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  2. Genetic history of Africa - Wikipedia

    en.wikipedia.org/wiki/Genetic_history_of_Africa

    [110] [109] The ancestral sickle cell haplotype to modern haplotypes (e.g., Cameroon/Central African Republic and Benin/Senegal haplotypes) may have first arose in the ancestors of modern West Africans, bearing haplogroups E1b1a1-L485 and E1b1a1-U175 or their ancestral haplogroup E1b1a1-M4732. [96]

  3. Anthony Clifford Allison - Wikipedia

    en.wikipedia.org/wiki/Anthony_Clifford_Allison

    At the time it was a scientific puzzle that the disease was prevalent even though it killed people before they reached puberty, before they can have children to pass on the lethal gene. [4] He found that the prevalence of sickle-cell trait (heterozygous condition) among people inhabiting coastal areas was higher than 20%. [8]

  4. Betibeglogene autotemcel - Wikipedia

    en.wikipedia.org/wiki/Betibeglogene_autotemcel

    Betibeglogene autotemcel, sold under the brand name Zynteglo, is a gene therapy for the treatment for beta thalassemia. [1] [5] [2] It was developed by Bluebird Bio and was given breakthrough therapy designation by the US Food and Drug Administration in February 2015.

  5. Geography of Iowa - Wikipedia

    en.wikipedia.org/wiki/Geography_of_Iowa

    Simplified map of Iowa Bedrock formations of Iowa The geography of Iowa includes the study of bedrock, landforms, rivers, geology, paleontology and urbanisation of the U.S. state of Iowa . The state covers an area of 56,272.81 sq mi (145,746 km 2 ).

  6. Health in Sudan - Wikipedia

    en.wikipedia.org/wiki/Health_in_Sudan

    In Sudan, sickle cell disease was first reported in 1926 by Archibald. [23] The disease is considered one of the major types of anemia, especially in Western Sudan where the sickle cell gene is frequent [24] Sickle cell disease is the major haemoglobinopathy seen in Khartoum, the capital of Sudan. This may be attributed to the migration of ...

  7. Balancing selection - Wikipedia

    en.wikipedia.org/wiki/Balancing_selection

    A well-studied case is that of sickle cell anemia in humans, a hereditary disease that damages red blood cells. Sickle cell anemia is caused by the inheritance of an allele (HgbS) of the hemoglobin gene from both parents. In such individuals, the hemoglobin in red blood cells is extremely sensitive to oxygen deprivation, which results in ...

  8. BCL11A - Wikipedia

    en.wikipedia.org/wiki/BCL11A

    The corresponding Bcl11a mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated.

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