Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fernando F Costa

Showing results (71-80 of 154) with videos related to

Pageof 16
Sort By:
British Journal of Haematology|May 25, 2019
Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignanciesBruno K L Duarte, Gabriela G Yamaguti-Hayakawa, Samuel S Medina, et al.
Leukemia & Lymphoma|June 27, 2009
New mutations detected by denaturing high performance liquid chromatography during screening of exon 6 bcr-abl mutations in patients with chronic myeloid leukemia treated with tyrosine kinase inhibitorsCintia C Mascarenhas, Anderson F Cunha, Eliana C Miranda, et al.
Cells|April 12, 2022
TGF-β1 Reduces Neutrophil Adhesion and Prevents Acute Vaso-Occlusive Processes in Sickle Cell Disease MiceLidiane S Torres, Hanan Chweih, Fernanda C Z Fabris, et al.
Hematology, Transfusion and Cell Therapy|March 17, 2024
Sickle cell disease and increased adverse maternal and perinatal outcomes in different genotypesCamilla Olivares Figueira, José Paulo S Guida, Fernanda G Surita, et al.
Biochimica Et Biophysica Acta|September 8, 2006
ANKHD1, ankyrin repeat and KH domain containing 1, is overexpressed in acute leukemias and is associated with SHP2 in K562 cellsFabíola Traina, Patricia M B Favaro, Samuel de Souza Medina, et al.
Thrombosis and Haemostasis|July 23, 2004
Platelet glycoprotein Ibalpha polymorphisms modulate the risk for myocardial infarctionMargareth C Ozelo, Andrea F Origa, Francisco J P Aranha, et al.
Journal of Leukocyte Biology|May 16, 2019
S100A8 acts as an autocrine priming signal for heme-induced human Mϕ pro-inflammatory responses in hemolytic inflammationAngélica A A Silveira, Olwyn R Mahon, Clare C Cunningham, et al.
European Journal of Haematology|August 7, 2009
PIP4KIIA and beta-globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H diseaseMarcia R S C Wenning, Maricilda P Mello, Tiago G Andrade, et al.
Hematology (Amsterdam, Netherlands)|August 13, 2002
Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosisMônica B Melo, Nilofer N Ahmad, Carmen S P Lima, et al.
Haematologica|January 18, 2015
Elevated hypercoagulability markers in hemoglobin SC diseaseMarina P Colella, Erich V de Paula, João A Machado-Neto, et al.
Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:
Pageof 16
British Journal of Haematology|May 25, 2019
Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignanciesBruno K L Duarte, Gabriela G Yamaguti-Hayakawa, Samuel S Medina, et al.
Leukemia & Lymphoma|June 27, 2009
New mutations detected by denaturing high performance liquid chromatography during screening of exon 6 bcr-abl mutations in patients with chronic myeloid leukemia treated with tyrosine kinase inhibitorsCintia C Mascarenhas, Anderson F Cunha, Eliana C Miranda, et al.
Cells|April 12, 2022
TGF-β1 Reduces Neutrophil Adhesion and Prevents Acute Vaso-Occlusive Processes in Sickle Cell Disease MiceLidiane S Torres, Hanan Chweih, Fernanda C Z Fabris, et al.
Hematology, Transfusion and Cell Therapy|March 17, 2024
Sickle cell disease and increased adverse maternal and perinatal outcomes in different genotypesCamilla Olivares Figueira, José Paulo S Guida, Fernanda G Surita, et al.
Biochimica Et Biophysica Acta|September 8, 2006
ANKHD1, ankyrin repeat and KH domain containing 1, is overexpressed in acute leukemias and is associated with SHP2 in K562 cellsFabíola Traina, Patricia M B Favaro, Samuel de Souza Medina, et al.
Thrombosis and Haemostasis|July 23, 2004
Platelet glycoprotein Ibalpha polymorphisms modulate the risk for myocardial infarctionMargareth C Ozelo, Andrea F Origa, Francisco J P Aranha, et al.
Journal of Leukocyte Biology|May 16, 2019
S100A8 acts as an autocrine priming signal for heme-induced human Mϕ pro-inflammatory responses in hemolytic inflammationAngélica A A Silveira, Olwyn R Mahon, Clare C Cunningham, et al.
European Journal of Haematology|August 7, 2009
PIP4KIIA and beta-globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H diseaseMarcia R S C Wenning, Maricilda P Mello, Tiago G Andrade, et al.
Hematology (Amsterdam, Netherlands)|August 13, 2002
Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosisMônica B Melo, Nilofer N Ahmad, Carmen S P Lima, et al.
Haematologica|January 18, 2015
Elevated hypercoagulability markers in hemoglobin SC diseaseMarina P Colella, Erich V de Paula, João A Machado-Neto, et al.
Pageof 16