P1066
Flexibility of a eukaryotic lipidome--insights from yeast lipidomicsInvolvement of caveolin-2 in caveolar biogenesis in MDCK cellsOrm family proteins mediate sphingolipid homeostasisLocalization of low molecular weight GTP binding proteins to exocytic and endocytic compartmentsIdentification of components of trans-Golgi network-derived transport vesicles and detergent-insoluble complexes by nanoelectrospray tandem mass spectrometryCholesterol, lipid rafts, and diseaseVIP21/caveolin is a cholesterol-binding proteinGlobal analysis of the yeast lipidome by quantitative shotgun mass spectrometryRab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membraneAmyloidogenic processing of the Alzheimer beta-amyloid precursor protein depends on lipid raftsGp135/podocalyxin and NHERF-2 participate in the formation of a preapical domain during polarization of MDCK cellsApical membrane targeting of Nedd4 is mediated by an association of its C2 domain with annexin XIIIbOn the entry of Semliki forest virus into BHK-21 cellsFunctional rafts in cell membranesPlasma membrane proton ATPase Pma1p requires raft association for surface delivery in yeast.Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast.Cell surface polarization during yeast mating.Lipid rafts and signal transductionA putative novel class of animal lectins in the secretory pathway homologous to leguminous lectinsModel systems, lipid rafts, and cell membranesProhibitin, an antiproliferative protein, is localized to mitochondriaProtein transport to the dendritic plasma membrane of cultured neurons is regulated by rab8pRaft-partitioning of the ubiquitin ligases Cbl and Nedd4 upon IgE-triggered cell signalingHopanoids as functional analogues of cholesterol in bacterial membranesAn automated shotgun lipidomics platform for high throughput, comprehensive, and quantitative analysis of blood plasma intact lipidsEngineering the future with cell biologyThe small GTPase rab5 functions as a regulatory factor in the early endocytic pathwayCell membranes: the lipid perspective.Accumulation of raft lipids in T-cell plasma membrane domains engaged in TCR signallingGolgi protein FAPP2 tubulates membranesQuantitative profiling of phospholipids by multiple precursor ion scanning on a hybrid quadrupole time-of-flight mass spectrometer.The effect of raft lipid depletion on microvilli formation in MDCK cells, visualized by atomic force microscopy.A genome-wide visual screen reveals a role for sphingolipids and ergosterol in cell surface delivery in yeastIdentification of glycosylated marker proteins of epithelial polarity in MDCK cells by homology driven proteomics.Controversy fuels trafficking of GPI-anchored proteinsMembrane raft association is a determinant of plasma membrane localizationMolecular cloning of YPT1/SEC4-related cDNAs from an epithelial cell lineDe novo formation of caveolae in lymphocytes by expression of VIP21-caveolin.Lipid rafts and membrane dynamics.The differential miscibility of lipids as the basis for the formation of functional membrane rafts.
P50
Q21134862-CDDD9F14-5CAF-4360-A946-C71F062F4930Q24297660-FE145CFB-C8D8-48A7-B2DB-702447D4109EQ24300979-F96B2699-8F85-42A6-9897-AEB2D4662FB2Q24316079-40A41E63-F185-48AC-BB3C-CBDDD303F2B4Q24321353-BFBA3D4C-243D-4AB8-93EC-EB7AC10525EBQ24553188-E866B053-1930-48D3-B230-E17CA7D45490Q24563474-30DC765C-0AB1-4D5F-BBF0-19DC7D340674Q24646313-B6BB30D9-D2D2-481F-8892-10B8A0E56533Q24673790-1E2ADF64-8EF2-439C-81D4-CCCF84A40183Q24675729-DEFBA681-CCB9-404E-B170-F2A584E9DE77Q24678887-C315B93A-04E8-466C-BD06-68D502E8CB69Q24685954-99A2131F-1157-4A78-85A7-A76C0864BC3AQ27482326-1EDE6FCB-A608-4D7D-9656-359EAB3AAEFBQ27860768-519D5516-0A95-4D79-879D-FA63F3226089Q27932251-337402D9-118D-42DD-ACAB-2CAF1821C6E5Q27932650-0AEC21F5-404B-462E-9BA9-AE5B18B9DF51Q27934709-89891AE1-FE50-4734-82D3-06F63FFE3D31Q28131735-C257AF2F-0FB5-4A5B-9018-14331E387EF6Q28254839-62DF9BA2-4AD1-49EC-943A-7D4B9C1FC364Q28261365-C37F610B-425E-439D-A5D2-84CEA2803DE4Q28306674-C803A2D4-BDC5-45D7-AD04-4FD7BFD12C9BQ28566824-6B4CCCBA-5A82-4074-A837-F5665FE60150Q28573083-2B405419-FCCD-46AD-B5E0-4E7CEAED6029Q28607147-4DA75CED-8896-47CF-A8B6-C7D963895C1DQ28611371-48BFB182-033E-44C3-B981-349B5C4FE653Q28748362-EE0B24D0-ED06-40B8-8020-7C17D7277D59Q29620272-DCB3BC3B-C63C-4A46-AA0C-EF67C3B90B69Q30409388-7149E0E8-EB4B-4918-80EC-467F98A1C560Q30486555-1D62A852-2924-406C-9347-F561C90236C5Q30492412-A0B1A9C3-E8C1-4CF8-A237-C2283A9CB3C7Q30700823-99B11E15-9E07-4025-87DB-CDF0397F1B4BQ33202774-134E482A-6548-4CB6-A6B8-6D4C07A037B9Q33228605-3925DB11-E9B7-420B-855E-3F0CEAB9F6D6Q33236260-62CAAC82-995A-4165-BA1A-E29B64502C0FQ33237790-02566682-E26A-4E7F-ABBA-FC86D4B882FAQ33767581-71C4E278-73D2-4B55-B267-C6776C94D4CDQ33792963-F2F31EAF-5342-49A8-9FC4-DB8E6FF96007Q33916325-4AD04EA9-1FD7-447A-9B25-639D71464EE0Q33985713-746D6392-F73B-489F-AD7E-9393DE23AA7DQ34067848-9A8ED0A9-CBAA-44B3-8135-31F7556B64F0
P50
subject
description
Finnish biochemist and molecular biologist
@en
Fins biochemicus
@nl
biochemik fiński
@pl
finnischer Mediziner und Biochemiker
@de
suomalainen biokemisti
@fi
name
Kai Simons
@ast
Kai Simons
@ca
Kai Simons
@de
Kai Simons
@en
Kai Simons
@es
Kai Simons
@fi
Kai Simons
@fr
Kai Simons
@ga
Kai Simons
@nl
Kai Simons
@pl
type
label
Kai Simons
@ast
Kai Simons
@ca
Kai Simons
@de
Kai Simons
@en
Kai Simons
@es
Kai Simons
@fi
Kai Simons
@fr
Kai Simons
@ga
Kai Simons
@nl
Kai Simons
@pl
altLabel
Kai Lennart Simons
@de
Kai Lennart Simons
@en
prefLabel
Kai Simons
@ast
Kai Simons
@ca
Kai Simons
@de
Kai Simons
@en
Kai Simons
@es
Kai Simons
@fi
Kai Simons
@fr
Kai Simons
@ga
Kai Simons
@nl
Kai Simons
@pl