TRISOMY 4G32->4GTER DUE TO A MATERNAL 4/21 TRANSLOCATIONBACCICHETTI C; TENCONI R; ANGLANI F et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 425-427; BIBL. 9 REF.Article

TRISOMY 1Q AND HEMATOLOGIC DISORDERSANGLANI F; ARTIFONI L; ZANESCO L et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 3; PP. 275-279; BIBL. 13 REF.Article

Association studies of genetic polymorphisms and complex diseaseGAMBARO, G; ANGLANI, F; D'ANGELO, A et al.Lancet (British edition). 2000, Vol 355, Num 9200, pp 308-311, issn 0140-6736Article

Screening for cystic fibrosis gene mutations by multiplex DNA amplificationPICCI, L; ANGLANI, F; SCARPA, M et al.Human genetics. 1992, Vol 88, Num 5, pp 552-556, issn 0340-6717Article

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 12 (P11;P13). REPORT OF A CASETENCONI R; BACCICHETTI C; ANGLANI F et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 95-98; ABS. FR.; BIBL. 13REF.Article

The guanine triphosphatase (GTPase) activating protein (GAP)-related domain of the neurofibromatosis type 1 gene is not mutated in neural crest-derived sporadic tumoursMURGIA, A; ANGLANI, F; VINANZI, C et al.European journal of cancer (1990). 1998, Vol 34, Num 4, pp 577-579, issn 0959-8049Article

Long-term treatment with CsA decreases INF-γ mRNA and increases pre-pro-ET-1 mRNA in rat kidneysMURER, L; GIACOMINI, A; GAMBARO, G et al.Transplantation proceedings. 1998, Vol 30, Num 4, pp 950-951, issn 0041-1345Conference Paper

A comparative kinetic RT/-PCR strategy for the quantitation of mRNAs in microdissected human renal biopsy specimensDEL PRETE, D; FORINO, M; GAMBARO, G et al.Experimental nephrology. 1998, Vol 6, Num 6, pp 563-567, issn 1018-7782Article

Functional polarity of Na⁺/H⁺ and Cl^-/HCO₃^- exchangers in a rat cholangiocyte cell lineSPIRLI, C; GRANATO, A; ZSEMBERY, A et al.American journal of physiology. Gastrointestinal and liver physiology. 1998, Vol 38, Num 6, pp G1236-G1245, issn 0193-1857Article

Frequency of abnormal karyotypes in relation to the ascertainment method in females referred for suspected sex chromosome abnormalityANGLANI, F; BACCICHETTI, C; ARTIFONI, L et al.Clinical genetics. 1984, Vol 25, Num 3, pp 242-247, issn 0009-9163Article

Linkage analysis of neurofibromatosis type 1. Study of a homogeneous North Italian population with five DNA markers of chromosome 17CLEMENTI, M; MURGIA, A; ANGLANI, F et al.Human genetics. 1991, Vol 87, Num 1, pp 91-94, issn 0340-6717Article

A new screening test for rotavirus infectionGIAQUINTO, C; VANIN, M; ANGLANI, F et al.Infection. 1985, Vol 13, Num 6, pp 260-262, issn 0300-8126Article

Direct effect of chronic cyclosporine treatment on collagen III mRNA expression and deposition in rat kidneysCEOL, M; ANGLANI, F; VIANELLO, D et al.Clinical nephrology. 2000, Vol 53, Num 4, pp A8-A9, issn 0301-0430Conference Paper

Molecular biology of diabetic glomerulosclerosisDEL PRETE, D; ANGLANI, F; CEOL, M et al.Nephrology, dialysis, transplantation (Print). 1998, Vol 13, pp 20-25, issn 0931-0509, SUP8Conference Paper

Replication patterns of human X isochromosomes by high-resolution bandingARTIFONI, L; BACCICHETTI, C; PIOVAN, E et al.Cytogenetics and cell genetics. 1983, Vol 36, Num 4, pp 649-651, issn 0301-0171Article

Down-regulation of glomerular matrix metalloproteinase-2 gene in human NIDDMDEL PRETE, D; ANGLANI, F; FORINO, M et al.Diabetologia (Berlin). 1997, Vol 40, Num 12, pp 1449-1454, issn 0012-186XArticle

Increased glomerular α1(IV) collagen expression and deposition in long-term diabetic rats is prevented by chronic glycosaminoglycan treatmentCEOL, M; NERLICH, A; BAGGIO, B et al.Laboratory investigation. 1996, Vol 74, Num 2, pp 484-495, issn 0023-6837Article

A new disease-causing mutation in the GAP-related domain of the NF1 geneANGLANI, F; MURGIA, A; BEDIN, S et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, pp 1057-1059, issn 0964-6906Article

The use of biotinylated probes in the DNA analysis for diagnostic purposeANGLANI, F; CAMPORESE, C; GREGGIO, N et al.Chimica oggi. 1990, Vol 8, Num 6, pp 65-68, issn 0392-839X, 4 p.Article