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

S T Saad

Showing results (61-70 of 91) with videos related to

Pageof 10
Sort By:
Leukemia Research|August 26, 1998
Molecular analysis of the retinoblastoma (RB1) gene in acute myeloid leukemia patientsM B Melo, F F Costa, S T Saad, et al.
Blood|November 5, 1997
Band 3 Campinas: a novel splicing mutation in the band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handlingP R Lima, J A Gontijo, J B Lopes de Faria, et al.
Acta Haematologica|January 1, 1994
Hb Lepore Baltimore (delta 50Ser beta 86Ala) identified by DNA analysis in a Brazilian familyS R Miranda, M S Figueiredo, J Kerbauy, et al.
American Journal of Hematology|May 20, 1998
Haplotype analysis and Agamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobinS Bordin, J T Martins, M S Gonçalves, et al.
Vox Sanguinis|January 1, 1993
Hepatitis C antibody (anti-HCV) prevalence in Brazilian patients with sickle cell diseasesV R Arruda, K A Eid, G C Zen, et al.
Human Mutation|January 11, 2000
Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutationsR C Leite, D S Basseres, J S Ferreira, et al.
American Journal of Hematology|July 14, 1998
Increased tyrosine phosphorylation of band 3 in hemoglobinopathiesH T Terra, M J Saad, C R Carvalho, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|December 26, 2006
Third-trimester erythrocytapheresis in pregnant patients with sickle cell diseaseS C Gilli, E V De Paula, F P Biscaro, et al.
Leukemia & Lymphoma|November 9, 2001
Lack of association between N-ras gene mutations and clinical prognosis in Brazilian children with acute lymphoblastic leukemiaN C Clementino, M Yamamoto, M B Viana, et al.
Clinical Genetics|October 27, 1998
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?V R Arruda, C E Grignolli, M S Gonçalves, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
Leukemia Research|August 26, 1998
Molecular analysis of the retinoblastoma (RB1) gene in acute myeloid leukemia patientsM B Melo, F F Costa, S T Saad, et al.
Blood|November 5, 1997
Band 3 Campinas: a novel splicing mutation in the band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handlingP R Lima, J A Gontijo, J B Lopes de Faria, et al.
Acta Haematologica|January 1, 1994
Hb Lepore Baltimore (delta 50Ser beta 86Ala) identified by DNA analysis in a Brazilian familyS R Miranda, M S Figueiredo, J Kerbauy, et al.
American Journal of Hematology|May 20, 1998
Haplotype analysis and Agamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobinS Bordin, J T Martins, M S Gonçalves, et al.
Vox Sanguinis|January 1, 1993
Hepatitis C antibody (anti-HCV) prevalence in Brazilian patients with sickle cell diseasesV R Arruda, K A Eid, G C Zen, et al.
Human Mutation|January 11, 2000
Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutationsR C Leite, D S Basseres, J S Ferreira, et al.
American Journal of Hematology|July 14, 1998
Increased tyrosine phosphorylation of band 3 in hemoglobinopathiesH T Terra, M J Saad, C R Carvalho, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|December 26, 2006
Third-trimester erythrocytapheresis in pregnant patients with sickle cell diseaseS C Gilli, E V De Paula, F P Biscaro, et al.
Leukemia & Lymphoma|November 9, 2001
Lack of association between N-ras gene mutations and clinical prognosis in Brazilian children with acute lymphoblastic leukemiaN C Clementino, M Yamamoto, M B Viana, et al.
Clinical Genetics|October 27, 1998
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?V R Arruda, C E Grignolli, M S Gonçalves, et al.
Pageof 10