Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rosalie M. Baine"'
Autor:
Elisabeth Paietta, Rosalie M. Baine, Frederick R. Rickles, Martin S. Tallman, David Green, Isaac Cohen, Hau C. Kwaan, Phil Lefebvre, Mamoru Shoji
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 2(8)
We studied the pathogenesis of the bleeding disorder in acute promyelocytic leukemia by measuring procoagulant, profibrinolytic, and proinflammatory mediators in peripheral blood and bone marrow cells from 25 previously untreated patients. Patients w
Publikováno v:
Hemoglobin. 3:293-298
Autor:
Rosalie M. Baine, Jane M. Benson, Winston F. Moo-Penn, T. K. Hine, D C Swan, Danny L. Jue, David M. Virshup, Mary H. Johnson, William H. Zinkham
Publikováno v:
Journal of Biological Chemistry. 264:21454-21457
Hb Catonsville is an unstable variant in which glutamic acid is inserted into the alpha-globin chain between Pro-37(C2) and Thr-38(C3). The peptide sequence data are consistent with the DNA sequence of the polymerase chain reaction-amplified fragment
Publikováno v:
Hemoglobin. 4:201-207
Autor:
Rosalie M. Baine, Danny L. Jue, Winston F. Moo-Penn, Jane M. Benson, James E. McGuffey, Mary H. Johnson
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 747:65-70
Hb Evanston (α14 Trp → Arg) was detected on cellulose acetate at pH 8.4 as a band with an electrophoretic mobility similar to that of Hb S. In addition, a band migrating cathodic to Hb A2 suggested the presence of a variant Hb A2 with a substituti
Publikováno v:
Hemoglobin. 2:443-445
Hemoglobin J Rovigo was first described by Alberti et al. (1) in an Italian family. Our report concerns the identification and fuctional properties of this variant in combination with β-thalassemia in a Brazilian family.
The extent of variability in the number of human hemoglobin (Hb) alpha chain loci has not yet been conclusively determined. There is evidence that in some populations individuals may possess two alpha-chain loci, while in other populations only one l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc408dbf1d0930f610a463b0af0ae087
https://europepmc.org/articles/PMC431172/
https://europepmc.org/articles/PMC431172/
Autor:
Ovidiu Platica, R. F. Rieder, Marisol M. Cedeno, David B. Rausher, Ismat U. Nawabi, Rosalie M. Baine, Gwen B. Sancar
Publikováno v:
Annals of internal medicine. 98(6)
Members of a Jewish family of Polish origin were found to have hypochromic, microcytic erythrocytes. By restriction endonuclease analysis of DNA, the propositus, a brother, and an aunt were found to have a single alpha-globin gene on each chromosome