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Advances on Scoliogeny, Diagnosis and Management of Scoliosis and Spinal Disorders
Advances on Scoliogeny, Diagnosis and Management of Scoliosis and Spinal Disorders
Autore Grivas Theodoros B
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (264 p.)
Soggetto topico Medicine
Soggetto non controllato idiopathic scoliosis
health-related quality of life
cultural adaptation
Italian Spine Youth Quality of Life Questionnaire
systematic review
meta-analysis
adolescent idiopathic scoliosis
brace therapy
brace concepts
rigid brace
night time brace
ring apophysis
maturation
ossification
fusion
scoliosis
nighttime orthotic treatment
surgery
quality of life
paraspinal muscles
cross-sectional area
posterior approach
computed tomography
Italian spine youth quality of life questionnaire
SRS-22
22q11.2 deletion syndrome
human model
neuromuscular scoliosis
radiography
MRI
curve morphology
intraspinal anomaly
body height
pulmonary function test
Cobb angle
iTRAQ
α-actin
progressive
differentially expressed proteins
bracing
physiotherapeutic scoliosis-specific exercise
physical activity
adherence
spinal appearance
shared decision-making
personalised approach
sclerostin
osteocytes
β-catenin
Wnt signaling pathway
scoliometer
truncal asymmetry
lateral spinal profile
surface topography
aetiology
spinal deformities
pathobiomechanics
follow-up study
Rett syndrome
motor skills
telerehabilitation
physical therapy modalities
home exercise program
neurodynamic functions
assessment
pain
treatment
early onset scoliosis
non-operative treatment
body posture
sports activity
corrective exercises
digital photography
ISBN 3-0365-6006-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910639996503321
Grivas Theodoros B  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Genome Editing in Neurosciences [[electronic resource] /] / edited by Rudolf Jaenisch, Feng Zhang, Fred Gage
Genome Editing in Neurosciences [[electronic resource] /] / edited by Rudolf Jaenisch, Feng Zhang, Fred Gage
Autore Feng Zhang
Edizione [1st ed. 2017.]
Pubbl/distr/stampa Springer Nature, 2017
Descrizione fisica 1 online resource (XI, 123 p. 16 illus. in color.)
Disciplina 611.01816
599.935
Collana Research and Perspectives in Neurosciences
Soggetto topico Human genetics
Neurosciences
Biomedical engineering
Human Genetics
Biomedical Engineering/Biotechnology
Soggetto non controllato CRISPR
muscular dystrophy
Parkinson's disease
DNA
Rett syndrome
double-strand breaks
Huntington's disease
genetic engineering
ISBN 3-319-60192-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction -- In vitro modeling of complex neurological diseases -- Aquatic model organisms in neurosciences : the genome editing revolution -- Genome-wide genetic screening in the mammalian CNS -- CRISPR/Cas9-mediated Knockin and Knockout in Zebrafish -- Dissecting the role of synaptic proteins with CRISPR -- Recurrently Breaking Genes in Neural Progenitors: Potential Roles of DNA Breaks in Neuronal Function, Degeneration and Cancer -- Neuroscience research using non-human primate models and genome editing -- Multiscale genome engineering: Genome-wide screens and targeted approaches -- Using Genome Engineering to Understand Huntington’s Disease -- Therapeutic gene editing in muscles and muscle stem cells.
Record Nr. UNINA-9910231247003321
Feng Zhang  
Springer Nature, 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Structure, Activity, and Function of Protein Methyltransferases
Structure, Activity, and Function of Protein Methyltransferases
Autore Jeltsch Albert
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (292 p.)
Soggetto topico Research & information: general
Biology, life sciences
Biochemistry
Soggetto non controllato protein lysine methylation
H3K9 methylation
PKMT
enzyme specificity
enzyme regulation
heterochromatin
protein post-translational modification
NSD3
WHSC1L1
structure and function
protein arginine methylation
PRMT7
epigenetics
cancer
immunity
pluripotency
SETDB1
methyltransferase
schizophrenia
Huntington's disease
Rett syndrome
Prader-Willi syndrome
congenital heart diseases
inflammatory bowel disease
MLL2
structure
H3K4me3
chromatin regulation
disease
dystonia
NSD1
H3K36
SOTOS
NUP98-NSD1
AML
PRMT6
post-translational modification
H3R2me2a
SETD3
posttranslational modifications
protein histidine methylation
actin
polymerization
cytoskeleton
enteroviruses
oncogenesis
PRMT5
cardiovascular disease
neurodegenerative diseases
diabetes
inflammation
G9a
GLP
EHMT2
EHMT1
post translational modification
lysine methylation
N-terminal methylation
translation
eEF1A
METTL13
neuron
synapse
dendritic spine
actin cytoskeleton
GTPase
PRMT1
arginine methylation
H4R3 methylation
transcriptional regulation
cell signaling
DNA damage repair
PRMT2
SH3
SETMAR
Metnase
H3K36me2
Hsmar1
non-homologous end joining repair
NHEJ
transposase
transposable elements
histone
SET7/9
SETD7
lysine-specific methyltransferase (PKMT)
cell proliferation
stress response
post-translational protein modification
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566479603321
Jeltsch Albert  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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The Amazing World of IDPs in Human Diseases
The Amazing World of IDPs in Human Diseases
Autore Monti Simona Maria
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (196 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato alpha-synuclein
NMR
secondary structure propensity
pre-structured motifs (PreSMos)
intrinsically disordered protein
ubiquitin-proteasome system
intrinsically disordered proteins
protein misfolding
molecular recognition features
cancer
neurodegenerative diseases
protein degradation
EPR spectroscopy
isothermal titration calorimetry
protein-ligand interaction
site-directed spin labeling
protein structural dynamics
WASp interacting protein
protein-protein interactions
actin
cytoskeleton remodeling
SH3 domain
proline-rich motif
single nucleotide variants
interface core and rim
human disease
intrinsically disordered regions
linear motifs
gene duplications
de novo
evolutionary origin
circular dichroism
flexibility
fluorescence
importin
isothermal titration calorimetry (ITC)
molecular docking
nuclear magnetic resonance (NMR)
nuclear protein 1 (NPR1)
peptide
Methyl-CpG-binding protein 2 (MeCP2)
Rett syndrome
intrinsically disordered protein (IDP)
protein stability
protein-DNA interaction
proteostasis
ubiquitin independent degradation
NADH-26S proteasome
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557334303321
Monti Simona Maria  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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