Answer:heredity
Explanation:something that’s passed on to some members
Answer:
Heredity
Explanation:
You get some of these traits from your parents such as hair color, eye color, height, etc
What percentage of the water entering the small intestine is absorbed by the small intestine?.
What happens along the neural pathway when the tongue detects the stimulus?
Nerve cells transmit taste signals to the brain.
Dna polymerase links nucleotides into a chain by helping __.
An excess of nitrates in a lake could lead to
Answer:
The growth and aquatic plants and algae, but also the death of fish and other invertebrates.
Hypothesize how the breakup of Pangaea might have contributed to the evolutionary history of primates? PLS HELP
Pangea began to split around 200 million years ago, and the first primates ensued around 85 million years ago.
What is Pangea?When a three-pronged fracture developed between Africa, South America, and North America, Pangea first started to split apart. A volcanic rift zone was formed when magma welled up through the crustal weakness and rifting started.
As these split, continent-sized pieces of Pangea divided, volcanic explosions threw ash and volcanic debris throughout the terrain.
North America was being gradually pushed away from the rift zone and westward. A sequence of down-dropped fault blocks that closely parallel today's coastline were created as a result of the heavy continental crust that made up the new east coast collapsing.
Therefore, Pangea began to split around 200 million years ago, and the first primates ensued around 85 million years ago.
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In the cross TT x Tt, which of the following is true about the offspring?
T = tall
t = short
tall is completely dominant to short
Although this single cell can produce the protein of interest, one cell
can't produce enough to really help people. How can this problem
be solved? Type your proposed solution below:
Answer:
Single-cell proteins develop when microbes ferment waste materials (including wood, straw, cannery, and food-processing wastes, residues from alcohol production, hydrocarbons, or human and animal excreta). They are found in very low concentrations, usually less than 5%. Engineers have developed ways to increase the concentrations including centrifugation, flotation, precipitation, coagulation, and filtration, or the use of semi-permeable membranes.
Explanation:
I believe this is right I'm sorry if it isn't
State 10 differences between sandy and clay soil
Answer:
1 . clay soil : contains finer particles
sandy soil : contains larger particles
2 . clay soil : it is fertile
sandy soil : it is not fertile
3 : clay soil : particles are tightly packed
sandy soil : Particles are loosely packed
4 : clay soil : High water retention capacity
sandy soil : Low water retention capacity
5 : clay soil : Good for growing various crops
sandy soil : Not suitable for growing crops
Mark as brainlest ... Hope it helps!!!
Amoeba Sisters Video Recap: DNA vs. RNA & Protein Synthesis UPDATED Protein Synthesis Summary Complete the missing information in the summary chart after watching the Amoeba Sisters Protein Synthesis video. Process Name Location (in eukaryotic cell) Brief and General Description End Result DNA directly involved? (yes or no?) List RNA type(s) involved (mRNA, rRNA, and/or tRNA?) Transcription 21. 22. 23. 24. mRNA only Translation 25. 26. 27. No 28. 29. Consider the illustration placed in the transcription box above. Identify and label on the illustration if any of the following are present: DNA, mRNA, rRNA, tRNA, and/or amino acid. 30. Consider the illustration placed in the translation box above. Identify and label on the illustration if any of the following are present: DNA, mRNA, rRNA, tRNA, and/or amino acid.
Transcription is the process of making RNA from DNA molecules and it occurs in the nucleus.
Translation is process of making proteins from mRNA and tRNA molecules .
What is transcription?Transcription is the process where DNA molecules are used to synthesize RNA molecules.
Transcription occurs in the nucleus and the RNA produced is mRNA.
What is translation?Translation is the process whereby mRNA is used to make proteins.
It is also known as protein synthesis.
Translation occurs at the ribosomes in the cytoplasm.
mRNA and tRNA molecules are used to synthesize proteins.
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Someone please help with this. It has to be at least a paragraph long answer
Answer:
during meiosis, an event known as chromosomal crossing over sometimes occurs as a part of recombination. In this process, a region of one chromosome is exchanged for a region of another chromosome, thereby producing unique chromosomal combinations that further divide into haploid daughter cells.
In the human ABO blood type system, which genotype would result in red blood cells that exhibit codominance
Based on information from the periodic table, what does this image
represent?
4 Protons
= 5 Neutrons
= 4 Electrons
Answer:
This is beryllium
Explanation:
If you had a periodic table to work off of, it would be a bit easier, because normally the protons and atomic number are the same.
Hope this helped!!
What is the best over-the-counter medicine for restless leg syndrome.
Answer:
Aspirin, ibuprofen, or acetaminophen.
Explanation:
One parent has dimples, which is a dominant trait. The other parent has no dimples which is a recessive trait.
Dd
d
d
What can be predicted about their offsprings' chances of having dimples?
A 75% will have dimples
B 25% will have dimples
0% will have dimples
50% will have dimples
E 100% will have dimples
Is this right, please help me?
Yeah this is right answer
Huqqa base, (1.9.3) uses repeated, stylized flowers and leaves of plants as a ________ to create a strong, unified design.
Pashmina carpet from northern India uses repeated, stylized flowers as MOTIFS to create a unified design. The Huqqa base is a type of Indian metalwork.
What are the Pashmina carpet and the Huqqa base?The pashmina carpets are a specific type of carpet developed in northern India around the 17th century.
Pashmina carpets are very popular around the world due they are developed using soft materials.
Moreover, the Huqqa base is a class of Indian metalwork called bidri, which was developed in Bidar (north-eastern part of Karnataka state in India) in the 19th century.
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For a mutation to affect evolution, it must:
a.
Provide a benefit to the organism
b. Involve more than one chromosome
C Be able to get passed from parent or offspring
d. Be neutralneither help nor harm the organism
Answer:
C
Explanation:
For mutation to occur
It must affect hereditary material
If the nucleotide or base sequence of the DNA strand used as a template for messenger RNA synthesis is ACGTT, then what would be the sequence of bases in the corresponding mRNA?
A) ACGTT.
B) TGCAA.
C) UGCAA.
D) GUACC.
Answer:
C
Explanation:
u pairs with a, a pairs with t, c pairs with g, and g pairs with c
Use this space to map your dystrophin analogy. Make sure to include sarcolemma (cell membrane),
dystrophin, myofibril, and the relationship between structure and function
Please help answer this question
Abstract
The dystrophin complex stabilizes the plasma membrane of striated muscle cells. Loss of function mutations in the genes encoding dystrophin, or the associated proteins, triggers instability of the plasma membrane and myofiber loss. Mutations in dystrophin have been extensively cataloged providing remarkable structure-function correlation between predicted protein structure and clinical outcomes. These data have highlighted dystrophin regions necessary for in vivo function and fueled the design of viral vectors and now, exon skipping approaches for use in dystrophin restoration therapies. However, dystrophin restoration is likely more complex, owing to the role of the dystrophin complex as a broad cytoskeletal integrator. This review will focus on dystrophin restoration, with emphasis on the regions of dystrophin essential for interacting with its associated proteins and discuss the structural implications of these approaches.
Keywords: muscular dystrophy, dystrophin, spectrin repeat, exon skipping, sarcoglycan, sarcolemma
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INTRODUCTION
Muscular dystrophy is a collection of inherited diseases characterized by skeletal muscle weakness and degeneration. Muscular dystrophies are progressive disorders because over time healthy muscle fibers are lost and replaced by fibrosis and fat, making muscle tissues less able to generate force for everyday activity. As muscle wasting ensues, patients experience weakness, although muscle groups may be targeted differently in specific forms of muscular dystrophy. Respiratory failure, resulting from the weakening of breathing muscles, may limit lifespan in muscular dystrophy unless mechanical support is instituted. In some forms of muscular dystrophy, the heart is also affected resulting in cardiac complications including heart failure and irregular heart rhythms.
Duchenne muscular dystrophy (DMD) is one of the most common forms of muscular dystrophy. DMD is caused by recessive mutations in the dystrophin gene on X chromosome, affecting 1 in 3,500 to 5,000 newborn males worldwide (82). Boys with DMD show signs of muscle weakness early in childhood, typically between 2 and 7 years of age, and often lose ambulation around the time of puberty. DMD boys may have delayed development of motor skills such as sitting, walking and talking. Becker muscular dystrophy (BMD) is also caused by mutations in the DMD gene that encodes dystrophin. Individuals with BMD share similar signs and symptoms with DMD boys but with later onset and more varied time course. Like DMD, the heart can be affected in BMD.
The dystrophin gene is the largest known human gene, containing 79 exons and spanning > 2,200 kb, roughly 0.1% of the whole genome (96). The most common mutation responsible for DMD and BMD is a deletion spanning one or multiple exons. Such deletions account for 60–70% of all DMD cases and 80~85% BMD cases (58, 147). Point mutations are responsible for around 26% of DMD cases and 13% BMD cases. Exonic duplications account for 10 to 15% of all DMD cases and 5% to 10% BMD cases. Subexonic insertions, deletions, splice mutations and missense mutations account for the rest of the cases. DMD is associated with mutations that disrupt the protein’s reading frame causing premature stop codons. These mutated transcripts are susceptible to nonsense mediate decay, and the carboxy-terminal truncated protein products are also unstable and subject to degradation, leaving little or no protein produced in cells. In contrast, BMD patients usually have in-frame deletions that maintain the correct reading frame. Furthermore, nonsense mutations have been associated with both BMD and DMD. However, nonsense mutations associated with BMD are more prone to induce exon skipping than those found in DMD (59). The resulting protein products in BMD are internally truncated and expressed at lower levels than normal muscle. However, these internally truncated proteins are expressed at higher levels than in DMD and remain partially functional. Within one BMD affected family, three males carrying the same nonsense mutation in exon 29 displayed phenotypes from severe, mild to asymptomatic. This nonsense mutation is located in an exon recognition sequence in exon 29 and induces partial skipping of exon 29, producing an internally truncated dystrophin. A considerable amount s
Dystrophin is a complex structure that acts as an anchor, which connects the muscle cell cytoskeleton to the lattice of the protein and other extracellular matrix molecules.
What is dystrophin?It acts as a subsarcolemmal rod-shaped protein having a function to stabilize the sarcolemma, by connecting the extracellular matrix to the actin cytoskeleton through the dystrophin-associated glycoprotein complex.
This connection through the dystrophin-associated glycoprotein complex for sarcolemma maintains muscle cells from contraction-induced damage.
Dystrophin myofibril is a protein complex located between the sarcolemma and the outermost layer of myofilaments in the muscle fiber (myofiber). This is located at the muscle sarcolemma.
Therefore, dystrophin is a complex structure that connects the muscle cell cytoskeleton to the extracellular matrix.
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An example formed by metamorphic rocks would be _________________. (Choose 2)
Group of answer choices:
the Grand Canyon of Yellowstone
Red Rock Canyon
Cedar Breaks
the Grand Canyon
Bryce Canyon
the Himalayas
Answer:
the Grand Canyon of Yellowstone and the Himalayas
Explanation:
i dont know why tbh but those are the answers :p
An example formed by Metamorphic rocks would be the Grand Canyon of Yellowstone, and the Himalayas. Thus, the correct options are A and F.
What is Metamorphic rock?
Metamorphic rocks is a type of rock which have been substantially changed from their original form such as igneous, sedimentary, or earlier metamorphic form into mature metamorphic rock. The metamorphic rocks are formed when rocks are subjected to high temperature, pressure, hot mineral-rich fluids and, more commonly combination of these factors.
Some common examples of Metamorphic rocks are the Grand Canyon of Yellowstone and the Himalayas. The most common forms of metamorphic rocks are slates, schists and gneisses.
Therefore, the correct options are A and F.
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ancient Greeks believed the body has four humors blood phlegm yellow bile and black bile if the Greeks were aware of modern biological practices what would their humours be responsible for
if the Greeks had knowledge of modern biological practices the humors responsible for fluids. nowadays we know that fluids are those substances that are permanently in the body and whose production does not depend on external stimuli.
What is the theory of the 4 Hippocrates humors?The Hippocratic theory of the four humors, present in the work On the Nature of Man, constitutes the human body from four fluids:
bloodphlegmyellow bile and black bile.According to the treaty, health would be maintained by a balance between these four humors.
With this information, we know that fluids are those substances that are permanently in the body and whose production does not depend on external stimuli.
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Answer:
transporting anitbodies
Explanation:
What are the small air sacs called that exchange gases in the lungs? valves chambers alveoli nodes.
Answer:
I would go for alveoli
Explanation:
Cus
11. Write the complete formula for photosynthesis:
Please help me please and thank you
6 CO2 + 6 H20 --> C6H12O6 + 6O2
6 Carbon dioxide + 6 Water -> Fructose + 6 Oxygen
Cells pass through a g2 checkpoint before entering mitosis. Ideally, if dna damage is detected, the cells do not enter mitosis until the damage is repaired. Why is dna damage repaired before cells enter mitosis?.
what forms of hydrogen are MOST common on earth?
A. solid
B. gas
C. liquid
D. plasma
Why is water vital to living organisms?
(i need to get an answer ASAP!)
Answer:
it helps break down food
Explanation:
:)
Which trait is DEFINITELY caused by genetics?
weight
height
tanned skin
the hardwork
Thank you
Answer: the height?
Explanation: not too sure on this one
What is biogeography & how does it
provide evidence of evolution?
Answer: Biogeography is the study of the geographical distribution of plants, animals, and other forms of life. (Second part of question is in explanation)
Explanation: Biogeography gives information about how as well as when species might have matured. Fossils provide evidence of extended evolutionary changes, noting the earlier actuality of species that are now extinct.
In a tube-within-a-tube body plan, what is the interior tube derived from?.
Answer:
endoderm!
Explanation:
The tube-within-a-tube plan allows specialization of parts along the tube, such as a stomach, intestine, etc.
Hope this helps! :)
How do organisms obtain what they need from the hydrosphere?