Bioquímica y Biología Molecular
Departamento
Icahn School of Medicine at Mount Sinai
Nueva York, Estados UnidosPublicaciones en colaboración con investigadoras/es de Icahn School of Medicine at Mount Sinai (17)
2024
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SUMOylation controls Hu antigen R posttranscriptional activity in liver cancer
Cell Reports, Vol. 43, Núm. 3
2023
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Master Transcription Factor Reprogramming Unleashes Selective Translation Promoting Castration Resistance and Immune Evasion in Lethal Prostate Cancer
Cancer discovery, Vol. 13, Núm. 12, pp. 2584-2609
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
2019
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Somatic mutations and cell identity linked by Genotyping of Transcriptomes
Nature, Vol. 571, Núm. 7765, pp. 355-360
2018
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Histone Native Chromatin Immunoprecipitation
Methods in Molecular Biology (Humana Press Inc.), pp. 77-104
2017
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MTORC1-dependent AMD1 regulation sustains polyamine metabolism in prostate cancer
Nature, Vol. 547, Núm. 7661, pp. 109-113
2016
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The metabolic co-regulator PGC1α suppresses prostate cancer metastasis
Nature Cell Biology, Vol. 18, Núm. 6, pp. 645-656
2015
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Methodological aspects of the molecular and histological study of prostate cancer: Focus on PTEN
Methods, Vol. 77, pp. 25-30
2014
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A unified nomenclature and amino acid numbering for human PTEN
Science Signaling, Vol. 7, Núm. 332
2013
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The octamer is the major form of CENP-A nucleosomes at human centromeres
Nature Structural and Molecular Biology, Vol. 20, Núm. 6, pp. 687-695
2011
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Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres
Chromosoma, Vol. 120, Núm. 6, pp. 621-632
2010
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A paucity of heterochromatin at functional human neocentromeres
Epigenetics and Chromatin, Vol. 3, Núm. 1
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Protein-protein interactions at an enzyme-substrate interface: Characterization of transient reaction intermediates throughout a full catalytic cycle of Escherichia coli thioredoxin reductase
Proteins: Structure, Function and Bioinformatics, Vol. 78, Núm. 1, pp. 36-51
2007
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Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres
Genome Biology, Vol. 8, Núm. 7
2006
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Independent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigs
Genome Biology, Vol. 7, Núm. 10
2003
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Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres
Human Molecular Genetics, Vol. 12, Núm. 20, pp. 2711-2721
2000
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Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere
American Journal of Human Genetics, Vol. 66, Núm. 6, pp. 1794-1806