What was most crucial to gregor mendel’s final analysis

According to some genetic researchers, the palindromic and repetitive sequences found in the Y chromosome.

oee [108]

A word pharse that read the same backward as forward . it's about genetic table

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3 years ago

The Scientific Metho

Xelga [282]

Answer:

a.)

Explanation:

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3 years ago

Description of change 2011 japan tsunami

Vinvika [58]

2011 Tōhoku earthquake and tsunami<span>The 2011 earthquake off the Pacific coast of Tōhoku was a magnitude 9.0–9.1 undersea megathrust earthquake off the coast of Japan that occurred at 14:46 JST on Friday 11 March 2011, with the epicentre approximately 70 kilometres east of the Oshika Peninsula of Tōhoku and the hypocenter at an underwater depth of approximately 29 km. The earthquake is also often referred to in Japan as the Great East Japan earthquake and also known as the 2011 Tōhoku earthquake, and the 3.11 earthquake. It was the most powerful earthquake ever recorded to have hit Japan, and the fourth most powerful earthquake in the world since modern record-keeping began in 1900. The earthquake triggered powerful tsunami waves that reached heights of up to 40.5 meters. got from Wikipedia, need anything else let me know</span>

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3 years ago

Read 2 more answers

Explain mutations and how they can cause genetic disease

nadya68 [22]

Answer:

A mutation is a change in a DNA sequence. Mutations can result from DNA copying mistakes made during cell division, exposure to ionizing radiation, exposure to chemicals
called mutagens, or infection by viruses. Germ line mutations occur in the eggs and sperm and can be passed on to offspring, while somatic mutations occur in body cells and are not passed on.

Mutation has been the source of many Hollywood movies, but it's really a simple process of a mistake made in a DNA sequence as it's being copied. Some of that's just the background noise that DNA copying is not perfect, and we should be glad of that or evolution couldn't operate. But mutation can also be induced by things like radiation or carcinogens in a way that can increase the risk of cancers or birth defects. But it's pretty simple; it's basically an induced misspelling of the DNA sequence.
That's a mutation.

When a variant alters a protein that plays a critical role in the body, it can disrupt normal development or cause a health condition. A condition caused by variants in one or more genes is called a genetic disorder. In some cases, gene variants are so severe that they prevent an embryo from surviving until birth.

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3 years ago

Predict phenotypes associated with nondisjunction of sex chromosomes.

Mnenie [13.5K]

Answer: The new daughter cells will have an abnormal amount of genetic material. That is called aneuploidy and it is the presence of an abnormal number of chromosomes. Different clinical conditions are the result of this nondisjunction.

Explanation:

Normal cells are diploids, that means they have two copies of each gene, one of each chromosome. So normal cells have two homologous chromosomes, one from each parent.

During anaphase of cell division, each pair of chromosomes is separated by the mitotic spindle. The separated chromosomes are then pulled by the spindle to opposite poles of the cell, and eventually will end up in the new daughter cells.

Nondisjunction is the failure of homologous chromosomes to separate properly during cell division, so it is the miss segregation of them. The new daughter cells will have an abnormal amount of genetic material. <u>Different clinical conditions are the result of this nondisjunction.</u>

Sex chromosomes participates in sex determination of an individual. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY) So nondisjunction of sex chromosomes could be:

XX: one cell with no chromosome and the other cell with two X chromosomes.
XY: one cell with no chromosomes and the other cell with XY chromosomes.

According to which gametes are fused during fertilization, different phenotypes can be given. For example, if a gamete with one chromosome fuses with another gamete with two chromosomes, the result will be an individual with three chromosomes (it could be XXY, or XXX) called trisomy.

Triple X syndrome is characterized by an extra X chromosome in females. Those affected are often taller than average, but most females have a normal sexual development. Klinefelter syndrome is known XXY individuals, and it causes infertility in males, breast growth, less body hair and weaker muscles.

And if a gamete with no chromosome fuses also with another gamete with no chromosome, the result is a nullisomy. But due to the lack of genetic material, the nullisomic gametes are rendered unviable for fertilization.

And if a gamete with no chromosome fuses with another gamete with one chromosome (normal) the result is a monosomy, the presence of only one chromosome from a pair. The result can be an individual who is X or Y. People with Turner syndrome have one X chromosome and it is the only monosomy that is seen in humans because other cases monosomy are lethal.

Any of those examples is called aneuploidy and it is the presence of an abnormal number of chromosomes.

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3 years ago