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Items: 34

1.

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.

de la Morena-Barrio ME, Ballesta-Martínez MJ, López-Gálvez R, Antón AI, López-González V, Martínez-Ribot L, Padilla J, Miñano A, García-Algar O, Del Campo M, Corral J, Guillén-Navarro E, Vicente V.

Pediatr Res. 2018 Jan;83(1-1):119-127. doi: 10.1038/pr.2017.201. Epub 2017 Sep 20.

PMID:
28820871
2.

Correction: Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.

Toderici M, de la Morena-Barrio ME, Padilla J, Miñano A, Antón AI, Iniesta JA, Herranz MT, Fernández N, Vicente V, Corral J.

PLoS One. 2016 Jul 21;11(7):e0159987. doi: 10.1371/journal.pone.0159987. eCollection 2016.

3.

Antithrombin controls tumor migration, invasion and angiogenesis by inhibition of enteropeptidase.

Luengo-Gil G, Calvo MI, Martín-Villar E, Águila S, Bohdan N, Antón AI, Espín S, Ayala de la Peña F, Vicente V, Corral J, Quintanilla M, Martínez-Martínez I.

Sci Rep. 2016 Jun 8;6:27544. doi: 10.1038/srep27544.

4.

Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.

Toderici M, de la Morena-Barrio ME, Padilla J, Miñano A, Antón AI, Iniesta JA, Herranz MT, Fernández N, Vicente V, Corral J.

PLoS One. 2016 Mar 22;11(3):e0152159. doi: 10.1371/journal.pone.0152159. eCollection 2016. Erratum in: PLoS One. 2016;11(7):e0159987.

5.

Genotype-guided therapy improves initial acenocoumarol dosing. Results from a prospective randomised study.

Cerezo-Manchado JJ, Roldán V, Corral J, Rosafalco M, Antón AI, Padilla J, Vicente V, González-Conejero R.

Thromb Haemost. 2016 Jan;115(1):117-25. doi: 10.1160/TH14-09-0814. Epub 2015 Nov 5.

PMID:
26538428
6.

Prognostic signature and clonality pattern of recurrently mutated genes in inactive chronic lymphocytic leukemia.

Hurtado AM, Chen-Liang TH, Przychodzen B, Hamedi C, Muñoz-Ballester J, Dienes B, García-Malo MD, Antón AI, de Arriba F, Teruel-Montoya R, Ortuño FJ, Vicente V, Maciejewski JP, Jerez A.

Blood Cancer J. 2015 Aug 28;5:e342. doi: 10.1038/bcj.2015.65.

7.

Impaired leucocyte activation is underlining the lower thrombotic risk of essential thrombocythaemia patients with CALR mutations as compared with those with the JAK2 mutation.

Torregrosa JM, Ferrer-Marín F, Lozano ML, Moreno MJ, Martinez C, Anton AI, Rivera J, Vicente V.

Br J Haematol. 2016 Mar;172(5):813-5. doi: 10.1111/bjh.13539. Epub 2015 Jun 30. No abstract available.

PMID:
26132594
8.

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.

Martínez C, Antón AI, Bernal A, Lozano ML, Ferrer-Marin F, Corral J, Iniesta JA, Vicente V, Rivera J.

J Clin Neurol. 2015 Jan;11(1):102-3. doi: 10.3988/jcn.2015.11.1.102. Epub 2015 Jan 2. No abstract available.

9.

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study.

Sánchez-Guiu I, Antón AI, Padilla J, Velasco F, Lucia JF, Lozano M, Cid AR, Sevivas T, Lopez-Fernandez MF, Vicente V, González-Manchón C, Rivera J, Lozano ML.

Orphanet J Rare Dis. 2014 Dec 24;9:213. doi: 10.1186/s13023-014-0213-6.

10.

The JAK2 46/1 haplotype does not predispose to CALR-mutated myeloproliferative neoplasms.

Soler G, Bernal-Vicente A, Antón AI, Torregrosa JM, Caparrós-Pérez E, Sánchez-Serrano I, Martínez-Pérez A, Sánchez-Vega B, Vicente V, Ferrer-Marin F.

Ann Hematol. 2015 May;94(5):789-94. doi: 10.1007/s00277-014-2266-y. Epub 2014 Dec 9.

PMID:
25482455
11.

Hermansky-Pudlak syndrome. Overview of clinical and molecular features and case report of a new HPS-1 variant.

Sánchez-Guiu I, Torregrosa JM, Velasco F, Antón AI, Lozano ML, Vicente V, Rivera J.

Hamostaseologie. 2014;34(4):301-9. doi: 10.5482/HAMO-14-06-0024. Epub 2014 Aug 13. Review.

PMID:
25117010
12.

Effect of VKORC1, CYP2C9 and CYP4F2 genetic variants in early outcomes during acenocoumarol treatment.

Cerezo-Manchado JJ, Roldan V, Rosafalco M, Anton AI, Arroyo AB, Garcia-Barbera N, Martínez AB, Padilla J, Corral J, Vicente V, Gonzalez-Conejero R.

Pharmacogenomics. 2014 May;15(7):987-96. doi: 10.2217/pgs.13.232.

PMID:
24956252
13.

Chediak-Higashi syndrome: description of two novel homozygous missense mutations causing divergent clinical phenotype.

Sánchez-Guiu I, Antón AI, García-Barberá N, Navarro-Fernández J, Martínez C, Fuster JL, Couselo JM, Ortuño FJ, Vicente V, Rivera J, Lozano ML.

Eur J Haematol. 2014 Jan;92(1):49-58. doi: 10.1111/ejh.12203. Epub 2013 Oct 24.

PMID:
24112114
14.

Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?

de la Morena-Barrio ME, Buil A, Antón AI, Martínez-Martínez I, Miñano A, Gutiérrez-Gallego R, Navarro-Fernández J, Aguila S, Souto JC, Vicente V, Soria JM, Corral J.

PLoS One. 2013 May 21;8(5):e64998. doi: 10.1371/journal.pone.0064998. Print 2013.

15.

Novel associations of VKORC1 variants with higher acenocoumarol requirements.

Anton AI, Cerezo-Manchado JJ, Padilla J, Perez-Andreu V, Corral J, Vicente V, Roldan V, Gonzalez-Conejero R.

PLoS One. 2013 May 17;8(5):e64469. doi: 10.1371/journal.pone.0064469. Print 2013.

16.

Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency.

Águila S, Martínez-Martínez I, Collado M, Llamas P, Antón AI, Martínez-Redondo C, Padilla J, Miñano A, de la Morena-Barrio ME, Garcia-Avello Á, Vicente V, Corral J.

Thromb Haemost. 2013 Mar;109(3):556-8. doi: 10.1160/TH12-09-0707. Epub 2013 Jan 17. No abstract available.

PMID:
23329010
17.

Creating a genotype-based dosing algorithm for acenocoumarol steady dose.

Cerezo-Manchado JJ, Rosafalco M, Antón AI, Pérez-Andreu V, Garcia-Barberá N, Martinez AB, Corral J, Vicente V, González-Conejero R, Roldán V.

Thromb Haemost. 2013 Jan;109(1):146-53. doi: 10.1160/TH12-08-0631. Epub 2012 Nov 29.

PMID:
23196355
18.

Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.

de la Morena-Barrio ME, Antón AI, Martínez-Martínez I, Padilla J, Miñano A, Navarro-Fernández J, Águila S, López MF, Fontcuberta J, Vicente V, Corral J.

Thromb Haemost. 2012 Mar;107(3):430-7. doi: 10.1160/TH11-10-0701. Epub 2012 Jan 11.

PMID:
22234719
19.

Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.

Guerrero JA, Rivera J, Quiroga T, Martinez-Perez A, Antón AI, Martínez C, Panes O, Vicente V, Mezzano D, Soria JM, Corral J.

Haematologica. 2011 Sep;96(9):1335-43. doi: 10.3324/haematol.2011.042077. Epub 2011 May 5.

20.

Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure.

Navarro-Núñez L, Teruel R, Antón AI, Nurden P, Martínez-Martínez I, Lozano ML, Rivera J, Corral J, Mezzano D, Vicente V, Martinez C.

Thromb Haemost. 2011 May;105(5):855-63. doi: 10.1160/TH10-08-0536. Epub 2011 Mar 8.

PMID:
21384078
21.

Influence of the F12 -4 C>T polymorphism on hemostatic tests.

Corral J, Antón AI, Quiroga T, González-Conejero R, Pereira J, Roldán V, Vicente V, Mezzano D.

Blood Coagul Fibrinolysis. 2010 Oct;21(7):632-9. doi: 10.1097/MBC.0b013e32833a9048.

PMID:
20814302
22.

CALU A29809G polymorphism in coronary atherothrombosis: Implications for coronary calcification and prognosis.

Hernández-Romero D, Ruiz-Nodar JM, Marín F, Tello-Montoliu A, Roldán V, Mainar L, Pérez-Andreu V, Antón AI, Bonaque JC, Valdés M, Vicente V, González-Conejero R.

Ann Med. 2010 Sep;42(6):439-46. doi: 10.3109/07853890.2010.499131.

PMID:
20673165
23.

Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders.

Antón AI, González-Conejero R, Roldán V, Quiroga T, Sánchez-Vega B, Corral J, Vicente V, Mezzano D.

Ann Hematol. 2010 Nov;89(11):1147-54. doi: 10.1007/s00277-010-1000-7. Epub 2010 Jun 9.

PMID:
20532885
24.

Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.

Pérez-Andreu V, Roldán V, López-Fernández MF, Antón AI, Alberca I, Corral J, Montes R, García-Barberá N, Ferrando F, Vicente V, González-Conejero R.

J Thromb Haemost. 2010 May;8(5):1012-7. doi: 10.1111/j.1538-7836.2010.03800.x. Epub 2010 Feb 9.

25.

Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause.

Martínez C, Antón AI, Corral J, Quiroga T, Panes O, Lozano ML, González-Conejero R, Teruel R, Navarro-Núñez L, Pereira J, Mezzano D, Vicente V, Rivera J.

Br J Haematol. 2009 Jun;146(1):95-103. doi: 10.1111/j.1365-2141.2009.07713.x. Epub 2009 Apr 21.

PMID:
19388931
26.

Pharmacogenetic relevance of CYP4F2 V433M polymorphism on acenocoumarol therapy.

Pérez-Andreu V, Roldán V, Antón AI, García-Barberá N, Corral J, Vicente V, González-Conejero R.

Blood. 2009 May 14;113(20):4977-9. doi: 10.1182/blood-2008-09-176222. Epub 2009 Mar 6.

PMID:
19270263
27.

Functional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levels.

Antón AI, Teruel R, Corral J, Miñano A, Martínez-Martínez I, Ordóñez A, Vicente V, Sánchez-Vega B.

Haematologica. 2009 Apr;94(4):589-92. doi: 10.3324/haematol.2008.000604. Epub 2009 Feb 19.

28.

Novel cassette-based shuttle vector system for gram-positive bacteria.

Charpentier E, Anton AI, Barry P, Alfonso B, Fang Y, Novick RP.

Appl Environ Microbiol. 2004 Oct;70(10):6076-85.

29.

Sequence microdiversity at the ribosomal RNA operons of Escherichia coli pyelonephritogenic strains.

Anton AI, Martinez-Murcia AJ, Rodriguez-Valera F, Dalet F.

Clin Microbiol Infect. 2001 Jul;7(7):345-51.

30.

Use of the 16S--23S ribosomal genes spacer region in studies of prokaryotic diversity.

García-Martínez J, Acinas SG, Antón AI, Rodríguez-Valera F.

J Microbiol Methods. 1999 May;36(1-2):55-64.

PMID:
10353800
31.

Patterns of sequence variation in two regions of the 16S rRNA multigene family of Escherichia coli.

Martínez-Murcia AJ, Antón AI, Rodríguez-Valera F.

Int J Syst Bacteriol. 1999 Apr;49 Pt 2:601-10.

PMID:
10319482
32.

Intraspecific diversity of the 23S rRNA gene and the spacer region downstream in Escherichia coli.

Antón AI, Martínez-Murcia AJ, Rodríguez-Valera F.

J Bacteriol. 1999 May;181(9):2703-9.

33.
34.

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