Gelpi E, Rojas-García R, Clarimón J, Lleó A, Diehl-Schmid J, Alexopoulos P, Perneczky R, Synofzik M, Just J, Schöls L, Graff C, Thonberg H, Borroni B, Padovani A, Jordanova A, Sarafov S, Tournev I, de Mendonça A, Miltenberger-Miltényi G, Simões do Couto F, Ramirez A, Jessen F, Heneka MT, Gómez-Tortosa E, Danek A, Cras P, Vandenberghe R, De Jonghe P, De Deyn PP, Sleegers K, Cruts M, Van Broeckhoven C, Goeman J, Nuytten D, Smets K, Robberecht W, Damme PV, Bleecker J, Santens P, Dermaut B, Versijpt J, Michotte A, Ivanoiu A, Deryck O, Bergmans B, Delbeck J, Bruyland M, Willems C, Salmon E, Pastor P, Ortega-Cubero S, Benussi L, Ghidoni R, Binetti G, Hernández I, Boada M, Ruiz A, Sorbi S, Nacmias B, Bagnoli S, Sorbi S, Sanchez-Valle R, Llado A, Santana I, Rosário Almeida M, Frisoni GB, Maetzler W, Matej R, Fraidakis MJ, Kovacs GG, Fabrizi GM, Testi S.

Hum Mutat. 2017 Mar;38(3):297-309. doi: 10.1002/humu.23161. Epub 2017 Jan 19.

8.

ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.

Bahena-Bahena D, López-Valdez J, Raymond K, Salinas-Marín R, Ortega-García A, Ng BG, Freeze HH, Ruíz-García M, Martínez-Duncker I.

Mol Genet Metab Rep. 2014 Apr 25;1:203-212. eCollection 2014.

9.

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.

10.

Glutamatergic stimulation induces GluN2B translation by the nitric oxide-Heme-Regulated eIF2α kinase in cortical neurons.

Ramos-Fernández E, Tajes M, Ill-Raga G, Vargas L, Busquets-García A, Bosch-Morató M, Guivernau B, Valls-Comamala V, Gomis M, Grau C, Fandos C, Rosen MD, Rabinowitz MH, Inestrosa N, Maldonado R, Altafaj X, Ozaita A, Alvarez A, Vicente R, Valverde MA, Muñoz FJ.

Oncotarget. 2016 Sep 13;7(37):58876-58892. doi: 10.18632/oncotarget.11417.

11.

Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.

Lucariello M, Vidal E, Vidal S, Saez M, Roa L, Huertas D, Pineda M, Dalfó E, Dopazo J, Jurado P, Armstrong J, Esteller M.

Hum Genet. 2016 Dec;135(12):1343-1354. Epub 2016 Aug 19.

12.

Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders.

Fokstuen S, Makrythanasis P, Hammar E, Guipponi M, Ranza E, Varvagiannis K, Santoni FA, Albarca-Aguilera M, Poleggi ME, Couchepin F, Brockmann C, Mauron A, Hurst SA, Moret C, Gehrig C, Vannier A, Bevillard J, Araud T, Gimelli S, Stathaki E, Paoloni-Giacobino A, Bottani A, Sloan-Béna F, Sizonenko LD, Mostafavi M, Hamamy H, Nouspikel T, Blouin JL, Antonarakis SE.

Hum Genomics. 2016 Jun 28;10(1):24. doi: 10.1186/s40246-016-0080-4.

13.

Prediction of the Risk for Essential Hypertension among Carriers of C825T Genetic Polymorphism of G Protein β3 (GNB3) Gene.

El Din Hemimi NS, Mansour AA, Abdelsalam MM.

Biomark Insights. 2016 May 17;11:69-75. doi: 10.4137/BMI.S38321. eCollection 2016.

14.

Genetics of PCOS: A systematic bioinformatics approach to unveil the proteins responsible for PCOS.

Panda PK, Rane R, Ravichandran R, Singh S, Panchal H.

Genom Data. 2016 Mar 31;8:52-60. doi: 10.1016/j.gdata.2016.03.008. eCollection 2016 Jun.

15.

Fyn Kinase regulates GluN2B subunit-dominant NMDA receptors in human induced pluripotent stem cell-derived neurons.

Zhang WB, Ross PJ, Tu Y, Wang Y, Beggs S, Sengar AS, Ellis J, Salter MW.

Sci Rep. 2016 Apr 4;6:23837. doi: 10.1038/srep23837.

16.

Novel Methodology for Rapid Detection of KRAS Mutation Using PNA-LNA Mediated Loop-Mediated Isothermal Amplification.

Itonaga M, Matsuzaki I, Warigaya K, Tamura T, Shimizu Y, Fujimoto M, Kojima F, Ichinose M, Murata S.

PLoS One. 2016 Mar 21;11(3):e0151654. doi: 10.1371/journal.pone.0151654. eCollection 2016.

17.

Subunit-selective N-Methyl-d-aspartate (NMDA) Receptor Signaling through Brefeldin A-resistant Arf Guanine Nucleotide Exchange Factors BRAG1 and BRAG2 during Synapse Maturation.

Elagabani MN, Briševac D, Kintscher M, Pohle J, Köhr G, Schmitz D, Kornau HC.

J Biol Chem. 2016 Apr 22;291(17):9105-18. doi: 10.1074/jbc.M115.691717. Epub 2016 Feb 16.

18.

Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population.

Edelman D, Kalia H, Delio M, Alani M, Krishnamurthy K, Abd M, Auton A, Wang T, Wolkoff AW, Morrow BE.

Mol Genet Genomic Med. 2015 Aug 11;3(6):558-69. doi: 10.1002/mgg3.168. eCollection 2015 Nov.

19.

Purification and Characterization of Recombinant Human Lysozyme from Eggs of Transgenic Chickens.

Wu H, Cao D, Liu T, Zhao J, Hu X, Li N.

PLoS One. 2015 Dec 29;10(12):e0146032. doi: 10.1371/journal.pone.0146032. eCollection 2015.

20.

Evolution of the highly networked deubiquitinating enzymes USP4, USP15, and USP11.

Vlasschaert C, Xia X, Coulombe J, Gray DA.

BMC Evol Biol. 2015 Oct 26;15:230. doi: 10.1186/s12862-015-0511-1.

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