about
More than 200 genes required for methane formation from H₂ and CO₂ and energy conservation are present in Methanothermobacter marburgensis and Methanothermobacter thermautotrophicusThe genome sequence of Methanosphaera stadtmanae reveals why this human intestinal archaeon is restricted to methanol and H2 for methane formation and ATP synthesis.Complete Genome Sequence of Methanothermobacter marburgensis, a Methanoarchaeon Model OrganismTwo different bacterial community types are linked with the low-methane emission trait in sheepStructure of coenzyme F420H2 oxidase (FprA), a di-iron flavoprotein from methanogenic Archaea catalyzing the reduction of O2 to H2ORIM-DB: a taxonomic framework for community structure analysis of methanogenic archaea from the rumen and other intestinal environmentsSimultaneous amplicon sequencing to explore co-occurrence patterns of bacterial, archaeal and eukaryotic microorganisms in rumen microbial communitiesPhylogeny of intestinal ciliates, including Charonina ventriculi, and comparison of microscopy and 18S rRNA gene pyrosequencing for rumen ciliate community structure analysis.Si-face stereospecificity at C5 of coenzyme F420 for F420H2 oxidase from methanogenic Archaea as determined by mass spectrometry.The Draft Genome of the Non-Host-Associated Methanobrevibacter arboriphilus Strain DH1 Encodes a Large Repertoire of Adhesin-Like Proteins.F420H2 oxidase (FprA) from Methanobrevibacter arboriphilus, a coenzyme F420-dependent enzyme involved in O2 detoxification.Methane yield phenotypes linked to differential gene expression in the sheep rumen microbiome.Bacteria from diverse habitats colonize and compete in the mouse gut.Few highly abundant operational taxonomic units dominate within rumen methanogenic archaeal species in New Zealand sheep and cattleCharacterizing the interactions between a naturally primed immunoglobulin A and its conserved Bacteroides thetaiotaomicron species-specific epitope in gnotobiotic mice.Natural variation in methane emission of sheep fed on a lucerne pellet diet is unrelated to rumen ciliate community type.The genome of Clostridium kluyveri, a strict anaerobe with unique metabolic features.Characterizing a model human gut microbiota composed of members of its two dominant bacterial phylaThe long-term stability of the human gut microbiota.Coupled ferredoxin and crotonyl coenzyme A (CoA) reduction with NADH catalyzed by the butyryl-CoA dehydrogenase/Etf complex from Clostridium kluyveri.Draft Genome Sequences of Methanobrevibacter curvatus DSM11111, Methanobrevibacter cuticularis DSM11139, Methanobrevibacter filiformis DSM11501, and Methanobrevibacter oralis DSM7256.Re-citrate synthase from Clostridium kluyveri is phylogenetically related to homocitrate synthase and isopropylmalate synthase rather than to Si-citrate synthase.Conformational similarities in the beta-ionone ring region of the rhodopsin chromophore in its ground state and after photoactivation to the metarhodopsin-I intermediate.Comparative Genomic Analysis of Members of the Genera and Reveals Distinct Clades with Specific Potential Metabolic FunctionsNutrient-based diet modifications impact on the gut microbiome of the Javan slow loris (Nycticebus javanicus)Insights into the microbiome of farmed Asian sea bass (Lates calcarifer) with symptoms of tenacibaculosis and description of Tenacibaculum singaporense sp. novComplete Genome Sequence of Sponge-Associated Tenacibaculum mesophilum DSM 13764TComplete Genome Sequence of Duncaniella muris Strain B8, Isolated from the Feces of C57/BL6 Mice
P50
Q21296736-B71C2634-27CE-4E10-BBA1-34B2D82F9353Q22065443-720D152C-4E1C-4A66-813C-E8B0F079CA1DQ22065483-2EF67805-4A53-4946-9CF2-C5E949C97A9DQ27318117-576D3438-DF6B-4E76-9A75-6C9F18CF0AC7Q27644704-50B215B4-387A-4361-BC21-1E643EA262FEQ28654454-8E44F0F0-8C0F-4F2D-8B64-F30387B4B82BQ28709077-DCF238DE-146E-40F7-9616-15879A9F3533Q30627366-DCD548D6-8494-4B57-B787-419FF4880BB1Q33225009-5F1319D5-A4A4-4AF5-B0A7-11CB4B67DE6CQ33786706-2230B641-DA7D-4D02-ABB6-70F0C8630480Q33981039-11417A80-A497-4287-83DA-3EA6EB5E93B0Q34153777-0F2FB875-DA8B-411D-BE67-0FB56D1AB44BQ34324792-BDC9B407-E0D2-45EB-B88D-514A161814E0Q34933462-A5AC7AC5-DE8A-43D8-9F3E-BDCF4AA02EB7Q35608094-952C6466-810D-4464-9A80-6F3045317F01Q35905275-749973A4-474E-47D6-81D9-406D6D0FE61FQ36890927-F62FB0D2-6E58-4B68-BFF4-E23B6B2C99B6Q37138595-703ED7EF-4F51-465C-9A7A-0485BD30B0F7Q37217949-71984409-F575-433B-94EC-5ECAB27F908FQ41898948-DCCEF5BC-EC29-401F-ADA2-392D91502C59Q42548285-38D74C06-2886-4E95-A17A-1A4104F9D2F8Q42618417-964A5F4F-31EB-44AE-8601-A1A4C6EED28FQ44657906-F39F93CF-5833-459F-B74C-06A3A000B3EBQ58766041-37435280-6858-4802-88B3-D0B7B12EC87CQ64110157-A6059648-6190-43B0-8E69-B4B0583375DBQ89813420-36050A8D-32DF-452D-98D5-11C641509F96Q91495810-39754F3D-520D-45AA-8C89-6FF5A45E8DB8Q92185032-D347B7A8-816C-40E2-A8C4-53F694BD1F9A
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Henning Seedorf
@ast
Henning Seedorf
@en
Henning Seedorf
@es
Henning Seedorf
@fr
Henning Seedorf
@nl
Henning Seedorf
@sl
type
label
Henning Seedorf
@ast
Henning Seedorf
@en
Henning Seedorf
@es
Henning Seedorf
@fr
Henning Seedorf
@nl
Henning Seedorf
@sl
prefLabel
Henning Seedorf
@ast
Henning Seedorf
@en
Henning Seedorf
@es
Henning Seedorf
@fr
Henning Seedorf
@nl
Henning Seedorf
@sl
P108
P106
P108
P1153
23480554500
P21
P31
P496
0000-0002-5763-0236