Duga S - Search Results

1

Saposin D variants are not a common cause of familial Parkinson's disease among Italians.

Facchi D, Rimoldi V, Straniero L, Paraboschi EM, Soldà G, Zecchinelli AL, Cilia R, Duga S, Pezzoli G, Asselta R. Facchi D, et al. Among authors: duga s. Brain. 2020 Sep 1;143(9):e71. doi: 10.1093/brain/awaa213. Brain. 2020. PMID: 32793950 No abstract available.

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

Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML. Duga S, et al. Blood. 2000 Feb 15;95(4):1336-41. Blood. 2000. PMID: 10666208 Free article.

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

Identification of four novel polymorphisms in the Aalpha and gamma fibrinogen genes and analysis of association with plasma levels of the protein.

Menegatti M, Asselta R, Duga S, Malcovati M, Bucciarelli P, Mannucci PM, Tenchini ML. Menegatti M, et al. Among authors: duga s. Thromb Res. 2001 Aug 15;103(4):299-307. doi: 10.1016/s0049-3848(01)00329-2. Thromb Res. 2001. PMID: 11562340

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

187 results

Search Page

Filters