PubRank

F Pasquali

Author PubWeight™ 40.40‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Trisomy 8 in Philadelphia chromosome (Ph1)-negative cells in the course of Ph1-positive chronic myelocytic leukemia. Genes Chromosomes Cancer 1992 1.37
2 Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages. Eur J Immunol 1975 1.24
3 Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile. Hum Genet 1977 1.24
4 The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome. Leukemia 2009 1.12
5 Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene. Cancer Genet Cytogenet 2001 1.02
6 Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases. Genes Chromosomes Cancer 1996 0.95
7 Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet 1982 0.94
8 Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies. Cancer Genet Cytogenet 1985 0.94
9 Male infertility and 13-14 translocation. Lancet 1973 0.94
10 Polyphosphoinositide metabolism is rapidly stimulated by activation of a temperature-sensitive mutant of Rous sarcoma virus in rat fibroblasts. Oncogene 1987 0.92
11 Transformation of BALB/3T3 cells with EJ/T24/H-ras oncogene inhibits adenylate cyclase response to beta-adrenergic agonist while increases muscarinic receptor dependent hydrolysis of inositol lipids. Biochem Biophys Res Commun 1985 0.90
12 OTX1 expression in breast cancer is regulated by p53. Oncogene 2011 0.88
13 The Mr 17500 region of the A chain of urokinase is required for interaction with a specific receptor in A431 cells. Biochim Biophys Acta 1986 0.88
14 Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases. Hum Genet 1982 0.88
15 Flow cytometric evaluation of proliferative activity and ploidy in myelodysplastic syndromes and acute leukemias. Basic Appl Histochem 1986 0.87
16 Point-mutated p21ras couples a muscarinic receptor to calcium channels and polyphosphoinositide hydrolysis. Biochem Biophys Res Commun 1986 0.86
17 Internalization and metabolism of endogenous heparin by cultured endothelial cells. Biochem Biophys Res Commun 1986 0.86
18 Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR. Leukemia 2007 0.84
19 Adhesion-dependent heparin production by platelets. Nature 1982 0.84
20 Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders. Cancer Genet Cytogenet 2000 0.83
21 Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14. Clin Genet 1988 0.83
22 17q21-qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia. Cancer Genet Cytogenet 2001 0.82
23 Effects of cortisone with and without heparin on angiogenesis induced by prostaglandin E1 and by S180 cells, and on growth of murine transplantable tumours. Int J Cancer 1985 0.81
24 Cytogenetic findings in a case of anaplastic carcinoma of the pancreas. Cancer Genet Cytogenet 1987 0.81
25 Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia. Eur Neurol 1992 0.80
26 Synthesis of diacylglycerol de novo is responsible for permanent activation and down-regulation of protein kinase C in transformed cells. Biochem Biophys Res Commun 1989 0.80
27 Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase. Genes Chromosomes Cancer 1990 0.80
28 Transformation by ras oncogene induces nuclear shift of protein kinase C. Biochem Biophys Res Commun 1990 0.80
29 Binding, internalization and degradation of heparin and heparin fragments by cultured endothelial cells. Thromb Res 1988 0.79
30 Inhibition of BC3H-1 cell growth by heparin is related to decreased mitogenic signalling. Biochem Biophys Res Commun 1990 0.79
31 Heparin inhibits A431 cell growth independently of serum and EGF mitogenic signalling. FEBS Lett 1991 0.79
32 Effect of heparin on proliferation and signalling in BC3H-1 muscle cells. Evidence for specific binding sites. FEBS Lett 1990 0.79
33 A 45,X male with a Yp/18 translocation. Hum Genet 1986 0.79
34 Immunodeficiency in Down's syndrome: relationship between presence of human thyroglobulin antibodies and HBsAg carrier status. Eur J Pediatr 1977 0.78
35 Modulation of growth of melanoma. Int J Dermatol 1988 0.78
36 [Pickwickian-narcoleptic disorders after brain concussion]. Riv Sper Freniatr Med Leg Alien Ment 1972 0.78
37 Reconstitution of the complement channel into lipid vesicles and planar bilayers starting from the fluid phase complex. Biosci Rep 1985 0.78
38 Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies. Am J Med Genet 1998 0.78
39 Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. Ann Genet 1991 0.77
40 Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia. Leukemia 2001 0.77
41 Centralized cytogenetic analysis of pediatric acute leukemia: results of an Italian collaborative experience. Haematologica 1998 0.77
42 Transposition of 9q34 and 22 (q11toqter) regions has a specific role in chronic myelocytic leukemia. Hum Genet 1979 0.77
43 Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. Cancer Genet Cytogenet 1999 0.77
44 Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma. Hum Genet 1986 0.77
45 Tandem translocation 15-13. Ann Genet 1973 0.76
46 Monozygotic twins discordant for cutaneous mastocytosis. Arch Dermatol 1983 0.75
47 Mechanism of origin of the isochromosome i(17q) Cancer Genet Cytogenet 1995 0.75
48 Signal transduction in EJ-H-ras-transformed cells: de novo synthesis of diacylglycerol and subversion of agonist-stimulated inositol lipid metabolism. FEBS Lett 1989 0.75
49 Cooperative effect of exogenous heparin-like compounds and secreted glucocorticoid-induced inhibitor on plasminogen activator in 3T3 cell cultures. Tumori 1984 0.75
50 Parental origin of chromosomes 9 and 22 involved in the Ph chromosome translocation in chronic myelocytic leukemia. Cancer Genet Cytogenet 1998 0.75
51 High-degree abnormalities of nuclear DNA distribution in SIg negative acute lymphoblastic leukemia with vacuolated blasts. Cancer 1986 0.75
52 Spontaneous remission from RAEB in a child. Leukemia 2001 0.75
53 Isochromosome (17q) in Philadelphia chromosome (Ph1)-negative juvenile chronic myelocytic leukemia. Cancer Genet Cytogenet 1981 0.75
54 Chromosome abnormalities and male sterility. J Genet Hum 1975 0.75
55 [Persistence in the adult of the primitive cervical segmental artery]. Riv Sper Freniatr Med Leg Alien Ment 1970 0.75
56 Monosomy 7 syndrome. N Engl J Med 1982 0.75
57 Partial trisomy 1 due to 1/17 translocation in Ph'-positive chronic myelocytic leukemia. Hum Genet 1979 0.75
58 Hot air treatment for surface decontamination of table eggs experimentally infected with Salmonella, Listeria, and Escherichia coli. Vet Res Commun 2010 0.75
59 [Spinal metasteses from intracranial oligodendroglioma]. Riv Sper Freniatr Med Leg Alien Ment 1971 0.75
60 Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome. Hum Genet 1978 0.75
61 Russell-Silver syndrome and XXY syndrome. Pediatrics 1983 0.75
62 Pharmacokinetics of dipyridamole-beta-cyclodextrin complex in healthy volunteers after single and multiple doses. Eur J Drug Metab Pharmacokinet 1992 0.75
63 Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation. Cancer Genet Cytogenet 2000 0.75
64 Gene dosage effect for beta-glucuronidase (GUSB) in monosomy 7 cells of patients with myeloproliferative disorders. Acta Anthropogenet 1983 0.75
65 Trisomy 12 in a case of large cell, immunoblastic, polymorphous non-Hodgkin's lymphoma with IgG kappa monoclonal paraprotein. Cancer Genet Cytogenet 1984 0.75
66 [Glycosaminoglycans in pleural effusions. Preliminary results]. Minerva Med 1985 0.75
67 Letter: Comment on Russell-Silver syndrome. Pediatrics 1974 0.75
68 Involvement of chondroitin sulphate in preventing adhesive cellular interactions. Biochim Biophys Acta 1983 0.75
69 Erythroleukemia in early childhood associated with monosomy 7 and defective neutrophil chemotaxis. Haematologica 1983 0.75
70 Loss of the Y chromosome in smoldering acute leukemia. Haematologica 1977 0.75
71 [Chromosome 6/17 translocation as a cause of repeated abortions]. Ann Ostet Ginecol Med Perinat 1975 0.75
72 Rearrangement of three chromosomes (nos. 2,8, and 21) in acute myeloblastic leukemia. Evidence for more than one specific event. Cancer Genet Cytogenet 1981 0.75
73 Cytogenetics in autologous bone marrow transplantation. Cancer Genet Cytogenet 1990 0.75
74 Involvement of chromosome No. 20 in a complex Ph1 translocation. Cancer Genet Cytogenet 1983 0.75
75 The 47,XXY karyotype and unrelated malformative patterns: an unusual association. Helv Paediatr Acta 1987 0.75
76 Electrical properties of ionic channels formed by Helix pomatia hemocyanin in planar lipid bilayers. Biophys Struct Mech 1984 0.75
77 Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosome. Cancer Genet Cytogenet 1992 0.75
78 8/21 translocation, loss of the Y chromosome and Philadelphia chromosome. Br J Haematol 1978 0.75
79 [True hermaphroditism, lateral variety. contribution to the ultrastructural study of the gonadal tissue]. Minerva Pediatr 1975 0.75
80 Different break-points in Philadelphia chromosome variant translocations and in constitutional and sporadic translocations. Ann Hum Genet 1986 0.75
81 [2:12 (p25;q21) translocation classed at first as 2/X]. Ann Genet 1975 0.75
82 Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss. Cancer Genet Cytogenet 1997 0.75
83 Masked Philadelphia chromosome caused by translocation (9;11;22). Cancer Genet Cytogenet 1983 0.75
84 [Complex chromosome translocation in a case of congenital monocytic leukemia]. Pathologica 1983 0.75
85 Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase. Hum Genet 1988 0.75
86 Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia. Hereditas 1989 0.75
87 Translocation (8;21) in two cases of refractory anemia with excess of blasts in transformation. Cancer Genet Cytogenet 1992 0.75
88 Plasminogen activator: morphological evidence of binding, internalization and delivery to lysosomes in 3T3 mouse fibroblasts. Histochem J 1985 0.75
89 The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution. Hum Genet 1982 0.75