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  1. Pubblicazioni

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Rivista
Codice:
E183623
ISSN:
1107-3756
  • Dati Generali

Dati Generali

Pubblicazioni (18)

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A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality
Articolo
Absence of Kir6.1/KCNJ8 mutations in Italian patients with abnormal coronary vasomotion
Articolo
Analysis of the apolipoprotein(a) size polymorphism in patients with systemic lupus erythematosus
Articolo
Analysis of the apolipoprotein(a) size polymorphism in patients with systemic lupus erythematosus.
Articolo
Analysis of the apoliporotein(a) size polymorphism in patients with systemic lupus erythematosus
Articolo
Apolipoprotein(a) phenotypes are reliable biomarkers for familial aggregation of coronary heart disease
Articolo
CR1 genotype and haplotype involvement in coronary artery disease: the pivotal role of hypertension and dyslipidemia
Articolo
Coronary artery disease and depression: possible role of brain-derived neurotrophic factor and serotonin transporter gene polymorphisms
Articolo
Development of a prion (PRNP)-based antisense therapy approach in human astrocytoma cell lines
Contributo in Atti di convegno
Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia.
Articolo
Effect of apoptogenic stimuli on colon carcinoma cell lines with a different c-myc expression level
Articolo
Effects of thermal water on skin regeneration
Articolo
Interleukin-2 at different concentrations induces the growth of selective lymphoid cells
Articolo
Non-muscle myosin heavy chain IIA and IIB interact and co-localize in living cells: Relevance for MYH9-related disease.
Articolo
Relationship between the -374T/A RAGE gene polymorphism and angiographic coronary artery disease
Articolo
Role of squamous cell carcinoma antigen-1 on liver cells after partial hepatectomy in transgenic mice
Articolo
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q131.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies.
Articolo
The effect of glycosaminoglycans and proteoglycans on lipid peroxidation
Articolo
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