Marobbio CMT - Search Results

1

Mitochondrial transport and metabolism of the major methyl donor and versatile cofactor S-adenosylmethionine, and related diseases: A review^†.

Monné M, Marobbio CMT, Agrimi G, Palmieri L, Palmieri F. Monné M, et al. Among authors: marobbio cmt. IUBMB Life. 2022 Jul;74(7):573-591. doi: 10.1002/iub.2658. Epub 2022 Jun 22. IUBMB Life. 2022. PMID: 35730628 Free article. Review.

2

Identification of mitochondrial carriers in Saccharomyces cerevisiae by transport assay of reconstituted recombinant proteins.

Palmieri F, Agrimi G, Blanco E, Castegna A, Di Noia MA, Iacobazzi V, Lasorsa FM, Marobbio CM, Palmieri L, Scarcia P, Todisco S, Vozza A, Walker J. Palmieri F, et al. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1249-62. doi: 10.1016/j.bbabio.2006.05.023. Epub 2006 May 23. Biochim Biophys Acta. 2006. PMID: 16844075 Free article. Review.

3

A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria.

Fiermonte G, Paradies E, Todisco S, Marobbio CM, Palmieri F. Fiermonte G, et al. J Biol Chem. 2009 Jul 3;284(27):18152-9. doi: 10.1074/jbc.M109.014118. Epub 2009 May 8. J Biol Chem. 2009. PMID: 19429682 Free PMC article.

4

Pathogenic potential of SLC25A15 mutations assessed by transport assays and complementation of Saccharomyces cerevisiae ORT1 null mutant.

Marobbio CM, Punzi G, Pierri CL, Palmieri L, Calvello R, Panaro MA, Palmieri F. Marobbio CM, et al. Mol Genet Metab. 2015 May;115(1):27-32. doi: 10.1016/j.ymgme.2015.03.003. Epub 2015 Mar 17. Mol Genet Metab. 2015. PMID: 25818551

5

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.

Kishita Y, Pajak A, Bolar NA, Marobbio CM, Maffezzini C, Miniero DV, Monné M, Kohda M, Stranneheim H, Murayama K, Naess K, Lesko N, Bruhn H, Mourier A, Wibom R, Nennesmo I, Jespers A, Govaert P, Ohtake A, Van Laer L, Loeys BL, Freyer C, Palmieri F, Wredenberg A, Okazaki Y, Wedell A. Kishita Y, et al. Am J Hum Genet. 2015 Nov 5;97(5):761-8. doi: 10.1016/j.ajhg.2015.09.013. Epub 2015 Oct 29. Am J Hum Genet. 2015. PMID: 26522469 Free PMC article.

6

Molecular identification and functional characterization of a novel glutamate transporter in yeast and plant mitochondria.

Porcelli V, Vozza A, Calcagnile V, Gorgoglione R, Arrigoni R, Fontanesi F, Marobbio CMT, Castegna A, Palmieri F, Palmieri L. Porcelli V, et al. Among authors: marobbio cmt. Biochim Biophys Acta Bioenerg. 2018 Nov;1859(11):1249-1258. doi: 10.1016/j.bbabio.2018.08.001. Epub 2018 Aug 8. Biochim Biophys Acta Bioenerg. 2018. PMID: 30297026 Free article.

7

KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growth.

Raho S, Capobianco L, Malivindi R, Vozza A, Piazzolla C, De Leonardis F, Gorgoglione R, Scarcia P, Pezzuto F, Agrimi G, Barile SN, Pisano I, Reshkin SJ, Greco MR, Cardone RA, Rago V, Li Y, Marobbio CMT, Sommergruber W, Riley CL, Lasorsa FM, Mills E, Vegliante MC, De Benedetto GE, Fratantonio D, Palmieri L, Dolce V, Fiermonte G. Raho S, et al. Among authors: marobbio cmt. Nat Metab. 2020 Dec;2(12):1373-1381. doi: 10.1038/s42255-020-00315-1. Epub 2020 Nov 23. Nat Metab. 2020. PMID: 33230296

8

Citrate Regulates the Saccharomyces cerevisiae Mitochondrial GDP/GTP Carrier (Ggc1p) by Triggering Unidirectional Transport of GTP.

Seccia R, De Santis S, Di Noia MA, Palmieri F, Miniero DV, Marmo R, Paradies E, Santoro A, Pierri CL, Palmieri L, Marobbio CMT, Vozza A. Seccia R, et al. Among authors: marobbio cmt. J Fungi (Basel). 2022 Jul 29;8(8):795. doi: 10.3390/jof8080795. J Fungi (Basel). 2022. PMID: 36012783 Free PMC article.

9

alpha-Isopropylmalate, a leucine biosynthesis intermediate in yeast, is transported by the mitochondrial oxalacetate carrier.

Marobbio CM, Giannuzzi G, Paradies E, Pierri CL, Palmieri F. Marobbio CM, et al. J Biol Chem. 2008 Oct 17;283(42):28445-53. doi: 10.1074/jbc.M804637200. Epub 2008 Aug 5. J Biol Chem. 2008. PMID: 18682385 Free PMC article.

10

A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein.

Ersoy Tunalı N, Marobbio CM, Tiryakioğlu NO, Punzi G, Saygılı SK, Onal H, Palmieri F. Ersoy Tunalı N, et al. Mol Genet Metab. 2014 May;112(1):25-9. doi: 10.1016/j.ymgme.2014.03.002. Epub 2014 Mar 20. Mol Genet Metab. 2014. PMID: 24721342 Free PMC article.

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

Text availability

Article attribute

Article type

Publication date

26 results

Search Page