The process of comparing currently experienced visual input with past visual memories takes place in association areas.
The part of the cerebral cortex that processes visual information is called the visual cortex. The occipital lobe is where it is situated. The visual cortex receives sensory information coming from the eyes after passing through the lateral geniculate nucleus of the thalamus. The primary visual cortex, also known as visual area 1 (V1), Brodmann area 17, or the striate cortex, is the region of the visual cortex that receives sensory information from the lateral geniculate nucleus. The visual areas 2, 3, 4, and 5 (also known as V2, V3, V4, and V5 or Brodmann area 18 and all of Brodmann area 19) make up the extrastriate regions.
A visual cortex exists in the left hemisphere of the brain as well as the right.
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You are attempting to synthesize rRNA in a test tube using DNA isolated from mouse cells. In addition to the template DNA, ribonucleotides, and the necessary transcription factors, you should also add what enzyme to the test tube?
poly-A polymerase
RNA polymerase III
RNA polymerase I
RNA polymerase II
In addition to the template DNA, ribonucleotides, and the necessary transcription factors, you should also add RNA polymerase I enzyme to the test tube.
The pace of protein synthesis, which is closely linked to ribosome production and rRNA transcription, directly affects the rate of cell development. Therefore, rRNA synthesis must be synchronised with other protein translational components using intracellular cues. It is known that Myc interacts with human ribosomal DNA to promote the transcription of rRNA by RNA polymerase I. To ensure that rRNA synthesis and Pol I-mediated transcription are properly regulated, two distinct mechanisms have been found. The first phase involves fluctuations in the amount of genes that are being transcribed at any particular time due to the enormous number of rDNA genes that are available for transcription (several hundreds).
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What are the four main causes of mutations?
Mutations are brought on by environmental factors, often known as mutagens. Mutagens include things like radiation, chemicals, and pathogenic agents. Mutations can happen spontaneously in nature.
An organism's phenotype, or outward traits, may or may not be affected by a mutation. Among the good and bad biological processes that mutations participate in include evolution, cancer, and the maturation of the immune system, including junctional variation. All genetic diversity is the outcome of mutation, which also justifies the actions of evolutionary processes like natural selection. For an adaptive immune response to be successful, antigen-presenting cells (APCs), which are necessary for the smooth operation of both cytotoxic and helper T cells, must be present.
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Which of the following statements about the distribution of sap throughout a plant is true?
a) The driving force for sugar movement is transpiration.
b) The mechanism that explains the movement of sugars throughout a plant is called the pressure-flow hypothesis.
c) Companion cells form the conducting tissue for sap.
d) The main component of phloem sap is glucose.
The statements that are true about the distribution of sap throughout a plant are:
a) The driving force for sugar movement is transpiration.
b) The mechanism that explains the movement of sugars throughout a plant is called the pressure-flow hypothesis.
c) Companion cells form the conducting tissue for sap.
Transpiration is the process where water is lost from the leaves of the plant and the resulting negative pressure in the leaves pulls water from the roots.
The pressure-flow hypothesis describes how the pressure difference in the leaves and roots is used to drive the movement of sugars through the plant.
Companion cells are specialized cells found in phloem tissue that help to support the sieve tube cells which are responsible for the actual transport of sap.
Phloem sap is a complex mixture of sugars and other substances and not only glucose.
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Help? I don't understand
Answer:
Secondary succession is more common and usually occurs faster than primary succession because the substrate is already present.
Explanation:
Hope it helped:)
A similar screening test was developed and evaluated on a similar population, and found to have a sensitivity of 38%, a specificity of 97%, with 63% positive predictive value and 91% negative predictive value. Pick the correct interpretations of these results: (Pick all answers that are true - you will get partial credit for whatever you get correct)
Students who do not genuinely have anorexia are more likely to be ruled out by this screening test than those who do.
The screening test indicates that anorexic children have a 38% chance of testing positive while anorexic students have a 97% chance of testing negative.
Those who test positive for disease have a 63% likelihood of having it, whereas those who test negative have a 91% chance of being disease-free. An unjustified fear of being overweight and a skewed body image are characteristics of anorexia.
Attempts to keep a weight below average by fasting or excessive activity are symptoms. To get back to normal weight, medical intervention could be required.
College students face a lot of pressure to be social and presentable because they are frequently in the company of people their own age. Numerous children decide when, what, and how much to eat for the first time. The two most typical eating disorders are bulimia and anorexia. Usually, eating disorders start between the ages of 18 and 21. In college, between 10 and 20% of women and 4 to 10% of males struggle with eating disorders, and the prevalence is rising.
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Growth hormone stimulates the liver and other tissues to produce growth stimulants called insulin-like growth factors which are also called what
Development chemical invigorates the liver and different tissues to deliver development energizers called insulin-like development factors which are additionally called Somatostatin is one more name for human development chemical.
Corticotropin-delivering chemical (CRH) is let out of the nerve center, which invigorates the foremost pituitary to deliver adrenocorticotropic chemical (ACTH). ACTH then, at that point, follows up on its objective organ, the adrenal cortex.
Development chemical animates the creation of insulin-like development factor 1in the liver and different organs, and this follows up on tissues in the body to control digestion and development. Notwithstanding its impact on the development of chemical discharge, the development chemical delivering chemicals additionally influences rest, food admission, and memory.
Human development chemical, otherwise called hGH and somatotropin, is a characteristic chemical your pituitary organ makes and delivers that follows up on many pieces of the body to advance development in youngsters.
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A high relative humidity and sunshine hinder heat loss from the body by their adverse effects on the body, respectively, as:
The correct option (C) decreased evaporation and increased radiation.
Why does relative humidity climb the most just before dawn?
The ability of the air to hold water vapor increases with temperature. As a result, relative humidity rises as the temperature rises and reduces as it approaches the dew point. Around daybreak, when the nighttime low temperature is generally quite close to the dew point, the relative humidity is typically at its peak.
How does a high relative humidity affect things?
The "Heat Index" is the name given to this combined impact. The heat index increases with increasing air temperature and/or relative humidity, making the outside air seem hotter to our bodies.
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A high relative humidity and sunshine hinder heat loss from the body by their adverse effects on the body, respectively, as:
A. increased condensation and radiation
B. increased convection and radiation
C. decreased evaporation and increased radiation
D. decreased condensation and decreased radiation
E. increased evaporation and increased convection
a host is not considered diseased until an infection changes one's state of health. true or false
Answer:
it Is true
Explanation:
because he wouldn't have a virus and feel well
What is the difference between cellular respiration and getting energy from a log by burning it?
The stored chemical energy is eventually released during cellular respiration through a sequence of enzyme-aided processes. When a log burns, chemical energy that has been stored is swiftly released as heat and light.
Living cells need respiration, a biological process, to release energy. A chemical reaction called combustion takes place outside of living organisms or cells. A controlled biological process, respiration. It is impossible to control combustion. When there is oxygen present, substances undergo a chemical reaction known as burning, which produces significant amounts of heat and light. Similarities between burning and respiration For the creation of energy, both processes need oxygen. As a byproduct, they emit carbon dioxide. The metabolic process known as respiration is when an organism obtains energy from the breakdown of glucose molecules in the form of ATP molecules.
When compounds are exposed to oxygen, a chemical reaction known as burning takes place.
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What are ome of the body' natural immune repone to injury that are cauing john ymptom
The body’s natural immune responses to injury that are causing John's symptoms are the innate immune response and the adaptive immune response.
The primаry function of the immune system is to defend the body from pаthogens, which аre diseаse-cаusing orgаnisms such аs viruses аnd bаcteriа. Tissues, cells, аnd proteins in the immune system work together to аchieve this function.
When а pаthogen gets into the body, the immune system reаcts in 2 wаys.
The innаte immune response is а rаpid reаction. Innаte immune cells recognize certаin molecules found on mаny pаthogens. These cells аlso reаct to signаling molecules releаsed by the body in response to infection.The аdаptive immune response is slower thаn the innаte response but is better аble to tаrget specific pаthogens. There аre 2 mаin cell types involved in this response: T cells аnd B cells.For more information about the immune system refers to the link: https://brainly.com/question/19843453
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What are the 3 factors that cause natural selection?
Natural selection is founded on three principles: most qualities are inherited inheritance, more children are born than can survive competition, and children with more desirable characteristics will survive and produce more offspring variation.
One of the four fundamental tenets of evolutionary theory, along with mutation, migration, and genetic drift, is natural selection. Populations that exhibit variety in features, such as colour, are subject to natural selection. Its core tenet is that individuals are more likely to reproduce when they possess a characteristic that makes them more likely to survive in a given environment than their counterparts. Four requirements must be met for natural selection to take place: reproduction, inheritance, variety in physical traits, and variation in the number of children produced by each person.
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Which of the following is true concerning the anatomy of a skeletal muscle fiber?
a. actin and myosin sliding past each other and partially overlapping
b. certain smooth muscle cells can actually divide to increase their numbers
c. tropomyosin
d. myofibrils contain thick and thin filaments
A protein which regulates the activity of the lactose locus is located outside the lac operator and is encroaching, a globular contractile protein, works with myosin to contract muscles.
The single cells are what?Unicellular creatures are sometimes known as single-cell organisms. In contrast to multicellular creatures, which are made up of many cells, single cell organisms were minuscule and consist of just one cell. They are capable of functioning as a single cell that is capable of sustaining life.
What are some uses for single cells?Single-cell sequencing technology may identify individual immune cells, making it possible to distinguish between distinct immune cell types and learn about the relationships between them.
This contributes to our understanding of the intricate immune system and suggests new disease-treating targets.
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Identify the organ systems in your body that need to work together when dancing, eating bread, writing on a piece of paper.
Answer:
Muscular system, nervous system, skeletal system
Digestive system, blood circulatory system, respiratory system
Nervous system, muscular system, skeletal system
Question 22 of 22 Several members of the family in the pedigree who suffered from a disease are colored in black. Currently deceased members of the family are struck out with a line. Based on the data in the pedigree, propose a Mendelian model that would explain the inheritance of this disease. Explain how the data is consistent with your model. A scientist hypothesizes that a mutation at a single locus is responsible for the pattern of inheritance seen in this pedigree. Explain how a mutation in a gene can arise during meiosis. Describe one strategy organisms use to prevent such mutations from arising.
A. Many families have Alzheimer's disease. From this we conclude that the disease is X-linked recessive.
B. Meiosis is the process of generating gamete cells. There are two choices: mutual break join and another non-reciprocal break copy.
Many families are affected by Alzheimer's disease. It cannot be autosomal inherited because it affects more men than women. Affected males in the second generation have many affected children with normal wives.
If it was autosomal dominant, the sick father would have passed it on to all his second-generation children, but that is not the case. Therefore, it cannot be autosomal dominant.
If it had been autosomal recessive, he would not have affected his children, as his wife appears normal. increase. Therefore, it is not an autosomal abnormality.
Not X-linked dominant, in which case the affected father passed his only X chromosome to his daughter, making her daughter sick. But in this case, the sons are involved. Therefore, it is not X-linked dominant.
From this we conclude that the disease is X-linked recessive.
B. Meiosis is the process of generating gamete cells. Mutations can occur during meiosis in various ways such as double-strand breaks, inversions and point mutations. Important mutation types include missense, nonsense, and point mutations. Cells use multiple repair mechanisms to repair DNA damage or mutations during meiosis. One of the most efficient mechanisms is double-strand break repair by homologous recombination (HR).
Here, the DNA is unwound at the mutated region by recA loading. Recombination with homologous pairs continues through the RecBCD complex.
Here are his two alternatives: reciprocal break join and another non-reciprocal break copy.
Repair normally occurs during her S phase of the cell cycle, when the cell divides its DNA. However, mutations that occur during meiosis, such as chromatid pairing and recombination, are not easily repaired. Cells stop dividing only when the mutation gets worse.
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A thoracentesis specimen was collected and sent to the laboratory for testing. What body area was this specimen collected
The body area where this specimen was collected is thorax when a thoracentesis specimen was collected and sent to the laboratory for testing.
The thorax is the place among the stomach inferiorly and the foundation of the neck superiorly. It paperwork from the thoracic wall, its superficial structures (breast, muscles, and skin) and the thoracic cavity. The location of the frame among the neck and the stomach. The thorax carries important organs, inclusive of the heart, fundamental blood vessels, and lungs. It is supported through the ribs, breastbone, and spine. A skinny muscle referred to as the diaphragm separates the thorax from the stomach. It gives a base for the muscle attachment of the higher extremities, the pinnacle and neck, the vertebral column, and the pelvis. The thorax additionally gives safety for the heart, lungs, and viscera.
Thus, the body area is known as thorax.
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A molecule that can be used as a molecular clock has a neutral mutation rate of one mutation per 40 million years. How many years ago did two species share a common ancestor if the molecules found in these two species differ by a total of eight mutations
The two species must have shared a common ancestor 320 million years ago, since the neutral mutation rate of the molecular clock is one mutation per 40 million years and the two species differ by a total of eight mutations.
A molecular clock is a tool used by scientists to estimate the time since two species have shared a common ancestor. This is done by measuring the number of genetic differences, or mutations, between the two species. The molecular clock is based on the assumption that the mutation rate is constant.
In this case, we know that the neutral mutation rate of the molecule being used as a molecular clock is one mutation per 40 million years. This means that for two species to have a difference of eight mutations, it must have been at least 320 million years ago that they shared a common ancestor.
To arrive at this conclusion, we can use the following formula:
Number of mutations × Neutral mutation rate = Time since common ancestor
In this case, 8 mutations × 40 million years = 320 million years. This means that two species must have shared a common ancestor at least 320 million years ago for them to have a difference of eight mutations.
The molecular clock can be a powerful tool for scientists to estimate the time since two species have shared a common ancestor. In this case, the neutral mutation rate of the molecule was known and used to calculate that two species must have shared a common ancestor at least 320 million years ago.
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How do you release chronically tight muscles?
Chronically tight muscles can be release by Stretching ,Massage ,Foam Rolling and Strengthening.
Chronically tight muscles can be caused by over using muscle , poor posture , stress , anxiety and depression . This stiffness can commonly occurs after extensive exercise or lifting weights. this stiffness can also occurs after periods of inactivity, like prolonged sitting and sleeping for long hours in the bed.
In general , Muscle pain can effect almost every part of your body, which may include your neck, back, legs and even your hands. These pain can be relived by various medication that includes relaxant and ointments that soothes the pain .
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At what heart rate should you start compressions on a newborn?
The current neonatal resuscitation guidelines recommend to start chest compression in a newborn infant if the heart rate remains <60 beats per minute despite adequate ventilation for 60 s .
A small percentage (less than 10%) of newborn babies need active resuscitative measures in order to establish a loud cry or consistent breathing, keep their heart rates over 100 beats per minute (bpm), and acquire acceptable color and tone.
The establishment of proper ventilation has to be your top priority. If stimulation does not result in the prompt commencement of spontaneous respirations or the heart rate is below 100 bpm, give assisted ventilation while paying close attention to oxygen delivery, inspiratory time, and effectiveness as determined by chest rise.
To obtain roughly 90 compressions and 30 breaths per minute, time chest compressions with ventilations at a 3:1 ratio at a rate of 120 events per minute. If the heart rate is below 60 beats per minute after 30 seconds of efficient aided breathing and circulation, provide epinephrine (chest compressions).
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What would happen if a mistake were not caught by the proofreading mechanism and became permanent in the DNA
If a mistake were not caught by the proofreading mechanism and became permanently incorporated into the DNA, the consequences could be catastrophic.
The DNA is the blueprint for all life, and any mutation or alteration can cause a range of problems, from minor to severe. If the mistake were to alter a gene that is important for cell survival, it could lead to a range of health problems, from mild to life-threatening.
For example, if a gene that is responsible for the production of a certain enzyme is altered, it can cause a metabolic disorder, leading to physical and mental disabilities. If the mistake were to alter a gene that is responsible for the functioning of a specific organ, such as the heart or brain, it could lead to serious health problems, such as heart defects or neurological disorders.
If the mistake were to alter a gene responsible for the development of an organism, it could lead to serious developmental defects or even death. For example, if a gene that provides instructions for the development of the body's organs is altered, it could lead to serious malformations or even death.
In addition to the health risks, a mistake in the DNA could also lead to changes in the species. For example, if a mutation alters a gene that is important for the survival of a species, it could lead to the extinction of the species. This could be due to a decrease in fertility, a decrease in the population size, or an inability to adapt to a changing environment.
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When a person looks at a bright light, tiny muscles in the eye contract so less light can enter the eye. Which are most likely the characteristics of this muscle
At the point when an individual glance at a brilliant light, minuscule muscles in the eye contract so less light can enter the eye. These are in all probability the attributes of this muscle nonstriated, compulsory, and connected to the eyeball.
They are smooth muscles (nonstriated) that are not controlled intentionally. You don't get those minuscule muscles on your own will when you check a brilliant light out. It is additionally connected to the eyeball since it agrees to guarantee the most un-conceivable measure of light gets to your eye.
A few capabilities are automatically performed, for example, breathing, processing, heart pulsating, eye reflexes, and so on, however, a few compulsory activities have intentional control partially - models are breathing, salivation, deglutition (gulping), poop, micturition (pee) and others.
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Data was collected concerning Galapagos bird beak size over time. There are several species finches, and they are also known as
Darwin's Finches. These finches share the same habits and characteristics except for one; they all have different shaped and sized
beaks. The differences in their beaks might be the most important aspect of their survival. Around 1977, there was a huge drop in
finches with small beaks while there was a great increase in large-beaked birds. How can you explain this?
A)
The small-beaked finches were prey for larger animals.
B)
The large-beaked birds preyed on the small-beaked birds.
Available food changed and the small beaked birds could not readily adapt.
D)
Competition for food favored large beaks; the small beaked birds died off.
The struggle among Darwin's Finches, which is especially fierce during dry spells due to food scarcity, benefits those who are most adapted to their environment, according to the best conclusion.
Different finches species have nutritional specializations that are characterized by variations in their beaks due to diverse ecological settings on the same island.
Additionally, it has been demonstrated that finches that live in highly planted zones have a distinct call than those that reside in less vegetated areas, expanding their spectrum of mating calls.
A couple that belongs to the same milieu (environment) is more likely to be discovered as a result of this event, and it is from that point that the stabilization of genetic traits unique to the ecological environment occurs.
With this information, we can conclude that competition, which is particularly severe in periods of drought due to food shortages, favors the individuals most adapted to their environment. Because they have a greater chance of survival and, therefore, of reproduction, their particular genetic characteristics tend to be passed on to subsequent generations.
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How does Hardin’s example of the herdsman and his mathematical justification (nearly +1 and fraction of -1) embody the tragedy of the commons?
Garrett Hardin used the expression for the first time in a 1968 Science article.
The Tragedy of theere is Commons' core claim is that when something is owned by a collective (rather than a single person), its overall sustainability may suffer since th no single entity that is legally in control of or responsible for it. This argument states that people frequently make decisions that advance their own interests, regardless of how those decisions could affect other people. Garrett James Hardin is an environmental expert from the United States. He wrote an essay with the same title that was published in Science in 1968, and after reading it, he decided to devote the remainder of his life to researching human behaviour.
Any attempt to control nature will result in a variety of consequences, many of which are unexpected. Several websites have referred to Garrett as a white nationalist because of his violently anti-immigrant attitudes, eugenics beliefs, and views on multiethnicity. The Southern Poverty Law Center characterised his writings as "frank in their bigotry and quasi-fascist ethnonationalism."
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Why aren’t the three rRNA genes of corn one another’s closest relatives?
A. Because corn is a hybrid of yeast, cyanobacteria, and E. coli
B. Endosymbiosis in the ancestor of corn gave it the ability to photosynthesize and respire
C. Endosymbiosis in the ancestors of eukaryotes, and again in photosynthetic eukaryotes led to the evolution of mitochondria and chloroplasts, which retain parts of their original genomes
The correct option (c) Endosymbiosis in the ancestors of eukaryotes, and again in photosynthetic eukaryotes led to the evolution of mitochondria and chloroplasts, which retain parts of their original genomes.
Ribosomal ribonucleic acid (rRNA) is a non-coding RNA that is the principal component of ribosomes, which are required by all cells. rRNA is a ribozyme that conducts protein synthesis in ribosomes.
Ribosomal RNA is transcribed from rDNA and then bound to ribosomal proteins to produce small and large ribosomal subunits. The ribosome's physical and mechanical element that causes transfer RNA (tRNA) and messenger RNA (mRNA) to process and translate the latter into proteins is rRNA.
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macroscopically visible growths or clusters of microorganisms on solid media are called __________.
The answer is:
Colonies
why does breathing become faster during exercise
Explanation:
When you exercise and your muscles work harder, your body uses more oxygen and produces more carbon dioxide. To cope with this extra demand, your breathing has to increase from about 15 times a minute (12 litres of air) when you are resting, up to about 40–60 times a minute (100 litres of air) during exercise.
Your body needs more oxygen and creates more carbon dioxide while you exercise because your muscles are working harder.
6. Prepare a dichotomous key for the five fish in Figure 3.
REMEMBER: 1.) Each step has only two options. 2.) The options should be about the same characteristic.
Instead of ending with the family name for these fish, you should end with the numbers I, II, III, IV, and V. To
help you get started, I have given you the first pair of statements.
1.A.
B.
2.A.
Figure 3.
If the fish has a long, tube like body
If the fish does not have a tube like body
IV
******
A dichotomous key is a tool that can be used to identify organisms or objects in the natural world, such as plants, animals, or rocks. The dichotomous key for the given question is as follows in the explanation part.
What is a dichotomous key?A dichotomous key may be characterized as a type of key that is significantly utilized for the identification of organisms based on a series of choices between alternative characters.
If the fish has a long, tube-like body: I and IV. If the fish does not have a tube-like body: II and V. If the fish has a spherical appearance: II and V.If the fish does not have a spherical appearance: I and IV. If the fish swims at a rapid speed: I and IV.If the fish does not swim at a rapid speed: II and V.Fish that possess proper gills: III and IV. Fish that do not possess proper gills: I and V. Fish that absorb more water: I and IV.Fish that do not absorb more water: II and V.Therefore, the dichotomous key for the given question is well described above.
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What is a point insertion and deletion mutation?
In Point insertion DNA sequence is changed by adding one or more nucleotides to the gene. In deletion DNA sequence changed by removing at least one nucleotide in a gene.
In general, a Point mutation refers to alteration in a single base pair of DNA by substitution, deletion, or insertion of a single nitrogenous base. most common example of point mutation is sickle cell anemia. that consists of mutation in a single base pair in the beta-globin chain of hemoglobin pigment in the blood cells.
While , deletion mutation generally takes place when part of a DNA molecule is not copied during DNA replication. Thus the uncopied part remains as small as a single nucleotide or as an entire chromosome.
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One well-known recessive disorder is __________, which affects the way the body breaks down proteins contained in many foods.
One well-known recessive disorder is Phenylketonuria (PKU), which affects the way the body breaks down proteins contained in many foods.
Phenylketonuria (PKU) is an extraordinary however doubtlessly severe inherited disease. Our our bodies smash down the protein in foods, consisting of meat and fish, into amino acids, that are the "constructing blocks" of protein. Phenylketonuria, additionally referred to as PKU, is an extraordinary inherited disease that reasons an amino acid referred to as phenylalanine to accumulate withinside the body. PKU is due to a alternate withinside the phenylalanine hydroxylase (PAH) gene. This gene allows create the enzyme wanted to interrupt down phenylalanine. Phenylketonuria is a genetic circumstance in which ranges of phenylalanine building up for your body. If left untreated, phenylketonuria can have an effect on a person's cognitive development. Treatment with medicines and/or nutritional modifications assist lessen symptoms.
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List all the possible genotypes of the offspring from your Punnett
square in question 4. Next to each genotype write the corresponding
phenotype---short stems or tall stems.
we see that there are three possible genotypes that could result from this crossing: AA, Aa, aa. The genotypes AA and Aa will result in the yellow pea phenotype because A is dominant. Only aa will produce the green pea phenotype.
A Punnett square is a graph that makes it simple to ascertain the anticipated proportion of various genotypes in children of two parents. Figure below illustrates a Punnett square for pea plants. In this instance, flowercolor is heterozygous for both parents (Bb). The top of the graph represents the gametes produced by the male parent, while the sides represent the gametes produced by the female parent. By correctly filling in the Punnett square's cells, we may identify the various possible allele combinations in their progeny (alleles).
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How is most ATP formed during respiration?
Most of the ATP produced by aerobic cellular respiration is made by oxidative phosphorylation
Oxidative phosphorylation is responsible for the majority of the ATP generated by aerobic cellular respiration. Protons are pumped through a membrane to produce a chemiosmotic potential using the energy released. Then, ATP synthase is engaged by this potential to synthesis ATP from ADP and a phosphate group. During aerobic respiration, glucose and oxygen combine to produce ATP, which the cell can utilise. As products, water and carbon dioxide are produced. In the general equation for aerobic cellular respiration, glucose and oxygen combine to create ATP. Oxidative phosphorylation is the biochemical cycle that generates a most net ATP per molecule of glucose. The majority of ATP synthesis takes place during cellular respiration in the mitochondrial matrix, producing about 32 ATP molecules for every glucose molecule.
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