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3 NOVEL MUTATIONS OF THE PKD1 GENE IN ITALIAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE
Human mutation
DETECTION OF 2 DIFFERENT NONSENSE MUTATIONS IN EXON-44 OF THE PKD1 GENE IN 2 UNRELATED ITALIAN FAMILIES WITH SEVERE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE
Nephrology, dialysis, transplantation
A COMMON POLYMORPHISM IN EXON-46 OF THE HUMAN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE-1 GENE (PKD1)
Molecular and cellular probes
AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) IN AN ITALIAN FAMILY CARRYING A NOVEL NONSENSE MUTATION AND 2 MISSENSE CHANGES IN EXON-44 AND EXON-45 OF THE PKD1 GENE
American journal of medical genetics
JUVENILE IDIOPATHIC STABBING HEADACHE
Headache
BETA-ENDORPHIN IN PLASMA AND MONOCYTES IN JUVENILE HEADACHE
Headache
A NOVEL NONSENSE MUTATION IN THE PKD1 GENE (C3817T) IS ASSOCIATED WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) IN A LARGE 3-GENERATION ITALIAN FAMILY
Human molecular genetics
COMPARISON OF HETERODUPLEX AND SINGLE-STRAND CONFORMATION ANALYSES, FOLLOWED BY ETHIDIUM FLUORESCENCE VISUALIZATION, FOR THE DETECTION OF MUTATIONS IN 4 HUMAN GENES
Molecular and cellular probes
ERRONEOUS GENETIC RISK ASSESSMENT OF ALPORT SYNDROME
Lancet
MODIFICATION OF ANTIGEN EXPRESSION IN HUMAN AND HAMSTER PANCREATIC-CANCER CELL-LINES INDUCED BY SODIUM-BUTYRATE
Teratogenesis, carcinogenesis, and mutagenesis
CLINICAL RELEVANCE OF THE HAMSTER PANCREATIC-CANCER MODEL
International journal of pancreatology
CHOLECYSTOKININ INHIBITS DNA ALKYLATION INDUCED BY N-NITROSOBIS (2-OXOPROPYL)AMINE (BOP) IN HAMSTER PANCREAS
Cancer letters