about
The pharmacological potential of mushrooms.Selectivity and potency of microcystin congeners against OATP1B1 and OATP1B3 expressing cancer cellsIsolation of Microcystins from the Cyanobacterium Planktothrix rubescens Strain No80.Anti-infective Natural Products from Cyanobacteria.Anti-MRSA-acting carbamidocyclophanes H-L from the Vietnamese cyanobacterium Nostoc sp. CAVN2.Novel penicillins synthesized by biotransformation using laccase from Trametes spec.Identification and activation of novel biosynthetic gene clusters by genome mining in the kirromycin producer Streptomyces collinus Tü 365.Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi.Anti-MRSA-acting carbamidocyclophanes H-L from the Vietnamese cyanobacterium Nostoc sp. CAVN2.Xanthocidin Derivatives from the Endophytic Streptomyces sp. AcE210 Provide Insight into the Xanthocidin BiosynthesisDraft Genome Sequence of the Novonestmycin-Producing Strain Streptomyces sp. Z26, Isolated from Potato Rhizosphere in MoroccoInhibition of human 5-lipoxygenase and anti-neoplastic effects by 2-amino-1,4-benzoquinonesNovel cephalosporins synthesized by amination of 2,5-dihydroxybenzoic acid derivatives using fungal laccases IINuclear amination catalyzed by fungal laccases: reaction products of p-hydroquinones and primary aromatic aminesDraft Genome Sequence of the Xanthocidin-Producing Strain Streptomyces sp. AcE210, Isolated from a Root Nodule of Alnus glutinosa (L.).Nostotrebin 6 Related Cyclopentenediones and δ-Lactones with Broad Activity Spectrum Isolated from the Cultivation Medium of the Cyanobacterium Nostoc sp. CBT1153Precursor-Directed Biosynthesis and Fluorescence Labeling of Clickable Microcystins
P50
Q24530116-7467A744-63CC-44D8-817A-77BB3230CC13Q28540711-595BF5E4-7B39-4051-AD18-60C6D1DED44EQ38306495-4CE8BA4E-09AE-4C32-8FD1-846FCC682B94Q38530577-ABFDA815-946F-41BA-B714-ADD37E4E8350Q38960403-BB53B883-57D8-44FF-B533-B35536D72E0EQ40284775-E3E463C4-0A3B-47D6-B376-9FB75A7B8C5FQ40967708-A29927EA-7947-43C5-95C7-F051E2B3E5D2Q46095828-F759603A-0C29-4184-B8F0-9984F977C0D4Q48733143-D5B40DFA-8B49-4195-8B7B-6A5471E1A474Q57288121-42A7F61A-3C61-4B41-B470-093C72C972F7Q60921768-8DBAD3CD-DB42-402F-BCD7-6D1A91A00CB9Q79359155-600FD352-A278-48F1-B423-2CD438D11B46Q79849182-3D93E166-9F7C-41B1-AB76-16E70145A175Q81507185-0F488B7F-3FC4-480F-B918-6D55264C09C5Q90383568-4C15108E-0A4A-405F-8460-6348A6B051C0Q92909300-D491A606-E596-4CAC-92FC-2B39B374B98CQ95942520-A4756D76-9348-4023-B21D-2A573A8015C5
P50
description
German pharmacist
@en
deutscher Pharmazeut
@de
investigador
@es
pharmacist German
@en-ca
pharmacist German
@en-gb
wetenschapper
@nl
صيدلي ألماني
@ar
name
Timo H J Niedermeyer
@nl
Timo Niedermeyer
@de
Timo Niedermeyer
@en
Timo Niedermeyer
@fr
type
label
Timo H J Niedermeyer
@nl
Timo Niedermeyer
@de
Timo Niedermeyer
@en
Timo Niedermeyer
@fr
altLabel
Timo H J Niedermeyer
@en
Timo H. J. Niedermeyer
@de
Timo H. J. Niedermeyer
@en
prefLabel
Timo H J Niedermeyer
@nl
Timo Niedermeyer
@de
Timo Niedermeyer
@en
Timo Niedermeyer
@fr
P214
P227
P106
P21
P214
P227
P31
P496
0000-0003-1779-7899
P569
1977-01-01T00:00:00Z