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Massimo Tatti

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Protein Expression and Purification|April 6, 2011
Efficient one-step chromatographic purification and functional characterization of recombinant human Saposin CMarialetizia Motta, Massimo Tatti, Simone Martinelli, et al.
Human Molecular Genetics|May 21, 2010
Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sortingAnna M Vaccaro, Marialetizia Motta, Massimo Tatti, et al.
The Biochemical Journal|April 14, 2005
The N370S (Asn370-->Ser) mutation affects the capacity of glucosylceramidase to interact with anionic phospholipid-containing membranes and saposin CRosa Salvioli, Massimo Tatti, Susanna Scarpa, et al.
Journal of Extracellular Vesicles|December 10, 2023
Metabolic labelling of a subpopulation of small extracellular vesicles using a fluorescent palmitic acid analogueValeria Barreca, Zaira Boussadia, Deborah Polignano, et al.
International Journal of Molecular Sciences|August 10, 2024
Whole Genome Sequencing Solves an Atypical Form of Bardet-Biedl Syndrome: Identification of Novel Pathogenic Variants of <i>BBS9</i>Emilia Stellacci, Marcello Niceta, Alessandro Bruselles, et al.
The Journal of Biological Chemistry|October 6, 2009
Microenvironmental pH is a key factor for exosome traffic in tumor cellsIsabella Parolini, Cristina Federici, Carla Raggi, et al.
International Journal of Molecular Sciences|December 11, 2022
Biallelic Inactivating <i>TUB</i> Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary CiliumLucia Ziccardi, Marcello Niceta, Emilia Stellacci, et al.
Human Molecular Genetics|September 11, 2021
Hyperactive HRAS dysregulates energetic metabolism in fibroblasts from patients with Costello syndrome via enhanced production of reactive oxidizing speciesGiovanna Carpentieri, Chiara Leoni, Donatella Pietraforte, et al.
Orphanet Journal of Rare Diseases|April 23, 2026
Muscle ultrasonography in costello syndrome: unveiling new clinical insights of a complex muscular phenotypeChiara Leoni, Germana Viscogliosi, Deborah Pajalunga, et al.
Clinical Genetics|May 17, 2020
Refinement of the clinical and mutational spectrum of UBE2A deficiency syndromeViviana Cordeddu, Erica L Macke, Francesca Clementina Radio, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Protein Expression and Purification|April 6, 2011
Efficient one-step chromatographic purification and functional characterization of recombinant human Saposin CMarialetizia Motta, Massimo Tatti, Simone Martinelli, et al.
Human Molecular Genetics|May 21, 2010
Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sortingAnna M Vaccaro, Marialetizia Motta, Massimo Tatti, et al.
The Biochemical Journal|April 14, 2005
The N370S (Asn370-->Ser) mutation affects the capacity of glucosylceramidase to interact with anionic phospholipid-containing membranes and saposin CRosa Salvioli, Massimo Tatti, Susanna Scarpa, et al.
Journal of Extracellular Vesicles|December 10, 2023
Metabolic labelling of a subpopulation of small extracellular vesicles using a fluorescent palmitic acid analogueValeria Barreca, Zaira Boussadia, Deborah Polignano, et al.
International Journal of Molecular Sciences|August 10, 2024
Whole Genome Sequencing Solves an Atypical Form of Bardet-Biedl Syndrome: Identification of Novel Pathogenic Variants of <i>BBS9</i>Emilia Stellacci, Marcello Niceta, Alessandro Bruselles, et al.
The Journal of Biological Chemistry|October 6, 2009
Microenvironmental pH is a key factor for exosome traffic in tumor cellsIsabella Parolini, Cristina Federici, Carla Raggi, et al.
International Journal of Molecular Sciences|December 11, 2022
Biallelic Inactivating <i>TUB</i> Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary CiliumLucia Ziccardi, Marcello Niceta, Emilia Stellacci, et al.
Human Molecular Genetics|September 11, 2021
Hyperactive HRAS dysregulates energetic metabolism in fibroblasts from patients with Costello syndrome via enhanced production of reactive oxidizing speciesGiovanna Carpentieri, Chiara Leoni, Donatella Pietraforte, et al.
Orphanet Journal of Rare Diseases|April 23, 2026
Muscle ultrasonography in costello syndrome: unveiling new clinical insights of a complex muscular phenotypeChiara Leoni, Germana Viscogliosi, Deborah Pajalunga, et al.
Clinical Genetics|May 17, 2020
Refinement of the clinical and mutational spectrum of UBE2A deficiency syndromeViviana Cordeddu, Erica L Macke, Francesca Clementina Radio, et al.
Pageof 2