Answer:
1. Verdadero
2. Falso
3. Falso
4. Falso
5. Verdadero
Explanation:
Los seres humanos, como así también la mayoría de los mamíferos, poseen dos cromosomas sexuales: un cromosoma X y un cromosoma Y. Las hembras poseen 2 cromosomas X (un cromosoma X es heredado de la madre y el otro cromosoma X es heredado del padre); mientras que los hombres tienen un cromosoma X y un cromosoma Y (el cromosoma X es heredado de la madre, mientras que el cromosoma Y es heredado del padre). La hemofilia es una enfermedad recesiva monogénica ligada al cromosoma X, la cual está caracterizada por cuadros hemorrágicos causados por el déficit parcial y/o total de factores de coagulación. Los hombres expresan el fenotipo recesivo con mayor frecuencia que las mujeres para aquellos genes que se encuentran en el cromosoma X y poseen un mecanismo de herencia recesivo, esto debido a que los hombres sólo poseen una copia del alelo ligado al X (lo que hace que el alelo recesivo se exprese con mayor frecuencia en el fenotipo). De este modo, los hombres manifiestan hemofilia con mayor frecuencia que las mujeres porque en mujeres el gen recesivo necesita la presencia de dos copias del alelo defectuoso recesivo para que se exprese en el fenotipo hemofílico (es decir, las mujeres heterocigotas son portadoras de un alelo defectuoso pero no expresan la condición en el fenotipo), mientras que en los hombres la presencia de un sólo alelo defectuoso localizado en su único cromosoma X es suficiente para la expresión del fenotipo recesivo. En hombres, los genes ligados al cromosoma X son siempre heredados de la madre (los hombres heredan del padre el cromosoma Y). Finalmente, la herencia de caracteres ligados al cromosoma Y es muy rara porque los genes localizados en la región diferencial del cromosoma Y son escasos y estos genes solamente pueden ser trasmitidos de padres a hijos varones (ya que se encuentran en el cromosoma Y).
<span>The major structure that supplies the cells with nutrients and removes their waste is the circulatory system. The circulatory system is composed of the heart, the blood vessels going from and back to the heart, and the blood that travels inside them. The blood vessels that carry nutrient and oxygen-rich blood to the cells are arteries. They become the thinner arterioles, and then the thinnest capillaries. With the exception of the pulmonary arteries, which carry non-oxygenated blood from the heart to the lungs, all arteries carry oxygenated blood. The capillaries disburse the nutrients and oxygen to the cells and pick up wastes and carbon dioxide, form into the thicker venules, then to form veins, which lead back to the heart (with the exception of the pulmonary veins, which carry oxygenated blood from the lungs to the heart). Veins also differ from arteries in that veins have valves to prevent blood from flowing backward.</span>
Answer:
The answer in B) The offspring have one allele that codes for red and one allele that codes for white.
Explanation:
Let's say that the red flower has Bb, and the white flower has bb. In a punnet square you'd get 50% being Bb and another 50% being bb. The allele bb would be pink.
I hope this helps!
Answer:
The correct answer is option C.
Explanation:
The human gastrointestinal microbiota or the gut microbiota or the gut flora refers to the microbes, which thrive in the digestive tracts of humans. The human gastrointestinal tract comprises the gathering of all the genomes of gut microbiota. It is the niche where the human microbiota is found.
The microbial composition of the gut microbiota differs across the digestive tract. In the small intestine and stomach, very small species of bacteria are found, while the colon comprises the densely populated microbial ecosystem. Of these over 99 percent of the bacteria found in the gut are anaerobes, as the space within the intestines is highly anaerobic.
These microbes are confined deep within the body where oxygen cannot reach as it is not supplied with the help of blood vessels. Thus, a highly anaerobic environment is witnessed deep within the intestinal regions.
In homo sapiens(humans), males are the heterogametic sex meaning their sex chromosomes are not the same(=XY) while females are homogametic(=XX).
Sex linked traits or x linked traits are traits whose genes are present on the X chromosome. So if there is a recessive mutation in those genes, males will express that recessive trait. Basically males express everything that’s on their X chromosome because they only have 1, but females have 2 which helps “hide” the mutation and to not express the particular recessive trait.
That is why sex linked traits are more evident in males in the population and an example of that would be colorblindness.
Hope this helps:)
