Pierotti MA - Search Results

1

The M581V mutation, associated with a mild form of congenital insensitivity to pain with anhidrosis, causes partial inactivation of the NTRK1 receptor.

Miranda C, Selleri S, Pierotti MA, Greco A. Miranda C, et al. Among authors: pierotti ma. J Invest Dermatol. 2002 Oct;119(4):978-9. doi: 10.1046/j.1523-1747.2002.00140.x. J Invest Dermatol. 2002. PMID: 12406349 Free article. No abstract available.

2

Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations.

Miranda C, Di Virgilio M, Selleri S, Zanotti G, Pagliardini S, Pierotti MA, Greco A. Miranda C, et al. Among authors: pierotti ma. J Biol Chem. 2002 Feb 22;277(8):6455-62. doi: 10.1074/jbc.M110016200. Epub 2001 Nov 21. J Biol Chem. 2002. PMID: 11719521 Free article.

3

Oncogenic rearrangements of the NTRK1/NGF receptor.

Pierotti MA, Greco A. Pierotti MA, et al. Cancer Lett. 2006 Jan 28;232(1):90-8. doi: 10.1016/j.canlet.2005.07.043. Epub 2005 Oct 20. Cancer Lett. 2006. PMID: 16242838 Review.

4

Gain of function mutations of RTK conserved residues display differential effects on NTRK1 kinase activity.

Miranda C, Zanotti G, Pagliardini S, Ponzetto C, Pierotti MA, Greco A. Miranda C, et al. Among authors: pierotti ma. Oncogene. 2002 Nov 28;21(54):8334-9. doi: 10.1038/sj.onc.1206052. Oncogene. 2002. PMID: 12447696

5

Functional characterization of NTRK1 mutations identified in melanoma.

Miranda C, Mazzoni M, Sensi M, Pierotti MA, Greco A. Miranda C, et al. Among authors: pierotti ma. Genes Chromosomes Cancer. 2014 Oct;53(10):875-80. doi: 10.1002/gcc.22200. Epub 2014 Jun 26. Genes Chromosomes Cancer. 2014. PMID: 24965840

6

A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis.

Greco A, Villa R, Tubino B, Romano L, Penso D, Pierotti MA. Greco A, et al. Among authors: pierotti ma. Am J Hum Genet. 1999 Apr;64(4):1207-10. doi: 10.1086/302319. Am J Hum Genet. 1999. PMID: 10090906 Free PMC article. No abstract available.

7

The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor.

Greco A, Villa R, Fusetti L, Orlandi R, Pierotti MA. Greco A, et al. Among authors: pierotti ma. J Cell Physiol. 2000 Jan;182(1):127-33. doi: 10.1002/(SICI)1097-4652(200001)182:1<127::AID-JCP14>3.0.CO;2-0. J Cell Physiol. 2000. PMID: 10567924

8

Rearrangements of NTRK1 gene in papillary thyroid carcinoma.

Greco A, Miranda C, Pierotti MA. Greco A, et al. Among authors: pierotti ma. Mol Cell Endocrinol. 2010 May 28;321(1):44-9. doi: 10.1016/j.mce.2009.10.009. Epub 2009 Oct 31. Mol Cell Endocrinol. 2010. PMID: 19883730 Review.

9

Analysis of SHP-1-mediated down-regulation of the TRK-T3 oncoprotein identifies Trk-fused gene (TFG) as a novel SHP-1-interacting protein.

Roccato E, Miranda C, Raho G, Pagliardini S, Pierotti MA, Greco A. Roccato E, et al. Among authors: pierotti ma. J Biol Chem. 2005 Feb 4;280(5):3382-9. doi: 10.1074/jbc.M407522200. Epub 2004 Nov 22. J Biol Chem. 2005. PMID: 15557341 Free article.

10

Genomic organization of the human NTRK1 gene.

Greco A, Villa R, Pierotti MA. Greco A, et al. Among authors: pierotti ma. Oncogene. 1996 Dec 5;13(11):2463-6. Oncogene. 1996. PMID: 8957089

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

472 results

Search Page

Filters