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R M Baine

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Clinical Chemistry|July 1, 1981
Evaluation of a commercial kit for microchromatographic quantitation of hemoglobin A2 in the presence of hemoglobin SR M Baine, H G Brown
Blood|May 1, 1981
Cultured erythroid cells as a model for Hb regulation: ability of cultured cells to synthesize Hb lepore and HbA2 and to maintain balanced globin synthesisR M Baine, J M Benson
Hemoglobin|January 1, 1979
HB G Waimanalo (alpha 64 Asp replaced by Asn) in a child with homozygous beta-thalassemiaR M Baine, J M Wright, R W Wilkinson
Hemoglobin|January 1, 1978
Hemoglobin J Rovigo (alpha53 Ala replaced by Asp) in association with beta-thalassemiaW F Moo-Penn, D L Jue, R M Baine
Clinical Chemistry|December 1, 1978
Microchromatographic methods for hemoglobin A2 quantitation comparedE M Brosious, J M Wright, R M Baine, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1976
Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain lociR M Baine, D L Rucknagel, P A Dublin, et al.
Hemoglobin|January 1, 1980
Biosynthetic evidence for instability of HB M SaskatoonR M Baine, J M Wright, M H Johnson, et al.
Progress in Clinical and Biological Research|January 1, 1978
Polymorphism in the number of hemoglobin alpha-chain loci and mechanisms governing the balance of chain synthesisD L Rucknagel, R M Baine, S M Hanash, et al.
The Journal of Clinical Investigation|August 1, 1983
Hemolytic disease of the newborn caused by a new deletion of the entire beta-globin clusterM Pirastu, Y W Kan, C C Lin, et al.
Annals of Internal Medicine|June 1, 1983
Alpha-thalassemia in Ashkenazi JewsG B Sancar, D B Rausher, R M Baine, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Clinical Chemistry|July 1, 1981
Evaluation of a commercial kit for microchromatographic quantitation of hemoglobin A2 in the presence of hemoglobin SR M Baine, H G Brown
Blood|May 1, 1981
Cultured erythroid cells as a model for Hb regulation: ability of cultured cells to synthesize Hb lepore and HbA2 and to maintain balanced globin synthesisR M Baine, J M Benson
Hemoglobin|January 1, 1979
HB G Waimanalo (alpha 64 Asp replaced by Asn) in a child with homozygous beta-thalassemiaR M Baine, J M Wright, R W Wilkinson
Hemoglobin|January 1, 1978
Hemoglobin J Rovigo (alpha53 Ala replaced by Asp) in association with beta-thalassemiaW F Moo-Penn, D L Jue, R M Baine
Clinical Chemistry|December 1, 1978
Microchromatographic methods for hemoglobin A2 quantitation comparedE M Brosious, J M Wright, R M Baine, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1976
Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain lociR M Baine, D L Rucknagel, P A Dublin, et al.
Hemoglobin|January 1, 1980
Biosynthetic evidence for instability of HB M SaskatoonR M Baine, J M Wright, M H Johnson, et al.
Progress in Clinical and Biological Research|January 1, 1978
Polymorphism in the number of hemoglobin alpha-chain loci and mechanisms governing the balance of chain synthesisD L Rucknagel, R M Baine, S M Hanash, et al.
The Journal of Clinical Investigation|August 1, 1983
Hemolytic disease of the newborn caused by a new deletion of the entire beta-globin clusterM Pirastu, Y W Kan, C C Lin, et al.
Annals of Internal Medicine|June 1, 1983
Alpha-thalassemia in Ashkenazi JewsG B Sancar, D B Rausher, R M Baine, et al.
Pageof 2