Luís A. Alcaraz - Search Results

Year	Number of Results
2004	1
2005	2
2007	3
2008	2
2009	1
2010	2
2012	1
2013	2
2014	1
2015	1
2018	1
2021	1
2024	0

1

Blue Copper Proteins: A rigid machine for efficient electron transfer, a flexible device for metal uptake.

Pérez-Henarejos SA, Alcaraz LA, Donaire A. Pérez-Henarejos SA, et al. Among authors: alcaraz la. Arch Biochem Biophys. 2015 Oct 15;584:134-48. doi: 10.1016/j.abb.2015.08.020. Epub 2015 Aug 31. Arch Biochem Biophys. 2015. PMID: 26334718 Review.

2

Neuroimaging Findings in Patients with EBF3 Mutations: Report of Two Cases.

Jiménez de la Peña M, Jiménez de Domingo A, Tirado P, Calleja-Pérez B, Alcaraz LA, Álvarez S, Williams J, Hagman JR, Németh AH, Fernández-Jaén A. Jiménez de la Peña M, et al. Among authors: alcaraz la. Mol Syndromol. 2021 Jun;12(3):186-193. doi: 10.1159/000513583. Epub 2021 Apr 9. Mol Syndromol. 2021. PMID: 34177436 Free PMC article.

3

Into the lipid realm: stability and thermodynamics of membrane proteins.

Barrera FN, Alcaraz LA, Hurtado-Gómez E, Neira JL. Barrera FN, et al. Among authors: alcaraz la. Curr Protein Pept Sci. 2008 Dec;9(6):626-37. doi: 10.2174/138920308786733949. Curr Protein Pept Sci. 2008. PMID: 19075751 Review.

4

Small RNAs of Haloferax mediterranei: Identification and Potential Involvement in Nitrogen Metabolism.

Payá G, Bautista V, Camacho M, Castejón-Fernández N, Alcaraz LA, Bonete MJ, Esclapez J. Payá G, et al. Among authors: alcaraz la. Genes (Basel). 2018 Feb 10;9(2):83. doi: 10.3390/genes9020083. Genes (Basel). 2018. PMID: 29439418 Free PMC article.

5

Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.

Acién P, Galán F, Manchón I, Ruiz E, Acién M, Alcaraz LA. Acién P, et al. Among authors: alcaraz la. Orphanet J Rare Dis. 2010 Apr 14;5:6. doi: 10.1186/1750-1172-5-6. Orphanet J Rare Dis. 2010. PMID: 20388228 Free PMC article.

6

Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion.

Penacho V, Galán F, Martín-Bayón TA, Mayo S, Manchón I, Carrasco A, Martínez-Castellano F, Alcaraz LA. Penacho V, et al. Among authors: alcaraz la. Cytogenet Genome Res. 2014;144(4):275-9. doi: 10.1159/000370256. Epub 2015 Feb 20. Cytogenet Genome Res. 2014. PMID: 25722017

7

Electron transfer from cytochrome c to cupredoxins.

Takayama SJ, Irie K, Tai H, Kawahara T, Hirota S, Takabe T, Alcaraz LA, Donaire A, Yamamoto Y. Takayama SJ, et al. Among authors: alcaraz la. J Biol Inorg Chem. 2009 Aug;14(6):821-8. doi: 10.1007/s00775-009-0494-8. Epub 2009 Mar 18. J Biol Inorg Chem. 2009. PMID: 19294434

8

The metal-binding properties of the blue crab copper specific CuMT-2: a crustacean metallothionein with two cysteine triplets.

Serra-Batiste M, Cols N, Alcaraz LA, Donaire A, González-Duarte P, Vasák M. Serra-Batiste M, et al. Among authors: alcaraz la. J Biol Inorg Chem. 2010 Jun;15(5):759-76. doi: 10.1007/s00775-010-0644-z. Epub 2010 Apr 2. J Biol Inorg Chem. 2010. PMID: 20361221

9

Electrochemical nitration of myoglobin at tyrosine 103: structure and stability.

Gómez-Mingot M, Alcaraz LA, Heptinstall J, Donaire A, Piccioli M, Montiel V, Iniesta J. Gómez-Mingot M, et al. Among authors: alcaraz la. Arch Biochem Biophys. 2013 Jan 1;529(1):26-33. doi: 10.1016/j.abb.2012.10.013. Epub 2012 Nov 27. Arch Biochem Biophys. 2013. PMID: 23200748

10

Copy number variations in endoglin locus: mapping of large deletions in Spanish families with hereditary hemorrhagic telangiectasia type 1.

Fontalba A, Fernández-Luna JL, Zarrabeitia R, Recio-Poveda L, Albiñana V, Ojeda-Fernández ML, Bernabéu C, Alcaraz LA, Botella LM. Fontalba A, et al. Among authors: alcaraz la. BMC Med Genet. 2013 Nov 25;14:121. doi: 10.1186/1471-2350-14-121. BMC Med Genet. 2013. PMID: 24267784 Free PMC article.

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