Résultat de recherche

NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development.

Annarita Miccio

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Transcription factor binding sites are genetic determinants of retroviral integration in the human genome.

Annarita Miccio

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In vivo selection of genetically modified erythroblastic progenitors leads to long-term correction of beta-thalassemia.

Annarita Miccio

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The homeodomain transcription factor Prep1 (pKnox1) is required for hematopoietic stem and progenitor cell activity.

Annarita Miccio

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Hot spots of retroviral integration in human CD34+ hematopoietic cells.

Annarita Miccio

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Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype.

Annarita Miccio

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Phosphorylation of synapsin I by cAMP-dependent protein kinase controls synaptic vesicle dynamics in developing neurons.

Annarita Miccio

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Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A.

Matias Simons, Gwenn Le Meur

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Filling the Gap: Drosophila Nephrocytes as Model System in Kidney Research.

Matias Simons, Zvonimir Marelja

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U-Net: deep learning for cell counting, detection, and morphometry.

Matias Simons

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A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.

Matias Simons

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