Bortoletto E - Search Results

1

Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.

Lombardi AM, Bortoletto E, Scarparo P, Scapin M, Santarossa L, Girolami A. Lombardi AM, et al. Among authors: bortoletto e. Blood Coagul Fibrinolysis. 2008 Oct;19(7):639-43. doi: 10.1097/MBC.0b013e32830d8629. Blood Coagul Fibrinolysis. 2008. PMID: 18832903

2

Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature.

Girolami A, Scandellari R, Lombardi AM, Girolami B, Bortoletto E, Zanon E. Girolami A, et al. Among authors: bortoletto e. Haemophilia. 2005 Jan;11(1):26-30. doi: 10.1111/j.1365-2516.2005.01056.x. Haemophilia. 2005. PMID: 15660985 Review.

3

Mild factor VII deficiency due to heterozygosis is not associated with a bleeding tendency.

Girolami A, Vettore S, Bortoletto E, Zanon E. Girolami A, et al. Among authors: bortoletto e. Blood Coagul Fibrinolysis. 2005 Sep;16(6):459-60; author reply 460. doi: 10.1097/01.mbc.0000179910.34914.fb. Blood Coagul Fibrinolysis. 2005. PMID: 16093739 No abstract available.

4

Different fatherhood as a possible explanation for difficult pedigrees in coagulation defects: only 'mater semper certa est'.

Girolami A, Vettore S, Bortoletto E, Lombardi AM. Girolami A, et al. Among authors: bortoletto e. Br J Haematol. 2005 Aug;130(3):458-9; author reply 459-60. doi: 10.1111/j.1365-2141.2005.05623.x. Br J Haematol. 2005. PMID: 16042698 Free article. No abstract available.

5

Transcriptional deregulation and a missense mutation define ANKRD1 as a candidate gene for total anomalous pulmonary venous return.

Cinquetti R, Badi I, Campione M, Bortoletto E, Chiesa G, Parolini C, Camesasca C, Russo A, Taramelli R, Acquati F. Cinquetti R, et al. Among authors: bortoletto e. Hum Mutat. 2008 Apr;29(4):468-74. doi: 10.1002/humu.20711. Hum Mutat. 2008. PMID: 18273862

6

Tumor and metastasis suppression by the human RNASET2 gene.

Acquati F, Possati L, Ferrante L, Campomenosi P, Talevi S, Bardelli S, Margiotta C, Russo A, Bortoletto E, Rocchetti R, Calza R, Cinquetti R, Monti L, Salis S, Barbanti-Brodano G, Taramelli R. Acquati F, et al. Among authors: bortoletto e. Int J Oncol. 2005 May;26(5):1159-68. Int J Oncol. 2005. PMID: 15809705

7

Genetic damage induced by in vitro irradiation of human G0 lymphocytes with low-energy protons (28 keV/microm): HPRT mutations and chromosome aberrations.

Mognato M, Bortoletto E, Ferraro P, Baggio L, Cherubini R, Canova S, Russo A, Celotti L. Mognato M, et al. Among authors: bortoletto e. Radiat Res. 2003 Jul;160(1):52-60. doi: 10.1667/0033-7587(2003)160[0052:gdibiv]2.0.co;2. Radiat Res. 2003. PMID: 12816523

8

Chromosome instability induced in the cell progeny of human T lymphocytes irradiated in G(0) with gamma-rays.

Bortoletto E, Mognato M, Ferraro P, Canova S, Cherubini R, Celotti L, Russo A. Bortoletto E, et al. Mutagenesis. 2001 Nov;16(6):529-37. doi: 10.1093/mutage/16.6.529. Mutagenesis. 2001. PMID: 11682645

9

Long-read transcriptomics of Ostreid herpesvirus 1 uncovers a conserved expression strategy for the capsid maturation module and pinpoints a mechanism for evasion of the ADAR-based antiviral defence.

Rosani U, Bortoletto E, Zhang X, Huang BW, Xin LS, Krupovic M, Bai CM. Rosani U, et al. Among authors: bortoletto e. Virus Evol. 2024 Oct 17;10(1):veae088. doi: 10.1093/ve/veae088. eCollection 2024. Virus Evol. 2024. PMID: 39555210 Free PMC article.

10

Bioinformatics for Inosine: Tools and Approaches to Trace This Elusive RNA Modification.

Bortoletto E, Rosani U. Bortoletto E, et al. Genes (Basel). 2024 Jul 29;15(8):996. doi: 10.3390/genes15080996. Genes (Basel). 2024. PMID: 39202357 Free PMC article. Review.

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