Duga S - Search Results

1

Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis.

Cardamone G, Paraboschi EM, Soldà G, Cantoni C, Supino D, Piccio L, Duga S, Asselta R. Cardamone G, et al. Among authors: duga s. Hum Mol Genet. 2019 May 1;28(9):1414-1428. doi: 10.1093/hmg/ddy438. Hum Mol Genet. 2019. PMID: 30566690

2

Identification of a glucocorticoid response element in the human gamma chain fibrinogen promoter.

Asselta R, Duga S, Modugno M, Malcovati M, Tenchini ML. Asselta R, et al. Among authors: duga s. Thromb Haemost. 1998 Jun;79(6):1144-50. Thromb Haemost. 1998. PMID: 9657439 Free article.

3

SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population.

Tenchini ML, Duga S, Bonati MT, Asselta R, Oldani A, Zucconi M, Malcovati M, Dalprà L, Ferini-Strambi L. Tenchini ML, et al. Among authors: duga s. Sleep. 1999 Aug 1;22(5):637-9. doi: 10.1093/sleep/22.5.637. Sleep. 1999. PMID: 10450598

4

The intron-containing L3 ribosomal protein gene (RPL3): sequence analysis and identification of U43 and of two novel intronic small nucleolar RNAs.

Duga S, Asselta R, Malcovati M, Tenchini ML, Ronchi S, Simonic T. Duga S, et al. Biochim Biophys Acta. 2000 Feb 29;1490(3):225-36. doi: 10.1016/s0167-4781(99)00237-7. Biochim Biophys Acta. 2000. PMID: 10684968

5

Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE.

Bonati MT, Asselta R, Duga S, Ferini-Strambi L, Oldani A, Zucconi M, Malcovati M, Dalprà L, Tenchini ML. Bonati MT, et al. Among authors: duga s. Neuroreport. 2000 Jul 14;11(10):2097-101. doi: 10.1097/00001756-200007140-00008. Neuroreport. 2000. PMID: 10923651

6

Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.

Asselta R, Duga S, Simonic T, Malcovati M, Santagostino E, Giangrande PL, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: duga s. Blood. 2000 Oct 1;96(7):2496-500. Blood. 2000. PMID: 11001902 Free article.

7

A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker.

Bonati MT, Duga S, Asselta R, Ferini-Strambi L, Oldani A, Zucconi M, Malcovati M, Dalprà L, Tenchini ML. Bonati MT, et al. Among authors: duga s. Mol Cell Probes. 2000 Dec;14(6):373-80. doi: 10.1006/mcpr.2000.0327. Mol Cell Probes. 2000. PMID: 11090267

8

A novel two base pair deletion in the factor V gene associated with severe factor V deficiency.

Montefusco MC, Duga S, Asselta R, Santagostino E, Mancuso G, Malcovati M, Mannucci PM, Tenchini ML. Montefusco MC, et al. Among authors: duga s. Br J Haematol. 2000 Dec;111(4):1240-6. doi: 10.1046/j.1365-2141.2000.02456.x. Br J Haematol. 2000. PMID: 11167768 Free article.

9

Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms.

Duga S, Soldà G, Asselta R, Bonati MT, Dalprà L, Malcovati M, Tenchini ML. Duga S, et al. J Hum Genet. 2001;46(11):640-8. doi: 10.1007/s100380170015. J Hum Genet. 2001. PMID: 11721883

10

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.

Asselta R, Duga S, Spena S, Santagostino E, Peyvandi F, Piseddu G, Targhetta R, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: duga s. Blood. 2001 Dec 15;98(13):3685-92. doi: 10.1182/blood.v98.13.3685. Blood. 2001. PMID: 11739173 Free article.

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