in the absence of chromosomal rearrangements, what are the most likely karyotypes of a newborn baby with 47 chromosomes? with 45 chromosomes?

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Answer 1

In the absence of chromosomal rearrangements, a newborn baby with 47 chromosomes will have a karyotype of 47,XX,+21 and a newborn baby with 45 chromosomes will have a karyotype of 45,X.


Karyotype is the number and appearance of chromosomes in the nucleus of a eukaryotic cell. The term is also used for the entire complement of chromosomes in a cell or an organism.

Karyotyping is the process of pairing and ordering all the chromosomes of an organism, thus providing a comprehensive picture of its karyotype. Chromosomal rearrangements occur when parts of a chromosome are lost, duplicated, or rearranged within or between chromosomes.

In the absence of chromosomal rearrangements, the most likely karyotype of a newborn baby with 47 chromosomes is 47,XX,+21. 47,XX,+21 is a chromosomal disorder that occurs when a baby is born with an extra chromosome 21. It is also known as Down syndrome.

In the absence of chromosomal rearrangements, the most likely karyotype of a newborn baby with 45 chromosomes is 45,X. 45,X is a chromosomal disorder that occurs when a baby is born with only one sex chromosome. It is also known as Turner syndrome.

Hence, in the absence of chromosomal rearrangements, a newborn baby with 47 chromosomes and 45 chromosomes will have karyotypes of 47,XX,+21 and 45,X respectively.

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Related Questions

which of the following are true of asexual reproduction? choose all that apply. the offspring are genetically different than the parents. there is only one parent. the offspring are genetically identical to the parent. there are two parents.

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Asexual reproduction is the process by which an organism reproduces by itself without requiring gamete cells from another organism. Asexual reproduction generates genetically identical offspring to the parent. Therefore, the correct answer to this question is: there is only one parent. the offspring are genetically identical to the parent.

Usually, in asexual reproduction, there is only one parent involved. This implies that there is no exchange of genetic information between two individuals. As a result, the offspring generated through asexual reproduction are genetically identical to the parent.

As a result, the genetic makeup of the parent is transferred to the offspring without alteration.In conclusion, asexual reproduction is a significant mode of reproduction among organisms that do not require the existence of the opposite sex to reproduce.

Asexual reproduction is advantageous in some ways since it does not necessitate locating a partner, and the offspring generated are often quick to mature and establish themselves in a new location.

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The following question may be like this:

Which of the following are true of asexual reproduction? choose all that apply.

the offspring are genetically different than the parents. there is only one parent. the offspring are genetically identical to the parent. there are two parents.

how does the body decrease the blood vessel radius? how does the body decrease the blood vessel radius? vasodilation vasoconstriction cardiac muscle contraction valve closure

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The body decreases the blood vessel radius by vasoconstriction.

A blood vessel is a tubular structure that transports blood throughout the body. Blood vessels are divided into three types: arteries, veins, and capillaries.

The heart pumps blood into the arteries, which then branch off into smaller arterioles that supply the capillaries.

Vasoconstriction is the process by which blood vessels constrict or narrow their diameter, increasing vascular resistance and decreasing blood flow.

It helps to control blood pressure and redirect blood flow to areas of the body that require it more urgently than other areas.

Blood vessels can constrict to various degrees, depending on the needs of the body. Vasoconstriction can be caused by a variety of factors, including hormones, drugs, and neurotransmitters.

For example, the hormone norepinephrine causes vasoconstriction by activating alpha-adrenergic receptors on the smooth muscle cells of blood vessels.

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onsuming foods with high glycemic index immediately after a bout of exercise will multiple choice question. ensure a slow rise in blood glucose. supply amino acids for muscle repair. rapidly restore glycogen stores. replenish sweat losses.

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Consuming foods with high glycemic index immediately after a bout of exercise will c. rapidly restore glycogen stores.

Consuming foods with a high glycemic index such as boiled potatoes, white rice, white bread after exercise can quickly restore glycogen stores that are depleted during exercise. The glycemic index value depends on several factors, including dietary fiber content, amylose and amylopectin levels, fat and protein content, starch digestibility, and processing methods.

Glycogen is a storage form of glucose, where glucose is a simple sugar, a form of carbohydrates. Glycogen is an important fuel for athletes, because it is quickly broken down and used for energy.

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which of the following is not an example of a consumer? herbivores omnivores heterotrophs carnivores photosynthesizers

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Herbivores, Omnivores, Carnivores, and Heterotrophs are all examples of consumers, while Photosynthesizers are an example of a producer.

A consumer is an organism that gets its food by eating other living beings. Consumers are the second level of a food chain. In addition, they are categorized into primary consumers, secondary consumers, and tertiary consumers.

Herbivores, omnivores, carnivores, and heterotrophs are all examples of consumers.Photosynthesis is the process in which plants and some other organisms use sunlight to produce food. Since they make their food, photosynthesizers are not consumers but producers.

The two basic types of organisms in an ecosystem are producers and consumers. The producers are those organisms that produce food through the process of photosynthesis, while the consumers are those organisms that feed on other organisms.

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How does the apparent brightness of a star differ from the star’s intrinsic luminosity? In your answer, describe how stellar distances are determined by comparing apparent brightness and intrinsic luminosity when astronomers use spectroscopic parallax and the Leavitt relation for variable stars.

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The apparent brightness of a star is how bright it appears to us from Earth, while the intrinsic luminosity of a star is the total amount of energy it emits per second.

What is a star?

A star is a massive, luminous object in space that generates energy through nuclear fusion reactions in its core. It is composed mainly of hydrogen and helium gas, with small amounts of other elements.

Astronomers use various methods to determine the distances to stars, including parallax measurements, spectroscopic parallax, and the Leavitt relation for variable stars.

Parallax measurements involve observing a star's position from two different points on Earth's orbit around the Sun, and measuring the apparent shift in the star's position relative to more distant stars. This allows astronomers to calculate the star's distance using trigonometry. However, this method is limited to relatively nearby stars.

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all hormones are all hormones are proteins. chemical messengers. steroids. cholesterol based. inorganic compounds.

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All hormones are chemical messengers. The correct option is b.

Hormones are signaling molecules produced by glands in the endocrine system and released into the bloodstream to regulate various physiological processes in the body.

Hormones are classified into different categories based on their chemical composition, but not all hormones are proteins or steroids. Hormones can also be made up of other organic or inorganic compounds, depending on their structure and function. Therefore, option B, chemical messengers, is the correct answer to the given question.

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you decide to join a lab working on osteocalcin because it works on this hormone. you know from this and the next lecture many of its functions, target organs and receptors. can you present in one page what is/are the question(s) you would want to address and how would you tackle it/them?

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My approach to investigating the functions of osteocalcin would involve a combination of molecular and cellular techniques, animal models, and clinical studies, with the ultimate goal of advancing our understanding of this hormone and its potential applications in medicine.

As a researcher joining a lab working on osteocalcin, there are several questions that I would want to address in order to further our understanding of this hormone and its role in the body.

Firstly, I would want to investigate the molecular mechanisms by which osteocalcin interacts with its target organs and receptors. This could involve studying the 3D structure of osteocalcin and its binding sites, as well as using techniques such as gene expression analysis and protein-protein interaction assays to better understand how osteocalcin influences cellular signaling pathways.

Secondly, I would be interested in exploring the functional roles of osteocalcin in various physiological processes, including bone formation, glucose metabolism, and energy homeostasis. This could involve using animal models and cell culture systems to study the effects of osteocalcin on different tissues and organs, as well as conducting clinical studies to investigate the potential therapeutic applications of osteocalcin in the treatment of metabolic disorders such as diabetes.

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which sequence of metabolic paths could a carbon atom take to go from a molecule of glucose to a molecule of dna?

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The conversion of glucose to DNA involves several metabolic pathways. A carbon atom from a molecule of glucose can take the metabolic pathways of glycolysis, pyruvate dehydrogenase, the citric acid cycle, aconitase, and thymidine synthetase to reach a molecule of DNA.

A carbon atom from a molecule of glucose can take a few different metabolic pathways to reach a molecule of DNA. First, it would have to be converted to pyruvate, a three-carbon molecule, by glycolysis. This would then be converted to Acetyl-CoA by the enzyme pyruvate dehydrogenase. Acetyl-CoA then enters the citric acid cycle, in which it combines with oxaloacetate to form citrate, a six-carbon molecule. Finally, citrate is converted to a five-carbon molecule, alpha-ketoglutarate, by the enzyme aconitase. Alpha-ketoglutarate is then converted to the four-carbon molecule succinyl-CoA, which is then converted to a molecule of DNA by the enzyme thymidine synthetase.

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Classify each interaction as mutualism, commensalism, or parasitism. Explain your answers.

A remora fish attaches itself to the underside of a shark without harming the shark, and eats leftover bits of food from the shark's meals.

A vampire bat drinks the blood of horses.

A bee collects pollen and pollinates a flower.

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The remora fish that frequently swim alongside the leopards shark and yet are bonded to its body exhibit mutualism. The Remora hangs out beneath the shark's belly & scavenges extra food that it has left behind.

What roles do blood cells play in the body?

The primary function for red blood cells, and erythrocytes, is to transport carbon dioxide, a waste product, from the tissues back to the lungs and deliver oxygen from the lung to the body's tissues.

What occurs when red blood cell levels are low?

The body's capacity to move nutrients and oxygen throughout the cardiovascular system can be impacted by anemia, commonly known as a low RBC count. It may result in weakness, lightheadedness, and palpitations.

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which of the following is a disadvantage associated with the genetic modification of crops? responses genetically modified crops have a decreased resistance to drought. genetically modified crops have a decreased resistance to drought. genetically modified crops have a shorter shelf life and are more difficult to transport long distances. genetically modified crops have a shorter shelf life and are more difficult to transport long distances. genetically modifications can decrease the genetic diversity of crop species. genetically modifications can decrease the genetic diversity of crop species. genetic modifications decrease nutritional content in foods.

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The disadvantage associated with the genetic modification of crops is that genetic modifications can decrease the genetic diversity of crop species. This means that plants containing the same transgenes are bred together and cross pollination with other varieties is discouraged.

How genetic modification occurs in crops?

Genetic modification of crops involves the use of recombinant DNA (rDNA) technology to modify the genetic makeup of a plant organism. This is usually done by introducing one or more gene sequences from a different organism in order to confer desirable traits, such as greater resistance to disease or improved nutritional content. The new gene sequences are created by isolating the desired gene from the donor organism and then inserting it into the plant using techniques such as viral vectoring, where the gene is incorporated into a viral genome, or direct DNA transfer, which involves directly transferring the gene into the plant's cells. The modified genes can be combined in various ways to produce new plants with desired characteristics.

What is cross pollination?

Cross pollination is the process in which pollen from the male reproductive organ of one flower is transferred to the female reproductive organ of another flower, leading to the production of new seeds or fruits. It is a form of natural pollination that is responsible for the reproductive success of flowering plants.

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hich gas began to increase in the atmosphere as a result of photosynthesis by autotrophic prokaryotes approximately 2.7 billion years ago?

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Oxygen began to increase in the atmosphere as a result of photosynthesis by autotrophic prokaryotes approximately 2.7 billion years ago. This process, called oxygenic photosynthesis, uses energy from sunlight to convert carbon dioxide and water into organic matter (carbohydrates) and oxygen gas. This new source of oxygen led to an increase in atmospheric oxygen, which had previously been low, and allowed for the evolution of more complex forms of life.

Oxygenic photosynthesis is carried out by autotrophic prokaryotes, or “oxygenic phototrophs”, which are organisms that use energy from sunlight to convert inorganic molecules into organic molecules. These phototrophs use light to break down carbon dioxide molecules, and form simple organic molecules, such as glucose. The byproducts of this process are organic molecules and oxygen gas. As a result of this reaction, the amount of oxygen in the atmosphere began to increase.

This increase in oxygen allowed for the evolution of more complex life forms. Before the rise of oxygenic photosynthesis, the atmosphere was largely composed of carbon dioxide and nitrogen, which prevented the evolution of complex organisms. With the rise of oxygen, more complex organisms could thrive, as oxygen allowed for respiration, which is the process of breaking down food molecules to create energy. As a result, the diversity of organisms increased and eventually led to the evolution of multicellular organisms.

In conclusion, oxygen began to increase in the atmosphere approximately 2.7 billion years ago as a result of oxygenic photosynthesis carried out by autotrophic prokaryotes. This allowed for the evolution of more complex forms of life and the development of multicellular organisms.

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vii. explain how a single neurotransmitter can elicit different responses at different postsynaptic cells.

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The neurotransmitter released by a neuron can elicit different responses at different postsynaptic cells due to different receptor proteins on the postsynaptic cell.

The receptors on the postsynaptic cell are activated by different neurotransmitters, which then cause the cell to produce different responses. For example, some receptors on the postsynaptic cell might activate certain ion channels that cause an influx of calcium ions, while others might cause an influx of sodium ions or other substances.

These different responses can be triggered by different concentrations of the same neurotransmitter, depending on the receptor proteins present on the postsynaptic cell.

Furthermore, postsynaptic cells can also have different expression levels of receptors, which can lead to different responses to the same neurotransmitter. Therefore, a single neurotransmitter can produce different responses at different postsynaptic cells depending on the types of receptors present on the cell.

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Which statement best explains why these freshwater Mesosaurus fossils are found today in some rock layers in both South America and Africa?

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Answer:

The continents were once connected as a single land mass

Explanation:

the lipid-containing outer envelope surrounding the viral capsid of many animal viruses is derived from...

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The outer envelope surrounding the viral capsid of many animal viruses is derived from the host cell's lipid bilayer.

This lipid bilayer is the same membrane that encloses the host cell. During the process of viral replication, the capsid and other components of the virus are assembled inside the host cell and a portion of the host cell's membrane is used to form the outer envelope of the virus.

This envelope, along with the capsid, helps to protect the genetic material of the virus, allowing it to be transported to another cell for infection. The envelope also contains viral proteins that aid in the attachment and fusion of the virus to the host cell.

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In 1981, a couple found a stray kitten whose unusual ears curled up and back from her head. They decided to breed her with their male cat who is homozygous for the allele for normal ears. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. Subsequent litters with the same parents showed the same ratio of curled ears to normal ears. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears. This new trait was determined to be the result of a new and unique mutation in the ear gene of cats, and cats with this trait were named American curl cats.
In American curl cats, the allele that produces the ear-curling trait is which?
The allele that produces normal ears is which?
Dominant
Recessive
Page 120

Answers

In American curl cats, the allele that produces the ear-curling trait is dominant, while the allele that produces normal ears is recessive. This can be determined from the fact that when curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears, indicating that the ear-curling trait is dominant over the normal ear trait.

In American curl cats, the allele that produces the ear-curling trait is dominant. Dominance is a characteristic of an allele that expresses its phenotype in a heterozygote, such that it masks the expression of a recessive allele. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears.

The allele that produces normal ears is recessive. Recessive traits are only expressed in a homozygous state, and that are not expressed in a heterozygous state because a dominant allele mask it. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. The parents were heterozygous, with one carrying the dominant curled allele and the other carrying the recessive normal allele.

In summary, in American curl cats, the allele that produces the ear-curling trait is dominant. The allele that produces normal ears is recessive.

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During crossing over, when the invading strand uses the invaded DNA as a _____, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected _____ ratio.

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The correct answer is: During crossing over, when the invading strand uses the invaded DNA as a template, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.

Explanation:

DNA is replicated through the process of crossing over, which involves the exchange of genetic material between two homologous chromosomes. During the process, one of the homologous chromosomes acts as the invading sequence, while the other acts as the invaded DNA. When the invading strand uses the invaded DNA as a template, it results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.
What is crossing over?

Crossing over is a process during meiosis where the chromosome arms of maternal and paternal homologous chromosomes swap DNA sections (recombination) to produce new allelic combinations of traits. The crossing-over process starts with the breakage of two homologous chromosomes, the migration of the broken ends toward each other, and the formation of crosslinks by the formation of single crossovers.

These crosslinks are eventually converted to chiasmata that keep the chromosomal arms connected until metaphase I. During this process, one chromosome might lose genetic material while the other might acquire genetic material. This event results in unique combinations of genes that might not be present in either parent. The frequency of crossovers is affected by the distance between the gene and the centromere. Chromosomes that are nearer to the centromere are less likely to cross over than those that are further away. Explaining the departure from the expected Mendelian ratio.

The ratio of offspring created by a cross that exhibits the dominant and recessive traits that Mendel observed is referred to as the Mendelian ratio. Crossing over might result in new allelic combinations of genes that deviate from the Mendelian ratios. This is because the transmission of genes is no longer controlled by a single gene pair on a chromosome. Chromosome segregation is disturbed in one way or another by crossovers.

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explain why the mango slices swell up when placed in water

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Because the process of osmosis is taking place.

After duplication, at what point does a cell become two cells with identical DNA?

starting in prophase

end of anaphase

end of cytokinesis

Answers

it is at the end of cytokinesis that a cell becomes two cells with identical DNA. During cytokinesis, the cytoplasm and other cell contents are divided between the two daughter cells, and each daughter cell receives a complete set of chromosomes that are identical to the parent cell.

What is DNA?

DNA stands for deoxyribonucleic acid, which is a molecule that carries the genetic instructions used in the growth, development, functioning, and reproduction of all living organisms. DNA is a long, double-stranded helix structure made up of four building blocks called nucleotides, which are adenine (A), guanine (G), cytosine (C), and thymine (T).

The process of cell duplication or cell division involves several stages, including interphase, mitosis, and cytokinesis. During mitosis, the cell undergoes a series of sub-stages, including prophase, metaphase, anaphase, and telophase.

During prophase, the chromatin in the nucleus condenses into chromosomes, and the nuclear membrane breaks down. The chromosomes then attach to spindle fibers at the centromere region.

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what did kennedy believe the government could do to solve the problem?

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Explanation:

To stimulate the economy, Kennedy pursued legislation to lower taxes, protect the unemployed, increase the minimum wage, and energize the business and housing sectors

which treatment of the heat-killed siii bacterial extract, when mixed with rii bacteria, resulted in mice surviving infection?

Answers

The treatment of the heat-killed SIII bacterial extract, when mixed with RII bacteria, that resulted in mice surviving infection is inoculation. When the heat-killed SIII bacterial extract was mixed with RII bacteria and inoculated into mice, the mice were able to survive the infection.

What is inoculation?

Inoculation is the introduction of a disease-causing agent or an antigenic substance into the body, stimulating the body's immune system to fight off the infection. It is a method of increasing the resistance to infection. In this case, the heat-killed SIII bacterial extract was used to inoculate mice, which increased the resistance of the mice to the RII bacteria infection.

The treatment resulted in mice surviving infection.RII is a type of bacteria that is pathogenic and can cause infections. It is a Gram-negative bacteria that has an outer membrane that makes it more resistant to antibiotics. RII bacteria can cause serious infections such as meningitis, sepsis, and pneumonia.

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do not add any more lactose and watch what transpires. note what happens and why this occurs. how could you re-activate the lacz gene?

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The lacZ gene is responsible for the enzyme β-galactosidase which breaks down lactose. When no more lactose is added, the lacZ gene is not activated and the β-galactosidase enzyme does not break down lactose. To re-activate the lacZ gene, you would need to add lactose back in so that the β-galactosidase enzyme is activated and lactose is broken down.

Lactose is a disaccharide sugar composed of glucose and galactose, which is found in milk. Lactose can be hydrolyzed into glucose and galactose through the catalytic action of lactase enzymes. This reaction occurs in the small intestine, and the glucose and galactose are then absorbed and used as energy by the body.

When lactose is present, the lac operon is activated, and the genes involved in lactose metabolism are transcribed into messenger RNA. When lactose is absent, the lac operon is turned off, and these genes are not expressed.

To re-activate the lacZ gene, it is necessary to add lactose or a lactose analog such as IPTG to the culture medium. IPTG is an inducer of the lac operon that does not bind to the repressor protein, allowing the genes involved in lactose metabolism to be expressed even in the absence of lactose.

When lactose is present, the lac operon is activated, and the genes involved in lactose metabolism are transcribed into messenger RNA. When lactose is absent, the lac operon is turned off, and these genes are not expressed.

Therefore, if no more lactose is added to the culture medium, the lac operon will turn off, and the genes involved in lactose metabolism will not be expressed. This occurs because the repressor protein binds to the operator site of the operon, preventing RNA polymerase from transcribing the genes involved in lactose metabolism.

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in red bone marrow newly formed blood cells enter the circulation. you would expect to see many type of capillaries in red bone marrow. group of answer choices fenestrated continuous metarterioles sinusoid

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The main answer is that you would expect to see sinusoid capillaries in red bone marrow.

Sinusoid capillaries are present in red bone marrow and serve to allow newly formed blood cells to enter the circulation. These are specialized capillaries that are made up of large, thin-walled, endothelial-lined vessels with wide lumens and a lack of a basement membrane. They allow for a high degree of permeability, which helps facilitate the transfer of blood cells from the red marrow into the circulation.

Additionally, the unique shape of sinusoid capillaries allows for a high degree of interaction between the blood cells and other cells in the red marrow. This interaction is necessary for red marrow to regulate the number and quality of blood cells in the circulation.

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new plants imported from the americas to europe, asia and africa included rice, onions and garlic. t or f

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The statement "new plants imported from the Americas to Europe, Asia, and Africa included rice, onions, and garlic" is: false.

The statement is false because rice did not originate from the Americas, but from Asia. Similarly, onions and garlic are not originally from the Americas as well. Therefore, the statement should be corrected as: New plants imported from the Americas to Europe, Asia, and Africa including maize, potatoes, sweet potatoes, and tomatoes.

In the 15th century, the discovery of the Americas by the Europeans brought about an era of plant exchange between the two regions. European explorers, conquerors, and merchants took a variety of American crops, including maize, potatoes, sweet potatoes, and tomatoes, back to Europe.

These crops spread quickly throughout the continent, and soon became staples of European cuisine. European plant species, including wheat, barley, and grapes, were similarly introduced to the Americas. The introduction of these new crops led to significant dietary changes across the globe.

Imported plants have played an essential role in human history, making it possible to grow crops in new areas, feed growing populations, and improve the quality of life in many parts of the world. While some imported plants can have negative effects on the environment and the economy, the overall impact of imported plants has been positive, helping to create a more diverse and resilient global food system.

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which of the statements describes a polygenic trait? a trait that is influenced by both alleles of a single gene a trait that is influenced by a single, dominant allele of a single gene a trait that is influenced entirely by environmental factors a trait that is influenced by more than one gene

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A trait influenced by two or more genes is referred to as a polygenic trait. Examples of such traits include height and skin tone.

Polygenic traits do not inherit according to Mendelian principles since numerous genes are involved. Multifactorial qualities, which include many polygenic features, also have environmental influences.

Many of the most significant health issues of our time, including diabetes, cancer, and heart disease, have a genetic component that results from the interaction of several genes. Thus, polygenic, or having numerous genes. As researchers have delved deeper into these disorders, they've come to the realisation that there is a huge possibility for improving human health by using the methods we already have for forecasting the dangers associated with polygenic features.

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behaviors can be affected by differences in protein structure. group of answer choices true false

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The statement 'behaviors can be affected by differences in protein structure' is true as different proteins are responsible for different functioning process of the body.

Behaviors can be affected by differences in protein structure as proteins are made up of chains of amino acids and their arrangement and function is determined by the sequence of the amino acids in the chain. Different types of proteins have different functions in the body, and even slight changes in the amino acid sequence can affect their function and structure.

When the structure and function of proteins change, they can alter how they interact with other molecules in the body, leading to changes in behavior.

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Select the correct statement about absorptiona. 30% ingested materials have been absorbed by the end of the large intestine.b. carbohydrates diffuse across the villus epithelium and are then passively transported into blood capillaries.c. if intact fats are transported across the villus epithelium, an immune response may be generated.d. Amino acid transport is linked to sodium transport.The answer could be one choice or multiple choices

Answers

The correct statement(s) about absorption is (D) Amino acid transport is linked to sodium transport.

Amino acids are transported across the villus epithelium in the small intestine, and this process is linked to sodium transport.

Amino acids, not proteins, are absorbed; proteins rely on prior digestion to amino acids. Most absorption of amino acids occurs in the jejunum; there is a lesser contribution from the ileum.

Amino acids are absorbed by a co-transport mechanism with sodium ions. Both sodium ion and amino acid combine with a cell surface protein receptor.

There are different receptors for the groups: neutral amino acids, basic amino acids, acidic amino acids

In addition, certain amino acids may have there own specific transporter e.g. proline. The receptor then conveys both molecules to the inside of the cell.

The energy for this transport is derived from the concentration gradient for sodium across the cell membrane. Na-K ATPase transporters actively and continuously pump sodium ions outwards to maintain the gradient.

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in addition to the important roles of natural variability and natural selection in the process of evolution, it is also important that

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In addition to the important roles of natural variability and natural selection in the process of evolution, it is also important that genetic drift plays a role.

There are several factors involved in the process of evolution, and natural variability and natural selection are two of the most important. Natural variability refers to the fact that no two individuals within a species are exactly alike, and this variation can give some individuals a survival advantage over others. Natural selection then works to increase the frequency of advantageous traits within a population over time.

However, there is another factor that plays a role in the process of evolution, and that is genetic drift.

Genetic drift refers to the random changes in gene frequency that can occur within a population due to chance events. This can have significant effects on the genetic makeup of a population over time, and can even lead to the creation of new species.In addition to these factors, other important factors that can contribute to the process of evolution include gene flow, mutation, and non-random mating. All of these factors can influence the genetic makeup of a population over time, leading to the creation of new species or the extinction of existing ones.

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1.3 Discuss the benefits of goal setting on your career choice.​

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Answer:

Here are a few reasons it's important to set long-term professional goals for yourself:

1.Provides motivation.

2.Gives you focus.

3.Shows your ambition.

4.Aligns your actions with your end targets.

5.Think about what's important to you.

6.Consider what you can realistically achieve.

7.Decide on the best methods for achieving your goals.

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which of the following would not result in an increase in arterial blood pressure? group of answer choices increased blood volume increased sympathetic stimulation increased heart rate increased stroke volume increased arteriolar vasodilation

Answers

Increased arteriolar vasodilation would not result in an increase in arterial blood pressure. Vasodilation is the widening of the blood vessels, which decreases the resistance to blood flow and thus decreases arterial blood pressure. Therefore, option E, increased arteriolar vasodilation would not result in an increase in arterial blood pressure.

Increased blood volume, sympathetic stimulation, heart rate, and stroke volume all lead to an increase in arterial blood pressure by increasing cardiac output and/or resistance to blood flow.  To elaborate further, an increase in blood volume increases the pressure within the cardiovascular system, while increased sympathetic stimulation increases the contractility of the heart, leading to higher cardiac output. Increased heart rate and stroke volume also lead to higher cardiac output. Conversely, vasodilation causes the opposite effect - reducing the pressure within the cardiovascular system by decreasing the resistance to blood flow.
Increased arteriolar vasodilation would not result in an increase in arterial blood pressure. Arteriolar vasodilation refers to the relaxation or widening of the arterioles, which are the small blood vessels that connect arteries and capillaries. When the arterioles dilate, they allow more blood to flow through them, which results in a decrease in blood pressure. As a result, increased arteriolar vasodilation would not result in an increase in arterial blood pressure.

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because it mixes with both maternal and paternal chromosomes has the homologous pair of chromosomes in the following figure undergone crossing over? explain your answer either way.

Answers

Crossing over is a process in which homologous chromosomes exchange genetic material with each other during meiosis.

This process results in the formation of recombinant chromosomes. These recombinant chromosomes have a combination of genes from both the maternal and paternal chromosomes.

The process of crossing over occurs during the prophase I stage of meiosis. During this stage, homologous chromosomes pair up with each other and exchange genetic material.

This exchange of genetic material occurs at specific sites called chiasmata. The occurrence of chiasmata is a clear indication that crossing over has taken place.

However, it is not possible to determine whether crossing over has taken place in the given figure because there are no chiasmata visible in the figure.

Therefore, it cannot be determined with certainty whether the homologous pair of chromosomes has undergone crossing over or not.

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