INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE SALAMANCA
Instituto
University of Michigan Medical School
Ann Arbor, Estados UnidosPublicaciones en colaboración con investigadores/as de University of Michigan Medical School (21)
2022
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Mast Cell Diseases in Practice and Research: Issues and Perspectives Raised by Patients and Their Recommendations to the Scientific Community and Beyond
Journal of Allergy and Clinical Immunology: In Practice, Vol. 10, Núm. 8, pp. 2039-2051
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Small-molecule inhibitors targeting Polycomb repressive complex 1 RING domain
Nature Chemical Biology, Vol. 17, Núm. 7, pp. 784-793
2016
2015
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A global reference for human genetic variation
Nature, Vol. 526, Núm. 7571, pp. 68-74
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Designing a broad-spectrum integrative approach for cancer prevention and treatment
Seminars in Cancer Biology, Vol. 35, pp. S276-S304
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Snail1-induced partial epithelial-to-mesenchymal transition drives renal fibrosis in mice and can be targeted to reverse established disease
Nature Medicine, Vol. 21, Núm. 9, pp. 989-997
2012
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Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
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The first European interdisciplinary Ewing sarcoma research summit
Frontiers in Oncology, Vol. 2 MAY
2007
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Standards and standardization in mastocytosis: Consensus statements on diagnostics, treatment recommendations and response criteria
European Journal of Clinical Investigation, Vol. 37, Núm. 6, pp. 435-453
2006
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Characterization of opioid-binding sites in zebrafish brain
Journal of Pharmacology and Experimental Therapeutics, Vol. 316, Núm. 2, pp. 900-904
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In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse
Human Molecular Genetics, Vol. 15, Núm. 11, pp. 1847-1857
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The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
Nature Genetics, Vol. 38, Núm. 6, pp. 674-681
2005
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Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
Nature Genetics, Vol. 37, Núm. 3, pp. 282-288
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RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins
Journal of Biological Chemistry, Vol. 280, Núm. 39, pp. 33580-33587
2003
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A nonlinear filter-bank model of the guinea-pig cochlear nerve: Rate responses
Journal of the Acoustical Society of America, Vol. 113, Núm. 6, pp. 3264-3274
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Adaptation in a revised inner-hair cell model
Journal of the Acoustical Society of America, Vol. 113, Núm. 2, pp. 893-901
2000
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Characterization of ZFOR1, a putative delta-opioid receptor from the teleost zebrafish (Danio rerio)
Neuroscience Letters, Vol. 288, Núm. 3, pp. 207-210