human | Q5 |
P496 | ORCID iD | 0000-0001-8459-3664 |
P1889 | different from | James McNew | Q6139539 |
P734 | family name | McNew | Q37438528 |
McNew | Q37438528 | ||
McNew | Q37438528 | ||
P735 | given name | James | Q677191 |
James | Q677191 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q27936546 | A t-SNARE of the endocytic pathway must be activated for fusion. |
Q36116836 | An intramolecular t-SNARE complex functions in vivo without the syntaxin NH2-terminal regulatory domain |
Q36236499 | An inventory of peroxisomal proteins and pathways in Drosophila melanogaster |
Q35141453 | Balancing ER dynamics: shaping, bending, severing, and mending membranes |
Q46451525 | Beneficial effects of rapamycin in a Drosophila model for hereditary spastic paraplegia |
Q37010711 | Binding interactions control SNARE specificity in vivo |
Q36342484 | Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors |
Q35083786 | Fusing a lasting relationship between ER tubules |
Q38123199 | GTP-dependent membrane fusion |
Q27936489 | Gos1p, a Saccharomyces cerevisiae SNARE protein involved in Golgi transport. |
Q54459561 | Hemifusion arrest by complexin is relieved by Ca2+-synaptotagmin I. |
Q27939669 | Hemifusion in SNARE-mediated membrane fusion |
Q34994215 | Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin |
Q43745603 | In Arabidopsis, the spatial and dynamic organization of the endoplasmic reticulum and Golgi apparatus is influenced by the integrity of the C-terminal domain of RHD3, a non-essential GTPase |
Q58025405 | In Vitro Fusion Catalyzed by the Sporulation-Specific t-SNARE Light-Chain Spo20p is Stimulated by Phosphatidic Acid |
Q79281029 | Liposome fusion assay to monitor intracellular membrane fusion machines |
Q34985639 | Lunapark stabilizes nascent three-way junctions in the endoplasmic reticulum |
Q44702894 | Membrane-bound fatty acid desaturases are inserted co-translationally into the ER and contain different ER retrieval motifs at their carboxy termini |
Q36992879 | Munc18a scaffolds SNARE assembly to promote membrane fusion |
Q28474414 | Negative regulation of syntaxin4/SNAP-23/VAMP2-mediated membrane fusion by Munc18c in vitro |
Q27322788 | Peroxisomes are required for lipid metabolism and muscle function in Drosophila melanogaster |
Q37140912 | Regulation of SNARE-mediated membrane fusion during exocytosis |
Q36323855 | Regulation of membrane fusion by the membrane-proximal coil of the t-SNARE during zippering of SNAREpins |
Q28742152 | SNARE proteins are required for macroautophagy |
Q27931711 | Sec1p directly stimulates SNARE-mediated membrane fusion in vitro |
Q34435795 | Specific cross-linking of the proline isomerase cyclophilin to a non-proline-containing peptide. |
Q57027952 | The atlastin membrane anchor forms an intramembrane hairpin that does not span the phospholipid bilayer |
Q36856961 | The effects of ER morphology on synaptic structure and function in Drosophila melanogaster |
Q73075597 | The length of the flexible SNAREpin juxtamembrane region is a critical determinant of SNARE-dependent fusion |
Q27931683 | The polybasic juxtamembrane region of Sso1p is required for SNARE function in vivo |
Q37071739 | The synaptobrevin homologue Snc2p recruits the exocyst to secretory vesicles by binding to Sec6p |
Q71641179 | The targeting and assembly of peroxisomal proteins: some old rules do not apply |
Q24315775 | Ykt6p, a Prenylated SNARE Essential for Endoplasmic Reticulum-Golgi Transport |
Q6139539 | James McNew | different from | P1889 |
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