Website Search
ID 15708
petri dish, nerve, red blood cells
Description:
Keywords:
red blood cells,petri dish,nerve
This work by Cold Spring Harbor Laboratory is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.Related content:
- 1715. Human (Homo sapiens) Cell Cutures
- When model organisms cannot provide the information needed to answer a particular research question, biologists can turn to cultured human cells.
- SOURCE: G2C
- 15967. What is sickle cell?
- Mutations in the HBB gene on chromosome 11 can cause sickle cell.
- SOURCE: DNAi
- 15968. What causes sickle cell?
- Mutations in the HBB gene on chromosome 11 can cause sickle cell.
- SOURCE: DNAi
- 548. Model Center
- Model organisms share with humans many key biochemical and physiological functions that have been conserved (maintained) by evolution.
- SOURCE: G2C
- 15907. Beta-thalassemia
- The HBB gene encodes an important blood protein called beta globin.
- SOURCE: DNAi
- 15498. Hemoglobin and sickle cell anemia, 3D animation with no audio
- This animation shows hemoglobin proteins of a person with sickle cell anemia.
- SOURCE: DNAi
- 15532. Sickle cell anemia, 3D animation with narration
- Sickle cell anemia is a genetic disease that affects hemoglobin, the oxygen transport molecule in the blood.
- SOURCE: DNAi
- 16625. Problem 28: Some types of mutations are automatically repaired.
- Learn how the cause of Xeroderma pigmentosum is caused by a defect in a DNA repair system.
- SOURCE: DNAFTB
- 15561. Katreece, sickle cell patient
- Katreece (here at right) has sickle cell anemia. The causes of sickle cell have been known since the 1940s.
- SOURCE: DNAi
- 15936. What is beta-thalassemia?
- The HBB gene encodes an important blood protein called beta globin. A person with beta-thalassemia carries a mutation in both copies of the HBB gene, completely halting production of the beta globin protein.
- SOURCE: DNAi
