Léon-del-Rio A - Search Results

1

Mutations participating in interallelic complementation in propionic acidemia.

Gravel RA, Akerman BR, Lamhonwah AM, Loyer M, Léon-del-Rio A, Italiano I. Gravel RA, et al. Am J Hum Genet. 1994 Jul;55(1):51-8. Am J Hum Genet. 1994. PMID: 8023851 Free PMC article.

2

Isolation of a cDNA encoding human holocarboxylase synthetase by functional complementation of a biotin auxotroph of Escherichia coli.

León-Del-Rio A, Leclerc D, Akerman B, Wakamatsu N, Gravel RA. León-Del-Rio A, et al. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4626-30. doi: 10.1073/pnas.92.10.4626. Proc Natl Acad Sci U S A. 1995. PMID: 7753853 Free PMC article.

3

Sequence requirements for the biotinylation of carboxyl-terminal fragments of human propionyl-CoA carboxylase alpha subunit expressed in Escherichia coli.

Leon-Del-Rio A, Gravel RA. Leon-Del-Rio A, et al. J Biol Chem. 1994 Sep 16;269(37):22964-8. J Biol Chem. 1994. PMID: 8083196 Free article.

4

Clustering of mutations in the biotin-binding region of holocarboxylase synthetase in biotin-responsive multiple carboxylase deficiency.

Dupuis L, Leon-Del-Rio A, Leclerc D, Campeau E, Sweetman L, Saudubray JM, Herman G, Gibson KM, Gravel RA. Dupuis L, et al. Hum Mol Genet. 1996 Jul;5(7):1011-6. doi: 10.1093/hmg/5.7.1011. Hum Mol Genet. 1996. PMID: 8817339

5

Coding sequence mutations in the alpha subunit of propionyl-CoA carboxylase in patients with propionic acidemia.

Campeau E, Dupuis L, León-Del-Rio A, Gravel R. Campeau E, et al. Mol Genet Metab. 1999 May;67(1):11-22. doi: 10.1006/mgme.1999.2850. Mol Genet Metab. 1999. PMID: 10329019

6

Assignment of holocarboxylase synthetase gene (HLCS) to human chromosome band 21q22.1 and to mouse chromosome band 16C4 by in situ hybridization.

Zhang XX, León-Del-Rio A, Gravel RA, Eydoux P. Zhang XX, et al. Cytogenet Cell Genet. 1997;76(3-4):179. doi: 10.1159/000134540. Cytogenet Cell Genet. 1997. PMID: 9186515 No abstract available.

7

Holocarboxylase Synthetase: A Moonlighting Transcriptional Coregulator of Gene Expression and a Cytosolic Regulator of Biotin Utilization.

León-Del-Río A, Valadez-Graham V, Gravel RA. León-Del-Río A, et al. Annu Rev Nutr. 2017 Aug 21;37:207-223. doi: 10.1146/annurev-nutr-042617-104653. Epub 2017 May 31. Annu Rev Nutr. 2017. PMID: 28564555 Review.

8

Paradoxical regulation of biotin utilization in brain and liver and implications for inherited multiple carboxylase deficiency.

Pacheco-Alvarez D, Solórzano-Vargas RS, Gravel RA, Cervantes-Roldán R, Velázquez A, León-Del-Río A. Pacheco-Alvarez D, et al. J Biol Chem. 2004 Dec 10;279(50):52312-8. doi: 10.1074/jbc.M407056200. Epub 2004 Sep 28. J Biol Chem. 2004. PMID: 15456772 Free article.

9

Impaired biotinidase activity disrupts holocarboxylase synthetase expression in late onset multiple carboxylase deficiency.

Pérez-Monjaras A, Cervantes-Roldán R, Meneses-Morales I, Gravel RA, Reyes-Carmona S, Solórzano-Vargas S, González-Noriega A, León-Del-Río A. Pérez-Monjaras A, et al. J Biol Chem. 2008 Dec 5;283(49):34150-8. doi: 10.1074/jbc.M806985200. Epub 2008 Oct 9. J Biol Chem. 2008. PMID: 18845537 Free PMC article.

10

Nuclear tristetraprolin acts as a corepressor of multiple steroid nuclear receptors in breast cancer cells.

Barrios-García T, Gómez-Romero V, Tecalco-Cruz Á, Valadéz-Graham V, León-Del-Río A. Barrios-García T, et al. Mol Genet Metab Rep. 2016 Mar 22;7:20-6. doi: 10.1016/j.ymgmr.2016.02.004. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27114912 Free PMC article.

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