In addition to atp, what are the products of glycolysis?.

OMG PLEASE HELP QUICK!!!

Anton [14]

Answer:

Maybe ores

Explanation:

8 0

3 years ago

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True or false. The absence of a trait cannot be used as a synapomorphy in phylogenetic analysis

kolbaska11 [484]

Answer:

False

Explanation:

Phylogenetic analysis is a means of establishing evolutionary relationships.

Synapomorphy is a shared ("syn") character that is different from the form found in an ancestor that distinguishes a clade (monophyletic group)from other organisms

The absence of a trait can be used as a synapomorphy in phylogenetic analysis. For example, the loss of a trait, such as the loss of legs in snakes, can be a valuable synapomorphy for a clade.

4 0

3 years ago

Help Nucleic acid Certain protein Cell membranes Certain carbohydrates

viktelen [127]

Certain Protiens, amino acids form protiens

8 0

3 years ago

What is the starfish experiment?

vitfil [10]

Answer:

When starfish were removed from their environment, the species richness of that area went down. This was because the starfish ate the mussels, and when the starfish were removed, the mussels became abundant and preyed on many of the other species.

This experiment showed that the starfish were a keystone species. A keystone species is a species that has a low biomass but a large impact on the community they are living in.

6 0

3 years ago

the couple is also concerned about their child inheriting hemophilia, another rare disease, which is x-linked. natalie’s brother

IgorC [24]

Hemophilia is a recessive X-linked condition and is inherited from parents. . The probability that Natalie and Daniel’s first child has hemophilia is 1/4, not 1/8. The statement is false.

<h3>What is an X-linked gene?</h3>

When talking about sex-linked genes, we refer to all those genes located in one of the sex-chromosomes and not in the somatic ones.

X-linked genes are the genes located specifically in the X sex chromosome.

Traits coded by these genes are inherited. This is, X-linked genes are transmitted from parents to children through generations.

According to this, X-linked genetic disorders will be inherited as well.

Men have a high probability of being affected since they only have one copy of the X chromosome.

In women, the effect of the mutation might be musk in heterozygous state if the mutation is recessive.

Hemophilia is a recessive X-linked disorder, which means it is coded by the recessive allele.

X+ ⇒ X chrosomosome with Dominant allele

X- ⇒ X chrosomosome with Recessive allele

Genotype Phenotype

X+X+ Healthy woman

X+X- Healthy carrier woman

X-X- Hemophilic woman

X+Y Healthy man

X-Y Hemophilic man

Let us make a pedigree of these families,

Natalie's family:

Mother healthy carrier X+X-

Father healthy X+Y

Brother hemophilic X-Y

Natalie Healthy X+X- or X+X+

Natalie has 1/2 chances of being carrier X+X- and 1/2 of being X+X+.

Daniel's family:

Mother healthy carrier X+X-

Father hemophilic X-Y

Sister hemophilic X-X-

Daniel Healthy X+Y

He has 1/2 chances of being healthy X+Y and 1/2 of being affected X-Y.

According to the product probability rule, if events A and B are independent from each other, the probability of occurrence of both events together is

P(A∩B) = P(A) x P(B)

In this case,

event A is Daniel being affected ⇒ 1/2
event B is Natalie being carrier ⇒ 1/2

P(A∩B) = P(A) x P(B) = 1/2 x 1/2 = 1/4

The probability that Natalie and Daniel’s first child has hemophilia is 1/4, not 1/8. The statement is false.

You can learn more about X-linked genes at

brainly.com/question/12420228

brainly.com/question/14704182

brainly.com/question/1387724

#SPJ1

7 0

1 year ago