Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanoma
Dono, M, Angelini, G, Cecconi, M, Amaro, A, Esposito, A I, Mirisola, V, Maric, I, Lanza, F, Nasciuti, F, Viaggi, S, Gualco, M, Bandelloni, R, Truini, M, Coviello, D A, Zupo, S, Mosci, C, Pfeffer, U
Published in British journal of cancer (18.02.2014)
Published in British journal of cancer (18.02.2014)
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The heritability of circulating testosterone, oestradiol, oestrone and sex hormone binding globulin concentrations in men: the Framingham Heart Study
Travison, T. G., Zhuang, W. V., Lunetta, K. L., Karasik, D., Bhasin, S., Kiel, D. P., Coviello, A. D., Murabito, J. M.
Published in Clinical endocrinology (Oxford) (01.02.2014)
Published in Clinical endocrinology (Oxford) (01.02.2014)
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First-trimester euploid miscarriages analysed by array-CGH
Viaggi, Chiara Donatella, Cavani, S, Malacarne, M, Floriddia, F, Zerega, G, Baldo, C, Mogni, M, Castagnetta, M, Piombo, G, Coviello, D. A, Camandona, F, Lijoi, D, Insegno, W, Traversa, M, Pierluigi, M
Published in Journal of applied genetics (01.08.2013)
Published in Journal of applied genetics (01.08.2013)
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Circulating Testosterone and SHBG Concentrations Are Heritable in Women: The Framingham Heart Study
Coviello, A. D, Zhuang, W. V, Lunetta, K. L, Bhasin, S, Ulloor, J, Zhang, A, Karasik, D, Kiel, D. P, Vasan, R. S, Murabito, J. M
Published in The journal of clinical endocrinology and metabolism (01.09.2011)
Published in The journal of clinical endocrinology and metabolism (01.09.2011)
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A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity
Bottinelli, R, Coviello, D.A, Redwood, C.S, Pellegrino, M.A, Maron, B.J, Spirito, P, Watkins, H, Reggiani, C
Published in Circulation research (01.01.1998)
Published in Circulation research (01.01.1998)
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17q23.3 de novo microdeletion involving only TANC2 gene: A new case
Tassano, E., Accogli, A., Ronchetto, P., Tortora, D., Tavella, E., Gimelli, G., Mancardi, M., Malacarne, M., Coviello, D.A.
Published in European journal of medical genetics (01.12.2020)
Published in European journal of medical genetics (01.12.2020)
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Generation of induced Pluripotent Stem Cells as disease modelling of NLSDM
Tavian, D., Missaglia, S., Castagnetta, M., Degiorgio, D., Pennisi, E.M., Coleman, R.A., Dell'Era, P., Mora, C., Angelini, C., Coviello, D.A.
Published in Molecular genetics and metabolism (01.05.2017)
Published in Molecular genetics and metabolism (01.05.2017)
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Androgen and estrogen receptors are present in primary cultures of human synovial macrophages
CUTOLO, M, ACCARDO, S, CARRUBA, G, CASTAGNETTA, L, VILLAGIO, B, BARONE, A, SULLI, A, COVIELLO, D. A, CARABBIO, C, FELLI, L, MICELLI, D, FARRUGGIO, R
Published in The journal of clinical endocrinology and metabolism (01.02.1996)
Published in The journal of clinical endocrinology and metabolism (01.02.1996)
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A novel dominant missense mutation - D179N - in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss
Primignani, P, Castorina, P, Sironi, F, Curcio, C, Ambrosetti, U, Coviello, DA
Published in Clinical genetics (01.06.2003)
Published in Clinical genetics (01.06.2003)
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Cumming syndrome with heterotaxia, campomelia and absent uterus/fallopian tubes
Bedeschi, M.F., Spaccini, L., Rizzuti, T., Coviello, D.A., Castorina, P., Natacci, F., Lalatta, F.
Published in American journal of medical genetics. Part A (30.01.2005)
Published in American journal of medical genetics. Part A (30.01.2005)
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Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene
Coviello, Domenico A, Maron, Barry J, Spirito, Paolo, Watkins, Hugh, Vosberg, Hans-Peter, Thierfelder, Ludwig, Schoen, Frederick J, Seidman, J.G, Seidman, Christine E
Published in Journal of the American College of Cardiology (01.03.1997)
Published in Journal of the American College of Cardiology (01.03.1997)
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An MBL2 haplotype and ABCB4 variants modulate the risk of liver disease in cystic fibrosis patients: A multicentre study
Tomaiuolo, R, Degiorgio, D, Coviello, D.A, Baccarelli, A, Elce, A, Raia, V, Motta, V, Seia, M, Castaldo, G, Colombo, C
Published in Digestive and liver disease (01.11.2009)
Published in Digestive and liver disease (01.11.2009)
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Estradiol inhibits growth of hormone-nonresponsive PC3 human prostate cancer cells
CARRUBA, G, PFEFFER, U, FECAROTTA, E, COVIELLO, D. A, D'AMATO, E, LO CASTO, M, VIDALI, G, CASTAGNETTA, L
Published in Cancer research (Chicago, Ill.) (01.03.1994)
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Published in Cancer research (Chicago, Ill.) (01.03.1994)
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Interferon therapy in chronic hepatitis C : evaluation of a low dose maintenance schedule in responder patients
PICCIOTTO, A, VARAGONA, G, VALLE, F, COVIELLO, D. A, LAPERTOSA, G, CELLE, G
Published in Journal of hepatology (01.03.1993)
Published in Journal of hepatology (01.03.1993)
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Terminal erythroid differentiation in the K-562 cell line by 1-β-D-arabinofuranosylcytosine: accompaniment by c-myc messenger RNA decrease
BIANCHI SCARRA, G. L, ROMANI, M, COVIELLO, D. A, GARRE, C, RAVAZZOLO, R, VIDALI, G, AJMAR, F
Published in Cancer research (Chicago, Ill.) (01.12.1986)
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Published in Cancer research (Chicago, Ill.) (01.12.1986)
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Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing familial hypercholesterolemia (FH-Salerno)
Bertolini, S, Patel, D D, Coviello, D A, Lelli, N, Ghisellini, M, Tiozzo, R, Masturzo, P, Elicio, N, Knight, B L, Calandra, S
Published in Journal of lipid research (01.08.1994)
Published in Journal of lipid research (01.08.1994)
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Characterization of three mutations of the low density lipoprotein receptor gene in Italian patients with familial hypercholesterolemia
Lelli, N, Ghisellini, M, Gualdi, R, Tiozzo, R, Calandra, S, Gaddi, A, Ciarrocchi, A, Arca, M, Fazio, S, Coviello, D A
Published in Arteriosclerosis and thrombosis (01.03.1991)
Published in Arteriosclerosis and thrombosis (01.03.1991)
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