Answer this question properly​

Answer:

D

Explanation:

Answer: flax seed whole wheat tortillas.

1⁄2 cup low-fat refried beans.

1⁄4 cup low-fat cheddar cheese.

leaves lettuce.

1⁄ cup salsa.

1⁄4 cup fat free sour cream.

Pinto beans are added to tacos, burritos, and soups that are high in fiber.

The body is unable to digest fiber, which is a form of carbohydrate. While fiber cannot be converted into glucose, the sugar that results from the breakdown of most carbs, fiber travels through the body undigested.

The solubility, viscosity, and fermentability of dietary fibers, which have an impact on how they are metabolized by the body, can be used to classify them in general. Dietary fibers have a wide range of chemical compositions.

Fibre comes in two varieties: soluble and insoluble. Both are crucial for good health, digestion, and illness prevention. Thus, Pinto beans are added to tacos, burritos, and soups that are high in fiber.

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Answer:

for healthy living and long life

Cell: A cell is the structural and fundamental unit of life. The study of cells from its basic structure to the functions of every cell organelle is called Cell Biology.

Atom:  atom is the smallest component of an element, characterized by a sharing of the chemical properties of the element and a nucleus with neutrons, protons and electrons. The protons and the neutrons reside in the nucleus.

whats the difference between atom and cell?

function wise atoms take part in every chemical reaction while cells are responsible for the development and growth of living existences. Atoms do not have life. They do not need food, water, and they do not reproduce. Cells are alive. Cells consume food and water and can reproduce. Atoms construct molecules and Cells make tissues for organs.

Answer:

c. a duplication of the C4 gene

Explanation:

Schizophrenia is a disease that affects the brain, which is characterized by an imbalance of neurotransmitters and the presence of damaged brain tissues. In humans, the Complement component 4 (C4) protein is found at the neurons (i.e., cell bodies, dendrites and axons), which are the most common brain cells, and neuronal synapses. Moreover, gene duplication can increase gene expression when repressive mechanisms (e.g., DNA methylation at promoter sites) capable of silencing the expression of the duplicated gene are lacking. Recently, it has been discovered that a chromosome rearrangement associated with a tandem duplication of a genomic region that contains a C4 gene may contribute to schizophrenia risk by increasing the expression of this gene​. In this example, a, b and d options are associated with a decrease in expression of the C4 gene, either by decreasing its transcription (options a and d) or by posttranscriptional mechanisms (option c).

Answer:

Answer:

Starts process with a glucose molecule (Obtaining ATP begins with a breakdown of a glucose molecule (hence the name of glycose), and this is in common with the anaerobic process since this step does not require oxygen.)

Explanation:

#keep learning!!

Answer:

If your doing the test on edgen then the answers are A.)consists of three stages, B.)yields 36 ATP molecules and, E.)starts process with a glucose molecule

Explanation:

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Answer:

Oxygen is carried by blood to all the cells of the body in the form of haemoglobin.​

Explanation:

Oxygen is carried in the blood in two forms:

(1) dissolved in plasma and red blood cells water (about 2% of the total)

(2) reversibly bound to haemoglobin (about 98% of the total).

Haemoglobin is a protein in the red blood cells and carries oxygen around our bodies. At the same time, carbon dioxide that is dissolved in the blood comes out of the capillaries back into the air sacs, ready to be breathed out.

Answer:

The first bar increases in length as compared to the second bar.

Explanation:

The length of the bar of control cages in graph increases because the number of bees per colony increases while on the other hand, the length of the bar of the cage that is exposed to fungicides decreases because the bees are negatively affected from the application of fungicides. They act abnormal in behaviour and adversely affected the reproduction of bees that greatly affected its population.

Answer:

- When a neuron is stimulated and sodium channels open, the process of depolarization has begun.  

- Structures of the nervous system surrounding, but not part of the central nervous system are part of the peripheral nervous system

- Two consecutive neurons communicate at a synapse, where they physically come together.  

- Endorphins are a group of natural chemicals that reduce the perception of pain.  

- Supporting cells of the nervous system are collectively called neuroglia

- When potassium channels have been open long enough to go below resting membrane potential, hyperpolarization has occurred.

Explanation:

Neurons undergo depolarization in response to diverse stimuli (e.g., heat, light, electrical, chemical, etc). The depolarization occurs when sodium (Na+) ions pass through specific channels  (i.e., open voltage-gated Na+ channels) into a neuron, which causes an increase in the positivity of membrane potential. On the other hand, hyperpolarization occurs when potassium (K+) channels remain open and Na+ channels reset, thereby producing an increase in negativity of membrane potential. The peripheral nervous system (PNS) is composed of the cranial nerves, spinal nerves, peripheral nerves, and neuromuscular junctions, which connect the Central nervous system (CNS) to the organs, limbs, and skin. Endorphins (e.g., serotonin) are polypeptides secreted by the pituitary gland and CNS to relieve stress and pain. Neuroglia refers to a class of neural cells that have ectodermal (e.g., astroglia, peripheral glial cells) or mesodermal (e.g., microglia) origins. Neuroglia cells are involved in diverse roles, including, among others, the formation of the blood-brain barrier, homeostatic support, provision of nutrients for neurons, structural support to nerve cells, etc.

Answer:

0.0177

Explanation:

Cystic fibrosis is an autosomal recessive disease, thereby an individual must have both copies of the CFTR mutant alleles to have this disease. The Hardy-Weinberg equilibrium states that p² + 2pq + q² = 1, where p² represents the frequency of the homo-zygous dominant genotype (normal phenotype), q² represents the frequency of the homo-zygous recessive genotype (cystic fibrosis phenotype), and 2pq represents the frequency of the heterozygous genotype (individuals that carry one copy of the CFTR mutant allele). Moreover, under Hardy-Weinberg equilibrium, the sum of the dominant 'p' allele frequency and the recessive 'q' allele frequency is equal to 1. In this case, we can observe that the frequency of the homo-zygous recessive condition for cystic fibrosis (q²) is 1/3200. In consequence, the frequency of the recessive allele for cystic fibrosis can be calculated as follows:

1/3200 = q² (have two CFTR mutant alleles) >>  

q = √ (1/3200) = 1/56.57 >>

- Frequency of the CFTR allele q = 1/56.57 = 0.0177  

- Frequency of the dominant 'normal' allele p = 1 - q = 1 - 0.0177 = 0.9823

Answer:

An enzyme is a type of protein found within a cell. Enzymes create chemical reactions in the body. They actually speed up the rate of a chemical reaction to help support life.

Answer:

ex. where you are standing now

a perspective that one uses to determine if an object is moving.

Explanation:

in physics, a frame of reference, or reference frame, is a perspective that one uses to determine if an object is moving. ... For example, when you see a ball roll down a street, you can tell the ball is moving because the frame of reference is the streets, whatever may be on the side of the roads, or the Earth.

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Complete question:

Two species of closely related frogs are found in the same pond high in the Andes of South America. Both species only have teeth on the top jaw. One has small teeth for holding small live prey prior to swallowing. The other species has very large sharp teeth for injuring and killing large prey prior to biting off pieces of flesh for consumption. The above is an example of:

Answer:

Explanation:

Competition is an ecological and evolutive process very common in nature. Competition might be intra- or interspecific. Competition between different species in a community or ecosystem might be due to the same resource use, or the same territory, shelter, etcetera. When a resource is useful for two or more species, and limited, they compete to gain it.

The principle of competitive exclusion states that different species with the same requirements sharing the niche can not coexist indefinitely based on the same limited resource. When two competing species coexist, this is because of niche partitioning or niche differentiation.

Differentiation of effective niche is closely related to character displacement.

Character displacement is the result of interspecific competition, in which two or more species that live in the same habitat manage to avoid competition by developing different traits. Morphological divergence, or any adaptative trait development, fixated genetically, is the product of niche segregation. Species tend to differentiate morphologically in the presence of strong competitors. Traits divergence favors coexistence in the same place.

In the exposed example, both species live in the same pond. But to avoid competition and competitive exclusion, species developed different teeth sizes to feed on different prey items.  

Answer:

Pisces are known as amazingly imaginative, creative, empathetic, and kind, they can also be overly sentimental, impressionable, and closed off.

Explanation:

Hope this helps!

Answer:

This is an example of gene translation.

Explanation:

Gene translation refers to the genetic process where a set of genes is used to create amino acids that will be responsible for creating a protein needed to perform some function or characteristic of the organism. In the question above, we can see that anthocyanin, responsible for the pigment of flowers, is created through the work of proteins that are created from gebes C and P. This is an example of gene translation, as it presents the formation of proteins regulated by genes.

Answer:

1. Phosphatases hydrolyze key phosphorylated residues.

Explanation:

Receptor Tyrosine Kinases (RTKs) are high-affinity transmembrane protein receptors that bind to a wide variety of ligands (e.g., growth factors, cytokines, hormones). These receptors (RTKs) have a transmembrane domain and therefore these proteins act as membrane receptors, as well as exhibit catalytic activity. The intracellular C terminal region of RTKs contains catalytic domains responsible for both autophosphorylation and tyrosine phosphorylation of their protein substrates. Moreover, Protein Tyrosine Phosphatase (PTPs) are critical enzymes that remove phosphate groups from tyrosine residues in different substrates (including RTKs), thereby regulating key signaling pathways such as cell proliferation, cell differentiation, and cell-cell adhesion.

Answer:

Mutations that cause the death of an organism are called lethals — and it doesn't get more negative than that.

Answer:

plss translate it in English so i Can easyly answer it.

Explanation:

Thank you.

Answer: Pyruvate would increase, NADH would decrease, and intermembrane H+ would decrease as well.

Explanation:

Glycolysis would raise pyruvate, but the Krebs Cycle would not produce NADH, decreasing it. No protons (H+) will be pushed into the intermembrane gap, lowering its H+ content and raising its pH.

The tricarboxylic acid (TCA) cycle, commonly referred to as the Krebs cycle or the citric acid cycle, is the primary route that cells use in order to acquire energy and is an essential component of aerobic respiration. The cycle transforms the oxidative potential of acetyl coenzyme A (acetyl CoA) into the reductive potential of nicotinamide adenine dinucleotide (NADH).

The synthesis of ATP via the Krebs cycle is disrupted when arsenic is present because it prevents pyruvate from being converted into acetyl coenzyme A (acetyl-CoA). In addition to the effects described above, arsenic also prevents glucose uptake at the cellular level, as well as gluconeogenesis, the oxidation of fatty acids, and additional acetyl-CoA formation.

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Answer:

yes

Explanation:

Because science &biology have a connection

Answer:

SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level  

Explanation:

Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.

Answer:

3:1

Explanation:

Due to technical problems, you will find the complete explanation in the attached files.

Answer:

D. A silent variant near the 5' end of the TBX1 gene.

Explanation:

TBX1 gene is wild type human being. It gives instructions for making protein called T-box 1. It plays an important role in tissue formation and organs during embryonic development.

Answer:

There are two differences that distinguish DNA from RNA: (a) RNA contains the sugar ribose, while DNA contains the slightly different sugar deoxyribose (a type of ribose that lacks one oxygen atom), and (b) RNA has the nucleobase uracil while DNA contains thymine.

Answer:

The correct answer is: automaticity.

Explanation:

Cardiac muscle has several properties. These properties are: automaticity (given by the pacemaker cells), conductivity (meaning that each cardiac cell can transmit the electrical impulse to the next cardiac cells), contractility (like other types of muscles, cardiac muscle cells can contract), and irritability (each cell can contract on its own without the external stimuli).

Cardiac pacemaker cells are the ones with the capacity to initiate the electrical impulse by creating rhythmic impulses called action potentials, and thus directly regulating heart rate.

Pacemaker cells are located in the sinoatrial (SA) node, in the upper portion of the right atrial wall. In these cells, depolarization of the cardiac muscle begins, and the electrical impulse generated by it is transmitted to the atrioventricular (AV) node, the His bundle and then the Purkinje fibers - this order of events is necessary for the correct contraction of the heart to occur. All of these structures are part of the Conduction System of the heart.

Answer:3/4

Explanation:4 possibilities, 3 dominant

If a pigmented and non-pigmented organism mate and produce a pigmented organism, which mate again and produce non-pigmented organisms, the probability that the next offspring will be pigmented is ¾ as P is the dominant, pigment-producing allele.

The association between two genetic variants is referred to as dominant. Each gene has two alleles that an individual inherits from each parent. One allele of a gene, known as the dominant gene, will be expressed if the alleles are different. The impact of the additional allele, known as the recessive one, is concealed.

If one is in charge, the other must be recessive. Then it is referred to as recessive. A dominant gene, or dominant form of a gene, is a specific variant of a gene that expresses itself more powerfully on its own than any other version of the gene that the individual is carrying—in this example, the recessive—for a variety of reasons.

Now, it mainly refers to patterns of inheritance typically used in combination with a Punnett square, where if a person has two copies of a gene and one is shown to frequently be passed down from one generation to another, it is referred to as dominant.

According to biochemistry, what is happening in this situation is that the genetic variant may, for a variety of reasons, cause a cell to perform a very advantageous or very disadvantageous function that the other version of the gene cannot cover up or counteract.

Therefore, the probability that the next offspring will be pigmented is ¾ as P is the dominant, pigment-producing allele.

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