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Updates on Molecular Targeted Therapies for CNS Tumors
Updates on Molecular Targeted Therapies for CNS Tumors
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2023
Descrizione fisica 1 online resource (368 p.)
Soggetto topico Medicine and Nursing
Oncology
Soggetto non controllato A172
A2AAR antagonist
adenosine
adenosine receptors
antigen processing and presentation
antioxidant
apoptosis
ATRX
bevacizumab
biomarker
blood-brain barrier
brain metastasis
brain tumor
cancer metabolism
cell cycle arrest
central nervous system
chemotherapy
CNS disease
CNS lymphoma
CpG island
diffuse midline gliomas
DNMT
EGFR
ependymoma
EPHB2
epidermal growth factor receptor
ERK/MAPK pathway
FGFR3
G-CIMP
GBM
germline mutation
glioblastoma
glioblastoma molecular classification
glioma
Group A
Group B
H3K27M
histone acetylation
IDH-mutant glioma
immune evasion
immune score
immunotherapy
intraparenchymal metastases
intrathecal
isotope labeling
KIF11
leptomeningeal
low grade glioma
low-grade glioma
LPS
lung cancer
lung carcinoma
lung malignancy
mass spectrometry
meningitis
MET
metastatic disease
Metformin
methotrexate
methylation
methylomics
methyltransferases
MGMT
molecular targets
molecular therapy
monoclonal antibodies
MYCN
myxopapillary
n/a
neoantigen
neoplastic
neurofibromatosis
NF1
novel therapeutics
novel therapies
patient avatars
PCNSL
PDGFRA
pediatric brain tumor
PFA
PFB
PI3K/PTEN pathway
plexiform neurofibroma
potential therapy development
preclinical models
progression
progression-free survival
radiotherapy
receptor tyrosine kinase
RELA
stereotactic radiosurgery
subependymoma
T cells
T lymphocytes
targeted therapy
temozolomide
tumor microenvironment
tumor mutation burden
tumor suppressor
tyrosine kinase inhibitors
U87MG
vestibular schwannoma
Warburg effect
whole-brain radiation therapy
YAP1
ZFTA
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9911053032003321
MDPI - Multidisciplinary Digital Publishing Institute, 2023
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Venom and Toxin as Targeted Therapy / Hang Fai Henry Kwok
Venom and Toxin as Targeted Therapy / Hang Fai Henry Kwok
Autore Kwok Hang Fai Henry
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (180 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato cane toad
B cell non-Hodgkin lymphoma
Malaysian cobras
complement system
decay accelerating factor
neuroblastoma
atopic dermatitis
complement dependent cytotoxicity
antioxidant enzymes
bacterial adhesion
cancer therapy
N. kaouthia
anuran skin secretion
frog
Apis mellifera syriaca
solid phase extraction
bee venom phospholipase A2 (bvPLA2)
disintegrin
toad toxins
immunotoxins
ribosome-inactivating proteins
antimicrobial peptide (AMP)
drug design
Moxetumomab pasudotox
snake venom
antiviral activity
in vitro effects
bombesin-related peptide
oxidative stress biomarkers
half-life
blood vessel formation
target therapy
2
MYCN
indolealkylamines
Huachansu
membrane attack complex
bouganin
bee venom
SEM
anticancer activity
antimicrobial peptide
house dust mite extract (DFE)
mannose receptor
O. hannah
bicarinalin
gastric cells
melittin
LC-ESI-MS
dermaseptin
smooth muscle
apoptosis
anticancer
N. sumatrana
Helicobacter pylori
inflammation
immunotherapy
atopic dermatitis (AD)
immunotoxin
mantle cell lymphoma
clearance
mass spectrometry
Bougainvillea
rRNA N-glycosylase activity
fungal toxin
skin inflammation
targeted therapy
4-dinitrochlorobenzene (DNCB)
Bee venom
VEGF
Chansu
bufadienolides
obsessive-compulsive disorder (OCD)
BLF1
antimicrobial activity
orellanine
VB6-845
acute lymphoblastic leukemia
ribosome-inactivating protein
CD206
molecular cloning
cancer
CD22
eIF4A
ISBN 9783039211906
3039211900
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367754703321
Kwok Hang Fai Henry  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui