Answer:
2) glycogen...................
Answer:Una célula pasa por cuatro etapas a lo largo de su vida, que son: el nacimiento, el crecimiento, la diferenciación y la reproducción o muerte celular.
El proceso por el cual nace una célula a partir de otra preexistente se denomina división celular. El mecanismo que da origen a un nuevo individuo, en organismos unicelulares, es decir, organismos formados por una sola célula, se produce para aumentar el tamaño de su población, mientras que en organismos pluricelulares, este proceso funciona para aumentar el número de células y el reemplazo de células que se encuentren dañadas o muertas.
El ciclo celular se define como el conjunto de transformaciones que sufren las células para generar dos células hijas.
Este ciclo está formado por tres fases: la interfase, la mitosis y la ciclo
Answer:
I am assuming that the mutant cells have mutated beta galactosidase activity hence the relative levels of enzymatic activity would be reduced.
Proteins are apart of this group
Answer: The correct answer to the question is option C
BECAUSE YOU HAVE HAD ONE CHILD WITH TAY-SACHS,YOU MUST EACH CARRY THE ALLELE.ANY CHILD YOU HAVE HAS A 25% CHANCE OF HAVING THE DISEASE.
Explanation: Tay- Sachs is a rare disorder that is inherited,it is characterised by a progressive destruction of the nerves of the brain and spinal cord.its onset is from around 6months of life to around 4-5years of age when the child affected eventually dies.
A Child that have Tay-Sachs experiences problem with coordination,muscle contraction, must stiffness and weakness.there is also difficulty is speaking, swallowing, wasting(uncontrolled weightloss), hearing loss,seizure, and vision loss.
Since the parents of the child in the question claims they don't have Tay- Sachs and no one in the family has it but they came down with a child having Tay-Sachs and one of the major factors to Tay-Sachs as stated above is heredity,the main point to counsel the couples on is that because they have had one child with Tay-Sachs,they most each carry the allele which is obviously recessive so any child they had have has 25% chance of having the disease.
