Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Clayton Natta"'
Autor:
Clayton Natta, Ingrid M. Outschoorn
Publikováno v:
Microbiology and Immunology. 36:977-982
Immunoglobulin levels were measured in serum samples of 12 black adult non-smoking asthmatic patients, 11 females and 1 male, and compared with 15 age-, sex-matched normal controls. Their total IgG, IgA and IgM levels were within the normal range. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f1adf05278e2fe9cc54326c7e683041
https://doi.org/10.1111/j.1348-0421.1992.tb02101.x
https://doi.org/10.1111/j.1348-0421.1992.tb02101.x
Publikováno v:
Annals of the New York Academy of Sciences. 585:505-509
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e79dc307e8cb34708634afb7c6a79ba
https://doi.org/10.1111/j.1749-6632.1990.tb28089.x
https://doi.org/10.1111/j.1749-6632.1990.tb28089.x
Publikováno v:
Annals of the New York Academy of Sciences. 669:365-367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1174dea549802e7f03aeb3a3de50ecba
https://doi.org/10.1111/j.1749-6632.1992.tb17125.x
https://doi.org/10.1111/j.1749-6632.1992.tb17125.x
Autor:
Clayton Natta, Leon T. Kremzner
Publikováno v:
AGE. 11:11-14
Aging of human red cells (RBC) appears to occur as a function of the age of the subject and time which is spent by the erythrocyte in the circulation. In SCA, there is a decrease in the time RBCs circulate. The polyamines, putrescine, spermidine and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3d7dfbcd8e216138974bd03c464dd95
https://doi.org/10.1007/bf02431759
https://doi.org/10.1007/bf02431759
Publikováno v:
Blood. 47:899-907
The alpha thalassemias are associated with a decrease in alpha chain synthesis. Hemoglobin H (HbH) disease is a moderately severe form of alpha thalassemia characterized by the production of 5%--20% of HbH, while alpha thalassemia trait is a milder f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e80d40fe384b915b048d7d68ce3c13
https://doi.org/10.1182/blood.v47.6.899.899
https://doi.org/10.1182/blood.v47.6.899.899
Autor:
Koji Nakanishi, Joseph I. Okogun, Clayton Natta, V. U. Enyenihi, D.E.U. Ekong, Valeria Balogh-Nair
Publikováno v:
Nature. 258:743-746
RECENT efforts to develop therapeutic agents for the treatment of sickle cell disease have led to the discovery of several antisickling agents1. We now report a new such agent, 3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-butyric acid (DBA) (Compound 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88264efa86a718f577bb515f5bb33bfe
https://doi.org/10.1038/258743a0
https://doi.org/10.1038/258743a0
Publikováno v:
Biochemical Medicine. 23:144-149
Sickle cell anemia, a chronic hemolytic disease characterized by severe pain and premature death, affects to varying degrees 1% of the world's black population. Although a number of biochemical alterations have previously been associated with this an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d157af0b9f11e8c96be72fdf1dc7418c
https://doi.org/10.1016/0006-2944(80)90065-4
https://doi.org/10.1016/0006-2944(80)90065-4
Autor:
Sol Spiegelman, Paul A. Marks, Clayton Natta, D. L. Kacian, Francesco Ramirez, George M. Maniatis, Arthur Bank, Roberto Gambino
Publikováno v:
Annals of the New York Academy of Sciences. 241:247-252
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98d75a2a7e593d9a3ea10f379f550e5b
https://doi.org/10.1111/j.1749-6632.1974.tb21883.x
https://doi.org/10.1111/j.1749-6632.1974.tb21883.x
Publikováno v:
Hemoglobin. 2:463-468
During the course o f screening for abnormal hemoglobins in the City of New York, an abnormal hemoglobin with fast electrophoretic mobility was discovered in an asymptomatic 16-year-old Black female high school student. Structural studies, performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53a60407d3d1a61b0e6de76c66e881a8
https://doi.org/10.3109/03630267809007082
https://doi.org/10.3109/03630267809007082
Publikováno v:
Journal of Clinical Investigation. 54:805-809
Sickle cell anemia (SS) is associated with abnormalities of the red cell membrane and decreased red cell deformability. The present study assesses globin chain binding to stroma in SS, sickle cell trait (AS), and nonsickling (AA) cells. The results i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d0276d3071cbbca6b7df9d277ef5389
https://doi.org/10.1172/jci107820
https://doi.org/10.1172/jci107820