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      <title>mutations by </title>
      <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4</link>
      <description>rubina wahab</description>
      <language>en-us</language>
      <pubDate>2021-10-20 05:56:42 UTC</pubDate>
      <lastBuildDate>2025-12-15 17:34:30 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>MUTATIONS</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829479436</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-10-20 06:00:54 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829479436</guid>
      </item>
      <item>
         <title>SINGLE GENE MUTATIONS </title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829493417</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-10-20 06:09:59 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829493417</guid>
      </item>
      <item>
         <title>TYPES OF MUTAGENS </title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829495298</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-10-20 06:11:10 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829495298</guid>
      </item>
      <item>
         <title>CHROMOSOME MUTATIONS</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829496538</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2021-10-20 06:11:56 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829496538</guid>
      </item>
      <item>
         <title>(1)  FRAMESHIFT</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829504436</link>
         <description><![CDATA[<div>- It is a genetic mutation that is caused by insertion or deletion of one or more nucleotides, that is not divisible by three<br>- This occurs to the nucleotides that has caused a shift in the reading frame <br><br></div>]]></description>
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         <pubDate>2021-10-20 06:17:07 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1829504436</guid>
      </item>
      <item>
         <title>(2) SILENT MUTATION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830261649</link>
         <description><![CDATA[<div>- Due to DNA redundancy, mutation will not change the amino acid sequence. The result is that the protein is still functional<br>- For amino acid, plenty of codons may code, but this does not lead to any changes in protein</div>]]></description>
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         <pubDate>2021-10-20 13:05:57 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830261649</guid>
      </item>
      <item>
         <title>(3) MISSENSE MUTATION  </title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830266053</link>
         <description><![CDATA[<div>- Missense mutation function is that changes are made to the amino acid due to the fact&nbsp; in the protein the wrong amino acid is being incorporated.&nbsp;</div>]]></description>
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         <pubDate>2021-10-20 13:07:18 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830266053</guid>
      </item>
      <item>
         <title>(4) NONSENSE MUTATION </title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830269481</link>
         <description><![CDATA[<div>- Introduction of stop codon leads this mutation to have a shortened protein</div>]]></description>
         <enclosure url="https://i.ytimg.com/vi/pLGOf6BDzf0/hqdefault.jpg" />
         <pubDate>2021-10-20 13:08:21 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830269481</guid>
      </item>
      <item>
         <title>(5) POINT MUTATION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830271984</link>
         <description><![CDATA[<div>- A change of a single nucleotide, that consists of insertion, deletion, or a substitution of one nucleotide in a gene<br><br></div>]]></description>
         <enclosure url="http://www.yourgenome.org/sites/default/files/illustrations/diagram/dna_mutations_point_mutation_yourgenome.png" />
         <pubDate>2021-10-20 13:09:02 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830271984</guid>
      </item>
      <item>
         <title>(1) DELETION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830279463</link>
         <description><![CDATA[<div>- In the DNA replication a chromosome or a sequence of DNA is then left out. In a single base, any amount of nucleotides can be removed.<br>- In the chromosome a piece of it is lost due to breakage</div>]]></description>
         <enclosure url="https://www.yourgenome.org/sites/default/files/illustrations/diagram/dna_mutations_deletion_yourgenome.png" />
         <pubDate>2021-10-20 13:10:58 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830279463</guid>
      </item>
      <item>
         <title>(2) INVERSION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830281487</link>
         <description><![CDATA[<div>- In inversion mutation the segments break off from the chromosome. This then flips the segment around backwards then reattaches.</div>]]></description>
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         <pubDate>2021-10-20 13:11:34 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830281487</guid>
      </item>
      <item>
         <title>(3) TRANSLOCATION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830283328</link>
         <description><![CDATA[<div>- This mutation consists of two chromosomes that are not homologous, parts of the chromosome are transferred to one another &nbsp;<br>- This sorta rearrangement can be known as a balanced<br>- When there is a loss or a gain of the genetic material, this is known as being unbalanced </div>]]></description>
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         <pubDate>2021-10-20 13:12:07 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830283328</guid>
      </item>
      <item>
         <title>(4) NONDISJUNCTION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830285876</link>
         <description><![CDATA[<div>- In this mutation, when the chromosome fails to separate it can cause gamete which can lead to having many or few chromosomes. This all occurs in the meiosis</div>]]></description>
         <enclosure url="http://desertbruchid.net/4_GB_Lecture_figs_f/4_GB_10_Genetics_Fig_f/13_2_NonDisjunction.GIF" />
         <pubDate>2021-10-20 13:12:54 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830285876</guid>
      </item>
      <item>
         <title>(5) DUPLICATION</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830288370</link>
         <description><![CDATA[<div>- In this mutation, one or more copies of a gene is produced. This occurs when a sequence is repeated and this is the gene sequence </div>]]></description>
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         <pubDate>2021-10-20 13:13:40 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830288370</guid>
      </item>
      <item>
         <title>(A) PHYSICAL </title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830309685</link>
         <description><![CDATA[<div>- This mutagen is a form of a physical substance and is responsible of physically change a structure of DNA. It is also like a short wave rays which then will penetrate through a living cell and the end results alter genetic material</div>]]></description>
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         <pubDate>2021-10-20 13:19:58 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830309685</guid>
      </item>
      <item>
         <title>(B) CHEMICAL</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830312682</link>
         <description><![CDATA[<div>- The nucleus in the cell has a induce mutation<br>- They are a important tool for mutagenesis in many different of organisms<br>- Chemicals that can cause mutations:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&gt;Mutagens<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &gt;Carcinogens<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&gt;Flame Retardants<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &gt;Hair dyes&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&gt;Hydrocarbons, Halogenated<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &gt;Fury Furamide<br>           &gt;Ethylene Dibromide DNA</div>]]></description>
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         <pubDate>2021-10-20 13:20:51 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1830312682</guid>
      </item>
      <item>
         <title>EXAMPLE</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1847195502</link>
         <description><![CDATA[<div>A disease that is caused by a single point mutation is sickle cell anemia</div>]]></description>
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         <pubDate>2021-10-27 04:53:45 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1847195502</guid>
      </item>
      <item>
         <title>EXAMPLE</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848490037</link>
         <description><![CDATA[<div>An example would be x-rays, ultra violet, etc all have high energy radiations. They are known to be extremely damaging because it can ripe through DNA molecules, which then causes point mutation a big portion of its chromosome</div>]]></description>
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         <pubDate>2021-10-27 14:49:26 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848490037</guid>
      </item>
      <item>
         <title>EXAMPLE</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848510227</link>
         <description><![CDATA[<div>A child can be born with translocation chromosome, which can result the child in having down syndrome also known as translocation down syndrome </div>]]></description>
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         <pubDate>2021-10-27 14:55:05 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848510227</guid>
      </item>
      <item>
         <title>EXAMPLE</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848558052</link>
         <description><![CDATA[<div>A rare genetic disorder of duplication is <strong>Pallister Killian </strong>syndrome</div>]]></description>
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         <pubDate>2021-10-27 15:09:11 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848558052</guid>
      </item>
      <item>
         <title>EXAMPLE</title>
         <author>rubinawahab</author>
         <link>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848599634</link>
         <description><![CDATA[<div>For a protein, when a single incorrect amino acid fully changes or alters how the protein functions, it can then result in the blood cells to be misshapen. This can cause sickle cell anemia</div>]]></description>
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         <pubDate>2021-10-27 15:21:20 UTC</pubDate>
         <guid>https://padlet.com/rubinawahab/ooy82p14s1xt8vb4/wish/1848599634</guid>
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