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AURORKA [14]
1 year ago
11

This graph shows three types of species based on the different patterns of survivorship.

Biology
2 answers:
nexus9112 [7]1 year ago
5 0

Answer: having few offspring

Masja [62]1 year ago
3 0

Answer: a having a high deathrate

Explanation:

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In this lab, you will figure out who was guilty of the classroom food mess by determining which macromolecules are present in th
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Answer: Which macromolecules from the mystery food sample will help you figure out who was guilty of making a mess in the classroom

Explanation:

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2 years ago
Which statement correctly describes the nuclear envelope of a eukaryotic cell? See Concept 6.3 (Page 102) View Available Hint(s)
netineya [11]

The correct answer is: The nuclear envelope is continuous with the endoplasmic reticulum

The nuclear envelope or nuclear membrane is composed of two phospholipid bilayers (outer and inner) that surround the nucleus in the eukaryotic cell. The space between the outer and inner membranes is called the perinuclear space. The nuclear envelop has nuclear pores that are responsible for the transport between nucleus and cytoplasm (e.g. transport of mRNA).

8 0
2 years ago
Suppose the following amino acid chain was created based on a student's transcription and translation: Tyr-Leu-Pro-Met In the ch
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Answer:

Error: The Methionine at the end of the chain

Explanation:

Hello! Let's solve this!

The start codon is AUG, this codon encodes Methionine. Therefore all proteins will start the amino acid sequence with Methionine.

In this case, the student placed the Methionine at the end of the chain, so that is the mistake. Methionine goes to the beginning of the chain.

7 0
2 years ago
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When Wendy was a baby, she was diagnosed with a gene-linked abnormality that left her unable to metabolize an important amino ac
Alex

<u>Phenylketonuria</u>

Explanation:

Phenylketonuria (PKU) is a type of a rare inherited metabolic disorder.  

Etiology: PKU results from excessive accumulation of the amino acid phenylalanine in the body. Normally, phenylalanine will be converted to tyrosine (forms neurotransmitters) by the action of the enzyme phenylalanine hydroxylase.

Among people with PKU, a defect in the PAH gene which codes to synthesize this enzyme occurs which leads to the absence of this enzyme. So the phenylalanine which is normally present in dietary protein is not metabolized and gets accumulated. This gene is inherited by the child only if both the parents are with the defective PAH gene.

Symptoms: Stunted growth, behaviroral disturbances, learning difficulties, seizures, tremors etc.

Treatment: Basic treatment is to follow a diet which limits dietary sources of phenylalanine. High protein foods like meat, egg should be avoided. Children can be given PKU formula to supplement their nutritional needs.

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2 years ago
Phosphatidylethanolamine has alternate pathways for synthesis. The reactions represent these pathways. Complete the reactions by
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Find the attachment for the answer.

Note: I have added the complete question in the attachment.

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2 years ago
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