15 biology your welcome

which describes the cells of a wilted plant?

the central vacuoles contain little water.

in general, what plant structure would have the most chloroplasts?

leaves

what causes rough endoplasmic reticulum to look “rough” under a microscope?

rough er has ribosomes attached to it.

which is the end result of photosynthesis?

the production of glucose

which describes a function of plasmodesmata?

they allow molecules to move between cells.

what chemical substance is used to power cellular activities?

atp

which cytoskeleton fibers are found in cilia and flagella?

microtubules

actin makes up cytoskeleton fibers called

microfilaments

what organelle controls information in the cell?

nucleus

what is a plant cell’s source of energy for photosynthesis?

sunlight

the glucose-making part of photosynthesis takes place in the

stroma

ribosomes are made up of

rna and proteins

what feature in a cell contains the dna sequence to make a specific protein?

gene

ribosomes are produced by the

nucleolus

what is the nucleolus?

a ball of fibers inside the nucleus

chemical because it warmed up which involves temperature and it bubbled which includes changing

mark me brainiest

the supermassive black hole is in the middle of the galaxy.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.

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