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J B Wilson

Showing results (191-200 of 363) with videos related to

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Hemoglobin|January 1, 1985
Hb Volga or alpha 2 beta 2 27(B9)Ala----Asp in an Italian familyG V Sciarratta, G Ivaldi, G Sansone, et al.
Hemoglobin|January 1, 1990
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adultD Plaseska, L H Gu, J B Wilson, et al.
British Journal of Haematology|October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.
Hemoglobin|January 1, 1990
Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----AlaD Plaseska, P A de Alarcon, S McMillan, et al.
Hemoglobin|January 1, 1979
The structure of goat hemoglobins. V. A fourth beta chain variant (beta-D-Malta; 69 Asp is replaced by Gly) with decreased oxygen affinity and occurring at a high frequency in MaltaJ V Bannister, W H Bannister, J B Wilson, et al.
Biochimica Et Biophysica Acta|October 9, 1974
Hemoglobin St. Claude or alpha2-127(H10)Lys leads to Thr-beta2F Vella, P Galbraith, J B Wilson, et al.
Biochimica Et Biophysica Acta|October 5, 1982
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infantZ Yi-Tao, M E Headlee, J Henson, et al.
Hemoglobin|January 1, 1984
Hb Beograd-beta zero thalassemia in a Turkish family from YugoslaviaM Aksoy, A Kutlar, F Kutlar, et al.
Hemoglobin|January 1, 1992
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from TunisiaT P Molchanova, J B Wilson, L H Gu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1973
Hb-Genova ( 2 2 28(B10)Leu leads to Pro ); methods for detection and analysis of unstable hemoglobinsR N Wrightstone, J B Wilson, C A Reynolds, et al.
Pageof 37

Showing results (191-200 of 363) with videos related to

Sort By:
Pageof 37
Hemoglobin|January 1, 1985
Hb Volga or alpha 2 beta 2 27(B9)Ala----Asp in an Italian familyG V Sciarratta, G Ivaldi, G Sansone, et al.
Hemoglobin|January 1, 1990
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adultD Plaseska, L H Gu, J B Wilson, et al.
British Journal of Haematology|October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.
Hemoglobin|January 1, 1990
Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----AlaD Plaseska, P A de Alarcon, S McMillan, et al.
Hemoglobin|January 1, 1979
The structure of goat hemoglobins. V. A fourth beta chain variant (beta-D-Malta; 69 Asp is replaced by Gly) with decreased oxygen affinity and occurring at a high frequency in MaltaJ V Bannister, W H Bannister, J B Wilson, et al.
Biochimica Et Biophysica Acta|October 9, 1974
Hemoglobin St. Claude or alpha2-127(H10)Lys leads to Thr-beta2F Vella, P Galbraith, J B Wilson, et al.
Biochimica Et Biophysica Acta|October 5, 1982
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infantZ Yi-Tao, M E Headlee, J Henson, et al.
Hemoglobin|January 1, 1984
Hb Beograd-beta zero thalassemia in a Turkish family from YugoslaviaM Aksoy, A Kutlar, F Kutlar, et al.
Hemoglobin|January 1, 1992
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from TunisiaT P Molchanova, J B Wilson, L H Gu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1973
Hb-Genova ( 2 2 28(B10)Leu leads to Pro ); methods for detection and analysis of unstable hemoglobinsR N Wrightstone, J B Wilson, C A Reynolds, et al.
Pageof 37