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THE JOURNAL OF CLINICAL INVESTIGATION
Rivista
Codice:
E091034
ISSN:
0021-9738
Dati Generali
Dati Generali
Pubblicazioni (27)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
Amniotic fluid biomarkers predict the severity of congenital cytomegalovirus infection
Articolo
BRUGADA SYNDROME AND CONDUCTION SYSTEM DISEASE ARE LINKED TO A SINGLE SODIUM CHANNEL MUTATION.
Articolo
Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca release channels
Articolo
Combinatorial drug design targeting multiple cancer signaling networks controlled by mitochondrial Hsp90
Articolo
Conversion of the major birch pollen allergen, Bet v 1, into two nonanaphylactic T cell epitope-containing fragments - Candidates for a novel form of specific immunotherapy
Articolo
Dendritic cells in intestinal homeostasis and disease.
Articolo
Dissociation of glomerulosclerosis, glomerular hypertrophy and cell proliferation in mouse strains heterozygous for a mutation (os) which induces a 50% reduction in nephron number.
Articolo
Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias
Articolo
Helicobacter pylori upregulates expression of epidermal growth factor-related peptides, but inhibits their proliferative effect in MKN 28 gastric mucosal cells
Articolo
Hepatic expansion of a virus-specific regulatory CD8+T cell population in chronic hepatitis C virus infection.
Articolo
High efficiency myogenic conversion of human fibroblasts by adenoviral vector-mediated MyoD gene transfer. An alternative strategy for ex vivo gene therapy of primary myopathies
Articolo
Histone deacetylase 9 promotes endothelial-mesenchymal transition and an unfavorable atherosclerotic plaque phenotype
Articolo
Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
Articolo
Hypoxia modulates the barrier and coagulant function of cultured bovine endothelium.
Articolo
Induced pluripotent stem cell-derived cardiomyocytes in studies of inherited arrhythmias.
Articolo
Inhibiting pathologically active ADAM10 rescues synaptic and cognitive decline in Huntington’s disease
Articolo
Liver X receptors a and b are in vivo pathophysiological regulators of renin
Articolo
Mesodermal iPSC-derived progenitor cells functionally regenerate cardiac and skeletal muscle
Articolo
Nuclear retention of COL1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta.
Articolo
PD-L1 negatively regulates CD4+CD25+Foxp3+ tregs by limiting STAT-5 phosphrylation in patients chronically infected with HCV
Articolo
Possible involvement of inefficient cleavage of preprovasopressin by signal peptidase as a cause for familial central diabetes insipidus.
Articolo
Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice
Articolo
Targeted ablation of IKK2 improves skeletal muscle strength, maintains mass, and promotes regeneration
Articolo
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
Articolo
The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.
Articolo
The immunoglobulin-like modules C epsilon 3 and alpha 2 are the minimal units necessary for human IgE-Fc epsilon RI interaction
Articolo
Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation
Articolo
No Results Found
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