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3 years ago

PLSSSSS ANSWER LOTS OF POINTS AND BRAINLYEST

Biology

2 answers:

zheka24 [161]3 years ago

5 0

Answer:

the first answer I believe but I could be wrong

Musya8 [376]3 years ago

3 0

Answer: It is unicellular, does not have a nucleus, and is missing most organelles.

Explanation:

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WHAT IS HOMESTASIS???? SOMETHING I CAN UNDERSTAND PLEASE!

finlep [7]

Explanation:

Homeostasis, from the Greek words for "same" and "steady," refers to any process that living things use to actively maintain fairly stable conditions necessary for survival. The term was coined in 1930 by the physician Walter Cannon.

Examples include thermoregulation, blood glucose regulation, baroreflex in blood pressure, calcium homeostasis, potassium homeostasis, and osmoregulation.

PROCESS OF HOMEOSTASIS IN THE HUMAN BODY

Homeostasis refers to the body's ability to maintain a stable internal environment (regulating hormones, body temp., water balance, etc.). ... As the body works to maintain homeostasis, any significant deviation from the normal range will be resisted and homeostasis restored through a process called a feedback loop.

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3 years ago

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What does NADP stand for and what does it do?

Firlakuza [10]

NationalSozialistische Deutsche ArbeiterPartei (National Socialist German Workers’ Party)

4 0

3 years ago

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What is Cell wall!?

Sholpan [36]

Explanation:

protective, semi-permeable outer layer of a plant cell
to give the cell strength and structure, and to filter molecules that pass in and out of the cell

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3 years ago

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A nectar-eating bird has a slightly more curved beak than average for its species. This allows the bird to more easily access ne

Verdich [7]

C.

Every change in a species is coded within the DNA. But the bird had lost a toe an accident. So the toe-loosing-option isn't true because not every bird looses his toe.

(Example: If a women gets bitten by a snake on the arm and gets the arm removed from her body and then in a year or so has a baby with her new husband. The baby won't be born with one arm because his/her mother lost her arm.)

6 0

3 years ago

Each of the four pedigrees that follow represents a human family within which a genetic disease is segregating. Affected individ

Ne4ueva [31]

Answer:

The following four traits are -:

Pedigree 1 - A recessive trait (autosomal recessive) is expressed by pedigree 1.
Pedigree 2- Recessive inheritance is defined by Pedigree 2.
Pedigree 3 - The inheritance of the dominant trait (autosomal dominant) is illustrated by Pedigree 3.
Pedigree 4- An X-like dominant trait is expressed by Pedigree 4.

Explanation:

Explaination of each pedigree chart-

Pedigree 1 demonstrates the recessive trait since their children have been affected by two unaffected individuals. If the characteristics were X-linked, in order to have an affected daughter, I-1 would have to be affected. $X^A$ In this, both parents are autosomal recessive trait carriers, so the child will be affected by a 1/4 (aa)
Recessive inheritance is defined by Pedigree 2. This is X-related inheritance as autosomal recessive inheritance has already been accounted for in part 1. This inference is confirmed by evidence showing that the father (I-1) is unaffected and that only the sons exhibit the characteristic in generation II, suggesting that the mother must be the carrier. The individual I-2 is a carrier for this X-linked trait. A typical Xa chromosome is attached to the unaffected father (I-1), so the chance of carrier II-5 is 1/2. Probability of an affected son = 1/2 (probability II-5 is a carrier) x 1/2 (probability II -5 contributes ( $X^A$ ) x 1/2 (probability of Y from father II-6) = 1/8. An affected daughter's likelihood is 0 because a typical $X^A$ must be contributed by II-6.
The inheritance of the dominant trait is demonstrated by Pedigree 3 because affected children still have affected parents (remember that all four diseases are rare). The trait must be autosomal dominant because it is passed down to the son by the affected father. There is a 1/2 risk that the heterozygous mother (II-5) would pass on mutant alleles to a child of either sex for an autosomal dominant feature.
Pedigree 4 is an X-linked dominant function characterized by the transmission to all of his daughters from the affected father but none of his son. On the mutant X chromosome, the father (I-1) passes on to all his daughters and none of his sons. As seen by his normal phenotype, II-6 therefore does not bear the mutation. An affected child's likelihood is 0.

In the question the pedigree chart was missing ,hence it is given below.

7 0

3 years ago