Angelo Notarangelo
Casa Sollievo della Sofferenza(IT)
Publications by Year
Research Areas
Glioma Diagnosis and Treatment, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, MicroRNA in disease regulation, Epigenetics and DNA Methylation
Most-Cited Works
- → MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss(2001)241 cited
- → Sedlin Controls the ER Export of Procollagen by Regulating the Sar1 Cycle(2012)171 cited
- → Ring chromosome 21 in healthy persons: different consequencies in females and in males(1986)109 cited
- → Regulation ofKEAP1expression by promoter methylation in malignant gliomas and association with patient’s outcome(2011)104 cited
- Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.(1995)
- → Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years(2010)77 cited
- → Fine Exon–Intron Structure of the Fanconi Anemia Group A (FAA) Gene and Characterization of Two Genomic Deletions(1998)50 cited
- → Design and synthesis of 2-oxindole based multi-targeted inhibitors of PDK1/Akt signaling pathway for the treatment of glioblastoma multiforme(2015)47 cited
- → High Specificity of Quantitative Methylation‐Specific PCR Analysis for MGMT Promoter Hypermethylation Detection in Gliomas(2009)28 cited
- → On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome(1993)27 cited