The term meaning situated nearest the midline or beginning of a body structure is proximal. Proximal is a medical term frequently used to mention to the distance of a body part such as shoulder, elbow, wrist, hand, fingers etc. in respects to its contiguity from the center of the body, normally the torso. In most circumstances, torso as the center point and the arms and legs as connections that prolong from the center. The further away an attachment or body part is from the center shoulder, elbow, wrist, hand, fingers the more distal it is and the closer the body part is to the center the more proximal it is. Therefore, when looking at the center of the human body, the shoulder is proximal in closer proximity to the torso when related to the elbow which is further away.
Embryonic stem cells have the potential to produce regenerated tissues, such as skin. They could provide means of healing diseases such as type 1 diabetes where a particular cell has been lost or is malfunctioning.
Answer:
D. the 23rd pair of chromosomes
Explanation:
Humans have a total of 23 pairs of chromosomes. Out of a total of 23 pairs, 22 pairs are autosomes. Autosomes are the chromosomes that carry the genes for all the genetic traits but are not involved in the sex determination of the individuals.
The 23rd pair of chromosomes in humans is of sex chromosomes as these chromosomes carry the genes to regulate the gender of the individuals. A human female has two copies of the X chromosome as sex chromosomes while human males have one X and one Y chromosome as their sex chromosomes. The Y chromosome carries "SRY" gene that codes for testes determining factor and regulates the development of testes in the embryo.
Complete question:
Imagine that a newly discovered, recessively inherited disease is expressed only in individuals with type O blood, although the disease and blood group are independently inherited.
A normal man with type A blood and a normal woman with type B blood have already had one child with the disease. The woman is now pregnant for a second time.
Assuming that both parents are heterozygous for the gene that causes the disease, what is the probability that the second child will also have the disease? Express your answer as a fraction using the slash symbol and no spaces (for example, 1/2).
Answer:
The probability that the second child will also have the disease is 1/16.
Explanation:
<u>Available data:</u>
- Two genes independently inherited: one for blood type, the other for disease
- Man with type A blood x Woman with type B blood
- Both parents are heterozygous for the gene that causes the disease; Dd
If the man has A blood, and the woman has B blood, and they already have an affected child, this means that they must be heterozygous for blood type too.
Cross:
Parentals) AiDd x BiDd
Gametes) AD Ad iD id BD Bd iD id
Punnett square) AD Ad iD id
BD ABDD ABDd BiDD BiDd
Bd ABDd ABdd BiDd Bidd
iD AiDD AiDd iiDD iiDd
id AiDd Aidd iiDd iidd
F1) <u>Genotype</u>:
1/16 ABDD
2/16 ABDd
1/16 ABdd
1/16 AiDD
1/16 BiDD
2/16 AiDd
2/16 BiDd
1/16 Aidd
1/16 Bidd
1/16 iiDD
2/16 iiDd
1/16 iidd
<u>Phenotype:</u>
3/16 A/B normal
4/16 A normal
4/16 B normal
3/16 0 normal
1/16 0 affected by the disease.
