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  2. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    Examples of this type of disorder are albinism, medium-chain acyl-CoA dehydrogenase deficiency, cystic fibrosis, sickle cell disease, Tay–Sachs disease, Niemann–Pick disease, spinal muscular atrophy, and Roberts syndrome. Certain other phenotypes, such as wet versus dry earwax, are also determined in an autosomal recessive fashion.

  3. Human variability - Wikipedia

    en.wikipedia.org/wiki/Human_variability

    Examples of human phenotypic variability: people with different levels of skin colors, a normal distribution of IQ scores, the tallest recorded man in history - Robert Wadlow - with his father. Human variability, or human variation, is the range of possible values for any characteristic, physical or mental, of human beings.

  4. Restriction fragment length polymorphism - Wikipedia

    en.wikipedia.org/wiki/Restriction_fragment...

    For example, the standard protocols for DNA fingerprinting involve PCR analysis of panels of more than a dozen VNTRs. RFLP is still used in marker-assisted selection. Terminal restriction fragment length polymorphism (TRFLP or sometimes T-RFLP) is a technique initially developed for characterizing bacterial communities in mixed-species samples.

  5. Chronic condition - Wikipedia

    en.wikipedia.org/wiki/Chronic_condition

    Obesity and body fat distribution for example contribute and are risk factors for many chronic diseases such as diabetes, heart, and kidney disease. [33] Other epidemiological factors, such as social, socioeconomic, and environment do not have a straightforward cause and effect relationship with chronic disease diagnosis.

  6. Globin - Wikipedia

    en.wikipedia.org/wiki/Globin

    The eight helices of the globin fold core share significant nonlocal structure, unlike other structural motifs in which amino acids close to each other in primary sequence are also close in space.

  7. Beta thalassemia - Wikipedia

    en.wikipedia.org/wiki/Beta_thalassemia

    Scientists at Weill Cornell Medical College have developed a gene therapy strategy that could feasibly treat both beta-thalassemia and sickle cell disease. The technology is based on delivery of a lentiviral vector carrying both the human β-globin gene and an ankyrin insulator to improve gene transcription and translation, and boost levels of ...

  8. Hemoglobin variants - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_variants

    The hemoglobin production stops at birth and decreases to adult levels by the age of one or two. The levels can be normal to increased in beta thalassemia. Hemoglobin F frequently increases in individuals with sickle cell anemia and sickle cell-beta thalassemia. Individuals with sickle cell and increase of Hb F have a milder case of the disease.

  9. Anisocytosis - Wikipedia

    en.wikipedia.org/wiki/Anisocytosis

    Anisocytosis is a medical term meaning that a patient's red blood cells are of unequal size. This is commonly found in anemia and other blood conditions. False diagnostic flagging may be triggered on a complete blood count by an elevated WBC count, agglutinated RBCs, RBC fragments, giant platelets or platelet clumps due to anisocytosis.