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Your search keyword '"del Senno, L."' showing total 19 results
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19 results on '"del Senno, L."'

1. Analysis of published PKD1 gene sequence variants

Author

Gout, A. M., ADPKD Gene Variant Consortium, Ravine, D., Harris, P. C., Rossetti, S., Peters, D., Breuning, M., Henske, E. P., Koizumi, A., Inoue, S., Shimizu, Y., Thongnoppakhun, W., Yenchitsomanus, P. T., Deltas, C., Sandford, R., Torra, R., Turco, Alberto, Jeffery, S., Fontes, M., Somlo, S., Furu, L. M., Smulders, Y. M., Mercier, B., Ferec, C., Burtey, S., Pei, Y., Kalaydjieva, L., Bogdanova, N., Mccluskey, M., Geon, L. J., Wouters, C. H., Reiterova, J., Stekrová, J., San Millan, J. L., Aguiari, G., and Del Senno, L.

Subjects
Genetics, sequence variants, Polymorphism, Genetic, TRPP Cation Channels, PKD1, Base Sequence, business.industry, Biology, Text mining, ADPKD, Polymorphism (computer science), Research Design, Humans, Base sequence, Gene sequence, business
Published
2007

2. [Huntington chorea in the province of Ferrara from 1971 to 1987. Descriptive study]

Author

Govoni V, Pavoni M, Enrico Granieri, Carreras M, Malagù S, Gandini E, and Del Senno L

Subjects
Male, Huntington Disease, Italy, Risk Factors, Humans, Female, Middle Aged, Aged
Abstract

In the context of a multidisciplinary study program whose purpose is to investigate the genetic aspects of Huntington's Chorea (HC), the authors conducted an epidemiological descriptive research extended to the population residing in the province of Ferrara in a time period including the years from 1971 to 1987. On December 31st, 1987 we estimated a prevalence rate of 1.89 cases of HC per 100,000 inhabitants; in the years 1971-1987 the incidence rate was of 0.11 per 100,000/year and the mortality rate of 0.06 per 100,000/year. In the last years considered for the study, the incidence and the prevalence showed a relative increase indicating that HC still exists in the ferrarese population, despite a greater public awareness. With the aim to organize preventive actions and to reach the preclinical diagnosis of the disease we singled out 83 subjects at risk the study area.

Published
1988

4. Hypomethylation of the human estrogen receptor gene in primary human breast cancers

Author

A P Rimondi, Roberta Piva, Iva Maestri, Giovannini G, del Senno L, and Castagnoli A

Subjects
Oncology, Cancer Research, medicine.medical_specialty, business.industry, Clinical Biochemistry, Breast Neoplasms, DNA, Neoplasm, Biology, Methylation, Pathology and Forensic Medicine, Text mining, Receptors, Estrogen, Internal medicine, medicine, Cancer research, Humans, business, Estrogen receptor alpha, Human breast, Estrogen receptor beta
Published
1988

16. Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme

Author

Bernardi, F., Marchetti, G, Patracchini, P, DEL SENNO, L, Tripodi, M, Fantoni, A, Bartolai, S, Vannini, F, Felloni, L, Rossi, L, Panicucci, F, and Conconi, F

Subjects
Male, animal structures, Factor XII Deficiency, TaqI, Immunology, Coagulation Factor XII, Biochemistry, NO, Restriction fragment, chemistry.chemical_compound, Restriction map, Humans, cardiovascular diseases, Gene, Genetics, Factor XII, Polymorphism, Genetic, biology, Genetic Carrier Screening, Collodion, Cell Biology, Hematology, Molecular biology, Pedigree, Restriction enzyme, chemistry, biology.protein, Electrophoresis, Polyacrylamide Gel, Partial Thromboplastin Time, Restriction fragment length polymorphism, Polymorphism, Restriction Fragment Length, circulatory and respiratory physiology
Abstract

A cDNA for coagulation factor XII has been used to investigate the presence of gene lesions and restriction fragment length polymorphisms in two brothers with Hageman trait and their family. A TaqI polymorphic fragment has been found in the two propositi and in 11 members of the paternal lineage. This polymorphism, absent in the normal population, is correlated with the reduction of factor XII activity and enables the identification of heterozygous factor XII deficiency. Factor XII gene deletion as the cause of Hageman trait in this family has been excluded. A restriction map has been constructed, and the TaqI polymorphic site has been localized within the 5′ portion of the gene. The mutation in the polymorphic site is probably the cause of the factor XII deficiency. Data suggest the presence of one factor XII gene per haploid genome.

19. ?-Globin gene is undermethylated in K-562 cells: Increased expression after treatment of the cells with 5-azacytidine

Author

Francesco Bernardi, del Senno L, Roberto Gambari, Amelotti F, and Raffaella Barbieri

Subjects
Leukemia, DNA, Recombinant, Nucleic Acid Hybridization, Tumor cells, DNA, DNA Restriction Enzymes, Cell Biology, Methylation, Biology, Molecular biology, Deoxyribonuclease HpaII, Cell Line, Globins, chemistry.chemical_compound, Gene Expression Regulation, chemistry, Gene expression, Azacitidine, Humans, RNA, Messenger, Globin gene, Gene, After treatment
Published
1984
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