Pontoglio A - Search Results

1

Gelfi C, Vigano A, Ripamonti M, Pontoglio A, Begum S, Pellegrino MA, Grassi B, Bottinelli R, Wait R, Cerretelli P. Gelfi C, et al. Among authors: pontoglio a. J Proteome Res. 2006 Jun;5(6):1344-53. doi: 10.1021/pr050414x. J Proteome Res. 2006. PMID: 16739986

2

Peptide and protein separations by capillary electrophoresis in the presence of mono- and diquaternarized diamines.

Pontoglio A, Viganò A, Sebastiano R, Citterio A, Maragnoli L, Righetti PG, Gelfi C. Pontoglio A, et al. Electrophoresis. 2004 Apr;25(7-8):1065-70. doi: 10.1002/elps.200305794. Electrophoresis. 2004. PMID: 15095449

3

Study of Innovative GO/PBI Composites as Possible Proton Conducting Membranes for Electrochemical Devices.

Di Virgilio M, Basso Peressut A, Pontoglio A, Latorrata S, Dotelli G. Di Virgilio M, et al. Among authors: pontoglio a. Membranes (Basel). 2023 Apr 13;13(4):428. doi: 10.3390/membranes13040428. Membranes (Basel). 2023. PMID: 37103855 Free PMC article.

4

Mitochondrial Respiratory Complexes as Targets of Drugs: The PPAR Agonist Example.

Bottoni P, Pontoglio A, Scarà S, Pieroni L, Urbani A, Scatena R. Bottoni P, et al. Among authors: pontoglio a. Cells. 2022 Mar 30;11(7):1169. doi: 10.3390/cells11071169. Cells. 2022. PMID: 35406733 Free PMC article.

5

Functional analysis of six uncharacterised mutations in LDLR gene.

Gomez A, Colombo R, Pontoglio A, Helman L, Kaeser L, Giunta G, Parolin ML, Toscanini U, Cuniberti L. Gomez A, et al. Among authors: pontoglio a. Atherosclerosis. 2019 Dec;291:44-51. doi: 10.1016/j.atherosclerosis.2019.10.013. Epub 2019 Oct 12. Atherosclerosis. 2019. PMID: 31689621

6

A STAG3 missense mutation in two sisters with primary ovarian insufficiency.

Colombo R, Pontoglio A, Bini M. Colombo R, et al. Among authors: pontoglio a. Eur J Obstet Gynecol Reprod Biol. 2017 Sep;216:269-271. doi: 10.1016/j.ejogrb.2017.08.005. Epub 2017 Aug 5. Eur J Obstet Gynecol Reprod Biol. 2017. PMID: 28802712 No abstract available.

7

Caution in interpretation of disease causality for heterozygous loss-of-function variants in the MYH8 gene associated with autosomal dominant disorder.

Dai Z, Whitt Z, Mighion LC, Pontoglio A, Bean LJH, Colombo R, Hegde M. Dai Z, et al. Among authors: pontoglio a. Eur J Med Genet. 2017 Jun;60(6):312-316. doi: 10.1016/j.ejmg.2017.03.012. Epub 2017 Apr 2. Eur J Med Genet. 2017. PMID: 28377322

8

Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.

Colombo R, Pontoglio A, Bini M. Colombo R, et al. Among authors: pontoglio a. Gynecol Obstet Invest. 2017;82(3):283-286. doi: 10.1159/000468934. Epub 2017 Mar 30. Gynecol Obstet Invest. 2017. PMID: 28355598

9

Mild orotic aciduria in UMPS heterozygotes: a metabolic finding without clinical consequences.

Wortmann SB, Chen MA, Colombo R, Pontoglio A, Alhaddad B, Botto LD, Yuzyuk T, Coughlin CR, Descartes M, Grűnewald S, Maranda B, Mills PB, Pitt J, Potente C, Rodenburg R, Kluijtmans LA, Sampath S, Pai EF, Wevers RA, Tiller GE; additional individual contributors. Wortmann SB, et al. Among authors: pontoglio a. J Inherit Metab Dis. 2017 May;40(3):423-431. doi: 10.1007/s10545-017-0015-9. Epub 2017 Feb 15. J Inherit Metab Dis. 2017. PMID: 28205048 Free PMC article.

10

The multikinase inhibitor Sorafenib enhances glycolysis and synergizes with glycolysis blockade for cancer cell killing.

Tesori V, Piscaglia AC, Samengo D, Barba M, Bernardini C, Scatena R, Pontoglio A, Castellini L, Spelbrink JN, Maulucci G, Puglisi MA, Pani G, Gasbarrini A. Tesori V, et al. Among authors: pontoglio a. Sci Rep. 2015 Mar 17;5:9149. doi: 10.1038/srep09149. Sci Rep. 2015. PMID: 25779766 Free PMC article.

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