Giuliano S - Search Results

1

A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.

Habbout K, Poulin H, Rivier F, Giuliano S, Sternberg D, Fontaine B, Eymard B, Morales RJ, Echenne B, King L, Hanna MG, Männikkö R, Chahine M, Nicole S, Bendahhou S. Habbout K, et al. Among authors: giuliano s. Neurology. 2016 Jan 12;86(2):161-9. doi: 10.1212/WNL.0000000000002264. Epub 2015 Dec 11. Neurology. 2016. PMID: 26659129 Free PMC article.

2

Substitutions of the S4DIV R2 residue (R1451) in Na_V1.4 lead to complex forms of paramyotonia congenita and periodic paralyses.

Poulin H, Gosselin-Badaroudine P, Vicart S, Habbout K, Sternberg D, Giuliano S, Fontaine B, Bendahhou S, Nicole S, Chahine M. Poulin H, et al. Among authors: giuliano s. Sci Rep. 2018 Feb 1;8(1):2041. doi: 10.1038/s41598-018-20468-0. Sci Rep. 2018. PMID: 29391559 Free PMC article.

3

The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis.

Sacco S, Giuliano S, Sacconi S, Desnuelle C, Barhanin J, Amri EZ, Bendahhou S. Sacco S, et al. Among authors: giuliano s. Hum Mol Genet. 2015 Jan 15;24(2):471-9. doi: 10.1093/hmg/ddu462. Epub 2014 Sep 8. Hum Mol Genet. 2015. PMID: 25205110

4

Andersen's syndrome mutants produce a knockdown of inwardly rectifying K⁺ channel in mouse skeletal muscle in vivo.

Simkin D, Robin G, Giuliano S, Vukolic A, Moceri P, Guy N, Wagner KD, Lacampagne A, Allard B, Bendahhou S. Simkin D, et al. Among authors: giuliano s. Cell Tissue Res. 2018 Feb;371(2):309-323. doi: 10.1007/s00441-017-2696-7. Epub 2017 Oct 10. Cell Tissue Res. 2018. PMID: 29018970 Free article.

5

Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein Pathway.

Pini J, Giuliano S, Matonti J, Gannoun L, Simkin D, Rouleau M, Bendahhou S. Pini J, et al. Among authors: giuliano s. J Bone Miner Res. 2018 Oct;33(10):1826-1841. doi: 10.1002/jbmr.3474. Epub 2018 Jun 29. J Bone Miner Res. 2018. PMID: 29813186 Free article.

6

Revisiting CFTR inhibition: a comparative study of CFTRinh -172 and GlyH-101 inhibitors.

Melis N, Tauc M, Cougnon M, Bendahhou S, Giuliano S, Rubera I, Duranton C. Melis N, et al. Among authors: giuliano s. Br J Pharmacol. 2014 Aug;171(15):3716-27. doi: 10.1111/bph.12726. Br J Pharmacol. 2014. PMID: 24758416 Free PMC article.

7

Ciglitazone negatively regulates CXCL1 signaling through MITF to suppress melanoma growth.

Botton T, Puissant A, Cheli Y, Tomic T, Giuliano S, Fajas L, Deckert M, Ortonne JP, Bertolotto C, Tartare-Deckert S, Ballotti R, Rocchi S. Botton T, et al. Among authors: giuliano s. Cell Death Differ. 2011 Jan;18(1):109-21. doi: 10.1038/cdd.2010.75. Epub 2010 Jul 2. Cell Death Differ. 2011. PMID: 20596077 Free PMC article.

8

Proteomic analysis of lymphoblastoid cells from Nasu-Hakola patients: a step forward in our understanding of this neurodegenerative disorder.

Giuliano S, Agresta AM, De Palma A, Viglio S, Mauri P, Fumagalli M, Iadarola P, Montalbetti L, Salvini R, Bardoni A. Giuliano S, et al. PLoS One. 2014 Dec 3;9(12):e110073. doi: 10.1371/journal.pone.0110073. eCollection 2014. PLoS One. 2014. PMID: 25470616 Free PMC article.

9

Mitf is the key molecular switch between mouse or human melanoma initiating cells and their differentiated progeny.

Cheli Y, Giuliano S, Botton T, Rocchi S, Hofman V, Hofman P, Bahadoran P, Bertolotto C, Ballotti R. Cheli Y, et al. Among authors: giuliano s. Oncogene. 2011 May 19;30(20):2307-18. doi: 10.1038/onc.2010.598. Epub 2011 Jan 31. Oncogene. 2011. PMID: 21278797

10

Hypoxia and MITF control metastatic behaviour in mouse and human melanoma cells.

Cheli Y, Giuliano S, Fenouille N, Allegra M, Hofman V, Hofman P, Bahadoran P, Lacour JP, Tartare-Deckert S, Bertolotto C, Ballotti R. Cheli Y, et al. Among authors: giuliano s. Oncogene. 2012 May 10;31(19):2461-70. doi: 10.1038/onc.2011.425. Epub 2011 Sep 26. Oncogene. 2012. PMID: 21996743

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