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Hemoglobin|November 14, 2018
Codon 14 (+T) (HBB: c.44_45insT): a Rare β-Thalassemia Mutation Reported Only in AzerbaijanGunay Aliyeva, Chingiz Asadov, Tahira Mammadova, et al.Hemoglobin|October 5, 2019
Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern VietnamTuan Mai Anh, Kanokwan Sanchaisuriya, Giang Nguyen Kieu, et al.Hemoglobin|August 8, 2019
Hb Gibbon [β124(H2)Pro→Thr (HBB: c.373C>A, p.P125T)], an Asymptomatic Novel Hemoglobin Variant Detected by Newborn ScreeningAlejandro Wolf, Joseph M Rohr, Catalina Amador, et al.Hemoglobin|May 14, 2008
Hb Agrinio [alpha29(B10)Le-->uPro (alpha2)] in combination with --(MED I). Results in a severe form of Hb H diseaseXenia Felekis, Marios Phylactides, Anthi Drousiotou, et al.Hemoglobin|May 14, 2008
A +8 (-->CT) mutation within the 5' untranslated region of beta-globin down-regulates the mRNA transcriptionNeil Van de Water, Tina Tan, George Chan, et al.Hemoglobin|May 14, 2008
Molecular basis of alpha-thalassemia in AlgeriaHamida Mesbah-Amroun, Fatiha Rouabhi, Rolande Ducrocq, et al.Hemoglobin|May 14, 2008
Analyses of expression of cytoglobin by immunohistochemical studies in human tissuesAkio Shigematsu, Yasushi Adachi, Junko Matsubara, et al.Hemoglobin|May 14, 2008
Compound heterozygosity for Hb S [beta6(A3)GluVal, GAG-->GTG] and a new thalassemic mutation [beta132(H10)Lys-->term, AAA-->TAA] detected in a family from West AfricaHannes Frischknecht, Heinz Troxler, Jeanette Greiner, et al.Hemoglobin|January 1, 1989
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemiaA Kutlar, F Kutlar, M Aksoy, et al.Hemoglobin|March 17, 2006
Erythropoietin administration may potentiate mobilization of storage iron in patients on oral iron chelation therapyJaroslav CermákPageof 240