Baldoin MC - Search Results

1

Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.

Doimo M, Desbats MA, Baldoin MC, Lenzini E, Basso G, Murphy E, Graziano C, Seri M, Burlina A, Sartori G, Trevisson E, Salviati L. Doimo M, et al. Among authors: baldoin mc. Hum Mutat. 2013 Jan;34(1):229-36. doi: 10.1002/humu.22233. Epub 2012 Oct 17. Hum Mutat. 2013. PMID: 23076989

2

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: baldoin mc. Hum Mutat. 2007 Jul;28(7):694-702. doi: 10.1002/humu.20498. Hum Mutat. 2007. PMID: 17326097

3

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: baldoin mc. Hum Genet. 2008 Oct;124(3):303. Hum Genet. 2008. PMID: 18846631 No abstract available.

4

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: baldoin mc. Hum Genet. 2008 Oct;124(3):303. Hum Genet. 2008. PMID: 18846632 No abstract available.

5

COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2.

Cerqua C, Morbidoni V, Desbats MA, Doimo M, Frasson C, Sacconi S, Baldoin MC, Sartori G, Basso G, Salviati L, Trevisson E. Cerqua C, et al. Among authors: baldoin mc. Biochim Biophys Acta Bioenerg. 2018 Apr;1859(4):244-252. doi: 10.1016/j.bbabio.2018.01.004. Epub 2018 Feb 3. Biochim Biophys Acta Bioenerg. 2018. PMID: 29355485 Free article.

6

A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like disease.

Salviati L, Trevisson E, Baldoin MC, Toldo I, Sartori S, Calderone M, Tenconi R, Laverda A. Salviati L, et al. Among authors: baldoin mc. Neurogenetics. 2007 Jan;8(1):57-60. doi: 10.1007/s10048-006-0065-x. Epub 2006 Oct 10. Neurogenetics. 2007. PMID: 17031678

7

hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assembly.

Sacconi S, Trevisson E, Pistollato F, Baldoin MC, Rezzonico R, Bourget I, Desnuelle C, Tenconi R, Basso G, DiMauro S, Salviati L. Sacconi S, et al. Among authors: baldoin mc. Biochem Biophys Res Commun. 2005 Nov 25;337(3):832-9. doi: 10.1016/j.bbrc.2005.09.127. Epub 2005 Sep 29. Biochem Biophys Res Commun. 2005. PMID: 16212937

8

Extracellular ATP signaling during differentiation of C2C12 skeletal muscle cells: role in proliferation.

Martinello T, Baldoin MC, Morbiato L, Paganin M, Tarricone E, Schiavo G, Bianchini E, Sandonà D, Betto R. Martinello T, et al. Among authors: baldoin mc. Mol Cell Biochem. 2011 May;351(1-2):183-96. doi: 10.1007/s11010-011-0726-4. Epub 2011 Feb 10. Mol Cell Biochem. 2011. PMID: 21308481

9

Effect of auranofin on the mitochondrial generation of hydrogen peroxide. Role of thioredoxin reductase.

Rigobello MP, Folda A, Baldoin MC, Scutari G, Bindoli A. Rigobello MP, et al. Among authors: baldoin mc. Free Radic Res. 2005 Jul;39(7):687-95. doi: 10.1080/10715760500135391. Free Radic Res. 2005. PMID: 16036347

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