Casarin A - Search Results

1

Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency.

Cogliati S, Frezza C, Soriano ME, Varanita T, Quintana-Cabrera R, Corrado M, Cipolat S, Costa V, Casarin A, Gomes LC, Perales-Clemente E, Salviati L, Fernandez-Silva P, Enriquez JA, Scorrano L. Cogliati S, et al. Among authors: casarin a. Cell. 2013 Sep 26;155(1):160-71. doi: 10.1016/j.cell.2013.08.032. Epub 2013 Sep 19. Cell. 2013. PMID: 24055366 Free PMC article.

2

LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability.

Dimmer KS, Navoni F, Casarin A, Trevisson E, Endele S, Winterpacht A, Salviati L, Scorrano L. Dimmer KS, et al. Among authors: casarin a. Hum Mol Genet. 2008 Jan 15;17(2):201-14. doi: 10.1093/hmg/ddm297. Epub 2007 Oct 9. Hum Mol Genet. 2008. PMID: 17925330

3

Optimization of respiratory chain enzymatic assays in muscle for the diagnosis of mitochondrial disorders.

Spinazzi M, Casarin A, Pertegato V, Ermani M, Salviati L, Angelini C. Spinazzi M, et al. Among authors: casarin a. Mitochondrion. 2011 Nov;11(6):893-904. doi: 10.1016/j.mito.2011.07.006. Epub 2011 Aug 9. Mitochondrion. 2011. PMID: 21855655

4

Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells.

Spinazzi M, Casarin A, Pertegato V, Salviati L, Angelini C. Spinazzi M, et al. Among authors: casarin a. Nat Protoc. 2012 May 31;7(6):1235-46. doi: 10.1038/nprot.2012.058. Nat Protoc. 2012. PMID: 22653162

5

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.

Spinazzi M, Cazzola S, Bortolozzi M, Baracca A, Loro E, Casarin A, Solaini G, Sgarbi G, Casalena G, Cenacchi G, Malena A, Frezza C, Carrara F, Angelini C, Scorrano L, Salviati L, Vergani L. Spinazzi M, et al. Among authors: casarin a. Hum Mol Genet. 2008 Nov 1;17(21):3291-302. doi: 10.1093/hmg/ddn225. Epub 2008 Aug 4. Hum Mol Genet. 2008. PMID: 18678599

6

Vitamin K2 cannot substitute Coenzyme Q₁₀ as electron carrier in the mitochondrial respiratory chain of mammalian cells.

Cerqua C, Casarin A, Pierrel F, Vazquez Fonseca L, Viola G, Salviati L, Trevisson E. Cerqua C, et al. Among authors: casarin a. Sci Rep. 2019 Apr 25;9(1):6553. doi: 10.1038/s41598-019-43014-y. Sci Rep. 2019. PMID: 31024065 Free PMC article.

7

Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation.

Boaretto F, Vettori A, Casarin A, Vazza G, Muglia M, Rossetto MG, Cavallaro T, Rizzuto N, Carelli V, Salviati L, Mostacciuolo ML, Martinuzzi A. Boaretto F, et al. Among authors: casarin a. Neurology. 2010 Jun 8;74(23):1919-21. doi: 10.1212/WNL.0b013e3181e240f9. Neurology. 2010. PMID: 20530328 No abstract available.

8

Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogene.

Trevisson E, Salviati L, Baldoin MC, Toldo I, Casarin A, Sacconi S, Cesaro L, Basso G, Burlina AB. Trevisson E, et al. Among authors: casarin a. Hum Mutat. 2007 Jul;28(7):694-702. doi: 10.1002/humu.20498. Hum Mutat. 2007. PMID: 17326097

9

Gene symbol: ASL. Disease: Argininosuccinate lyase deficiency.

Trevisson E, Salviati L, Baldoin MC, Casarin A, Basso G, Burlina A. Trevisson E, et al. Among authors: casarin a. Hum Genet. 2008 Oct;124(3):303. Hum Genet. 2008. PMID: 18846631 No abstract available.

10

Gene symbol: ASL. Disease: Argininosuccinate lyase deficiency.

Trevisson E, Salviati L, Baldoin MC, Casarin A, Basso G, Burlina A. Trevisson E, et al. Among authors: casarin a. Hum Genet. 2008 Oct;124(3):303. Hum Genet. 2008. PMID: 18846632 No abstract available.

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