Alain Martelli - Search Results

Year	Number of Results
2004	1
2005	2
2006	1
2007	2
2008	2
2009	1
2011	1
2012	2
2013	1
2014	2
2015	1
2017	1
2018	1
2019	4
2022	1
2023	1
2024	1

1

Understanding the genetic and molecular pathogenesis of Friedreich's ataxia through animal and cellular models.

Martelli A, Napierala M, Puccio H. Martelli A, et al. Dis Model Mech. 2012 Mar;5(2):165-76. doi: 10.1242/dmm.008706. Dis Model Mech. 2012. PMID: 22382366 Free PMC article. Review.

2

A modified mouse model of Friedreich's ataxia with conditional Fxn allele homozygosity delays onset of cardiomyopathy.

Perfitt TL, Huichalaf C, Gooch R, Kuperman A, Ahn Y, Chen X, Ullas S, Hirenallur-Shanthappa D, Zhan Y, Otis D, Whiteley LO, Bulawa C, Martelli A. Perfitt TL, et al. Among authors: martelli a. Am J Physiol Heart Circ Physiol. 2024 Feb 1;326(2):H357-H369. doi: 10.1152/ajpheart.00496.2023. Epub 2023 Dec 1. Am J Physiol Heart Circ Physiol. 2024. PMID: 38038720

3

Dysregulation of cellular iron metabolism in Friedreich ataxia: from primary iron-sulfur cluster deficit to mitochondrial iron accumulation.

Martelli A, Puccio H. Martelli A, et al. Front Pharmacol. 2014 Jun 3;5:130. doi: 10.3389/fphar.2014.00130. eCollection 2014. Front Pharmacol. 2014. PMID: 24917819 Free PMC article. Review.

4

In vivo overexpression of frataxin causes toxicity mediated by iron-sulfur cluster deficiency.

Huichalaf C, Perfitt TL, Kuperman A, Gooch R, Kovi RC, Brenneman KA, Chen X, Hirenallur-Shanthappa D, Ma T, Assaf BT, Pardo I, Franks T, Monarski L, Cheng TW, Le K, Su C, Somanathan S, Whiteley LO, Bulawa C, Pregel MJ, Martelli A. Huichalaf C, et al. Among authors: martelli a. Mol Ther Methods Clin Dev. 2022 Feb 7;24:367-378. doi: 10.1016/j.omtm.2022.02.002. eCollection 2022 Mar 10. Mol Ther Methods Clin Dev. 2022. PMID: 35252470 Free PMC article.

5

ISCA1 is essential for mitochondrial Fe₄S₄ biogenesis in vivo.

Beilschmidt LK, Ollagnier de Choudens S, Fournier M, Sanakis I, Hograindleur MA, Clémancey M, Blondin G, Schmucker S, Eisenmann A, Weiss A, Koebel P, Messaddeq N, Puccio H, Martelli A. Beilschmidt LK, et al. Among authors: martelli a. Nat Commun. 2017 May 11;8:15124. doi: 10.1038/ncomms15124. Nat Commun. 2017. PMID: 28492233 Free PMC article.

6

Structure of the human frataxin-bound iron-sulfur cluster assembly complex provides insight into its activation mechanism.

Fox NG, Yu X, Feng X, Bailey HJ, Martelli A, Nabhan JF, Strain-Damerell C, Bulawa C, Yue WW, Han S. Fox NG, et al. Among authors: martelli a. Nat Commun. 2019 May 17;10(1):2210. doi: 10.1038/s41467-019-09989-y. Nat Commun. 2019. PMID: 31101807 Free PMC article.

7

Zinc(II) binding on human wild-type ISCU and Met140 variants modulates NFS1 desulfurase activity.

Fox NG, Martelli A, Nabhan JF, Janz J, Borkowska O, Bulawa C, Yue WW. Fox NG, et al. Among authors: martelli a. Biochimie. 2018 Sep;152:211-218. doi: 10.1016/j.biochi.2018.07.012. Epub 2018 Jul 20. Biochimie. 2018. PMID: 30031876 Free PMC article.

8

Iron regulatory protein 1 sustains mitochondrial iron loading and function in frataxin deficiency.

Martelli A, Schmucker S, Reutenauer L, Mathieu JRR, Peyssonnaux C, Karim Z, Puy H, Galy B, Hentze MW, Puccio H. Martelli A, et al. Cell Metab. 2015 Feb 3;21(2):311-323. doi: 10.1016/j.cmet.2015.01.010. Cell Metab. 2015. PMID: 25651183 Free article.

9

4'-Phosphopantetheine and long acyl chain-dependent interactions are integral to human mitochondrial acyl carrier protein function.

Majmudar JD, Feng X, Fox NG, Nabhan JF, Towle T, Ma T, Gooch R, Bulawa C, Yue WW, Martelli A. Majmudar JD, et al. Among authors: martelli a. Medchemcomm. 2019 Jan 8;10(2):209-220. doi: 10.1039/c8md00489g. eCollection 2019 Feb 1. Medchemcomm. 2019. PMID: 30881609 Free PMC article.

10

GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia.

Daher R, Mansouri A, Martelli A, Bayart S, Manceau H, Callebaut I, Moulouel B, Gouya L, Puy H, Kannengiesser C, Karim Z. Daher R, et al. Among authors: martelli a. Mol Genet Metab. 2019 Nov;128(3):342-351. doi: 10.1016/j.ymgme.2018.12.012. Epub 2019 Jan 7. Mol Genet Metab. 2019. PMID: 30660387

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

23 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

23 results

Results by year