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WKP|Q91143063
(VIAF cluster)
(Authority/Source Record)
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WKP |
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20241120235931.0 |
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(WKP)Q91143063
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0000-0003-0790-3133
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orcid
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7201855583
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scopus
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(OCoLC)Q91143063
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100
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0 |
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Giuliana Ferrari
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researcher (ORCID 0000-0003-0790-3133)
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en
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375
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2
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iso5218
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400
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Giuliana Ferrari
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wetenschapper
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nl
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670
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Author's Bone marrow as a source of hematopoietic stem cells for human gene therapy of β-thalassemia
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670
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Author's Inhibition of FGF23 is a therapeutic strategy to target hematopoietic stem cell niche defects in β-thalassemia
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670
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‡a
Author's Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia
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670
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Author's Mesenchymal cells appearing in pancreatic tissue culture are bone marrow-derived stem cells with the capacity to improve transplanted islet function
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670
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Author's Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease
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(scopus) 7201855583
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(orcid) 0000000307903133
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1
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mesenchymalcellsappearinginpancreatictissueculturearebonemarrowderivedstemcellswiththecapacitytoimprovetransplantedisletfunction
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Mesenchymal cells appearing in pancreatic tissue culture are bone marrow-derived stem cells with the capacity to improve transplanted islet function
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1
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919
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quantitativelydifferentredcellnucleatedcellchimerisminpatientswithlongtermpersistenthematopoieticmixedchimerismafterbonemarrowtransplantationforthalassemiamajororsicklecelldisease
‡A
Quantitatively different red cell/nucleated cell chimerism in patients with long-term, persistent hematopoietic mixed chimerism after bone marrow transplantation for thalassemia major or sickle cell disease
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1
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919
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intrabonehematopoieticstemcellgenetherapyforadultandpediatricpatientsaffectedbytransfusiondependentssthalassemia
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Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia
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1
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919
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inhibitionoffgf23isatherapeuticstrategytotargethematopoieticstemcellnichedefectsinβthalassemia
‡A
Inhibition of FGF23 is a therapeutic strategy to target hematopoietic stem cell niche defects in β-thalassemia
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1
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919
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bonemarrowasasourceofhematopoieticstemcellsforhumangenetherapyofβthalassemia
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Bone marrow as a source of hematopoietic stem cells for human gene therapy of β-thalassemia
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