about
Exploring the avian gut microbiota: current trends and future directionsMarine sponges as microbial fermentersDiversity, structure and convergent evolution of the global sponge microbiomeSponge-associated microorganisms: evolution, ecology, and biotechnological potential.Thermal stress responses in the bacterial biosphere of the Great Barrier Reef sponge, Rhopaloeides odorabile.Could some coral reefs become sponge reefs as our climate changes?Genomic and phenotypic insights into the ecology of Arthrobacter from Antarctic soils.'Candidatus Protochlamydia amoebophila', an endosymbiont of Acanthamoeba spp.Host specificity in marine sponge-associated bacteria, and potential implications for marine microbial diversity.Biogeography of bacteria associated with the marine sponge Cymbastela concentrica.Soaking it up: the complex lives of marine sponges and their microbial associates.Diversity and mode of transmission of ammonia-oxidizing archaea in marine sponges.Activity profiles for marine sponge-associated bacteria obtained by 16S rRNA vs 16S rRNA gene comparisons.Characterizing the avian gut microbiota: membership, driving influences, and potential functionMeeting report: 1st international symposium on sponge microbiology.Deciphering the evolution and metabolism of an anammox bacterium from a community genome.Deep sequencing reveals exceptional diversity and modes of transmission for bacterial sponge symbionts.Assessing the complex sponge microbiota: core, variable and species-specific bacterial communities in marine spongesChloroflexi bacteria are more diverse, abundant, and similar in high than in low microbial abundance sponges.Sponge-specific clusters revisited: a comprehensive phylogeny of sponge-associated microorganisms.Influence of hand rearing and bird age on the fecal microbiota of the critically endangered kakapo.Gut microbiome of the critically endangered New Zealand parrot, the kakapo (Strigops habroptilus).Genomic insights into the marine sponge microbiome.Bacterial community profiles in low microbial abundance sponges.'Sponge-specific' bacteria are widespread (but rare) in diverse marine environments.Sponge-microbe associations survive high nutrients and temperaturesTemporal molecular and isotopic analysis of active bacterial communities in two New Zealand sponges.Pyrosequencing reveals regional differences in fruit-associated fungal communities.Successional development of biofilms in moving bed biofilm reactor (MBBR) systems treating municipal wastewater.Diverse honeydew-consuming fungal communities associated with scale insects.Quantifying the impact of storage procedures for faecal bacteriotherapy in the critically endangered New Zealand parrot, the kakapo (Strigops habroptilus).Paenibacillus darwinianus sp. nov., isolated from gamma-irradiated Antarctic soil.Evaluating variation in human gut microbiota profiles due to DNA extraction method and inter-subject differences.Influence of environmental variation on symbiotic bacterial communities of two temperate sponges.dsrAB-based analysis of sulphate-reducing bacteria in moving bed biofilm reactor (MBBR) wastewater treatment plants.Genome-based comparative analyses of Antarctic and temperate species of Paenibacillus.Diversity of Actinobacteria Associated with the Marine Ascidian Eudistoma toealensis.Microbial community structure in the gut of the New Zealand insect Auckland tree weta (Hemideina thoracica).Paired analysis of the microbiota of surface mucus and whole-tissue specimens in patients with chronic rhinosinusitis.In four shallow and mesophotic tropical reef sponges from Guam the microbial community largely depends on host identity
P50
Q26801978-E0A1BD01-2F46-4A38-B5DC-184FA0DE9ABDQ27345294-6CFDCD6F-080A-4D6F-8655-44DE81C6146CQ28601066-841BC98F-EE0E-4920-9692-26E8E86AA6D2Q28757510-3A375CE3-DEF1-494A-ACC4-ABB46DFC4FBAQ30575216-C3375A59-8F07-4B38-A5F7-3CF25A24E21EQ30611785-F818E838-485A-4BD3-BC7B-43C8E2DC7D9CQ30620331-19A44374-6325-4F8C-8865-E66EE5E55178Q31004808-A033F343-469C-4789-AA1E-E838035EA9D1Q31039805-7082EAB8-AA05-4F80-912A-91ECD0692705Q33211359-864C019B-040D-41BA-8BD0-0379DB57A975Q33307500-38D00DF7-91AD-4A86-B4CF-4866B7B4529AQ33313406-FE40E932-BEB3-4D91-95EE-8BCBEA0DF5B3Q33522374-C3DC00F8-E8ED-42A1-AAFD-CB0B0C9062B9Q33658088-677B6648-33E8-4635-A615-820C17502829Q33966109-9711910E-8F49-43D8-816F-510CB01BB3ADQ33994876-0D50EF36-9780-41B8-924D-06A214AA6ED1Q34038454-019405AF-2B49-4E92-9E19-0FE022E8079DQ34047356-52C6DB97-E694-42D2-A021-68C495EB6FCEQ34069899-2B35001B-B494-454E-8AC6-2063ED865F22Q34094192-E468EDAA-68F1-460D-A7DA-A7FA8DB5808CQ34106990-36E0D667-B1BC-4A2A-B8AE-F4D976F406AEQ34244003-90A46CDD-EB77-4A94-B3D2-B8DD4CEED0D1Q34355776-5A8B633A-9E51-4BF0-80AF-1E99C0EA5DE9Q34375342-A08EA852-8BBF-47EC-9D69-E26246542949Q34434393-DD6BD650-20F0-4E96-A821-E44EF1B48EF5Q34533369-EA819DE5-A3D9-4649-AED0-C1848CCF0E10Q34619981-9D397054-8E6E-43F1-8086-E8638E5F8386Q34639677-DA818E0A-4B1B-46C9-A2BD-439645D6C7B9Q34803834-157C5546-65CB-4961-9B49-1467FCE5DAEDQ34906881-92DC171E-4B0D-4FFF-B176-E72365C7210AQ34982476-A03F4539-F7F2-4CAD-BC68-A90504156AC1Q35085918-3AC248BF-F34B-4497-BF7B-29D148DABDB5Q35094598-C27C9DFA-D8B3-46E5-9431-55180D13AA40Q35117185-B90AC6FA-FDE2-4B02-BADC-73ACFB0837D9Q35161477-EBEB97F7-6790-4C68-B037-765A8B7847B8Q35304665-40C11202-5A5B-458D-962C-2E40A2495CE1Q35560389-202C33C2-D328-4788-810B-0F143BF8EA15Q35564780-C65B4CFA-3CA3-4C5B-AF1B-518F85B9E0ADQ35717558-EBF3A6A4-00CE-4912-BC42-BD3253117C32Q35999194-4062C209-2437-4357-A93A-01334C747A5C
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Michael W Taylor
@es
Michael W Taylor
@nl
Michael W Taylor
@sl
Michael W. Taylor
@en
type
label
Michael W Taylor
@es
Michael W Taylor
@nl
Michael W Taylor
@sl
Michael W. Taylor
@en
prefLabel
Michael W Taylor
@es
Michael W Taylor
@nl
Michael W Taylor
@sl
Michael W. Taylor
@en
P106
P1153
7406242798
P21
P31
P496
0000-0002-0463-7813