Asselta R - Search Results

1

Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.

Zadra G, Asselta R, Malcovati M, Santagostino E, Peyvandi F, Mannucci PM, Tenchini ML, Duga S. Zadra G, et al. Among authors: asselta r. Haematologica. 2004 Nov;89(11):1332-40. Haematologica. 2004. PMID: 15531455 Free article.

2

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.

Oldani A, Zucconi M, Asselta R, Modugno M, Bonati MT, Dalprà L, Malcovati M, Tenchini ML, Smirne S, Ferini-Strambi L. Oldani A, et al. Among authors: asselta r. Brain. 1998 Feb;121 ( Pt 2):205-23. doi: 10.1093/brain/121.2.205. Brain. 1998. PMID: 9549500

3

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. Thromb Haemost. 1998 Jun;79(6):1144-50. Thromb Haemost. 1998. PMID: 9657439 Free article.

4

Analysis of the 16S rRNA gene sequence of the coryneform bacterium associated with hyperkeratotic dermatitis of athymic nude mice and development of a PCR-based detection assay.

Duga S, Gobbi A, Asselta R, Crippa L, Tenchini ML, Simonic T, Scanziani E. Duga S, et al. Among authors: asselta r. Mol Cell Probes. 1998 Aug;12(4):191-9. doi: 10.1006/mcpr.1998.0168. Mol Cell Probes. 1998. PMID: 9727194

5

A new exon in the 5' untranslated region of the connexin32 gene.

Duga S, Asselta R, Del Giacco L, Malcovati M, Ronchi S, Tenchini ML, Simonic T. Duga S, et al. Among authors: asselta r. Eur J Biochem. 1999 Jan;259(1-2):188-96. doi: 10.1046/j.1432-1327.1999.00029.x. Eur J Biochem. 1999. PMID: 9914492 Free article.

6

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: asselta r. Sleep. 1999 Aug 1;22(5):637-9. doi: 10.1093/sleep/22.5.637. Sleep. 1999. PMID: 10450598

7

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. Among authors: asselta r. Blood. 2000 Feb 15;95(4):1336-41. Blood. 2000. PMID: 10666208 Free article.

8

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. Among authors: asselta r. Biochim Biophys Acta. 2000 Feb 29;1490(3):225-36. doi: 10.1016/s0167-4781(99)00237-7. Biochim Biophys Acta. 2000. PMID: 10684968

9

cDNA cloning of turtle prion protein.

Simonic T, Duga S, Strumbo B, Asselta R, Ceciliani F, Ronchi S. Simonic T, et al. Among authors: asselta r. FEBS Lett. 2000 Mar 3;469(1):33-8. doi: 10.1016/s0014-5793(00)01232-1. FEBS Lett. 2000. PMID: 10708751 Free article.

10

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: asselta r. Neuroreport. 2000 Jul 14;11(10):2097-101. doi: 10.1097/00001756-200007140-00008. Neuroreport. 2000. PMID: 10923651

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