Question 31 Marks: 1 The Muerto Canyon virus causes disease of the ______ in humans.Choose one answer. a. lungs b. kidneys c. intestine d. brain

Answers

Answer 1

The Muerto Canyon virus causes disease of the lungs in humans.The Muerto Canyon virus is a type of hantavirus that is known to cause disease in humans. This virus is typically transmitted to humans through contact with infected rodents or their excreta. Option A is correct.

The Muerto Canyon virus is found primarily in the southwestern United States and has been known to cause a severe respiratory illness in humans. The disease caused by the Muerto Canyon virus affects the lungs of humans. The virus is known to cause a condition called hantavirus pulmonary syndrome (HPS), which is characterized by severe respiratory distress, fever, and muscle aches. The disease progresses rapidly and can lead to severe respiratory failure and death in a significant number of cases.

While the Muerto Canyon virus primarily affects the lungs of humans, it is important to note that other types of hantaviruses can cause disease in other organs. For example, the Seoul virus, which is another type of hantavirus, is known to cause renal failure in humans. The Hantaan virus, which is found primarily in Asia, is known to cause a severe hemorrhagic fever that affects multiple organs, including the lungs, kidneys, and brain.

In summary, the Muerto Canyon virus is a hantavirus that primarily affects the lungs of humans. It is important to take precautions when dealing with rodents and their excreta to reduce the risk of infection with this and other types of hantaviruses. If you suspect that you may have been exposed to the Muerto Canyon virus, seek medical attention immediately to receive prompt treatment and prevent the progression of the disease. Option A is correct.

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Related Questions

9. What is a tumor suppressor gene?In general, how do they function? What is apoptosis? Can you give examples of tumor suppressor genes?

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A tumor suppressor gene is a type of gene that helps regulate cell growth and division. These genes are also referred to as anti-oncogenes because their normal function is to prevent the development of cancer.

Tumor suppressor genes function to inhibit the uncontrolled growth of cells, which can lead to the formation of tumors. When a tumor suppressor gene is mutated or deleted, it can no longer perform its function, which can result in uncontrolled cell growth and the development of cancer. Apoptosis is a process of programmed cell death that occurs in multicellular organisms. Apoptosis is important for regulating cell growth and eliminating damaged or abnormal cells. Tumor suppressor genes can trigger apoptosis if they detect that a cell has suffered irreparable DNA damage or if a cell is growing uncontrollably.

Tumor suppressor genes function in several ways, including:

Regulating the cell cycle: Tumor suppressor genes help regulate the cell cycle by promoting the repair of damaged DNA or triggering cell death (apoptosis) if the DNA damage cannot be repaired.

Inhibiting cell proliferation: Tumor suppressor genes can also inhibit cell proliferation by preventing cells from dividing too rapidly or inappropriately.

Examples of tumor suppressor genes include:

TP53: This is one of the most well-known tumor suppressor genes. It encodes the p53 protein, which plays a critical role in regulating the cell cycle and triggering apoptosis in cells with DNA damage.

RB1: This gene encodes the retinoblastoma protein, which helps regulate the progression of cells through the cell cycle. Mutations in this gene can lead to the development of retinoblastoma and other types of cancer.

BRCA1 and BRCA2: These genes are involved in DNA repair and help prevent the development of breast and ovarian cancer. Mutations in these genes can lead to an increased risk of developing these types of cancer.

PTEN: This gene helps regulate cell growth and division by inhibiting a signaling pathway called the PI3K/AKT/mTOR pathway. Mutations in this gene can lead to the development of several types of cancer, including prostate, breast, and colorectal cancer.

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What unifying lab theme does protein electrophoresis incorperate

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The unifying lab theme that protein electrophoresis incorporates is the separation and analysis of proteins based on their physical properties, such as size and charge, using an electric field.

This technique is widely used in various fields, including biochemistry, molecular biology, and clinical diagnostics, to identify and quantify proteins in complex mixtures. During protein electrophoresis, a sample containing proteins is loaded onto a gel, typically made of polyacrylamide, and an electric current is applied. Proteins migrate through the gel in response to the electric field, with smaller proteins moving more quickly than larger proteins. The gel can be stained to visualize the separated proteins, and different techniques can be used to analyze the separated proteins, such as Western blotting or mass spectrometry.

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during a ____ cross, an individual with the dominant phenotype and unknown genotype is crossed with a ___ individual to determine the unknown genotype.a. monohybrid, homozygous recessiveb. dihybrid,heterozygous c. test, homozygous dominante. test, homozygous recessive

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During a test cross, an individual with the dominant phenotype and unknown genotype is crossed with a homozygous recessive individual to determine the unknown genotype.

This cross helps to determine whether the dominant phenotype is due to homozygosity or heterozygosity. If all offspring display the dominant phenotype, then the individual with the dominant phenotype is likely homozygous dominant. However, if some offspring display the recessive phenotype, then the individual with the dominant phenotype is likely heterozygous.

For example, let's consider a monohybrid test cross where a plant with tall height (dominant phenotype) and unknown genotype is crossed with a homozygous recessive plant with short height. If all offspring are tall, then the plant with tall height is likely homozygous dominant for height. However, if some offspring are short, then the plant with tall height is likely heterozygous for height. In summary, a test cross is a useful tool in genetics to determine the genotype of an individual with a dominant phenotype. During a test cross, an individual with the dominant phenotype and unknown genotype is crossed with a homozygous recessive individual to determine the unknown genotype, so the correct answer is d. test, homozygous recessive.

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Question 35 Marks: 1 Transportation is the largest source of air pollution.Choose one answer. a. True b. False

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The given statement "Transportation is the largest source of air pollution." is True because the emissions generated by vehicles contribute significantly to the degradation of air quality.

The exhaust fumes released by cars, trucks, buses, and other modes of transportation contain harmful pollutants such as carbon monoxide, nitrogen oxides, and particulate matter. These pollutants have detrimental effects on human health, including respiratory problems, heart disease, and cancer.

Moreover, transportation emissions also contribute to the formation of ground-level ozone and fine particulate matter, which are major components of smog. These pollutants are particularly harmful to children, older adults, and people with existing respiratory and cardiovascular diseases.

To combat the negative impacts of transportation-related air pollution, governments and organizations have implemented various policies and initiatives. These include incentivizing the use of cleaner vehicles, promoting public transportation and active modes of transportation such as walking and cycling, and implementing stricter emissions standards for vehicles.

In conclusion, it is true that transportation is one of the largest sources of air pollution. However, it is also important to recognize that we can take action to mitigate its negative impacts and promote cleaner, healthier modes of transportation.

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In humans, a gene for free earlobes dominates a gene for attached earlobes. These alternative forms of a gene for earlobe shape are examples of

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In humans, a gene for free earlobes dominates a gene for attached earlobes. These alternative forms of a gene for earlobe shape are examples of alleles.

Alleles are alternative forms of a gene that are located at the same place on a chromosome. Alleles may produce different characteristics in an organism, such as the shape of earlobes. In humans, the allele for a free earlobes dominates over the allele for attached earlobes.

This means that the free earlobes trait will be expressed, regardless of the genotype. A person can be homozygous for free earlobes, meaning they have two free earlobes alleles, or heterozygous for free earlobes, meaning they have one free earlobes allele and one attached earlobes allele. In either case, the trait that will be expressed is free earlobes.

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A _____ is the functional unit of muscle that produces muscular contraction and consists of repeating sections of actin and myosin.

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A sarcomere is the functional unit of muscle that produces muscular contraction and consists of repeating sections of actin and myosin. The sarcomere is the basic unit of striated muscle tissue, which includes skeletal muscle and cardiac muscle.

It is bounded by two Z discs and contains overlapping filaments of actin and myosin, which generate the force required for muscular contraction. When the muscle contracts, the actin filaments slide past the myosin filaments, causing the sarcomere to shorten and the muscle to contract. The length of the sarcomere is critical for optimal muscle function, as it determines the degree of overlap between the actin and myosin filaments. Overlapping filaments generate more force, so a sarcomere that is too short or too long may not be able to generate maximal force. Changes in sarcomere length can occur in response to training, injury, or disease, which can affect muscle function and performance.

Understanding the structure and function of the sarcomere is critical for understanding the physiology of muscle contraction and for developing effective strategies for training and rehabilitation. By manipulating the length of the sarcomere through training or other interventions, it is possible to optimize muscle function and improve athletic performance or functional outcomes in patients with muscle-related injuries or diseases.

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Explain the importance of meiosis in the production of gametes (4)

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Meiosis specifically produces novel genetic material combinations in each of the four daughter cells. These novel pairings are the consequence of DNA switching between linked chromosomes.

Because of this interaction, the gametes created during meiosis display a remarkable diversity of genetic variation. Since meiosis involves two distinct cell divisions, a parent cell can generate four gametes (eggs in females, sperm in males).

The process of meiosis is what creates the gametes, which are essential for sexual reproduction. - It activates the genetic material required for gamete development. It helps to maintain a consistent number of chromosomes by cutting the number of chromosomes in gametes cells in half.

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Question 67 Marks: 1 Biological effects of radiation on all living organisms, including human beings, are termed somatic or genetic.Choose one answer. a. True b. False

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The given statement " Biological effects of radiation on all living organisms, including human beings, are termed somatic or genetic" is True because Radiation can have various effects on living organisms, including human beings. These effects are categorized into two main types: somatic and genetic.

Option (a) is correct.

Somatic effects are those that affect the organism that was exposed to the radiation. These effects can include skin burns, radiation sickness, and an increased risk of developing cancer later in life.

On the other hand, genetic effects refer to changes that occur in the DNA of reproductive cells, which can then be passed down to future generations. These changes can include mutations, chromosomal abnormalities, and an increased risk of genetic disorders in offspring.

Both somatic and genetic effects can occur at various levels of radiation exposure. High levels of radiation exposure can result in immediate and severe somatic effects, while low levels of exposure may not cause immediate harm but can still result in long-term effects, including an increased risk of cancer.

It is important to note that the biological effects of radiation depend on several factors, including the type and amount of radiation, the duration of exposure, and the sensitivity of the exposed organism.

Therefore, option (a) is correct.

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Question 17
Which is not considered a single dose rodenticide?
a. ANTU
b. strychnine
c. red squill
d. warfarin

Answers

Strychnine is not considered a single dose rodenticide. The correct option is "B".

Strychnine is a highly toxic alkaloid that is used primarily as a pesticide and as a poison for rodents and other small animals. However, it is not commonly used as a single-dose rodenticide, which is a type of poison that is designed to kill rodents with a single exposure.

Examples of commonly used single-dose rodenticides include warfarin, brodifacoum, bromadiolone, and difenacoum. These compounds work by interfering with blood clotting and causing internal bleeding, ultimately leading to the death of the rodent. Another example of a non-anticoagulant single-dose rodenticide is zinc phosphide, which reacts with stomach acid to release phosphine gas, causing respiratory failure in the rodent.

The correct option is "B".

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what primary active transporter drives the formation of hcl? group of answer choices na /k transporter (na goes into the parietal cell and k goes into the stomach lumen) h /k transporter (h goes into lumen of the stomach and k goes into the parietal cell) na /k transporter (na goes into lumen of the stomach and k goes into the parietal cell) h /k transporter (h goes into the parietal cell and k goes into the lumen of the stomach)

Answers

The primary active transporter that drives the formation of HCl is the H/K transporter. This transporter moves hydrogen ions (H+) from the parietal cell into the lumen of the stomach, while simultaneously moving potassium ions (K+) from the stomach lumen into the parietal cell. This results in the production of hydrochloric acid (HCl) in the stomach.

The most well-known component of gastric juice is HCl, which the parietal cells then release. When the parietal cells are triggered, they release hydrochloric acid into enormous canaliculi, which are the deep folds in the plasma membrane and extend into the lumen of the stomach.  

The concentration of hydrogen ions in parietal cell secretions is approximately 3 million times higher than in blood, and chloride is secreted against both an electric and a concentration gradient. As a result, active transport is necessary for the parietal cell's propensity to discharge acid.  

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Individuals do not evolve. The smallest ecological unit in which evolution can occur is the population. true or false

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True. Individuals do not evolve. Evolution is a change in the genetic makeup of a population over time.

It occurs due to various factors such as genetic mutation, genetic drift, natural selection, gene flow, and non-random mating. Individuals do not evolve because they do not undergo changes in their genetic makeup during their lifetime. It is the frequency of alleles or genes within a population that changes, leading to the evolution of the population as a whole. Therefore, evolution occurs at the level of populations, not individuals. A genetic mutation is a change in the DNA sequence that makes up a gene. Mutations can occur spontaneously or be caused by external factors such as exposure to radiation, chemicals, or certain viruses.

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"In the ratio 1:1 homozygotes to heterozygotes** In a cross between two heterozygotes (Aa), the next generation will be in the ratio 1:1 homozygotes (AA, aa) to heterozygotes (2 Aa)."true or false

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The given statement "In the ratio 1:1 homozygotes to heterozygotes, in a cross between two heterozygotes (Aa), the next generation will be in the ratio 1:1 homozygotes (AA, aa) to heterozygotes (2 Aa)" is false.

When two heterozygous people (Aa) cross, the offspring can acquire either the dominant allele (A) or the recessive allele (a) from each parent. The offspring's genotypes are thus AA, Aa, or aa, with the chance of each genotype given by probability rules.

In the progeny of a cross between two heterozygotes, the correct genotype ratio is 1:2:1, with one AA homozygote, two Aa heterozygotes, and one aa homozygote. This ratio results from the fact that each allele's inheritance is independent and follows Mendelian genetics principles.

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Pharmacological and Parenteral Therapies
Intravenous Therapy: Intervention to Reduce the Risk of Infection ( RM FUND 9.0 Ch 49)
-hand hygiene before and after
-standard precautions
change IV sites according to the facility's policy
-replacement fo the administration set is dependent upon the infusion
-remove catheters as soon as there is no clinical need for them
-replace catheters when suspecting any break in surgical aseptic techniques, such as during emergency insertions
-use sterile needs or catheter for each attempt
-avoid writing on IV bags with pen or markers
-change tubing immediately for potential contamination
-do not allow fluids to hand for more than 24 hrs unless it is a closed system
-wipe all ports with alcohol before connecting IV lines or inserting a syringe
-never disconnect tubing for convenience or to reposition the client

Answers

Intravenous (IV) therapy is a common medical intervention used to deliver medications, fluids, and nutrients directly into the bloodstream. However, the use of IV therapy can also pose risks to patients, including the risk of infection.

To reduce the risk of infection associated with IV therapy, healthcare providers should follow specific interventions and guidelines. These interventions include hand hygiene before and after the procedure, using standard precautions, changing IV sites according to facility policies, using sterile equipment, avoiding writing on IV bags with pen or markers, and replacing tubing and catheters as soon as there is no clinical need for them. Proper implementation of these interventions can help prevent the transmission of infections and promote patient safety during IV therapy.

This passage outlines guidelines for safe intravenous therapy to reduce the risk of infection. The guidelines include:

Hand hygiene before and after IV administration to prevent the spread of infection.

Standard precautions should be followed to minimize the risk of infection transmission.

Change IV sites according to the facility's policy to reduce the risk of infection.

Replacement of the administration set is dependent upon the infusion.

Remove catheters as soon as there is no clinical need for them to prevent the risk of infection.

Replace catheters when suspecting any break in surgical aseptic techniques, such as during emergency insertions.

Use sterile needles or catheters for each attempt to reduce the risk of infection.

Avoid writing on IV bags with pen or markers as it can lead to contamination.

Change tubing immediately for potential contamination.

Do not allow fluids to hang for more than 24 hrs unless it is a closed system to prevent the growth of bacteria.

Wipe all ports with alcohol before connecting IV lines or inserting a syringe to minimize the risk of infection.

Never disconnect tubing for convenience or to reposition the client to prevent the risk of infection.

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Surfactant is produced by what cell type in the alveolus?

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Surfactant is produced by specialized cells called Type II alveolar cells, also known as surfactant-producing cells.

These cells are responsible for synthesizing and secreting the surfactant, which helps to reduce surface tension in the alveoli and prevent their collapse during expiration. Surfactant is produced by a specific cell type in the alveolus called Type II alveolar cells, also known as Type II pneumocytes. These cells synthesize, store, and secrete surfactant, which plays a crucial role in reducing surface tension within the alveoli and preventing their collapse during exhalation.

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A(n) ______ is a cluster of genes that perform related functions, found in ______.

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A(n) gene is a cluster of genes that perform related functions, found in organisms. These clusters are found in a variety of organisms, including bacteria, fungi, plants, and animals.

Gene clusters can be made up of as few as two genes or as many as several hundred, and they can be located on either the same or different chromosomes. One common type of gene cluster is the operon, which is found in bacteria and regulates the expression of multiple genes involved in a specific metabolic pathway.

Another example is the Hox gene cluster found in animals, which controls the development of body segments along the anterior-posterior axis. Gene clusters can also be involved in the synthesis of secondary metabolites, such as antibiotics, pigments, and toxins.

In fungi and plants, these gene clusters are often located in specialized structures known as secondary metabolite biosynthetic gene clusters (SMBGCs). Studying gene clusters can provide insight into the evolution and function of biological systems, as well as potential applications in biotechnology and medicine.

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The amount of available Amorphous Data Parallelism of DMR may increase and decrease during the computation.true/false

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True. The amount of available Amorphous Data Parallelism of DMR may increase or decrease during the computation, depending on factors such as the number of available processors, the complexity of the computation, and the amount of data being processed at any given time.


True. The amount of available Amorphous Data Parallelism in DMR (Data-parallel Model Reduction) may increase and decrease during the computation, as it refers to the parallel execution of tasks on diverse data sets.

Changes in the data or the nature of the tasks being processed can lead to variations in the level of parallelism throughout the computation.

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For a variations to be inheritable, where must changes in chromosomes occur?

Answers

The answer is B. Sex Cells. Changes in chromosomes must occur in sex cells in order for variation to be inherited, as they that unite during fertilization, and the union of the two parent sex cells is what produces the unique combination of chromosomes in each individual's genome.

What are chromosomes?

Chromosomes are structures in the nucleus of cells that contain long strands of DNA. They contain all of the genetic information that makes us who we are. There are usually two matched sets of chromosomes (one from each parent) which carry the genetic information that determines our physical attributes like eye, hair and skin color.

What is fertilization?

Fertilization is the process through which a sperm meets and merges with an egg. This process typically occurs within the female reproductive system and is necessary for sexual reproduction in most species. During fertilization, the sperm and egg combine to form a single cell called a zygote. This single cell contains genetic material from both the sperm and egg and is the first stage of development.

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Gene regulation in eukaryotes often involves which of the following, which are not also used by prokaryotes? Bacteriophages Lysogeny replicase Formyi-methionine Histone modification

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Gene regulation in eukaryotes often involves histone modification, which is not commonly used by prokaryotes.

Histones are proteins that help to package DNA into a compact structure known as chromatin. Changes to the structure of histones can have a major impact on gene expression.

In eukaryotes, histone modification is a key mechanism of gene regulation, and it involves the addition or removal of chemical groups to histone proteins.

These modifications can affect the way that DNA is packaged, making it more or less accessible to transcription factors and other proteins involved in gene expression.

While some prokaryotes do have histone-like proteins that can help to package DNA, histone modification is not commonly used as a mechanism of gene regulation in these organisms. Instead, prokaryotes often rely on other mechanisms, such as changes in DNA supercoiling or the binding of regulatory proteins to specific DNA sequences.

Therefore, Histone modification is the right response.

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Question 30
Which organisms are most resistant to unfavorable environmental conditions and indicate past or possibly intermittent pollution?
a. Fecal streptococci
b. Escherichia coli
c. Aerobacter aerogenes
d. Clostridium sporulates

Answers

The correct answer to the question is option (d) Clostridium sporulates.

Clostridium is a genus of bacteria that is known for its ability to form endospores. Endospores are highly resistant to unfavorable environmental conditions, including high temperatures, desiccation, and exposure to chemicals and radiation. Clostridium sporulates is particularly known for its ability to form endospores, which makes it one of the most resistant organisms to unfavorable environmental conditions. It can survive in extreme environments and can even tolerate high levels of pollution.Fecal streptococci, Escherichia coli, and Aerobacter aerogenes are not as resistant as Clostridium sporulates to unfavorable environmental conditions. Fecal streptococci and Escherichia coli are both bacteria that are commonly used as indicators of fecal contamination in water. While they are able to survive in a range of conditions, they are not as resistant as Clostridium sporulates to environmental stressors. Similarly, Aerobacter aerogenes is a bacterium that is often found in soil and water, but it is not known for its ability to resist unfavorable environmental conditions.

The basic mechanism of osmoregulation is ________, the movement of water from areas of a higher concentration of water to an area of lower concentration of water.A) myogenic transferB) osmosisC) facilitated diffusionD) photonephridic transferE) active transport

Answers

The basic mechanism of osmoregulation is osmosis,  the movement of water from an areas of a  higher concentration to an area of lower concentration of water. Option B is correct.

Osmosis is an important process for maintaining fluid balance and regulating the concentration of solutes in the body, particularly in aquatic animals where there is a constant exchange of water and ions with the environment.

Osmosis occurs through the movement of water molecules across a membrane in response to a concentration gradient. The concentration of solutes on either side of the membrane determines the direction of water movement, with water moving from areas of lower solute concentration to areas of higher solute concentration.

This process is driven by the natural tendency of water to move from an area of high concentration to an area of low concentration, known as the concentration gradient. In order to regulate osmosis and maintain fluid balance, organisms have developed a range of osmoregulatory mechanisms.

These mechanisms include active transport, facilitated diffusion, myogenic transfer, and photonephridic transfer, which allow for the selective uptake and elimination of ions and water as needed to maintain the appropriate balance of solutes within the body.

Overall, osmoregulation is a critical process for ensuring proper physiological function and survival in a range of organisms, and osmosis plays a key role in this process by allowing for the movement of water across cell membranes to maintain proper fluid balance and concentration of solutes within the body.

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Autotrophs in aquatic food webs have _____ rates of production

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Autotrophs in aquatic food webs have Primary consumer rates of production.

Autotrophs include algae, plants, certain bacteria, and fungus. Autotrophs are the food chain's producers since they make their own energy and nutrients. Like the majority of autotrophs, kelp produces energy through a process known as photosynthesis. Depending on the magnitude of the ecosystem, a food web can contain billions or even trillions of producers.

The trophic level with the most producers often has the most biomass. They have the most direct access to energy since they produce their own food using the Sun's energy or the energy from chemical processes. The primary autotrophs in aquatic habitats are phytoplankton. These autotrophs utilize carbon dioxide, light, and minerals to make nutrients and oxygen while they are found in seas all over the world.

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Question 59
The incidence of tuberculosis in English laboratory workers working with M. tuberculosis was reported to be __ higher than for the general population
a. 2 times
b. 3 times
c. 5 times
d. 10 times

Answers

The incidence of tuberculosis in English laboratory workers working with M. tuberculosis was reported to be c. 5 times higher than for the general population.

Historically, laboratory workers who handle Mycobacterium tuberculosis, the bacteria that causes tuberculosis, have been at increased risk for contracting the disease. This is because exposure to the bacteria in the laboratory can occur through inhalation of infectious aerosols or accidental injury with contaminated needles or other sharp instruments. Studies have shown that laboratory workers who handle M. tuberculosis are at higher risk of developing tuberculosis than the general population. One study conducted in England in the 1980s found that the incidence of tuberculosis among laboratory workers was approximately five times higher than in the general population.

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Spirogyra are green algae that can reproduce sexually. Which of the following identifies reproduction in Spirogyra as sexual reproduction? A. The cells of parent algae have nuclei. B. Each offspring contains chloroplasts. C. Several offspring may be produced at once. D. Genetic material is contributed by two parent ​

Answers

The option that identifies reproduction in Spirogyra as sexual reproduction is as follows: genetic material is contributed by two parent (option D).

What is sexual reproduction?

Sexual reproduction is the process whereby a new organism is created by combining the genetic material of two organisms.

Spirogyra are any of the group of freshwater, filamentous green algae, of the genus Spirogyra, having chloroplasts arranged in spirals. These organisms are capable of sexual reproduction called fragmentation.

In this process, the genetic material (DNA) is contributed by two parents (male and female).

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What is the frequency for any individual person to have a SNP base-pair variant that is different from the general population "consensus" wild-type chromosome?

Answers

The frequency for any individual person to have a SNP base-pair variant that is different from the general population "consensus" wild-type chromosome can vary depending on various factors such as genetic predisposition, environmental exposures, and random mutations.

It is generally estimated that each person may have around 3-4 million SNPs, and the frequency of these SNPs can range from being very common to very rare. In general, the frequency of a SNP variant can be determined by comparing the individual's genome sequence to a reference genome of the general population, and the frequency can range from being present in more than 1% of the population (common variant) to being present in less than 0.1% of the population (rare variant).

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How does active transport help a cell maintain homeostasis?
O A. Cells are moved to areas where the concentrations of substances are the most stable.
OB. Molecules flow rapidly from an area of higher concentration to one of lower concentration to meet the needs of the cell.
O C. Large molecules flow through channel proteins to keep their concentrations stable.
O D. Carrier proteins use energy to move molecules from an area of lower concentration to one of higher concentration.​

Answers

Molecules are transported by carrier proteins using energy from a region of lower concentration to one of higher concentration.

Active transport benefits the cell in what ways?

When molecules move actively, they do so in opposition to a gradient or other sort of resistance, like migrating from a region of lower to higher charge. Cells use active transport to store essential substances like amino acids and glucose.

What supports cellular homeostasis?

A number of control systems that operate at the organ, tissue, or cellular level work together to maintain homeostasis. Substrate supply, individual enzyme and receptor activation or inhibition, enzyme synthesis and breakdown, and compartmentalization are some of these regulatory mechanisms.

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enveloped viruses are released from the host cell by lysing the host cell which results in immediate cell death.T/F

Answers

The given statement "enveloped viruses are released from the host cell by lysing the host cell which results in immediate cell death." is False.

Enveloped viruses:

Enveloped viruses can be released from the host cell by both lytic and non-lytic processes, such as the budding process. The budding process allows the virus to exit the host cell without immediately causing cell death. During the budding process, the virus acquires its envelope from the host cell membrane, and the newly formed virus particles then leave the cell. This process allows the host cell to remain alive and continue producing more viruses. Lysis of host cell refers to the destruction of the cell, which is more commonly associated with non-enveloped viruses.

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What happened in the experiment when Observing Movement through a Selectively Permeable Membrane?

Answers

When observing movement through a selectively permeable membrane in an experiment, it was observed that certain molecules or ions were able to pass through the membrane while others were not.

This selective permeability is due to the structure of the membrane, which allows only certain molecules to pass through based on their size, charge, and other factors. In the experiment, it was observed that smaller molecules like water and oxygen were able to pass through the membrane, while larger molecules like glucose and proteins were not able to pass through as easily. The movement of molecules through the membrane was also affected by factors like concentration gradients and pressure differentials, which caused the molecules to move from areas of high concentration to areas of low concentration. This process is known as diffusion and it is one of the main mechanisms by which molecules move through selectively permeable membranes.

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Can a protein be removed from the membrane after insertion? What degree of flexibility does the portein have once inserted?

Answers

Yes, a protein be removed from the membrane after insertion the process is called extraction.

Extraction is the process of removing a protein from a membrane, and it can be carried out using detergents or other techniques that damage the membrane's lipid bilayer. Detergents can help to solubilize membrane proteins and aid in membrane separation.

When a protein is inserted into a membrane, the membrane type and the particular protein will affect how flexible the protein is. When the membrane environment changes or when they interact with other proteins or ligands. some membrane proteins which have a fixed structure become more flexible and can change conformation.

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Practice 1: Asexual Reproduction
Which of the following describes asexual reproduction?
Passing an identical set of genes to the offspring
Sorting only the best genes to pass on to the offspring
Passing unique sets of genes to the offspring
Engineering new sets of genes for the offspring
SUBMIT

Answers

Answer:

Passing And Identical Set Of Genes To The Offspring

Explanation:

A person sweats on a hot day. This is an example of . . .A) negative feedbackB) signal transductionC) effector linkageD) positive feedbackE) orthogonal feedback

Answers

Sweating on a hot day is an example of positive feedback because the body's response amplifies the stimulus. The correct answer to the question is D) positive feedback.

In this case, as the body temperature rises, sweat glands release sweat onto the skin, which then evaporates and cools the body down.

This cooling effect sends a signal to the hypothalamus in the brain to continue producing sweat, further cooling the body.

This process continues until the body's temperature returns to normal.

Positive feedback mechanisms are typically self-amplifying and can lead to rapid and sometimes irreversible changes in the body.

In contrast, negative feedback mechanisms work to maintain homeostasis by counteracting changes in the body and returning it to a stable state.

Signal transduction and effector linkage refer to the processes by which signals are transmitted and responses are elicited in the body, respectively.

Orthogonal feedback refers to a feedback mechanism that operates independently of other feedback pathways. Therefore, the right answer is D, positive feedback.

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