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Literature citations Results

A defect of the vacuolar putative lipase Atg15 accelerates degradation of lipid droplets through lipolysis.

Maeda Y., Oku M., Sakai Y.

Autophagy 0:0-0(2015)

Necrotic Cells Actively Attract Phagocytes through the Collaborative Action of Two Distinct PS-Exposure Mechanisms.

Li Z., Venegas V., Nagaoka Y., Morino E., Raghavan P., Audhya A., Nakanishi Y., Zhou Z.

PLoS Genet. 11:e1005285-e1005285(2015) · Mapped (6)

Ligand regulation of a constitutively dimeric EGF receptor.

Freed D.M., Alvarado D., Lemmon M.A.

Nat Commun 6:7380-7380(2015) · Mapped (6)

Neurodegeneration in C. elegans models of ALS requires TIR-1/Sarm1 immune pathway activation in neurons.

Veriepe J., Fossouo L., Parker J.A.

Nat Commun 6:7319-7319(2015) · Mapped (21)

Characterization of skn-1/wdr-23 phenotypes in Caenorhabditis elegans; pleitrophy, aging, glutathione, and interactions with other longevity pathways.

Tang L., Choe K.P.

Mech. Ageing Dev. 0:0-0(2015) · Mapped (6)

Yeast FEX1 is a Constitutively Expressed Fluoride Channel with Functional Asymmetry of its Two Homologous Domains.

Smith K.D., Gordon P.B., Rivetta A., Allen K.E., Berbasova T., Slayman C., Strobel S.A.

J. Biol. Chem. 0:0-0(2015)

The DAF-7/TGF-beta signaling pathway regulates abundance of the Caenorhabditis elegans glutamate receptor GLR-1.

McGehee A.M., Moss B.J., Juo P.

Mol. Cell. Neurosci. 67:66-74(2015) · Mapped (4)

The unfolded protein response is required for dendrite morphogenesis.

Wei X., Howell A.S., Dong X., Taylor C.A., Cooper R.C., Zhang J., Zou W., Sherwood D.R., Shen K.

Elife 4:0-0(2015) · Mapped (3)

Dynamic Microtubules Drive Circuit Rewiring in the Absence of Neurite Remodeling.

Kurup N., Yan D., Goncharov A., Jin Y.

Curr. Biol. 25:1594-1605(2015) · Mapped (2)

Saccharomyces cerevisiae Ski7 Is a GTP-Binding Protein Adopting the Characteristic Conformation of Active Translational GTPases.

Kowalinski E., Schuller A., Green R., Conti E.

Structure 0:0-0(2015)

LSY-2 is essential for maintaining the germ-soma distinction in C. elegans.

Lin L., Li Y., Yan L., Zhang G., Zhao Y., Zhang H.

Protein Cell 0:0-0(2015) · Mapped (4)

Effect of different N7 substitution of dinucleotide cap analogs on the hydrolytic susceptibility towards scavenger decapping enzymes (DcpS).

Piecyk K., Darzynkiewicz Z.M., Jankowska-Anyszka M., Ferenc-Mrozek A., Stepinski J., Darzynkiewicz E., Bojarska E.

Biochem. Biophys. Res. Commun. 0:0-0(2015) · Mapped (2)

N(6)-methyladenosine modulates messenger RNA translation efficiency.

Wang X., Zhao B.S., Roundtree I.A., Lu Z., Han D., Ma H., Weng X., Chen K., Shi H., He C.

Cell 161:1388-1399(2015) · UniProtKB (2)

Myristoylated CIL-7 Regulates Ciliary Extracellular Vesicle Biogenesis.

Maguire J.E., Silva M., Nguyen K.C., Hellen E., Kern A.D., Hall D.H., Barr M.M.

Mol. Biol. Cell 0:0-0(2015) · Mapped (1)

Lifespan extension and increased resistance to environmental stressors by N-Acetyl-L-Cysteine in Caenorhabditis elegans.

Oh S.I., Park J.K., Park S.K.

Clinics (Sao Paulo) 70:380-386(2015) · Mapped (3)

Cdk1 plays matchmaker for the Polo-like kinase and its activator SPAT-1/Bora.

Tavernier N., Panbianco C., Gotta M., Pintard L.

Cell Cycle 0:0-0(2015) · Mapped (5)

A Mutation in Caenorhabditis elegans NDUF-7 Activates the Mitochondrial Stress Response, and Prolongs Lifespan via ROS and CED-4.

Rauthan M., Ranji P., Abukar R., Pilon M.

G3 (Bethesda) 0:0-0(2015) · Mapped (6)

An internal thioester in a pathogen surface protein mediates covalent host binding.

Walden M., Edwards J.M., Dziewulska A.M., Bergmann R., Saalbach G., Kan S.Y., Miller O.K., Weckener M., Jackson R.J., Shirran S.L. et al.

Elife 4:0-0(2015) · UniProtKB (2)

Polyamine-independent expression of Caenorhabditis elegans antizyme.

Stegehake D., Kurosinski M.A., Schuermann S., Daniel J., Luersen K., Liebau E.

J. Biol. Chem. 0:0-0(2015) · Mapped (3)

Somatic expression of unc-54 and vha-6 mRNAs declines but not pan-neuronal rgef-1 and unc-119 expression in aging Caenorhabditis elegans.

Adamla F., Ignatova Z.

Sci Rep 5:10692-10692(2015) · Mapped (9)

Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming.

Yang X., Wang S., Sheng Y., Zhang M., Zou W., Wu L., Kang L., Rizo J., Zhang R., Xu T. et al.

Nat. Struct. Mol. Biol. 0:0-0(2015) · Mapped (2)

C. elegans Punctin Clusters GABAA Receptors via Neuroligin Binding and UNC-40/DCC Recruitment.

Tu H., Pinan-Lucarre B., Ji T., Jospin M., Bessereau J.L.

Neuron 86:1407-1419(2015) · Mapped (5)

MADD-4/Punctin and Neurexin Organize C. elegans GABAergic Postsynapses through Neuroligin.

Maro G.S., Gao S., Olechwier A.M., Hung W.L., Liu M., Ozkan E., Zhen M., Shen K.

Neuron 86:1420-1432(2015) · Mapped (20)

Environmental Temperature Differentially Modulates C. elegans Longevity through a Thermosensitive TRP Channel.

Zhang B., Xiao R., Ronan E.A., He Y., Hsu A.L., Liu J., Xu X.Z.

Cell Rep 11:1414-1424(2015) · Mapped (2)

The longevity effect of echinacoside in Caenorhabditis elegans mediated through daf-16.

Wang X., Zhang J., Lu L., Zhou L.

Biosci. Biotechnol. Biochem. 2015:1-8(2015) · Mapped (1)

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