Pinotti M - Search Results

1

The effect of the chemical chaperone 4-phenylbutyrate on secretion and activity of the p.Q160R missense variant of coagulation factor FVII.

Andersen E, Chollet ME, Baroni M, Pinotti M, Bernardi F, Skarpen E, Sandset PM, Skretting G. Andersen E, et al. Among authors: pinotti m. Cell Biosci. 2019 Aug 27;9:69. doi: 10.1186/s13578-019-0333-8. eCollection 2019. Cell Biosci. 2019. PMID: 31467667 Free PMC article.

2

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).

Marchetti G, Patracchini P, Gemmati D, DeRosa V, Pinotti M, Rodorigo G, Casonato A, Girolami A, Bernardi F. Marchetti G, et al. Among authors: pinotti m. Hum Genet. 1992 Jul;89(5):497-502. doi: 10.1007/BF00219173. Hum Genet. 1992. PMID: 1634227

3

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.

Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, Pinotti M, Redaelli R, Ballerini G, Pemberton S, et al. Bernardi F, et al. Among authors: pinotti m. Br J Haematol. 1994 Mar;86(3):610-8. doi: 10.1111/j.1365-2141.1994.tb04793.x. Br J Haematol. 1994. PMID: 8043443

4

In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.

Bernardi F, Patracchini P, Gemmati D, Pinotti M, Schwienbacher C, Ballerini G, Marchetti G. Bernardi F, et al. Among authors: pinotti m. Hum Mol Genet. 1993 May;2(5):545-8. doi: 10.1093/hmg/2.5.545. Hum Mol Genet. 1993. PMID: 8518792

5

Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.

Bernardi F, Castaman G, Pinotti M, Ferraresi P, Di Iasio MG, Lunghi B, Rodeghiero F, Marchetti G. Bernardi F, et al. Among authors: pinotti m. Hum Mutat. 1996;8(2):108-15. doi: 10.1002/(SICI)1098-1004(1996)8:2<108::AID-HUMU2>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8844208

6

Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations.

Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, Prydz H, Samama M, Sandset PM, Strom R, Garcia VV, Mariani G. Bernardi F, et al. Among authors: pinotti m. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2548-53. doi: 10.1161/01.atv.17.11.2548. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409226

7

Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.

Pinotti M, Toso R, Redaelli R, Berrettini M, Marchetti G, Bernardi F. Pinotti M, et al. Blood. 1998 Sep 1;92(5):1646-51. Blood. 1998. PMID: 9716592 Free article.

8

Molecular and clinical aspects of factor VII deficiency.

Mariani G, Lo Coco L, Bernardi F, Pinotti M. Mariani G, et al. Among authors: pinotti m. Blood Coagul Fibrinolysis. 1998 Mar;9 Suppl 1:S83-8. Blood Coagul Fibrinolysis. 1998. PMID: 9819034

9

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.

Pinotti M, Toso R, Girelli D, Bindini D, Ferraresi P, Papa ML, Corrocher R, Marchetti G, Bernardi F. Pinotti M, et al. Blood. 2000 Jun 1;95(11):3423-8. Blood. 2000. PMID: 10828024 Free article.

10

Residual factor VII activity and different hemorrhagic phenotypes in CRM(+) factor VII deficiencies (Gly331Ser and Gly283Ser).

Pinotti M, Etro D, Bindini D, Papa ML, Rodorigo G, Rocino A, Mariani G, Ciavarella N, Bernardi F. Pinotti M, et al. Blood. 2002 Feb 15;99(4):1495-7. doi: 10.1182/blood.v99.4.1495. Blood. 2002. PMID: 11830508 Free article.

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

231 results

Search Page

Filters