Gagliardi L - Search Results

1

ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humans.

Luo H, Lao L, Au KS, Northrup H, He X, Forget D, Gauthier MS, Coulombe B, Bourdeau I, Shi W, Gagliardi L, Fragoso MCBV, Peng J, Wu J. Luo H, et al. Among authors: gagliardi l. Genome Biol. 2024 Jan 15;25(1):19. doi: 10.1186/s13059-023-03147-w. Genome Biol. 2024. PMID: 38225631 Free PMC article.

2

ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasia.

Lao L, Bourdeau I, Gagliardi L, He X, Shi W, Hao B, Tan M, Hu Y, Peng J, Coulombe B, Torpy DJ, Scott HS, Lacroix A, Luo H, Wu J. Lao L, et al. Among authors: gagliardi l. Nucleic Acids Res. 2022 Jun 24;50(11):6343-6367. doi: 10.1093/nar/gkac483. Nucleic Acids Res. 2022. PMID: 35687106 Free PMC article.

3

ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II).

De Sousa SMC, Stowasser M, Feng J, Schreiber AW, Wang P, Hahn CN, Gordon RD, Torpy DJ, Scott HS, Gagliardi L. De Sousa SMC, et al. Among authors: gagliardi l. J Hum Hypertens. 2017 Dec;31(12):857-859. doi: 10.1038/jhh.2017.71. Epub 2017 Oct 12. J Hum Hypertens. 2017. PMID: 29022889 No abstract available.

4

ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia.

Gagliardi L, Schreiber AW, Hahn CN, Feng J, Cranston T, Boon H, Hotu C, Oftedal BE, Cutfield R, Adelson DL, Braund WJ, Gordon RD, Rees DA, Grossman AB, Torpy DJ, Scott HS. Gagliardi L, et al. J Clin Endocrinol Metab. 2014 Sep;99(9):E1784-92. doi: 10.1210/jc.2014-1265. Epub 2014 Jun 6. J Clin Endocrinol Metab. 2014. PMID: 24905064

5

A case of Aromatase deficiency due to a novel CYP19A1 mutation.

Gagliardi L, Scott HS, Feng J, Torpy DJ. Gagliardi L, et al. BMC Endocr Disord. 2014 Feb 19;14:16. doi: 10.1186/1472-6823-14-16. BMC Endocr Disord. 2014. PMID: 24552606 Free PMC article.

6

Corticosteroid-binding globulin: the clinical significance of altered levels and heritable mutations.

Gagliardi L, Ho JT, Torpy DJ. Gagliardi L, et al. Mol Cell Endocrinol. 2010 Mar 5;316(1):24-34. doi: 10.1016/j.mce.2009.07.015. Epub 2009 Jul 28. Mol Cell Endocrinol. 2010. PMID: 19643166 Review.

7

Exenatide corrects postprandial hyperglycaemia in young people with cystic fibrosis and impaired glucose tolerance: A randomized crossover trial.

Geyer MC, Sullivan T, Tai A, Morton JM, Edwards S, Martin AJ, Perano SJ, Gagliardi L, Rayner CK, Horowitz M, Couper JJ. Geyer MC, et al. Among authors: gagliardi l. Diabetes Obes Metab. 2019 Mar;21(3):700-704. doi: 10.1111/dom.13544. Epub 2018 Oct 25. Diabetes Obes Metab. 2019. PMID: 30259623 Clinical Trial.

8

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.

Hahn CN, Chong CE, Carmichael CL, Wilkins EJ, Brautigan PJ, Li XC, Babic M, Lin M, Carmagnac A, Lee YK, Kok CH, Gagliardi L, Friend KL, Ekert PG, Butcher CM, Brown AL, Lewis ID, To LB, Timms AE, Storek J, Moore S, Altree M, Escher R, Bardy PG, Suthers GK, D'Andrea RJ, Horwitz MS, Scott HS. Hahn CN, et al. Among authors: gagliardi l. Nat Genet. 2011 Sep 4;43(10):1012-7. doi: 10.1038/ng.913. Nat Genet. 2011. PMID: 21892162 Free PMC article.

9

Management of obesity in patients with type 2 diabetes mellitus.

Gagliardi L, Wittert G. Gagliardi L, et al. Curr Diabetes Rev. 2007 May;3(2):95-101. doi: 10.2174/157339907780598207. Curr Diabetes Rev. 2007. PMID: 18220660 Review.

10

Screening for subclinical Cushing's syndrome in type 2 diabetes mellitus: low false-positive rates with nocturnal salivary cortisol.

Gagliardi L, Chapman IM, O'Loughlin P, Torpy DJ. Gagliardi L, et al. Horm Metab Res. 2010 Apr;42(4):280-4. doi: 10.1055/s-0029-1246191. Epub 2010 Jan 29. Horm Metab Res. 2010. PMID: 20119887

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