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Items: 1 to 50 of 151

1.

Multilayer scaffolds for cartilage tissue engineering.

Campos Y, Almirall A, Fuentes G, Bloem HL, Kaijzel E, Cruz LJ.

Tissue Eng Part B Rev. 2019 Mar 27. doi: 10.1089/ten.TEB.2018.0330. [Epub ahead of print]

PMID:
30913997
2.

Palmitoylation is a post-translational modification of Alix regulating the membrane organization of exosome-like small extracellular vesicles.

Romancino DP, Buffa V, Caruso S, Ferrara I, Raccosta S, Notaro A, Campos Y, Noto R, Martorana V, Cupane A, Giallongo A, d'Azzo A, Manno M, Bongiovanni A.

Biochim Biophys Acta Gen Subj. 2018 Dec;1862(12):2879-2887. doi: 10.1016/j.bbagen.2018.09.004. Epub 2018 Sep 7.

PMID:
30251702
3.

Apparent isocitrate lyase activity in Leishmania amazonensis.

Hernández-Chinea C, Maimone L, Campos Y, Mosca W, Romero PJ.

Acta Parasitol. 2017 Dec 20;62(4):701-707. doi: 10.1515/ap-2017-0084.

PMID:
29035856
4.

Congenital Melanocytic Nevus Syndrome: A Case Series.

Recio A, Sánchez-Moya AI, Félix V, Campos Y.

Actas Dermosifiliogr. 2017 Nov;108(9):e57-e62. doi: 10.1016/j.ad.2016.07.025. Epub 2017 Jan 19. English, Spanish.

PMID:
28110826
5.

Exposure to pesticides and mental disorders in a rural population of Southern Brazil.

Campos Ÿ, Dos Santos Pinto da Silva V, Sarpa Campos de Mello M, Barros Otero U.

Neurotoxicology. 2016 Sep;56:7-16. doi: 10.1016/j.neuro.2016.06.002. Epub 2016 Jun 24.

PMID:
27350176
6.

Alix-mediated assembly of the actomyosin-tight junction polarity complex preserves epithelial polarity and epithelial barrier.

Campos Y, Qiu X, Gomero E, Wakefield R, Horner L, Brutkowski W, Han YG, Solecki D, Frase S, Bongiovanni A, d'Azzo A.

Nat Commun. 2016 Jun 23;7:11876. doi: 10.1038/ncomms11876.

7.

Neuroleptic Malignant Syndrome Associated with Refractory Acute Disseminated Encephalomyelitis.

Delgado SR, Tornes L, Maldonado J, Hernandez J, Campos Y, Rammohan K.

Case Rep Neurol. 2016 Apr 28;8(1):97-101. doi: 10.1159/000446106. eCollection 2016 Jan-Apr.

8.

Regulated lysosomal exocytosis mediates cancer progression.

Machado E, White-Gilbertson S, van de Vlekkert D, Janke L, Moshiach S, Campos Y, Finkelstein D, Gomero E, Mosca R, Qiu X, Morton CL, Annunziata I, d'Azzo A.

Sci Adv. 2015 Dec 18;1(11):e1500603. doi: 10.1126/sciadv.1500603. eCollection 2015 Dec.

9.

Alcohol use behaviors among indigenous migrants: a transnational study on communities of origin and destination.

Pinedo M, Campos Y, Leal D, Fregoso J, Goldenberg SM, Zúñiga ML.

J Immigr Minor Health. 2014 Jun;16(3):348-55. doi: 10.1007/s10903-013-9964-8.

10.

Preparation and characterization of hydrophilic composites AA/EPMA loaded with hydroxyapatite.

Campos Y, Fuentes G, Delgado JA, Almirall A.

J Biomed Mater Res A. 2013 Dec;101(12):3607-15. doi: 10.1002/jbm.a.34658. Epub 2013 Aug 26.

PMID:
23982885
11.

European mitochondrial haplogroups are associated with CD4+ T cell recovery in HIV-infected patients on combination antiretroviral therapy.

Guzmán-Fulgencio M, Berenguer J, Micheloud D, Fernández-Rodríguez A, García-Álvarez M, Jiménez-Sousa MA, Bellón JM, Campos Y, Cosín J, Aldámiz-Echevarría T, Catalán P, López JC, Resino S.

J Antimicrob Chemother. 2013 Oct;68(10):2349-57. doi: 10.1093/jac/dkt206. Epub 2013 Jun 7.

PMID:
23749950
12.

Mitochondrial haplogroups are associated with clinical pattern of AIDS progression in HIV-infected patients.

Guzmán-Fulgencio M, Jiménez JL, García-Álvarez M, Bellón JM, Fernández-Rodriguez A, Campos Y, Rodríguez C, González-Garcia J, Riera M, Viciana P, Muñoz-Fernández MÁ, Resino S.

J Acquir Immune Defic Syndr. 2013 Jun 1;63(2):178-83. doi: 10.1097/QAI.0b013e3182893f74.

PMID:
23666137
13.

Identification and characterization of the nano-sized vesicles released by muscle cells.

Romancino DP, Paterniti G, Campos Y, De Luca A, Di Felice V, d'Azzo A, Bongiovanni A.

FEBS Lett. 2013 May 2;587(9):1379-84. doi: 10.1016/j.febslet.2013.03.012. Epub 2013 Mar 20.

14.

Emphysema in an adult with galactosialidosis linked to a defect in primary elastic fiber assembly.

Lehman A, Mattman A, Sin D, Pare P, Zong Z, d'Azzo A, Campos Y, Sirrs S, Hinek A.

Mol Genet Metab. 2012 May;106(1):99-103. doi: 10.1016/j.ymgme.2012.02.004. Epub 2012 Feb 8.

PMID:
22386972
15.

Alix protein is substrate of Ozz-E3 ligase and modulates actin remodeling in skeletal muscle.

Bongiovanni A, Romancino DP, Campos Y, Paterniti G, Qiu X, Moshiach S, Di Felice V, Vergani N, Ustek D, d'Azzo A.

J Biol Chem. 2012 Apr 6;287(15):12159-71. doi: 10.1074/jbc.M111.297036. Epub 2012 Feb 13.

16.

Clinical and cellular consequences of the mutation m.12300G>A in the mitochondrial tRNA(Leu(CUN)) gene.

Martín-Jiménez R, Martín-Hernández E, Cabello A, García-Silva MT, Arenas J, Campos Y.

Mitochondrion. 2012 Mar;12(2):288-93. doi: 10.1016/j.mito.2011.10.004. Epub 2011 Nov 7.

PMID:
22094595
17.

European mitochondrial DNA haplogroups and metabolic disorders in HIV/HCV-coinfected patients on highly active antiretroviral therapy.

Micheloud D, Berenguer J, Guzmán-Fulgencio M, Campos Y, García-Álvarez M, Catalán P, Cosín J, Miralles P, López JC, Resino S.

J Acquir Immune Defic Syndr. 2011 Dec 1;58(4):371-8. doi: 10.1097/QAI.0b013e31822d2629.

PMID:
21792063
18.

European mitochondrial DNA haplogroups and liver fibrosis in HIV and hepatitis C virus coinfected patients.

García-Álvarez M, Guzmán-Fulgencio M, Berenguer J, Micheloud D, Campos Y, López JC, Cosín J, Miralles P, Alvarez E, Resino S.

AIDS. 2011 Aug 24;25(13):1619-926. doi: 10.1097/QAD.0b013e328349820f.

PMID:
21673559
19.

Drug-resistant HIV-1 in Cuban children and their seropositive mothers.

Pérez L, Correa C, Campos YA, González I, Pérez J, Martínez PA, Alvarez A, Soto Y, Kourí V.

MEDICC Rev. 2011 Apr;13(2):24-31. Erratum in: MEDICC Rev. 2011 Oct;13(4):13. Alemán, Joan [corrected to Campos, Yoan Alemán].

20.

An inexpensive antigen for serodiagnosis of Chagas' disease.

Briceño L, Rodríguez EM, Medina M, Campos Y, Mosca W, Briceño A, León G.

Invest Clin. 2010 Mar;51(1):101-13.

PMID:
20815160
21.

Ozz-E3 ubiquitin ligase targets sarcomeric embryonic myosin heavy chain during muscle development.

Campos Y, Qiu X, Zanoteli E, Moshiach S, Vergani N, Bongiovanni A, Harris AJ, d'Azzo A.

PLoS One. 2010 Mar 24;5(3):e9866. doi: 10.1371/journal.pone.0009866.

22.

Serological diagnosis of Chagas disease: evaluation and characterisation of a low cost antigen with high sensitivity and specificity.

Campos Y, Briceño L, Reina K, Figarella K, Pérez JL, Mosca W.

Mem Inst Oswaldo Cruz. 2009 Sep;104(6):914-7.

23.

Heterodimerization of the sialidase NEU1 with the chaperone protective protein/cathepsin A prevents its premature oligomerization.

Bonten EJ, Campos Y, Zaitsev V, Nourse A, Waddell B, Lewis W, Taylor G, d'Azzo A.

J Biol Chem. 2009 Oct 9;284(41):28430-41. doi: 10.1074/jbc.M109.031419. Epub 2009 Aug 7.

24.

Cyfip1 is a putative invasion suppressor in epithelial cancers.

Silva JM, Ezhkova E, Silva J, Heart S, Castillo M, Campos Y, Castro V, Bonilla F, Cordon-Cardo C, Muthuswamy SK, Powers S, Fuchs E, Hannon GJ.

Cell. 2009 Jun 12;137(6):1047-61. doi: 10.1016/j.cell.2009.04.013.

25.

Mitochondrial alterations in dynamin 2-related centronuclear myopathy.

Zanoteli E, Vergani N, Campos Y, Vainzof M, Oliveira AS, d'Azzo A.

Arq Neuropsiquiatr. 2009 Mar;67(1):102-4. No abstract available.

26.

Lethal hepatopathy and leukodystrophy caused by a novel mutation in MPV17 gene: description of an alternative MPV17 spliced form.

Navarro-Sastre A, Martín-Hernández E, Campos Y, Quintana E, Medina E, de Las Heras RS, Lluch M, Muñoz A, del Hoyo P, Martín R, Gort L, Briones P, Ribes A.

Mol Genet Metab. 2008 Jun;94(2):234-9. doi: 10.1016/j.ymgme.2008.01.012. Epub 2008 Mar 10. Erratum in: Mol Genet Metab. 2012 Aug;106(4):504.

PMID:
18329934
27.

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La Morgia C, Montagna P, Liguori M, Zanna C, Rugolo M, Cossarizza A, Wissinger B, Verny C, Schwarzenbacher R, Martín MA, Arenas J, Ayuso C, Garesse R, Lenaers G, Bonneau D, Carelli V.

Brain. 2008 Feb;131(Pt 2):338-51. Epub 2007 Dec 24.

28.
29.

Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase.

Rivera H, Blázquez A, Carretero J, Alvarez-Cermeño JC, Campos Y, Cabello A, Gonzalez-Vioque E, Borstein B, Garesse R, Arenas J, Martín MA.

Neuromuscul Disord. 2007 Oct;17(9-10):677-80. Epub 2007 Jul 5.

PMID:
17614277
30.

A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy.

Maeso E, Rueda A, Jiménez S, Del Hoyo P, Martín R, Cabello A, Mendoza LM, Arenas J, Campos Y.

Neuromuscul Disord. 2007 May;17(5):415-8. Epub 2007 Mar 23.

PMID:
17363246
31.
32.

NARP-MILS syndrome caused by 8993 T>G mitochondrial DNA mutation: a clinical, genetic and neuropathological study.

Rojo A, Campos Y, Sánchez JM, Bonaventura I, Aguilar M, García A, González L, Rey MJ, Arenas J, Olivé M, Ferrer I.

Acta Neuropathol. 2006 Jun;111(6):610-6. Epub 2006 Mar 9.

PMID:
16525806
33.

Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.

González-Vioque E, Blázquez A, Fernández-Moreira D, Bornstein B, Bautista J, Arpa J, Navarro C, Campos Y, Fernández-Moreno MA, Garesse R, Arenas J, Martín MA.

Arch Neurol. 2006 Jan;63(1):107-11.

PMID:
16401742
34.

Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE.

Blazquez A, Martín MA, Lara MC, Martí R, Campos Y, Cabello A, Garesse R, Bautista J, Andreu AL, Arenas J.

Neuromuscul Disord. 2005 Nov;15(11):775-8. Epub 2005 Sep 28.

PMID:
16198108
35.

Gene symbol: GLB1. Disease: GM1 gangliosidosis infantile.

Drousiotou A, Georgiou T, Drousiotou A, Campos Y, Caciotti A, Sztriha L, Gururaj A, Ozand P, Zammarchi E, Morrone A, d Azzo A.

Hum Genet. 2005 May;116(6):542. No abstract available.

PMID:
15991327
36.

Gene symbol: GLB1. Disease: GM1 gangliosidosis infantile.

Drousiotou A, Georgiou T, Drousiotou A, Campos Y, Caciotti A, Sztriha L, Gururaj A, Ozand P, Zammarchi E, Morrone A, d Azzo A.

Hum Genet. 2005 May;116(6):542. No abstract available.

PMID:
15991326
37.

Gene symbol: GLB1. Disease: GM1 gangliosidosis infantile.

Drousiotou A, Georgiou T, Drousiotou A, Campos Y, Caciotti A, Sztriha L, Gururaj A, Ozand P, Zammarchi E, Morrone A, d Azzo A.

Hum Genet. 2005 May;116(6):534. No abstract available.

PMID:
15988828
38.

Renal pathology in children with mitochondrial diseases.

Martín-Hernández E, García-Silva MT, Vara J, Campos Y, Cabello A, Muley R, Del Hoyo P, Martín MA, Arenas J.

Pediatr Nephrol. 2005 Sep;20(9):1299-305. Epub 2005 Jun 24.

PMID:
15977024
39.

Exercise training in mitochondrial myopathy: a randomized controlled trial.

Cejudo P, Bautista J, Montemayor T, Villagómez R, Jiménez L, Ortega F, Campos Y, Sánchez H, Arenas J.

Muscle Nerve. 2005 Sep;32(3):342-50.

PMID:
15962332
40.

The Arg482His mutation in the beta-galactosidase gene is responsible for a high frequency of GM1 gangliosidosis carriers in a Cypriot village.

Georgiou T, Stylianidou G, Anastasiadou V, Caciotti A, Campos Y, Zammarchi E, Morrone A, D'azzo A, Drousiotou A.

Genet Test. 2005 Summer;9(2):126-32.

PMID:
15943552
41.

Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase.

Loren DJ, Campos Y, d'Azzo A, Wyble L, Grange DK, Gilbert-Barness E, White FV, Hamvas A.

J Perinatol. 2005 Jul;25(7):491-4.

PMID:
15908988
42.

Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.

Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T.

Proc Natl Acad Sci U S A. 2005 May 17;102(20):7127-32. Epub 2005 May 3.

43.

Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.

Martín MA, Blázquez A, Gutierrez-Solana LG, Fernández-Moreira D, Briones P, Andreu AL, Garesse R, Campos Y, Arenas J.

Arch Neurol. 2005 Apr;62(4):659-61.

PMID:
15824269
44.

Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosis.

Gururaj A, Sztriha L, Hertecant J, Johansen JG, Georgiou T, Campos Y, Drousiotou A, d'Azzo A.

J Child Neurol. 2005 Jan;20(1):57-60.

PMID:
15791924
45.

Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyria.

Navarro S, Del Hoyo P, Campos Y, Abitbol M, Morán-Jiménez MJ, García-Bravo M, Ochoa P, Grau M, Montagutelli X, Frank J, Garesse R, Arenas J, de Salamanca RE, Fontanellas A.

Exp Dermatol. 2005 Jan;14(1):26-33.

PMID:
15660916
46.

Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.

Bornstein B, Mas JA, Patrono C, Fernández-Moreno MA, González-Vioque E, Campos Y, Carrozzo R, Martín MA, del Hoyo P, Santorelli FM, Arenas J, Garesse R.

Biochem J. 2005 May 1;387(Pt 3):773-8.

47.

Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE.

Martín MA, Blázquez A, Martí R, Bautista J, Lara MC, Cabello A, Campos Y, Belda O, Andreu AL, Arenas J.

Neurology. 2004 Oct 26;63(8):1536-7. No abstract available.

PMID:
15505189
48.

Four novel mutations in patients from the Middle East with the infantile form of GM1-gangliosidosis.

Georgiou T, Drousiotou A, Campos Y, Caciotti A, Sztriha L, Gururaj A, Ozand P, Zammarchi E, Morrone A, D'Azzo A.

Hum Mutat. 2004 Oct;24(4):352. Erratum in: Hum Mutat. 2004 Dec;24(6):536-7.

PMID:
15365997
49.

Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes).

Berbel-Garcia A, Barbera-Farre JR, Etessam JP, Salio AM, Cabello A, Gutierrez-Rivas E, Campos Y.

Clin Neuropharmacol. 2004 Jul-Aug;27(4):187-91.

PMID:
15319706
50.

Single fiber electromyography (SFEMG) in mitochondrial diseases (MD).

Cruz-Martínez A, Arpa J, Santiago S, Pérez-Conde C, Gutiérrez-Molina M, Campos Y.

Electromyogr Clin Neurophysiol. 2004 Jan-Feb;44(1):35-8.

PMID:
15008023

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