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Molecular and cellular pathogenesis of hemoglobin SC disease.

Solution and cell studies were performed to ascertain why individuals with hemoglobin (Hb) SC have disease whereas those with Hb AS do not. The polymerization of deoxygenated mixtures containing sickle cell Hb (Hb S; alpha 2 beta 2(6)Glu leads to Val) and Hb C (alpha 2 beta 2(6)Glu leads to Lys) was...

Whakaahuatanga katoa

I tiakina i:
Ngā taipitopito rārangi puna kōrero
I whakaputaina i:Proc Natl Acad Sci U S A
Ngā kaituhi matua: Bunn, H F, Noguchi, C T, Hofrichter, J, Schechter, G P, Schechter, A N, Eaton, W A
Hōputu: Artigo
Reo:Inglês
I whakaputaina: National Academy of Sciences 1982
Ngā marau:
Urunga tuihono:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC347373/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6961429/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.23.7527
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