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 Masala

Showing results (51-60 of 63) with videos related to

Pageof 7
Sort By:
Pathologica|March 1, 1975
[Research on the structure and biological properties of the nuclear DNA of Galliera sarcoma. 1. Chromatography of hydroxyapatite of native and heat denaturated DNA]G Ivaldi, F Vargiu, G M Cherchi, et al.
Hemoglobin|September 26, 2001
Hb Tigraye [beta79(EF3)Asp --> His] in a Caucasian family from SardiniaP Pistidda, L Cherchi, M Corda, et al.
Biochemical Genetics|October 1, 1986
DNA polymorphisms in North Sardinian newborns and their linkage with abnormal gamma globin gene arrangements and with beta (0) -thalassemiaY Hattori, F Kutlar, S S Chen, et al.
American Journal of Hematology|August 1, 1995
Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemiaP Pistidda, L Frogheri, L Oggiano, et al.
The Journal of Biological Chemistry|July 15, 1994
Functional alterations in adult and fetal hemoglobin Sassari Asp-alpha 126(H9)-->His. The role of alpha 1 alpha 2 contactM T Sanna, B Giardina, R Scatena, et al.
Hemoglobin|January 1, 1988
Biochemical and molecular aspects of beta-thalassemia types in northern SardiniaB Masala, L Manca, D Gallisai, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Hemoglobin|January 1, 1987
Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern SardiniaB Masala, L Manca, A Stangoni, et al.
Hemoglobin|January 1, 1981
Hematological and biosynthetic features of beta 0-thalassemia with an associated alpha-thalassemia heterozygosity in SardiniaM Longinotti, B Masala, M Tidore, et al.
Hemoglobin|January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newbornsY J Fei, F Kutlar, H F Harris, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Pathologica|March 1, 1975
[Research on the structure and biological properties of the nuclear DNA of Galliera sarcoma. 1. Chromatography of hydroxyapatite of native and heat denaturated DNA]G Ivaldi, F Vargiu, G M Cherchi, et al.
Hemoglobin|September 26, 2001
Hb Tigraye [beta79(EF3)Asp --> His] in a Caucasian family from SardiniaP Pistidda, L Cherchi, M Corda, et al.
Biochemical Genetics|October 1, 1986
DNA polymorphisms in North Sardinian newborns and their linkage with abnormal gamma globin gene arrangements and with beta (0) -thalassemiaY Hattori, F Kutlar, S S Chen, et al.
American Journal of Hematology|August 1, 1995
Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemiaP Pistidda, L Frogheri, L Oggiano, et al.
The Journal of Biological Chemistry|July 15, 1994
Functional alterations in adult and fetal hemoglobin Sassari Asp-alpha 126(H9)-->His. The role of alpha 1 alpha 2 contactM T Sanna, B Giardina, R Scatena, et al.
Hemoglobin|January 1, 1988
Biochemical and molecular aspects of beta-thalassemia types in northern SardiniaB Masala, L Manca, D Gallisai, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Hemoglobin|January 1, 1987
Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern SardiniaB Masala, L Manca, A Stangoni, et al.
Hemoglobin|January 1, 1981
Hematological and biosynthetic features of beta 0-thalassemia with an associated alpha-thalassemia heterozygosity in SardiniaM Longinotti, B Masala, M Tidore, et al.
Hemoglobin|January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newbornsY J Fei, F Kutlar, H F Harris, et al.
Pageof 7