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Irene Roberts

Showing results (41-50 of 129) with videos related to

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Transfusion|November 8, 2002
RBC T activation and hemolysis in a neonatal intensive care population: implications for transfusion practiceHarischandra Boralessa, Neena Modi, Hazel Cockburn, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|August 29, 2002
High transduction efficiency of circulating first trimester fetal mesenchymal stem cells: potential targets for in utero ex vivo gene therapyCesare Campagnoli, Ilaria Bellantuono, Sailesh Kumar, et al.
Blood Advances|April 18, 2025
Genome-wide association study of somatic GATA1s mutations in newborns with Down SyndromeYunqi Li, Natalina Elliott, Patricia Lein, et al.
British Journal of Haematology|February 3, 2005
GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorderEmily Carpenter, Veronica Valverde-Garduno, Alex Sternberg, et al.
British Journal of Haematology|November 12, 2005
The expression of minichromosome maintenance protein-2 in normal and abnormal megakaryocytes and comparison with the proliferative marker Ki-67Irvin A Lampert, Donna Horncastle, Steven Dilworth, et al.
Frontiers in Immunology|April 19, 2021
Development of LT-HSC-Reconstituted Non-Irradiated NBSGW Mice for the Study of Human Hematopoiesis <i>In Vivo</i>George Adigbli, Peng Hua, Masateru Uchiyama, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 1, 2011
Managing the difficult case of fetal anemiaEko G Zhang, Fiona Regan, Mark Layton, et al.
Journal of Pediatric Hematology/Oncology|April 2, 2019
A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid TreatmentRoula A Farah, Lojine Kamel, Noemi Roy, et al.
Human Molecular Genetics|April 18, 2013
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutationValentina S Caputo, Joana R Costa, Kalliopi Makarona, et al.
Leukemia|December 20, 2023
Backtracking to the future: unraveling the origins of childhood leukemiaAdam J de Smith, Joseph L Wiemels, Adam J Mead, et al.
Pageof 13

Showing results (41-50 of 129) with videos related to

Sort By:
Pageof 13
Transfusion|November 8, 2002
RBC T activation and hemolysis in a neonatal intensive care population: implications for transfusion practiceHarischandra Boralessa, Neena Modi, Hazel Cockburn, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|August 29, 2002
High transduction efficiency of circulating first trimester fetal mesenchymal stem cells: potential targets for in utero ex vivo gene therapyCesare Campagnoli, Ilaria Bellantuono, Sailesh Kumar, et al.
Blood Advances|April 18, 2025
Genome-wide association study of somatic GATA1s mutations in newborns with Down SyndromeYunqi Li, Natalina Elliott, Patricia Lein, et al.
British Journal of Haematology|February 3, 2005
GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorderEmily Carpenter, Veronica Valverde-Garduno, Alex Sternberg, et al.
British Journal of Haematology|November 12, 2005
The expression of minichromosome maintenance protein-2 in normal and abnormal megakaryocytes and comparison with the proliferative marker Ki-67Irvin A Lampert, Donna Horncastle, Steven Dilworth, et al.
Frontiers in Immunology|April 19, 2021
Development of LT-HSC-Reconstituted Non-Irradiated NBSGW Mice for the Study of Human Hematopoiesis <i>In Vivo</i>George Adigbli, Peng Hua, Masateru Uchiyama, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 1, 2011
Managing the difficult case of fetal anemiaEko G Zhang, Fiona Regan, Mark Layton, et al.
Journal of Pediatric Hematology/Oncology|April 2, 2019
A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid TreatmentRoula A Farah, Lojine Kamel, Noemi Roy, et al.
Human Molecular Genetics|April 18, 2013
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutationValentina S Caputo, Joana R Costa, Kalliopi Makarona, et al.
Leukemia|December 20, 2023
Backtracking to the future: unraveling the origins of childhood leukemiaAdam J de Smith, Joseph L Wiemels, Adam J Mead, et al.
Pageof 13