Which region of the scapula is found on the anterior surface.

Answers

Answer 1

Answer:

The subscapular fossa is located on the anterior surface of the scapula.

Explanation:


Related Questions

Based on information from the periodic table, what does this image
represent?
4 Protons
= 5 Neutrons
= 4 Electrons

Answers

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!!

Is this right, please help me?

Answers

Yeah this is right answer

How can tools be useful to scientists who study minerals?
They help scientists build structures.
They help scientists see very large things.
They help scientists research on the internet.
They help scientists observe things that are very small.

Answers

Answer:

They help scientists observe things that are very small.

Explanation:

Geologists use a lot of tools to aid their studies. Some of the most common tools used are compasses, rock hammers, hand lenses, and field books.

Answer: it’s “They help Scientists observe thing that are very small”

Explanation: mostly the last one if I’m right! I hope this helps!!!

How do organisms obtain what they need from the hydrosphere?

Answers

3.4 The importance of the hydrosphere (ESAHT)

Water is a part of living cells Each cell in a living organism is made up of almost 75% water, and this allows the cell to function normally. ... Water provides a habitat The hydrosphere provides an important place for many animals and plants to live.

What happens along the neural pathway when the tongue detects the stimulus?​

Answers

Nerve cells transmit taste signals to the brain.

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?.

Answers

if a cell is damaged, it will not be able to successfully go through mitosis due to it being weak.

what forms of hydrogen are MOST common on earth?
A. solid
B. gas
C. liquid
D. plasma

Answers

C Liquid I believe it is

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

Answers

Answer:

C

Explanation:

For mutation to occur

It must affect hereditary material


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

Answers

The correct answer is B.25%

If a water source has a high pH (9-14) then it is considered?
Acidic
Basic

Answers

Not sure what basic means in this context but it would be considered alkaline and definitely not acidic so I'd say basic.

Put these steps in order
Unzip DNA
Editing and splicing
Translation
Transcription
Finished protein

Answers

Say that again please

Then
construct a graph of the number of bacteria vs. time in hours.

Answers

Answer:

A bacteria culture starts with 500 bacteria and doubles in size every half hour. (a) How many bacteria are there after 3 hours? (b) How many bacteria are there after hours? (c) How many bacteria are there after 40 minutes? (d) Graph the population function and estimate the time for the population to reach 100,000.

Explanation:

it hope it helps

11. Write the complete formula for photosynthesis:
Please help me please and thank you

Answers

6 CO2 + 6 H20 -->  C6H12O6 + 6O2

6 Carbon dioxide + 6 Water -> Fructose + 6 Oxygen

Facts about preventing Hazardous Waste

Answers

Buy and use multipurpose cleaners.

Buy the least harmful product. Read labels.

Wipe up spills when they happen.

Hope this was Helpful! :)

In the human ABO blood type system, which genotype would result in red blood cells that exhibit codominance

Answers

if an individual inherits allele A from their mother and allele B from their father, they have blood type AB.

Mangrove have two types of specialized root systems. Please select the best answer from the choices provided T F.

Answers

Answer:

True

Explanation:


What is biogeography & how does it
provide evidence of evolution?

Answers

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.

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:

Answers

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

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

Answers

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

Go to:

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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Why is water vital to living organisms?

(i need to get an answer ASAP!)

Answers

Answer:

it helps break down food

Explanation:

:)

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

Answers

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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Which one of water's unique properties allows living organisms to maintain a constant internal temperature?

A: it is held together by ionic bonds
B: it has a high specific heat

Answers

Answer:

B: it has a high specific heat

Which trait is DEFINITELY caused by genetics?

weight
height
tanned skin
the hardwork
Thank you

Answers

Answer: the height?

Explanation: not too sure on this one

Hypothesize how the breakup of Pangaea might have contributed to the evolutionary history of primates? PLS HELP​

Answers

Pangea began to split around 200 million years ago, and the first primates ensued around 85 million years ago.

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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What percentage of the water entering the small intestine is absorbed by the small intestine?.

Answers

90 percent
The small intestine absorbs about 90 percent of the water you ingest (either as liquid or within solid food)

16 - Albinism: Prom Genotype to Phenotype
Supplemental activity: Flow Chart
Name:
By creating a flow chart below, trace the steps from DNA through to the resulting phenotype. It has been started for you
below The following words must appear in this flow chart transcription, translation, amino acid(s), protein, gene, mRNA,
TRNA, phenotype
DNA

Answers

A correct flow chart is DNA i.e., gene (transcription) >> mRNA + tRNAs (translation) >> amino acids or protein >> phenotype.  It is the flow of the genetic information.

What is the flow of genetic information?

The flow of genetic information refers to the molecular process from DNA to the final phenotype (i.e., protein product).

During gene transcription, a particular fragment of DNA called gene is used as a template to generate an mRNA.

Subsequently, the mRNA serves as a template to generate a linear chain of amino acids, i.e., a protein, by a process called translation.

The final protein can be considered as the phenotype (in this case, the albinism trait) because it is the observable feature.

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Which of the following would provide the best evidence that genetic factors influence the growth of plants?

Answers

Seeds from several different plants are planted under identical conditions and found to grow at similar rates.

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

Answers

It would be C

Hope this helps!!

Please help if u know

Answers

Answer:

False

Hope it help! Please mark as BRAINLIEST!

What are the small air sacs called that exchange gases in the lungs? valves chambers alveoli nodes.

Answers

Answer:

I would go for alveoli

Explanation:

Cus

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