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New developments at INFN-LNS on TOF–DOI PET based on SiPM detectors

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2013-02, Vol.702, p.10-12

2013

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MASA syndrome: ultrasonographic evidence in a male fetus

Prenatal diagnosis, 2000-12, Vol.20 (12), p.1012-1014

2000

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Phenotype of in vitro human otosclerotic cells and its modulation by TGF beta

Cellular and molecular biology (Noisy-le-Grand, France), 1995-12, Vol.41 (8), p.1039

1995

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Molecular characterization of an unusual variant t(15;17) detected in an APL patient

Leukemia, 1995-10, Vol.9 (10), p.1787-1789

1995

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Glycosaminoglycan metabolism in otosclerotic bone cells

Biology of the cell, 1996, Vol.86 (1), p.73-78

1996

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Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories

Genetics in medicine, 2005-11, Vol.7 (9), p.620-625

2005

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PTH induces modification of transductive events in otosclerotic bone cell cultures

Cell biochemistry and function, 1993-12, Vol.11 (4), p.257-261

1993

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Interleukin-1 alpha: regulation of cellular proliferation and collagen synthesis in cultured human osteoblast-like cells

Cellular and molecular biology (Noisy-le-Grand, France), 1992-08, Vol.38 (5-6), p.679

1992

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Glycosaminoglycan metabolism in otosclerotic bone cells

Biology of the cell, 1996, Vol.86 (1), p.73-78

1996

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Synthesis and secretion of glycosaminoglycans and proteins in human normal and otosclerotic bone cells

Cellular and molecular biology (Noisy-le-Grand, France), 1992-08, Vol.38 (5-6), p.635

1992

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X-Ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect

Journal of endocrinological investigation, 1989-04, Vol.12 (4), p.257-263

1989

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Search for cytogenetic markers in chemically xenogenized murine lymphomas

Pharmacological research, 1989-09, Vol.21 (5), p.667-668

1989

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Human bone cell cultures: A new model for studying the mechanism of action of calcitonin

Cell biochemistry and function, 1985-07, Vol.3 (3), p.179-184

1985

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DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation)

Journal of medical genetics, 1982-10, Vol.19 (5), p.349-353

1982

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Trisomy 6p22?6pter due to familial t(6;13)(p22;q34 or 33) translocation

Human genetics, 1979-01, Vol.51 (1), p.67-72

1979

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Glycosaminoglycan Metabolism and Cytokine Release in Normal and Otosclerotic Human Bone Cells Interleukin-1 Treated

Connective tissue research, 1997, Vol.36 (3), p.231-240

1997

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Altered adenylate cyclase activity in human otosclerotic bone cell cultures

Molecular and cellular endocrinology, 1989-03, Vol.62 (1), p.119-123

1989

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A case of complete testicular feminisation and 47,XXY karyotype

Journal of medical genetics, 1979-12, Vol.16 (6), p.480-483

1979

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Acute myeloblastic leukemia after adjuvant chemotherapy with melphalan in breast cancer. Case report with cytogenetic analysis

Tumori, 1983-04, Vol.69 (2), p.117-122

1983

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Morphological and functional characteristics of human temporal-bone cell cultures

Cell and tissue research, 1983-01, Vol.229 (3), p.505-513

1983

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The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG)

Human genetics, 1979-01, Vol.48 (1), p.53-59

1979

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Hormonal receptor site alterations in the etiopathogenesis of otosclerosis

Annals of otology, rhinology & laryngology, 1986-05, Vol.95 (3 Pt 1), p.294-297

1986

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Molecular characterization of an unusal variant t(15; 17) detected in an APL patient

Leukemia, 1995-01, Vol.9 (10), p.1787-1798

1995

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Yq--in a family with several cases of complete testicular feminization

Rivista di biologia, 1979-01, Vol.72 (1-2), p.39

1979

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Mapping of chromosome 17 breakpoints in acute myeloid leukemias

Oncogene, 1990-10, Vol.5 (10), p.1557-1563

1990

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New developments at INFN-LNS on TOF–DOI PET based on SiPM detectors

MASA syndrome: ultrasonographic evidence in a male fetus

Phenotype of in vitro human otosclerotic cells and its modulation by TGF beta

Molecular characterization of an unusual variant t(15;17) detected in an APL patient

Glycosaminoglycan metabolism in otosclerotic bone cells

Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories

PTH induces modification of transductive events in otosclerotic bone cell cultures

Interleukin-1 alpha: regulation of cellular proliferation and collagen synthesis in cultured human osteoblast-like cells

Glycosaminoglycan metabolism in otosclerotic bone cells

Synthesis and secretion of glycosaminoglycans and proteins in human normal and otosclerotic bone cells

X-Ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect

Search for cytogenetic markers in chemically xenogenized murine lymphomas

Human bone cell cultures: A new model for studying the mechanism of action of calcitonin

DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation)

Trisomy 6p22?6pter due to familial t(6;13)(p22;q34 or 33) translocation

Glycosaminoglycan Metabolism and Cytokine Release in Normal and Otosclerotic Human Bone Cells Interleukin-1 Treated

Altered adenylate cyclase activity in human otosclerotic bone cell cultures

A case of complete testicular feminisation and 47,XXY karyotype

Acute myeloblastic leukemia after adjuvant chemotherapy with melphalan in breast cancer. Case report with cytogenetic analysis

Morphological and functional characteristics of human temporal-bone cell cultures

The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG)

Hormonal receptor site alterations in the etiopathogenesis of otosclerosis

Molecular characterization of an unusal variant t(15; 17) detected in an APL patient

Yq--in a family with several cases of complete testicular feminization

Mapping of chromosome 17 breakpoints in acute myeloid leukemias

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