Ads
related to: sickle cell anemia scholarly articles- Mechanism Of Action
Learn About The LYFGENIA
MOA & How It Works.
- Treatment Pathway
Get An Overview Of The Treatment
Steps With LYFGENIA.
- Support & Resources
Support For Your Patients During
Their Consideration & Treatment.
- FAQs
Get Answers To Questions
About Treatment With LYFGENIA.
- Request A Representative
Fill Out The Online Form To Be
Contacted About LYFGENIA.
- Safety Information
Review Information On Adverse
Reactions & Additional Safety Data.
- Mechanism Of Action
Search results
Results From The WOW.Com Content Network
Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] The most common type is known as sickle cell anemia. [2] It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2] This leads to a rigid, sickle -like shape under ...
Sickle Cell Anemia, a Molecular Disease" is a 1949 scientific paper by Linus Pauling, Harvey A. Itano, Seymour J. Singer and Ibert C. Wells that established sickle-cell anemia as a genetic disease in which affected individuals have a different form of the metalloprotein hemoglobin in their blood.
Roland Boyd Scott (April 18, 1909 – December 10, 2002) was an American researcher, pediatrician and authority on sickle cell disease. [1] Scott authored a key paper in 1948 describing the incidence of sickle cell in infants that eventually led to the establishment of routine screening for newborns. [1] He established the Howard University ...
In November 1949, Pauling, Harvey Itano, S. J. Singer and Ibert Wells published "Sickle Cell Anemia, a Molecular Disease" [64] in the journal Science. It was the first proof of a human disease being caused by an abnormal protein, and sickle cell anemia became the first disease understood at the
His contribution to clinical research includes genetic analysis of the TMPRSS6 gene in women with iron deficiency anemia; determining antigen levels in plasma and the genotypes of PAI-2 in pregnancy associated with homozygous sickle cell anemia; investigating genetic variants in the leptin gene linked to obesity; studying the effects of post ...
Hematology. Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous). Those who are heterozygous for the sickle cell allele produce both ...
Ad
related to: sickle cell anemia scholarly articles