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A novel missense mutation 15747 T>C in the mitochondrial cytochrome b gene.
Aguilera I, García-Lozano JR, Bautista J, Campos Y, Arenas J, Núñez-Roldán A. Aguilera I, et al. Hum Mutat. 1999 Dec;14(6):545. doi: 10.1002/(SICI)1098-1004(199912)14:6<545::AID-HUMU18>3.0.CO;2-J. Hum Mutat. 1999. PMID: 10571957 No abstract available.
A human monoclonal antibody reacting against HLA-DQ1-, DQ4-, and a subset of DQ7-bearing cells.
Sánchez B, de la Calle O, Yélamos J, Aguilera I, Sánchez F, Dessi V, Siervo S, García-Lozano JR, Melero J, Magariño R, et al. Sánchez B, et al. Hum Immunol. 1993 Feb;36(2):81-90. doi: 10.1016/0198-8859(93)90110-m. Hum Immunol. 1993. PMID: 7681815
Identification of cation-independent mannose 6-phosphate receptor/insulin-like growth factor type-2 receptor as a novel target of autoantibodies.
Tarrago D, Aguilera I, Melero J, Wichmann I, Nuñez-Roldan A, Sanchez B. Tarrago D, et al. Immunology. 1999 Dec;98(4):652-62. doi: 10.1046/j.1365-2567.1999.00889.x. Immunology. 1999. PMID: 10594701 Free PMC article.
A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy.
Garcia-Lozano JR, Aguilera I, Bautista J, Nuñez-Roldan A. Garcia-Lozano JR, et al. Hum Mutat. 2000 Jan;15(1):120-1. doi: 10.1002/(SICI)1098-1004(200001)15:1<120::AID-HUMU33>3.0.CO;2-8. Hum Mutat. 2000. PMID: 10612844 No abstract available.
[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy].
Franco E, Bautista J, Luque R, Chinchón I, García-Lozano R, Aguilera I, Campos Y, Arenas J. Franco E, et al. Neurologia. 1999 Nov;14(9):463-6. Neurologia. 1999. PMID: 10613022 Spanish.
Respiratory chain studies were consistent with complex I deficiency. Point mutations or deletions in mitochondrial DNA were not found. ...
Respiratory chain studies were consistent with complex I deficiency. Point mutations or deletions in mitochondrial DNA were not found …
Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?
Muñoz-Málaga A, Bautista J, Salazar JA, Aguilera I, Garcia R, Chinchon I, Segura MD, Campos Y, Arenas J. Muñoz-Málaga A, et al. Muscle Nerve. 2000 Apr;23(4):538-42. doi: 10.1002/(sici)1097-4598(200004)23:4<538::aid-mus12>3.0.co;2-t. Muscle Nerve. 2000. PMID: 10716764
Molecular structure of eight human autoreactive monoclonal antibodies.
Aguilera I, Melero J, Nuñez-Roldan A, Sanchez B. Aguilera I, et al. Immunology. 2001 Mar;102(3):273-80. doi: 10.1046/j.1365-2567.2001.01159.x. Immunology. 2001. PMID: 11298825 Free PMC article.
Mitochondrial disease and stroke.
Martínez-Fernández E, Gil-Peralta A, García-Lozano R, Chinchón I, Aguilera I, Fernández-López O, Arenas J, Campos Y, Bautista J. Martínez-Fernández E, et al. Stroke. 2001 Nov;32(11):2507-10. doi: 10.1161/hs1101.098328. Stroke. 2001. PMID: 11692008
Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease.
Aguilera I, García-Lozano JR, Muñoz A, Arenas J, Campos Y, Chinchón I, Roldán AN, Bautista J. Aguilera I, et al. J Neurol Sci. 2001 Nov 15;192(1-2):81-4. doi: 10.1016/s0022-510x(01)00634-7. J Neurol Sci. 2001. PMID: 11701156
Her muscle biopsy also revealed signs of mitochondrial proliferation, scattered RRF, and a deficit in complex I of the respiratory chain. ...Mitochondrial DNA analysis of muscle tissue revealed an additional G-to-A transition at nucleotide position 7444 in the cytochrome c …
Her muscle biopsy also revealed signs of mitochondrial proliferation, scattered RRF, and a deficit in complex I of the respiratory ch …
Antibodies against glutathione S-transferase T1 (GSTT1) in patients with de novo immune hepatitis following liver transplantation.
Aguilera I, Wichmann I, Sousa JM, Bernardos A, Franco E, García-Lozano JR, Núñez-Roldán A. Aguilera I, et al. Clin Exp Immunol. 2001 Dec;126(3):535-9. doi: 10.1046/j.1365-2249.2001.01682.x. Clin Exp Immunol. 2001. PMID: 11737073 Free PMC article.
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