about
Crystal Structure of an Ammonia-Permeable AquaporinHigh-resolution x-ray structure of human aquaporin 5Algal MIPs, high diversity and conserved motifsUnexpected complexity of the aquaporin gene family in the moss Physcomitrella patensStructure and stability of the spinach aquaporin SoPIP2;1 in detergent micelles and lipid membranes.Increasing gene dosage greatly enhances recombinant expression of aquaporins in Pichia pastoris.Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time.Aquaporin-9 protein is the primary route of hepatocyte glycerol uptake for glycerol gluconeogenesis in miceA new subfamily of major intrinsic proteins in plants.Structural mechanism of plant aquaporin gating.Human TRPA1 is intrinsically cold- and chemosensitive with and without its N-terminal ankyrin repeat domainSingle amino acid substitutions in the selectivity filter render NbXIP1;1α aquaporin water permeableAquaporin gating.Phylogeny of major intrinsic proteins.In vitro selection of RNA aptamers directed against protein E: a Haemophilus influenzae adhesin.Transcriptional regulation of aquaporins in accessions of Arabidopsis in response to drought stress.Whole gene family expression and drought stress regulation of aquaporins.The complete set of genes encoding major intrinsic proteins in Arabidopsis provides a framework for a new nomenclature for major intrinsic proteins in plants.The Aquaporin Splice Variant NbXIP1;1α Is Permeable to Boric Acid and Is Phosphorylated in the N-terminal Domain.A new mutation in 16S rRNA of Escherichia coli conferring spectinomycin resistance.The N-terminal Ankyrin Repeat Domain Is Not Required for Electrophile and Heat Activation of the Purified Mosquito TRPA1 Receptor.Increased Permeability of the Aquaporin SoPIP2;1 by Mercury and Mutations in Loop AThe 5A structure of heterologously expressed plant aquaporin SoPIP2;1.Human TRPA1 is a heat sensor displaying intrinsic U-shaped thermosensitivity.Annotation of Selaginella moellendorffii Major Intrinsic Proteins and the Evolution of the Protein Family in Terrestrial Plants.Corrigendum: Increased Permeability of the Aquaporin SoPIP2;1 by Mercury and Mutations in Loop A.Solute transport on the sub 100 ms scale across the lipid bilayer membrane of individual proteoliposomes.A novel plant major intrinsic protein in Physcomitrella patens most similar to bacterial glycerol channels.Affinity tags can reduce merohedral twinning of membrane protein crystals.MADS-box genes active in developing pollen cones of Norway spruce (Picea abies) are homologous to the B-class floral homeotic genes in angiosperms.Comparison of the complete sequence of the str operon in Salmonella typhimurium and Escherichia coli.The MADS-box gene DAL1 is a potential mediator of the juvenile-to-adult transition in Norway spruce (Picea abies).The DAL10 gene from Norway spruce (Picea abies) belongs to a potentially gymnosperm-specific subclass of MADS-box genes and is specifically active in seed cones and pollen cones.A structural preview of aquaporin 8 via homology modeling of seven vertebrate isoforms.The dynamic structure of EF-G studied by fusidic acid resistance and internal revertants.Fusidic acid-resistant mutants define three regions in elongation factor G of Salmonella typhimurium.Endogenous insensitivity to the Orco agonist VUAA1 reveals novel olfactory receptor complex properties in the specialist fly Mayetiola destructor.Purification and characterization of two protein kinases acting on the aquaporin SoPIP2;1.Arabidopsis genes encoding mitochondrial type II NAD(P)H dehydrogenases have different evolutionary origin and show distinct responses to light.The effects of the loss of TIP1;1 and TIP1;2 aquaporins in Arabidopsis thaliana.
P50
Q27344647-734184F0-7EFE-46CA-A6EA-6B21BB5160A3Q27651968-7E157204-ADA2-4F83-993C-CB8E0E7A0D7BQ28743824-198F4C65-68D8-4DFB-B9F8-9DAF823A95C9Q28754551-A04D726D-2980-495D-AC0E-223DDDF21264Q33826117-C0C5C85A-2406-4A13-9103-C09DE96163C1Q33898335-311320D9-A671-45D4-8919-778D3D6973F2Q33921320-70214289-43D7-4116-B13E-A8A5D886BFD0Q34073957-8181D4BC-0B48-4276-9200-92CD3035610CQ34120893-52519DD0-2C27-44DA-BB1D-9BA34CFD396FQ34474817-70289BFF-424D-44FC-978E-3CC63EF29946Q34601695-59E3E651-8C97-40A7-80A2-DD6AC2D1A7AAQ36303231-8D377320-1E02-4C08-A3A3-B40760B8B31AQ36534479-1B690836-4BE1-4314-9DF4-382139D3DC5CQ37776241-E4600ACD-7CF0-43CE-AE7A-D50B2C9A0D01Q38308093-A46D6FFC-8B9A-42F7-B012-6DCB94CF59F1Q38868262-B13E9432-3859-4A79-AE5D-E72423BEA834Q38868266-06FF809C-E7F4-464E-B436-80ACD4E6B489Q39576339-BE8AAE03-1EC6-461C-AE20-B08C05C545D1Q39631191-4526EC35-B1A8-441A-9103-E8E324E7F923Q40392885-56DD3D93-9278-47AE-AC34-605925984A94Q40392885-9A16A094-690A-4F4B-82DB-C1F1E505188AQ40422795-13605F36-929E-448F-AFAE-204C7BCACF0EQ40972446-B4151AB4-C50F-49C6-9CED-304E3A1D865CQ41627120-E8301340-5393-428C-A6AB-07F863A75587Q41790400-FDDF3CE9-B45F-470D-94C3-113627C0BFCFQ42174706-F2AB4F0C-BDD3-42C1-BFD7-702FC5D337AAQ42349342-EEC57524-8BC5-496B-B745-DBFA4A520293Q45908587-1B49B30B-7530-4DF4-8ECA-49FE2C385F33Q46661334-3AEA41F2-C105-48A6-8943-CDE3DAC31038Q47227462-DD803943-09D4-4DA3-ABC8-9BDDDA1FAFF4Q47918476-7EFE1DAB-6483-4E2E-BEF2-004AC29FA484Q48153498-92F1DE9F-A769-4DE0-A40F-9C6E868DA4FDQ48166987-2F1EE120-3CDC-4382-A258-1924C798BE94Q48203801-86D46EE6-F251-49C2-90D2-B9A4C14BD780Q49900832-BABE7C99-A27F-4AB2-A742-6F9AD42C48F9Q50138974-00ECC4EB-4F06-4FC9-8944-C6CE8A952C62Q50148687-55CB32C6-FC2E-4C73-9086-CB9E9BBB5A8AQ50325747-19E5788D-5797-4F75-8D74-56F35CFD5459Q50646506-F7A358EF-B57B-413B-B7EA-94EBDC314FE4Q51654190-5408000F-CD3A-4544-A91A-7891B928C696
P50
description
Zweeds onderzoeker
@nl
hulumtues
@sq
researcher
@en
հետազոտող
@hy
name
Urban Johanson
@ast
Urban Johanson
@en
Urban Johanson
@es
Urban Johanson
@nl
Urban Johanson
@sl
type
label
Urban Johanson
@ast
Urban Johanson
@en
Urban Johanson
@es
Urban Johanson
@nl
Urban Johanson
@sl
prefLabel
Urban Johanson
@ast
Urban Johanson
@en
Urban Johanson
@es
Urban Johanson
@nl
Urban Johanson
@sl
P106
P108
P21
P27
P31
P496
0000-0001-8862-128X
P569
2000-01-01T00:00:00Z