29 results on '"Gennaro, Elena"'
Search Results
2. HSP90 identified by a proteomic approach as druggable target to reverse platinum resistance in ovarian cancer
3. A novel mutation in KCNQ3 ‐related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome
4. Synthesis and Evaluation of the Antitumor Properties of a Small Collection of PtIIComplexes with 7-Deazaadenosine as Scaffold
5. A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients
6. The crucial role ofFBXO28in the pathogenesis of the 1q41q42 microdeletion syndrome
7. Synthesis and Evaluation of the Antiproliferative Properties of a Tethered Tubercidin-Platinum(II) Complex
8. Endothelial progenitor cells, defined by the simultaneous surface expression of VEGFR2 and CD133, are not detectable in healthy peripheral and cord blood
9. Maternal germinal mosaicism forSCN1Ain sibs with a mild form of Dravet syndrome
10. Mild Lafora disease: Clinical, neurophysiologic, and genetic findings
11. Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance
12. Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygousCSTBpoint and indel mutations
13. Caveolin‐1 overexpression is associated with simultaneous abnormal expression of the E‐cadherin/α–β catenins complex and multiple erbb receptors and with lymph nodes metastasis in head and neck squamous cell carcinomas
14. Proteomic analysis identifies differentially expressed proteins after HDAC vorinostat and EGFR inhibitor gefitinib treatments in Hep‐2 cancer cells
15. HDAC inhibitor vorinostat enhances the antitumor effect of gefitinib in squamous cell carcinoma of head and neck by modulating ErbB receptor expression and reverting EMT
16. SCN1Aduplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
17. Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype?Phenotype Correlations
18. Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations
19. Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families
20. Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease
21. Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
22. Frequent overexpression of multiple ErbB receptors by head and neck squamous cell carcinoma contrasts with rare antibody immunity in patients
23. Familial severe myoclonic epilepsy of infancy: truncation of Na v 1.1 and genetic heterogeneity
24. Critical role of both p27KIP1and p21CIP1/WAF1 in the antiproliferative effect of ZD1839 (‘Iressa’), an epidermal growth factor receptor tyrosine kinase inhibitor, in head and neck squamous carcinoma cells
25. Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
26. Lack of SCN1A Mutations in Familial Febrile Seizures
27. No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
28. HSP90 identified by a proteomic approach as druggable target to reverse platinum resistance in ovarian cancer
29. Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.