Besse A - Search Results

1

TRAF6 ubiquitin ligase is essential for RANKL signaling and osteoclast differentiation.

Lamothe B, Webster WK, Gopinathan A, Besse A, Campos AD, Darnay BG. Lamothe B, et al. Among authors: besse a. Biochem Biophys Res Commun. 2007 Aug 10;359(4):1044-9. doi: 10.1016/j.bbrc.2007.06.017. Epub 2007 Jun 11. Biochem Biophys Res Commun. 2007. PMID: 17572386 Free PMC article.

2

Site-specific Lys-63-linked tumor necrosis factor receptor-associated factor 6 auto-ubiquitination is a critical determinant of I kappa B kinase activation.

Lamothe B, Besse A, Campos AD, Webster WK, Wu H, Darnay BG. Lamothe B, et al. Among authors: besse a. J Biol Chem. 2007 Feb 9;282(6):4102-12. doi: 10.1074/jbc.M609503200. Epub 2006 Nov 29. J Biol Chem. 2007. PMID: 17135271 Free PMC article.

3

TAK1-dependent signaling requires functional interaction with TAB2/TAB3.

Besse A, Lamothe B, Campos AD, Webster WK, Maddineni U, Lin SC, Wu H, Darnay BG. Besse A, et al. J Biol Chem. 2007 Feb 9;282(6):3918-28. doi: 10.1074/jbc.M608867200. Epub 2006 Dec 8. J Biol Chem. 2007. PMID: 17158449 Free PMC article.

4

TRAF-interacting protein (TRIP) is a RING-dependent ubiquitin ligase.

Besse A, Campos AD, Webster WK, Darnay BG. Besse A, et al. Biochem Biophys Res Commun. 2007 Aug 3;359(3):660-4. doi: 10.1016/j.bbrc.2007.05.149. Epub 2007 May 30. Biochem Biophys Res Commun. 2007. PMID: 17544371

5

TRAFs in RANK signaling.

Darnay BG, Besse A, Poblenz AT, Lamothe B, Jacoby JJ. Darnay BG, et al. Among authors: besse a. Adv Exp Med Biol. 2007;597:152-9. doi: 10.1007/978-0-387-70630-6_12. Adv Exp Med Biol. 2007. PMID: 17633024 Review.

6

Personalized medicine approach confirms a milder case of ABAT deficiency.

Besse A, Petersen AK, Hunter JV, Appadurai V, Lalani SR, Bonnen PE. Besse A, et al. Mol Brain. 2016 Dec 1;9(1):93. doi: 10.1186/s13041-016-0273-8. Mol Brain. 2016. PMID: 27903293 Free PMC article.

7

The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism.

Besse A, Wu P, Bruni F, Donti T, Graham BH, Craigen WJ, McFarland R, Moretti P, Lalani S, Scott KL, Taylor RW, Bonnen PE. Besse A, et al. Cell Metab. 2015 Mar 3;21(3):417-27. doi: 10.1016/j.cmet.2015.02.008. Cell Metab. 2015. PMID: 25738457 Free PMC article.

8

Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease.

Stiles AR, Ferdinandusse S, Besse A, Appadurai V, Leydiker KB, Cambray-Forker EJ, Bonnen PE, Abdenur JE. Stiles AR, et al. Among authors: besse a. Mol Genet Metab. 2015 Aug;115(4):161-7. doi: 10.1016/j.ymgme.2015.05.008. Epub 2015 May 15. Mol Genet Metab. 2015. PMID: 26026795 Free PMC article.

9

Loss-of-function mutations in ISCA2 disrupt 4Fe-4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion.

Alaimo JT, Besse A, Alston CL, Pang K, Appadurai V, Samanta M, Smpokou P, McFarland R, Taylor RW, Bonnen PE. Alaimo JT, et al. Among authors: besse a. Hum Mutat. 2018 Apr;39(4):537-549. doi: 10.1002/humu.23396. Epub 2018 Jan 22. Hum Mutat. 2018. PMID: 29297947 Free PMC article.

10

LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity.

Besse A, Brezavar D, Hanson J, Larson A, Bonnen PE. Besse A, et al. Mitochondrion. 2020 Mar;51:68-78. doi: 10.1016/j.mito.2020.01.004. Epub 2020 Jan 7. Mitochondrion. 2020. PMID: 31923470 Free PMC article.

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