Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J B Wilson

Showing results (281-290 of 363) with videos related to

Pageof 37
Sort By:
Hemoglobin|January 1, 1989
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1979
Hb P-Nilotic in association with beta0-thalassemia: cis-mutation of a hemoglobin betaA chain regulatory determinant?A Abu-Sin, A E Felice, M E Gravely, et al.
Hemoglobin|January 1, 1982
Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian maleG V Sciarratta, G Sansone, M Valbonesi, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1978
Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb RampaT H Huisman, M E Gravely, J Henson, et al.
Biochimica Et Biophysica Acta|January 31, 1984
Hb J-Singa (alpha-78 Asn leads to Asp), a newly discovered hemoglobin variant with the same amino acid substitution as one of the two present in Hb J-Singapore (alpha-78 Asn leads to, alpha-79 Ala leads to Gly)S C Wong, M A Ali, J R Pond, et al.
Hemoglobin|January 1, 1986
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black familyJ E Bowman, R Bloom, S S Chen, et al.
Hemoglobin|January 1, 1979
The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newbornT H Huisman, G D Efremov, A L Reese, et al.
Hemoglobin|January 1, 1992
A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----TyrT P Molchanova, J B Wilson, L H Gu, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
The Journal of Clinical Investigation|November 1, 1971
Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemiaM M Keeling, L L Ogden, R N Wrightstone, et al.
Pageof 37

Showing results (281-290 of 363) with videos related to

Sort By:
Pageof 37
Hemoglobin|January 1, 1989
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1979
Hb P-Nilotic in association with beta0-thalassemia: cis-mutation of a hemoglobin betaA chain regulatory determinant?A Abu-Sin, A E Felice, M E Gravely, et al.
Hemoglobin|January 1, 1982
Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian maleG V Sciarratta, G Sansone, M Valbonesi, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1978
Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb RampaT H Huisman, M E Gravely, J Henson, et al.
Biochimica Et Biophysica Acta|January 31, 1984
Hb J-Singa (alpha-78 Asn leads to Asp), a newly discovered hemoglobin variant with the same amino acid substitution as one of the two present in Hb J-Singapore (alpha-78 Asn leads to, alpha-79 Ala leads to Gly)S C Wong, M A Ali, J R Pond, et al.
Hemoglobin|January 1, 1986
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black familyJ E Bowman, R Bloom, S S Chen, et al.
Hemoglobin|January 1, 1979
The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newbornT H Huisman, G D Efremov, A L Reese, et al.
Hemoglobin|January 1, 1992
A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----TyrT P Molchanova, J B Wilson, L H Gu, et al.
Hemoglobin|January 1, 1982
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemiaA L Reese, C Altay, M E Headlee, et al.
The Journal of Clinical Investigation|November 1, 1971
Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemiaM M Keeling, L L Ogden, R N Wrightstone, et al.
Pageof 37