Johan Flygare

Affiliated with

Research Area

Developmental Biology

Biography

Johan Flygare has not added Biography.
If you are Johan Flygare and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2018

Other Publications

Article	Year
Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis. Blood\| PubMed ID: 12393514	2003
Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia. Blood\| PubMed ID: 15626736	2005
Development of cellular models for ribosomal protein S19 (RPS19)-deficient diamond-blackfan anemia using inducible expression of siRNA against RPS19. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 15771965	2005
Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits. Blood\| PubMed ID: 16990592	2007
Diamond-Blackfan anemia: erythropoiesis lost in translation. Blood\| PubMed ID: 17164339	2007
Endoglin is not critical for hematopoietic stem cell engraftment and reconstitution but regulates adult erythroid development. Stem cells (Dayton, Ohio)\| PubMed ID: 17673527	2007
Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia... Stem cells (Dayton, Ohio)\| PubMed ID: 17962699	2008
Gene therapy of Diamond Blackfan anemia CD34(+) cells leads to improved erythroid development and engraftment following transplantation. Experimental hematology\| PubMed ID: 18715690	2008
Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia. Blood\| PubMed ID: 21989989	2011
From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications. Blood\| PubMed ID: 21998215	2011
Progress towards mechanism-based treatment for Diamond-Blackfan anemia. TheScientificWorldJournal\| PubMed ID: 22619618	2012
Dietary L-leucine improves the anemia in a mouse model for Diamond-Blackfan anemia. Blood\| PubMed ID: 22791294	2012
Fetal hepatic progenitors support long-term expansion of hematopoietic stem cells. Experimental hematology\| PubMed ID: 23415675	2013
Gene therapy cures the anemia and lethal bone marrow failure in a mouse model of RPS19-deficient Diamond-Blackfan anemia. Haematologica\| PubMed ID: 25216681	2014
Glucocorticoids improve erythroid progenitor maintenance and dampen Trp53 response in a mouse model of Diamond-Blackfan anaemia. British journal of haematology\| PubMed ID: 26305041	2015
Defining the Minimal Factors Required for Erythropoiesis through Direct Lineage Conversion. Cell reports\| PubMed ID: 27264182	2016
Direct Conversion of Fibroblasts to Megakaryocyte Progenitors. Cell reports\| PubMed ID: 27732845	2016
Direct lineage reprogramming: a useful addition to the blood cell research toolbox. Expert review of hematology\| PubMed ID: 27967256	2017
Lentiviral Vectors with Cellular Promoters Correct Anemia and Lethal Bone Marrow Failure in a Mouse Model for Diamond-Blackfan Anemia. Molecular therapy : the journal of the American Society of Gene Therapy\| PubMed ID: 28434866	2017