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J B Wilson

Showing results (301-310 of 363) with videos related to

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Hemoglobin|January 1, 1984
The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatographyG V Sciarratta, G Ivaldi, G L Molaro, et al.
American Journal of Hematology|January 1, 1994
Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia traitW B Qin, E Baysal, K F Wong, 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|January 1, 1992
A Canadian family with Hb Wayne; characterization by HPLC and DNA sequencingM L Salkie, T Higgins, D M Morrison, et al.
Biochimica Et Biophysica Acta|November 10, 1988
Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140V B Jogessar, K Westermeyer, B B Webber, et al.
Hemoglobin|January 1, 1976
Hb-Alberta or alpha2beta2 (101(G3) Glu replaced by Gly), a new high-oxygen-affinity hemoglobin variant causing erythrocytosisM J Mant, M L Salkie, N Cope, et al.
Hemoglobin|September 1, 1994
Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp)W B Qin, D D Pobedimskaya, T P Molchanova, et al.
British Journal of Haematology|May 1, 1989
Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia majorK G Yang, F Kutlar, E George, et al.
Hemoglobin|January 1, 1982
Hemoglobin Queens (alpha 34 (B15) Leu replaced by Arg) found in two Chinese familiesY T Zeng, S Z Huang, Y K Yen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 29, 1998
ELISA detection of restriction site polymorphisms in the pig ryanodine receptor locusG E Truett, J A Walker, J B Wilson, et al.
Pageof 37

Showing results (301-310 of 363) with videos related to

Sort By:
Pageof 37
Hemoglobin|January 1, 1984
The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatographyG V Sciarratta, G Ivaldi, G L Molaro, et al.
American Journal of Hematology|January 1, 1994
Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia traitW B Qin, E Baysal, K F Wong, 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|January 1, 1992
A Canadian family with Hb Wayne; characterization by HPLC and DNA sequencingM L Salkie, T Higgins, D M Morrison, et al.
Biochimica Et Biophysica Acta|November 10, 1988
Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140V B Jogessar, K Westermeyer, B B Webber, et al.
Hemoglobin|January 1, 1976
Hb-Alberta or alpha2beta2 (101(G3) Glu replaced by Gly), a new high-oxygen-affinity hemoglobin variant causing erythrocytosisM J Mant, M L Salkie, N Cope, et al.
Hemoglobin|September 1, 1994
Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp)W B Qin, D D Pobedimskaya, T P Molchanova, et al.
British Journal of Haematology|May 1, 1989
Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia majorK G Yang, F Kutlar, E George, et al.
Hemoglobin|January 1, 1982
Hemoglobin Queens (alpha 34 (B15) Leu replaced by Arg) found in two Chinese familiesY T Zeng, S Z Huang, Y K Yen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 29, 1998
ELISA detection of restriction site polymorphisms in the pig ryanodine receptor locusG E Truett, J A Walker, J B Wilson, et al.
Pageof 37