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Mechanisms of ER Protein Import
Mechanisms of ER Protein Import
Autore Zimmermann Richard
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (258 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato chaperones
contact sites
endoplasmic reticulum
ER-SURF
membrane extraction
mitochondria
protein targeting
bimolecular luminescence complementation
competition
split luciferase
membrane proteins
protein-protein interactions
Sec61 complex
Sec63
synthetic peptide complementation
TRAP complex
ER protein translocase
signal peptide
protein translocation
nascent peptide chain
membrane insertion
molecular modelling
molecular dynamics simulations
molecular docking
signal peptidase
ER translocon
signal recognition particle dependent protein targeting
Sec61 dependent translocation
co-translational translocation
inhibitor
high throughput screening
Sec61
Sec62
folding
insertion
membrane protein
translocon
ribosome
transmembrane segment
lipid droplets
peroxisomes
PEX3
membrane protein insertion
label-free quantitative mass spectrometry
differential protein abundance analysis
Zellweger syndrome
GET
protein transport
SND
SRP
EMC
positive-inside rule
hydrophobicity
transmembrane helix
signal recognition particle
nascent polypeptide-associated complex
fidelity
cyclotriazadisulfonamide
ER quality control
DNAJC3
preprotein
Sec61 translocon
ribosome stalling
signal sequence
Sec61 translocase
NAC
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910576886203321
Zimmermann Richard  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Neuromuscular Disorders in Children and Adolescents
Neuromuscular Disorders in Children and Adolescents
Autore Korinthenberg Rudolf
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (146 p.)
Soggetto topico Medicine
Neurology & clinical neurophysiology
Soggetto non controllato Pompe disease
GAA gene
general population database
carrier frequency
genetic prevalence
spinal muscular atrophy
quality of life
child neurology
patient-reported outcomes
neuromuscular
carpal tunnel syndrome
median nerve neuropathy
electrodiagnostic studies
neuromuscular ultrasound
mucopolysaccharidosis
neuropathy
children
adolescents
Charcot-Marie-Tooth disease
traumatic neuropathy
inflammatory neuropathy
metabolic neuropathy
posterior spinal fusion
kyphosis
sagittal plane deformity
signal recognition particle
3-hydroxy-3-methylglutaryl
coenzyme A reductase
juvenile myositis
therapy
clinical course
chaperone-assisted autophagy
clinical trials
Duchenne muscular dystrophy
public health surveillance
distal arthrogryposis
AMC
ECEL1
contractures
muscle MRI
spinal muscular atrophy (SMA)
nusinersen
fine manual dexterity
ultrasonographic elastography
neuromuscular disease
muscle
brachial plexus neuritis
hereditary sensory and motor neuropathy
paralysis
vaccination
pediatrics
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566465903321
Korinthenberg Rudolf  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui