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

B Tatsis

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Blood|June 1, 1977
Circulating antibody to transcobalamin II causing retention of vitamin B12 in the bloodR Carmel, B Tatsis, L Baril
New York State Journal of Medicine|December 1, 1979
Hematuria and hemoglobin C traitG L Ohri, F Rosner, B Tatsis
Blood|May 1, 1976
Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin SB Tatsis, K Sofroniadou, C I Stergiopoulos
JAMA|March 13, 1972
Screening for sickle cell disease and related disordersF Rosner, B Tatsis, C F Calas
New York State Journal of Medicine|October 1, 1982
A decade of experience with a sickle cell programF Rosner, L St Clair, G Karayalcin, et al.
Journal of Immunological Methods|January 1, 1981
Toward a system for detecting somatic-cell mutations. V. Preparation of fluorescent antibodies to hemoglobin hasharon, a human alpha-chain variantP E Nute, T Papayannopoulou, B Tatsis, et al.
Nature|May 3, 1984
A haemoglobin switching activity modulates hereditary persistence of fetal haemoglobinT Papayannopoulou, B Tatsis, S Kurachi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1980
Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletionsG B Sancar, B Tatsis, M M Cedeno, et al.
American Journal of Human Genetics|July 1, 1983
Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variantM Farquhar, R Gelinas, B Tatsis, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Blood|June 1, 1977
Circulating antibody to transcobalamin II causing retention of vitamin B12 in the bloodR Carmel, B Tatsis, L Baril
New York State Journal of Medicine|December 1, 1979
Hematuria and hemoglobin C traitG L Ohri, F Rosner, B Tatsis
Blood|May 1, 1976
Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin SB Tatsis, K Sofroniadou, C I Stergiopoulos
JAMA|March 13, 1972
Screening for sickle cell disease and related disordersF Rosner, B Tatsis, C F Calas
New York State Journal of Medicine|October 1, 1982
A decade of experience with a sickle cell programF Rosner, L St Clair, G Karayalcin, et al.
Journal of Immunological Methods|January 1, 1981
Toward a system for detecting somatic-cell mutations. V. Preparation of fluorescent antibodies to hemoglobin hasharon, a human alpha-chain variantP E Nute, T Papayannopoulou, B Tatsis, et al.
Nature|May 3, 1984
A haemoglobin switching activity modulates hereditary persistence of fetal haemoglobinT Papayannopoulou, B Tatsis, S Kurachi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1980
Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletionsG B Sancar, B Tatsis, M M Cedeno, et al.
American Journal of Human Genetics|July 1, 1983
Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variantM Farquhar, R Gelinas, B Tatsis, et al.
Pageof 1