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Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
(2010-05-26)
We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures. The 2020 blood samples were of ...
Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America.
(2010-05-26)
We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures. The 2020 blood samples were of ...
Desnaturação de oxihemoglobinas humanas A, A2 e S pelo metodo de tampão isopropanol
(1978-12-01)
Human oxyhaemoglobin A and A2 from normal individuals and oxyhaemoglobin S from patients with sickle cell anaemia and sickle cell trait were studied using Isopropanol/buffer method at 37°C and 40°C. Hb S was less stable ...
HB D Los Angeles in a Brazilian family
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2001-09-01)
As doenças hereditária da hemoglobina são as mais comuns doenças monogênicas e atualmente bem conhecidas do ponto de vista molecular, fato este que propiciou um avanço no seu controle e manuseio. A população brasileira ...
HB D Los Angeles in a Brazilian family
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2001-09-01)
As doenças hereditária da hemoglobina são as mais comuns doenças monogênicas e atualmente bem conhecidas do ponto de vista molecular, fato este que propiciou um avanço no seu controle e manuseio. A população brasileira ...
Amplificação gênica alelo-específica na caracterização das hemoglobinas S, C e D e as interaçõ es entre elas e talassemias beta
(2006-10-13)
Background: The hemoglobinopathies are a group of hereditary hemoglobin disorders in worldwide distribution, affecting Brazilian population significantly; they are decurrent of alterations in structural genes, responsible ...
Spin Label Studies of the Hemoglobin–Membrane Interaction During Sickle Hemoglobin Polymerization
(Springer Wien, 2010-05)
An enhanced hemoglobin–membrane association has been previously documented in sickle cell anemia. However, it is not known how this interaction is modified during the hemoglobin S polymerization process. In this work, we ...