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Advances in Chemical Crystallography: A Themed Issue Honoring Professor Alexandra M. Z. Slawin on the Occasion of Her 60th Birthday
Advances in Chemical Crystallography: A Themed Issue Honoring Professor Alexandra M. Z. Slawin on the Occasion of Her 60th Birthday
Autore Harrison William T. A
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (214 p.)
Soggetto topico Chemistry
Organic chemistry
Research and information: general
Soggetto non controllato 1,6-conjugate addition
2D Cu-MOF
3d metal complex
amide groups
ammonium enolate
arsenic
aryloxide
azetidinium
band gap modification
bandgap tuning
benchmark
bioMOF
bond activation
calcium MOF
Claisen rearrangement
Click reaction
Comparative DEER Analyzer
DEER
DFT
electrochemistry
EPR spectroscopy
ESI-MS studies
ester functionalization
green chemistry
heterometallic clusters
hydricity
indoloquinoline
intramolecular cyclization
isomers
isothiourea
Knoevenagel reaction
late-transition metals
layered perovskite
low oxidation state complexes
magnesium
magnetometry
metallacycles
MMM
MOF
molecular magnetism
mtsslSuite
multinuclear NMR
N-Substituted Benzamides
natural product
nitroxide spin label
organophosphorus
oxazoline
P-ligands
PDS
PELDOR
peri-substitution
perophoramidine
phenols
photoluminescence
pnictine
quinone methide
reduction reagent
ring system
Ruddlesden-Popper
scXRD
secondary interactions
selenation reagent
single crystal X-ray crystallography
single crystal X-ray structures
square grid structure
structure-property relations
supramolecular chemistry
thieno[2,3-c]pyrrolone
thiophene
titanium(IV) oxo-clusters
VTXRD
Wittig rearrangement
Woollins' reagent
X-ray crystallography
X-ray structure
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Advances in Chemical Crystallography
Record Nr. UNINA-9910576882403321
Harrison William T. A  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Advances in Plant Alkaloid Research
Advances in Plant Alkaloid Research
Autore D'Auria John C
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (278 p.)
Soggetto topico Biology, life sciences
Research & information: general
Soggetto non controllato 8-oxo-9-dihydromakomakine
AChE
acridone alkaloids
acridones
alkaloids
antiplasmodial activity
Aristotelia chilensis Molina Stuntz
Aspergillus flavus
benzylisoquinoline alkaloids
Berberidaceae
biodiscovery
bioprospecting
biosynthesis
biotechnological production
Borago officinalis
BuChE
Buxaceae
calystegine
cambial meristematic cells
canthin-6-one
catharanthine
Catharanthus roseus
chemistry
Chl a fluorescence
cocaine
Copper-dependent diamine oxidase
Crassocephalum
cyclopamine
cytochrome P450 monooxygenase
cytotoxicity
dereplication
dichlorocarbene
dimer alkaloids
DiversinateTM
endothelium-independent
epoxidation
Erythroxylaceae
Erythroxylum coca
GC-MS
Gynura bicolor
halogencyclopropane
hedgehog signaling
Hill reaction inhibitors
Homospermidine synthase
HPLC-MS
indole alkaloid
isoquinoline alkaloid
late-stage functionalization
library
Lolium perenne
mahimbrine A
Mahonia imbricata
medicinal chemistry
medicinal properties
methyltransferase
molecular docking
natural product
Necic acids
Necine bases
Nelumbo nucifera
next generation sequencing
norcoclaurine synthase
papaverine
pharmacology
phenylacrylamides
photosystem II
Picrolemma huberi
Pyrrolizidine alkaloid biosynthesis
Rhodophiala
Ruta graveolens
sacred lotus
sarchookloides A-C
Sarcococca hookeriana
scaffold
scopolamine
Senecionine
Shh-Light II cells
Simaroubaceae
stereochemistry
steroidal alkaloid
sulfinate
Swinglea glutinosa
terpenoid indole alkaloids
traditional medicine
tropane
tropane alkaloids
vascular activity
Veratrum californicum
vindoline
vindoline trimer
voltage-dependent calcium channels
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557109903321
D'Auria John C  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
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Anticancer Agents : Design, Synthesis and Evaluation
Anticancer Agents : Design, Synthesis and Evaluation
Autore Chen Qiao-Hong
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (606 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 1,2,3-triazole
2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
3,6-dibromocarbazole
4-(pyridin-4-yloxy)benzamide
5-bromoindole
5-fluorouracil
ABCB1 (P-glycoprotein)
actin
ADME
allene
amides/esters
androgen receptor
anti-cancer activity
anti-neuroinflammation
anti-ovarian cancer
anti-tumor
anticancer
anticancer activity
anticancer agent
anticancer agents
anticancer compounds
antimitotic agents
antioxidant activity
antiproliferative activity
antiproliferative agent
antitumor
antitumor activity
apalutamide
apoptosis
aromatase
benzimidazole
benzofuran-pyrazole
benzofurans
beta-lapachone
bivalency
breast cancer
c-Met
carbazole
cell cycle
chemical synthesis
chemoresistance
chrysin analogues
colchiceine
colchicine amide
colchicine analogs
colchicine sulfonamide
colon cancer
computational docking
coumarin
crystal structure
cyanopyridone
cytotoxic activity
cytotoxic properties
cytotoxicity
darolutamide
DFT study
dihydroartemisinin
dihydropyranoindole
docking
docking studies
drug discovery
drug resistance
E-stereoselective
enzalutamide
enzyme inhibition
estrone derivatives
flavonoid
flavonoids
gemcitabine
HDAC inhibitors
HeLa
HepG2
hydrates
hydrazine
IGF-1R
IL-12
immune modulation
indoleamine 2,3-dioxygenase
inflammation
inhibitor
K562
kinase inhibitor
MCF-7
MDM2-p53 interaction
migration
mimetics
molecular simulation
MOLT-4
multidrug resistance (MDR) reversal
N-substituted pyrazoline
nanoparticles
natural product
neuroblastoma
NIH3T3
o-nitro-benzyl
organosilicon compounds
ortho-quinones
ovarian cancer
overcoming drug resistance
P-glycoprotein
P-MAPA
PARP inhibitor
PARP-1 inhibition
phenylpyrazolopyrimidine
photoactivatable protecting groups
PI3Ks
PI3Kα inhibitor
PI3Kδ inhibitors
polyvalency
prodrug
prostate cancer
PROTACs
protein degradation
protein kinase
protein-protein interactions
Pyrazole
pyrazolopyridine
pyridotriazine
quinazolin-4(3H)-one
quinazolin-4(3H)-thione
regioselective
salinomycin
Schiff base
SILA-409 (Alis-409)
SILA-421 (Alis-421)
Src
substituted pyridine
synergy
synthesis
Talazoparib
tanshione IIA
taxoids
thiazolidinone
Thienopyrimidine
thienopyrimidinone
thiocolchicine
thiopene
thioxotriazopyridine
TLR signaling
topoisomerase II inhibitor
triazolothiadiazine
triple-negative breast cancer
tryptophan metabolism
tubulin inhibitors
tumor specificity
urea
virtual screening
xanthones
yeast-based assays
zampanolide
βIII-tubulin
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Anticancer Agents
Record Nr. UNINA-9910557129103321
Chen Qiao-Hong  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Anticancer Properties of Natural and Derivative Products
Anticancer Properties of Natural and Derivative Products
Autore Lupiáñez José Antonio
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (312 p.)
Soggetto topico Research and information: general
Soggetto non controllato 1,3-dipolar cycloaddition
3-hydroxy-β-ionone
actin cytoskeleton
Adenosma bracteosum
AKT/PI3K signaling pathway
anti-cancer
anti-inflammatory agent
anti-proliferative activity
anticancer activity
anticancer agent
antioxidant
antioxidant activity
antioxidant enzymes
apoptosis
autophagy
betulin glycoconjugates
betulinic acid
bioactive compounds
breast cancer
cancer
caspase-3
Caveolin-1
cell cycle
cell line
chemoprevention
chemotherapy
click chemistry
complementary medicine
cytotoxicity
danthron
DNA
DPPH
Elaeagnus angustifolia
emodin
EMT
extract
GC-MS
gingival fibroblasts
glioblastoma (GBM)
grapes
hepatocellular carcinoma (HCC)
human hepatocarcinoma HepG2 cells
hypericin
in vivo
interaction
isolated compounds
lactucopicrin (LCTP)
lung metastases
maslinic acid
medicinal mushrooms
melanoma
metabolites
migration activity
Moringa oleifera
n/a
natural compounds
natural extract
natural photosensitive compounds
natural product
NF-κB
Olea europaea L.
oleanolic acid
oral cancer
oxidative stress
p62/SQSM1
photodynamic therapy
photosensitiser
Pogostemon cablin (PPa extract)
proliferation
quinizarin
rhodamine B
ROS level
ROS levels
squamous cell carcinoma
synergism
temozolomide (TMZ)
therapeutic triglyceride
tormentic acid
total flavonoid content
total phenolic content
triterpenoic acid
uvaol
wine
xenograft study
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557370303321
Lupiáñez José Antonio  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Bioactive Marine Heterocyclic Compounds
Bioactive Marine Heterocyclic Compounds
Autore Usami Yoshihide
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (132 p.)
Soggetto topico Medicine
Soggetto non controllato acetylcholinesterase
Agelas
agesasines
altercrasins
Alternaria sp
Anthocidaris crassispina
antibiotics
antimicrobial activity
azole-based peptide
bioactivity
bromopyrrole alkaloid
Chrysosporium lobatum
Cladosporium cladosporioides
cyanobacteria
cytotoxicity
decalin derivatives
endophytic fungus
enzymatic inhibitory activity
gene disruption
genome mining
genome sequencing
lobophorin
mangrove plant
marine fungi
marine sponge
metabolic engineering
methicillin-resistant S. aureus
natural product
P. gingivalis
peptide synthesis
phenalenone derivatives
polyketides
solid-state extraction
solid-state fermentation
thiazole
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557762703321
Usami Yoshihide  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Biological Efficacy of Natural and Chemically Modified Products against Oral Inflammatory Lesions / Hiroshi Sakagami
Biological Efficacy of Natural and Chemically Modified Products against Oral Inflammatory Lesions / Hiroshi Sakagami
Autore Sakagami Hiroshi
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (212 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato gargle
oral lichen planus
angiotensin II blocker
quantitative structure-activity relationship
metabolomics
CCN2
anti-human immunodeficiency virus (HIV)
oral cell
arachidonic acid cascade
Kampo medicine
lignin-carbohydrate complex
traditional medicine
eugenol
QSAR analysis
constituent plant extract
polyphenol
benzaldehyde
glucosyltransferase
infective endocarditis
antiviral
periodontitis
nutritionally variant streptococci
Kampo
quantitative structure-activity relationship (QSAR) analysis
traditional Japanese herbal medicine
technical terms
allergic rhinitis
nasal epithelial cell
antimicrobial susceptibilities
alkaline extract
mastic
stomatitis
thioredoxin
production
oral microbiota
Jixueteng
oral inflammation
random forest
mice
chromone
natural products
Chinese herbal remedies
inflammation
quercetin
in vivo
kampo formula
glucocorticoids
Hangeshashinto
recurrent aphthous stomatitis
anti-osteoclast activity
cytotoxicity
dental application
tongue diagnosis
natural product
alkaloids
inflammatory disease
pathogenic factors
increase
machine learning
human virus
cepharanthin
mucositis
oral diseases
Juzentaihoto
in vitro
herbal medicine
tumour-specificity
ISBN 9783038979937
3038979937
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346850803321
Sakagami Hiroshi  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chromatography-the Ultimate Analytical Tool
Chromatography-the Ultimate Analytical Tool
Autore Samanidou Victoria
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (200 p.)
Soggetto topico Analytical chemistry
Chemistry
Research and information: general
Soggetto non controllato almonds
authenticity
biomarker
biomarkers
biotin acceptor peptide (BAP)
biotin ligase BirA
breast cancer
caffeine
catechins
cosmetics
derivatization
epidermal layer
flavonoids
functional
gallic acid
genomics
greener HPTLC
hemopexin
HPLC
HPLC-DAD
keratinocytes
LC-MS/MS
limited sampling strategy
liquid chromatography tandem mass spectrometry (LC-MS/MS)
liquid chromatography-tandem mass spectrometry
liver fibrosis
metabolomics
method validation
Miang
microflow LC-MS
mLC-MS/MS
multiple linear regression
multiple reaction monitoring (MRM)
mycophenolate mofetil
mycophenolic acid
natural product
nontargeted analysis
paracetamol
PCA
pediatric patients
phenolics
photoaging
polyamine
protein-protein interactions (PPIs)
proteomics
proximity utilizing biotinylation (PUB)
sample preparation
serum
simultaneous determination
SPE
steroid
Swietenia macrophylla
targeted analysis
therapeutic drug monitoring
tocopherols
UAE
UV irradiation
validation
walnut septum
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910576887103321
Samanidou Victoria  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Marine Compounds and Cancer 2020
Marine Compounds and Cancer 2020
Autore Honecker Friedemann
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (480 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 12-deacetyl-12-epi-scalaradial
3-alkylpyridinium polymers
A375 and HeLa cell lines
A549 cells
ABC transporter
actinomycin
AD0157
adriamycin resistance
Aeroplysinin
Akt
angiogenesis
angiogenesis inhibitor
ansamycins
anthranilic acid
anti-angiogenesis
anti-angiogenic
anti-cancer
anti-metastatic activity
anti-proliferation
anti-proliferative
antiangiogenesis
antiangiogenic
antibacterial
Antibody Drug Conjugates (ADCs)
anticancer
anticancer activity
anticancer agent
anticancer immunity
anticarcinogenic
anticoagulant
anticoagulation
antifouling
Antimicrobial peptide (AMP)
antioxidant
antiproliferative
antiproliferative activity
antitumor
antitumor activities
antitumoral
antitumour
AP-1
apoptosis
apoptosis-inducing activity
approved antitumor agents
araguspongine C
arrest of cell cycle
Aspergillus
autophagy
autophagy inducers
autophagy inhibitors
azoxymethane
BCRP/ABCG2
BEL-7402 cell
benzo[a]pyrene
bioactive natural product
bioanalysis
bis (2,3-dibromo-4,5-dihydroxy-phenyl)-methane (BDDPM)
bonnethead shark
breast cancer
breast cancer cells
Brevianamide
brominated indoles
bromophenol
buccal gland
c-JUN
c-Met
C15 acetogenins
camptothecin
cancer
Cancer
cancer genes
cancer preventive
cancer progression
Cantabrian Sea-derived actinobacteria
carbocyclic analogue
carcinoembryonic antigen
Caribbean sponge
carotenoid
carotenoids
caspase cascade
cell adhesion
cell adhesion molecules
cell cycle
cell cycle arrest
cell migration
cembranoids
chemical conjugation
chemoprevention
chemopreventive
chemosensitization
chemotherapy
chimera
CHOP
chromatography
circulating tumor cells
cisplatin
clinical trials
colorectal cancer
cooperative binding
cyclin D1
cyclin-dependent kinase
CYP1A1
cystatin F
cystatin superfamily
cytokine release
cytoskeleton
cytotoxic activity
cytotoxicity
deep-sea
depolymerisation
dibromotyrosine
dieckol
divergolides
DNA minor groove binder
drug discovery
Ecklonia cava
elisidepsin
EMT
endoperoxide
endophytic fungus
endothelial cells
energy stress
epigonal organ
epithelial-mesenchymal transition
ER-stress
ET-743
evolution
FAK
fascaplysin
fatty acid 2-hydroxylase
fatty acids
FAU
FBDD
fucoidan
fucoxanthin
fumigaclavine C
gemcitabine
gene expression
glioblastoma
gliotoxin
glucocorticoid receptor
glycosaminoglycans
gorgonian
Haliclona gracilis
HeLa cells
heparan sulphate
heparanase
hepatocellular carcinoma
HER2
HIF-1
hippuristanol
HSP90
human lung cancer
human normal diploid fibroblast (TIG-1 cells)
human sarcoma cell line (HT1080 cells)
humulane sesquiterpenoids
hybridization
hydroxylated lipids
hypoxia
hypoxia-inducible factor-1
IL-6
in vivo model
inflammation
inhibitor
integrin β1
invasion
isatin
Isofistularin
itampolin A
jaspine B
JNK1/2
Jurkat
kalkitoxin
kunitz type inhibitor
Lampetra morii
Leathesia nana
Leptogorgia
leukemia
lipid rafts
low molecular weight fucoidan extract
low toxic
LS-1
lung cancer
lung metastasis
Lyngbya majuscula
macrolide
mangrove-derived actinomycete
manzamine A
MAPK/ERK pathway
marangucyclines
marine antitumor agents
marine biotechnology
marine compound
marine drug
marine drugs
marine fungus
marine metabolites
marine mollusc
marine natural products
marine organisms
marine sponges
marine-derived drugs
Marthasterias glacialis L.
MCP-1
mechanisms of action
melanoma
membrane permeabilization
metastasis
microalgae
Micromonospora
migration
mitochondria
mitochondria toxin
mitochondrial pathway
mitochondrial dysfunction
molecular docking
molecular mechanisms
molecular modeling
molecular oncology
Moorea producens
MRP1/ABCC1
multi-drug resistant leukemia
multidrug resistance
Mycalin A
Mycochromenic acid derivative
N-Ras
n/a
nanoparticle
naphthopyrones
natural marine compounds
natural product
natural products
neuroblastoma-rat sarcoma
NF-κB
NF-κB signaling
nicotine
nicotinic acetylcholine receptor
non-small cell lung cancer
non-small cell lung cancer (NSCLC)
non-small cell lung carcinoma
nonfunctioning pituitary adenomas
novel inhibitor
NSCLC
Nur77
osteosarcoma
oxidative stress
oxidative stress
P-gp/ABCB1
P2X7 receptor
p38
p38/ERK
p38α
p65
pachastrissamine
palmitic acid
paulomycins
pazopanib
PEL
Penicillium brevicompactum
Penicillium paneum
phase I
pheochromocytoma and paraganglioma
phlorotannins
phycocyanin
PI3K/Akt
plakortide
plitidepsin
pollution
poly(ADP-ribose)-polymerase inhibitor
polyoxygenated steroids
polyphenols
polysaccharides
Porifera
porifera/sponge
preclinical
programmed cell death
programmed cell death-ligand 1
programmed cell death-ligand 2
proliferation
prostate cancer
proteasomal degradation
proteomic
pseudopterosin
puupehenones
pyrrolidinedione
reactive oxygen species
RGD motif
ribosomal protein genes
ROS
RPS30
safety
Sarcophyton ehrenbergi
sea anemone
sea cucumbers
seaweed
secondary metabolites
sediment
selenium-containing polysaccharide-protein complex
Sepia ink polysaccharides
shrimp
signal transduction
sinulariolide
sipholenol A
small cell lung cancer
SNORA62
snoRNA
SNU-C5/5-FU
soft coral
soft tissue sarcoma
soft tissue sarcoma
sphingosine kinase inhibitor
sponge
sponges
STAT3
Streptomyces sp. SCSIO 11594
synergism
synthetic analogues
SZ-685C
targeted therapy
terpenes
tetracenomycin X
TGF-β signaling
Thalassia testudinum
thalassiolin B
therapeutic compounds
Tilapia piscidin 4 (TP4)
TNFα
Topo I inhibitor
topoisomerase
trabectedin
triterpene glycosides
TRPM7
tumor cell line
tumor microenvironment
tumor-associated macrophages
Ulva fasciata
uveal melanoma
VEGF
virtual screening
xyloketal B
α9-nicotinic acetylcholine receptors (nAChRs)
αO-conotoxin GeXIVA
β1-integrin
λ-carrageenan
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557339303321
Honecker Friedemann  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Marine Natural Products as Anticancer Agents
Marine Natural Products as Anticancer Agents
Autore Alves Celso
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (150 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato alga
anti-cancer
antitumor
aplysinopsin analogs
apoptosis
astaxanthin
BH3 mimetics
bioactive compounds
biscembranoid-type metabolites
BT20
cancer stem cells
cancer therapy
chronic myeloid leukemia
colony formation
cytotoxicity
Ehlich's tumor
environment
epigenetic signaling
epigenome
epithelial-mesenchymal transition
flaccidoxide-13-acetate
gram-scale
hepatocellular carcinoma
hydroxyphenylacetic acid
indole alkaloids
inflammation
inflammatory factor production
invasion
LPS-stimulated murine macrophage
marine source
marine species
marine-derived fungus
meroterpenoids
migration
mutp53
n/a
nannocystin
Nanog
natural product
Oct4
P. purpurogenum
Penicillium chrysogenum
polyketide
pontin
proliferation
prostate cancer
Sarcophyton digitatum
secondary metabolites
siRNA
STAT3
T47D
total synthesis
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557595603321
Alves Celso  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Metabolomics in Neurodegenerative Disease
Metabolomics in Neurodegenerative Disease
Autore Green Brian
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (184 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato ?-synuclein aggregates
13C-labeled succinate
1H NMR
6-OHDA
age-related macular degeneration
Alzheimer's disease
bile acids
biomarkers
C. elegans
cerebral ischemia
cerebral palsy
dementia with Lewy bodies
direct mass spectrometry
drusen
endothelin-1
energy metabolism
excitotoxicity
fatty acid
fatty acid metabolism
GC-MS
glutamic acid
imaging mass spectrometry
LC-MS
lipidomics
malonate
mass spectrometry
metabolic pathways
metabolism
metabolomics
micro-dialysis
midbrain
mitochondrial dysfunction
myo-inositol
n/a
natural product
neurodegeneration
Parkinson's disease
Parkinson's disease dementia
pathogenesis
plasma
prodromal Parkinson's disease
reperfusion
retinal pigment epithelium
Streptomyces venezuelae
subacute mild traumatic brain injury
targeted mass spectrometry
tricarboxylic acid cycle
ISBN 3-03928-041-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910404087203321
Green Brian  
MDPI - Multidisciplinary Digital Publishing Institute, 2020
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