ºÝºÝߣshows by User: magendiramanivinayag / http://www.slideshare.net/images/logo.gif ºÝºÝߣshows by User: magendiramanivinayag / Fri, 11 Sep 2020 12:17:30 GMT ºÝºÝߣShare feed for ºÝºÝߣshows by User: magendiramanivinayag Homocystinuria /slideshow/homocystinuria-238455286/238455286 homocystinuria-200911121730
Homocystinuria is a disorder of methionine metabolism, leading to an abnormal accumulation of homocysteine and its metabolites (homocystine, homocysteine-cysteine complex, and others) in blood and urine. Normally, these metabolites are not found in appreciable quantities in blood or urine.]]>

Homocystinuria is a disorder of methionine metabolism, leading to an abnormal accumulation of homocysteine and its metabolites (homocystine, homocysteine-cysteine complex, and others) in blood and urine. Normally, these metabolites are not found in appreciable quantities in blood or urine.]]>
Fri, 11 Sep 2020 12:17:30 GMT /slideshow/homocystinuria-238455286/238455286 magendiramanivinayag@slideshare.net(magendiramanivinayag) Homocystinuria magendiramanivinayag Homocystinuria is a disorder of methionine metabolism, leading to an abnormal accumulation of homocysteine and its metabolites (homocystine, homocysteine-cysteine complex, and others) in blood and urine. Normally, these metabolites are not found in appreciable quantities in blood or urine. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/homocystinuria-200911121730-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Homocystinuria is a disorder of methionine metabolism, leading to an abnormal accumulation of homocysteine and its metabolites (homocystine, homocysteine-cysteine complex, and others) in blood and urine. Normally, these metabolites are not found in appreciable quantities in blood or urine.
Homocystinuria from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Maple syrup urine disease (msud) /slideshow/maple-syrup-urine-disease-msud/238455278 maplesyrupurinediseasemsud-200911121639
Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly. The condition gets its name from the distinctive sweet odor of affected infants' urine.]]>

Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly. The condition gets its name from the distinctive sweet odor of affected infants' urine.]]>
Fri, 11 Sep 2020 12:16:39 GMT /slideshow/maple-syrup-urine-disease-msud/238455278 magendiramanivinayag@slideshare.net(magendiramanivinayag) Maple syrup urine disease (msud) magendiramanivinayag Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly. The condition gets its name from the distinctive sweet odor of affected infants' urine. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/maplesyrupurinediseasemsud-200911121639-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly. The condition gets its name from the distinctive sweet odor of affected infants&#39; urine.
Maple syrup urine disease (msud) from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Albinism /magendiramanivinayag/albinism-238455259 albinism-200911121407
Albinism is a genetic condition where people are born without the usual pigment (color) in their bodies. Their bodies aren't able to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair color. So most people with albinism have very pale skin, hair, and eyes.]]>

Albinism is a genetic condition where people are born without the usual pigment (color) in their bodies. Their bodies aren't able to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair color. So most people with albinism have very pale skin, hair, and eyes.]]>
Fri, 11 Sep 2020 12:14:07 GMT /magendiramanivinayag/albinism-238455259 magendiramanivinayag@slideshare.net(magendiramanivinayag) Albinism magendiramanivinayag Albinism is a genetic condition where people are born without the usual pigment (color) in their bodies. Their bodies aren't able to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair color. So most people with albinism have very pale skin, hair, and eyes. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/albinism-200911121407-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Albinism is a genetic condition where people are born without the usual pigment (color) in their bodies. Their bodies aren&#39;t able to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair color. So most people with albinism have very pale skin, hair, and eyes.
Albinism from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Phenylketonuria /magendiramanivinayag/phenylketonuria-238342489 phenylketonuria-200831131324
Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. A birth defect that causes an amino acid called phenylalanine to build up in the body. Newborns should be screened for PKU. Untreated phenylketonuria can lead to brain damage, intellectual disabilities, behavioural symptoms or seizures. Treatment includes a strict diet with limited protein.]]>

Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. A birth defect that causes an amino acid called phenylalanine to build up in the body. Newborns should be screened for PKU. Untreated phenylketonuria can lead to brain damage, intellectual disabilities, behavioural symptoms or seizures. Treatment includes a strict diet with limited protein.]]>
Mon, 31 Aug 2020 13:13:24 GMT /magendiramanivinayag/phenylketonuria-238342489 magendiramanivinayag@slideshare.net(magendiramanivinayag) Phenylketonuria magendiramanivinayag Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. A birth defect that causes an amino acid called phenylalanine to build up in the body. Newborns should be screened for PKU. Untreated phenylketonuria can lead to brain damage, intellectual disabilities, behavioural symptoms or seizures. Treatment includes a strict diet with limited protein. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/phenylketonuria-200831131324-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. A birth defect that causes an amino acid called phenylalanine to build up in the body. Newborns should be screened for PKU. Untreated phenylketonuria can lead to brain damage, intellectual disabilities, behavioural symptoms or seizures. Treatment includes a strict diet with limited protein.
Phenylketonuria from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Tyrosinosis /slideshow/tyrosinosis/238342471 tyrosinosis-200831131150
a condition of faulty metabolism of tyrosine marked by the excretion of unusual amounts of tyrosine in the urine.]]>

a condition of faulty metabolism of tyrosine marked by the excretion of unusual amounts of tyrosine in the urine.]]>
Mon, 31 Aug 2020 13:11:50 GMT /slideshow/tyrosinosis/238342471 magendiramanivinayag@slideshare.net(magendiramanivinayag) Tyrosinosis magendiramanivinayag a condition of faulty metabolism of tyrosine marked by the excretion of unusual amounts of tyrosine in the urine. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tyrosinosis-200831131150-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> a condition of faulty metabolism of tyrosine marked by the excretion of unusual amounts of tyrosine in the urine.
Tyrosinosis from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Alkaptonuria /slideshow/alkaptonuria-238342456/238342456 alkaptonuria-200831131036
Alkaptonuria is a rare genetic metabolic disorder characterized by the accumulation of homogentisic acid in the body. Affected individuals lack enough functional levels of an enzyme required to breakdown homogentisic acid. Affected individuals may have dark urine or urine that turns black when exposed to air.]]>

Alkaptonuria is a rare genetic metabolic disorder characterized by the accumulation of homogentisic acid in the body. Affected individuals lack enough functional levels of an enzyme required to breakdown homogentisic acid. Affected individuals may have dark urine or urine that turns black when exposed to air.]]>
Mon, 31 Aug 2020 13:10:36 GMT /slideshow/alkaptonuria-238342456/238342456 magendiramanivinayag@slideshare.net(magendiramanivinayag) Alkaptonuria magendiramanivinayag Alkaptonuria is a rare genetic metabolic disorder characterized by the accumulation of homogentisic acid in the body. Affected individuals lack enough functional levels of an enzyme required to breakdown homogentisic acid. Affected individuals may have dark urine or urine that turns black when exposed to air. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/alkaptonuria-200831131036-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Alkaptonuria is a rare genetic metabolic disorder characterized by the accumulation of homogentisic acid in the body. Affected individuals lack enough functional levels of an enzyme required to breakdown homogentisic acid. Affected individuals may have dark urine or urine that turns black when exposed to air.
Alkaptonuria from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Immuno deficiency disorder Associated with purine metabolism /slideshow/immuno-deficiency-disorder-associated-with-purine-metabolism/237682110 immunodeficiencydisorder-200809051601
Xanthinuria Xanthinuria, also known as xanthine oxidase deficiency, is a rare genetic disorder causing the accumulation of xanthine. It is caused by a deficiency of the enzyme xanthine oxidase. Orotic aciduria Orotic aciduria is a disease caused by an enzyme deficiency resulting in a decreased ability to synthesize pyrimidines. It is the only known enzyme deficiency of the de novo pyrimidine synthesis pathway. Gout Gout is caused by a condition known as hyperuricemia, where there is too much uric acid in the body. ]]>

Xanthinuria Xanthinuria, also known as xanthine oxidase deficiency, is a rare genetic disorder causing the accumulation of xanthine. It is caused by a deficiency of the enzyme xanthine oxidase. Orotic aciduria Orotic aciduria is a disease caused by an enzyme deficiency resulting in a decreased ability to synthesize pyrimidines. It is the only known enzyme deficiency of the de novo pyrimidine synthesis pathway. Gout Gout is caused by a condition known as hyperuricemia, where there is too much uric acid in the body. ]]>
Sun, 09 Aug 2020 05:16:01 GMT /slideshow/immuno-deficiency-disorder-associated-with-purine-metabolism/237682110 magendiramanivinayag@slideshare.net(magendiramanivinayag) Immuno deficiency disorder Associated with purine metabolism magendiramanivinayag Xanthinuria Xanthinuria, also known as xanthine oxidase deficiency, is a rare genetic disorder causing the accumulation of xanthine. It is caused by a deficiency of the enzyme xanthine oxidase. Orotic aciduria Orotic aciduria is a disease caused by an enzyme deficiency resulting in a decreased ability to synthesize pyrimidines. It is the only known enzyme deficiency of the de novo pyrimidine synthesis pathway. Gout Gout is caused by a condition known as hyperuricemia, where there is too much uric acid in the body. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/immunodeficiencydisorder-200809051601-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Xanthinuria Xanthinuria, also known as xanthine oxidase deficiency, is a rare genetic disorder causing the accumulation of xanthine. It is caused by a deficiency of the enzyme xanthine oxidase. Orotic aciduria Orotic aciduria is a disease caused by an enzyme deficiency resulting in a decreased ability to synthesize pyrimidines. It is the only known enzyme deficiency of the de novo pyrimidine synthesis pathway. Gout Gout is caused by a condition known as hyperuricemia, where there is too much uric acid in the body.
Immuno deficiency disorder Associated with purine metabolism from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Tumour markers /slideshow/tumour-markers-237569504/237569504 tumourmarkers-200805071053
Tumor markers are substances, such as proteins, biochemicals, hormones or enzymes, produced by tumor cells or by the body in response to tumor cells. As tumor cells multiply, cancer spreads, and tissue is damaged, these substances increase and leak into the bloodstream. Tumor marker levels in blood help physicians evaluate people for certain types of cancer ]]>

Tumor markers are substances, such as proteins, biochemicals, hormones or enzymes, produced by tumor cells or by the body in response to tumor cells. As tumor cells multiply, cancer spreads, and tissue is damaged, these substances increase and leak into the bloodstream. Tumor marker levels in blood help physicians evaluate people for certain types of cancer ]]>
Wed, 05 Aug 2020 07:10:53 GMT /slideshow/tumour-markers-237569504/237569504 magendiramanivinayag@slideshare.net(magendiramanivinayag) Tumour markers magendiramanivinayag Tumor markers are substances, such as proteins, biochemicals, hormones or enzymes, produced by tumor cells or by the body in response to tumor cells. As tumor cells multiply, cancer spreads, and tissue is damaged, these substances increase and leak into the bloodstream. Tumor marker levels in blood help physicians evaluate people for certain types of cancer <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tumourmarkers-200805071053-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Tumor markers are substances, such as proteins, biochemicals, hormones or enzymes, produced by tumor cells or by the body in response to tumor cells. As tumor cells multiply, cancer spreads, and tissue is damaged, these substances increase and leak into the bloodstream. Tumor marker levels in blood help physicians evaluate people for certain types of cancer
Tumour markers from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Free radicals /slideshow/free-radicals-237569475/237569475 freeradicals-200805071000
Free radicals damage contributes to the etiology of many chronic health problems such as cardiovascular and inflammatory disease, cataract, and cancer. Antioxidants prevent free radical induced tissue damage by preventing the formation of radicals, scavenging them, or by promoting their decomposition.]]>

Free radicals damage contributes to the etiology of many chronic health problems such as cardiovascular and inflammatory disease, cataract, and cancer. Antioxidants prevent free radical induced tissue damage by preventing the formation of radicals, scavenging them, or by promoting their decomposition.]]>
Wed, 05 Aug 2020 07:10:00 GMT /slideshow/free-radicals-237569475/237569475 magendiramanivinayag@slideshare.net(magendiramanivinayag) Free radicals magendiramanivinayag Free radicals damage contributes to the etiology of many chronic health problems such as cardiovascular and inflammatory disease, cataract, and cancer. Antioxidants prevent free radical induced tissue damage by preventing the formation of radicals, scavenging them, or by promoting their decomposition. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/freeradicals-200805071000-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Free radicals damage contributes to the etiology of many chronic health problems such as cardiovascular and inflammatory disease, cataract, and cancer. Antioxidants prevent free radical induced tissue damage by preventing the formation of radicals, scavenging them, or by promoting their decomposition.
Free radicals from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Carcinogenic agents /slideshow/carcinogenic-agents-237569451/237569451 carcinogenicagents-200805070910
A carcinogenic agents or carcinogen is any substances, chemicals, medical or environmental radiation, some viruses, lifestyle factors, and even some medications that promotes carcinogenesis, the formation of cancer. This may be due to the ability to damage the genome or to the disruption of cellular metabolic processes]]>

A carcinogenic agents or carcinogen is any substances, chemicals, medical or environmental radiation, some viruses, lifestyle factors, and even some medications that promotes carcinogenesis, the formation of cancer. This may be due to the ability to damage the genome or to the disruption of cellular metabolic processes]]>
Wed, 05 Aug 2020 07:09:10 GMT /slideshow/carcinogenic-agents-237569451/237569451 magendiramanivinayag@slideshare.net(magendiramanivinayag) Carcinogenic agents magendiramanivinayag A carcinogenic agents or carcinogen is any substances, chemicals, medical or environmental radiation, some viruses, lifestyle factors, and even some medications that promotes carcinogenesis, the formation of cancer. This may be due to the ability to damage the genome or to the disruption of cellular metabolic processes <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/carcinogenicagents-200805070910-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> A carcinogenic agents or carcinogen is any substances, chemicals, medical or environmental radiation, some viruses, lifestyle factors, and even some medications that promotes carcinogenesis, the formation of cancer. This may be due to the ability to damage the genome or to the disruption of cellular metabolic processes
Carcinogenic agents from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Cancer character and types /slideshow/cancer-character-and-types-237569412/237569412 cancercharacterandtypes-200805070709
Cancer is the uncontrolled growth of abnormal cells anywhere in a body Causative agents – chemical, toxic compound exposures, ionizing radiation, some pathogens Most cancer form tumors, but not all tumors are cancerous. ]]>

Cancer is the uncontrolled growth of abnormal cells anywhere in a body Causative agents – chemical, toxic compound exposures, ionizing radiation, some pathogens Most cancer form tumors, but not all tumors are cancerous. ]]>
Wed, 05 Aug 2020 07:07:09 GMT /slideshow/cancer-character-and-types-237569412/237569412 magendiramanivinayag@slideshare.net(magendiramanivinayag) Cancer character and types magendiramanivinayag Cancer is the uncontrolled growth of abnormal cells anywhere in a body Causative agents – chemical, toxic compound exposures, ionizing radiation, some pathogens Most cancer form tumors, but not all tumors are cancerous. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/cancercharacterandtypes-200805070709-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Cancer is the uncontrolled growth of abnormal cells anywhere in a body Causative agents – chemical, toxic compound exposures, ionizing radiation, some pathogens Most cancer form tumors, but not all tumors are cancerous.
Cancer character and types from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Biosensor /slideshow/biosensor-88617203/88617203 biosensor-180222150450
BIOSENSOR AND ITS APPLICATIONS]]>

BIOSENSOR AND ITS APPLICATIONS]]>
Thu, 22 Feb 2018 15:04:50 GMT /slideshow/biosensor-88617203/88617203 magendiramanivinayag@slideshare.net(magendiramanivinayag) Biosensor magendiramanivinayag BIOSENSOR AND ITS APPLICATIONS <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/biosensor-180222150450-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> BIOSENSOR AND ITS APPLICATIONS
Biosensor from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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2 d page /slideshow/2-d-page/88616996 2dpage-180222150255
ELECTROPHORESIS - TWO DIMENSIONAL]]>

ELECTROPHORESIS - TWO DIMENSIONAL]]>
Thu, 22 Feb 2018 15:02:55 GMT /slideshow/2-d-page/88616996 magendiramanivinayag@slideshare.net(magendiramanivinayag) 2 d page magendiramanivinayag ELECTROPHORESIS - TWO DIMENSIONAL <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/2dpage-180222150255-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> ELECTROPHORESIS - TWO DIMENSIONAL
2 d page from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Inborn errors of metabolism /slideshow/inborn-errors-of-metabolism-78823314/78823314 inbornerrorsofmetabolism-170814113333
PHENYLKETONURIA TYROSINOSIS ALKAPTONURIA MAPLE SYRUP URINE DISEASE HARTNUP DISEASE HOMOCYSTINURIA ALBINISM ]]>

PHENYLKETONURIA TYROSINOSIS ALKAPTONURIA MAPLE SYRUP URINE DISEASE HARTNUP DISEASE HOMOCYSTINURIA ALBINISM ]]>
Mon, 14 Aug 2017 11:33:33 GMT /slideshow/inborn-errors-of-metabolism-78823314/78823314 magendiramanivinayag@slideshare.net(magendiramanivinayag) Inborn errors of metabolism magendiramanivinayag PHENYLKETONURIA TYROSINOSIS ALKAPTONURIA MAPLE SYRUP URINE DISEASE HARTNUP DISEASE HOMOCYSTINURIA ALBINISM <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/inbornerrorsofmetabolism-170814113333-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> PHENYLKETONURIA TYROSINOSIS ALKAPTONURIA MAPLE SYRUP URINE DISEASE HARTNUP DISEASE HOMOCYSTINURIA ALBINISM
Inborn errors of metabolism from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Hemoglobinopathy & erythrocyte enzyme disorder /slideshow/hemoglobinopathy-erythrocyte-enzyme-disorder/78823170 hemoglobinopathyerythrocyteenzymedisorder-170814112714
Sickle cell anemia, thalassemia, erythrocyte enzyme disorder]]>

Sickle cell anemia, thalassemia, erythrocyte enzyme disorder]]>
Mon, 14 Aug 2017 11:27:14 GMT /slideshow/hemoglobinopathy-erythrocyte-enzyme-disorder/78823170 magendiramanivinayag@slideshare.net(magendiramanivinayag) Hemoglobinopathy & erythrocyte enzyme disorder magendiramanivinayag Sickle cell anemia, thalassemia, erythrocyte enzyme disorder <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/hemoglobinopathyerythrocyteenzymedisorder-170814112714-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Sickle cell anemia, thalassemia, erythrocyte enzyme disorder
Hemoglobinopathy & erythrocyte enzyme disorder from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Guidelines to scientific writing thesis (1) /slideshow/guidelines-to-scientific-writing-thesis-1/70550590 guidelinestoscientificwriting-thesis1-161230133018
How to write Thesis - Ph.D life Science etc]]>

How to write Thesis - Ph.D life Science etc]]>
Fri, 30 Dec 2016 13:30:18 GMT /slideshow/guidelines-to-scientific-writing-thesis-1/70550590 magendiramanivinayag@slideshare.net(magendiramanivinayag) Guidelines to scientific writing thesis (1) magendiramanivinayag How to write Thesis - Ph.D life Science etc <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/guidelinestoscientificwriting-thesis1-161230133018-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> How to write Thesis - Ph.D life Science etc
Guidelines to scientific writing thesis (1) from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Guidelines to scientific paper writing /slideshow/guidelines-to-scientific-paper-writing/70550544 guidelinestoscientificpaperwriting-161230132827
How to write research article (Manuscript)]]>

How to write research article (Manuscript)]]>
Fri, 30 Dec 2016 13:28:27 GMT /slideshow/guidelines-to-scientific-paper-writing/70550544 magendiramanivinayag@slideshare.net(magendiramanivinayag) Guidelines to scientific paper writing magendiramanivinayag How to write research article (Manuscript) <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/guidelinestoscientificpaperwriting-161230132827-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> How to write research article (Manuscript)
Guidelines to scientific paper writing from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Overview of Electrophoresis /slideshow/overview-of-electrophoresis/66622313 electrophoresis-161001103243
SDS-PAGE, Agarose gel electrophoresis, factors affecting electrophoresis]]>

SDS-PAGE, Agarose gel electrophoresis, factors affecting electrophoresis]]>
Sat, 01 Oct 2016 10:32:43 GMT /slideshow/overview-of-electrophoresis/66622313 magendiramanivinayag@slideshare.net(magendiramanivinayag) Overview of Electrophoresis magendiramanivinayag SDS-PAGE, Agarose gel electrophoresis, factors affecting electrophoresis <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/electrophoresis-161001103243-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> SDS-PAGE, Agarose gel electrophoresis, factors affecting electrophoresis
Overview of Electrophoresis from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Agarose gel electrophoresis /slideshow/agarose-gel-electrophoresis-66622262/66622262 agarosegelelectrophoresis-161001102825
DNA electrophoresis]]>

DNA electrophoresis]]>
Sat, 01 Oct 2016 10:28:24 GMT /slideshow/agarose-gel-electrophoresis-66622262/66622262 magendiramanivinayag@slideshare.net(magendiramanivinayag) Agarose gel electrophoresis magendiramanivinayag DNA electrophoresis <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/agarosegelelectrophoresis-161001102825-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> DNA electrophoresis
Agarose gel electrophoresis from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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Sodium Dodecyl Poly Acryl AMide Gel electrophoresis (SDS-PAGE) /slideshow/sodium-dodecyl-poly-acryl-amide-gel-electrophoresis-sdspage/66622211 sds-pageelectrophoresis-161001102435
SDS-PAGE electrophoresis]]>

SDS-PAGE electrophoresis]]>
Sat, 01 Oct 2016 10:24:34 GMT /slideshow/sodium-dodecyl-poly-acryl-amide-gel-electrophoresis-sdspage/66622211 magendiramanivinayag@slideshare.net(magendiramanivinayag) Sodium Dodecyl Poly Acryl AMide Gel electrophoresis (SDS-PAGE) magendiramanivinayag SDS-PAGE electrophoresis <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/sds-pageelectrophoresis-161001102435-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> SDS-PAGE electrophoresis
Sodium Dodecyl Poly Acryl AMide Gel electrophoresis (SDS-PAGE) from Marudhar Kesari Jain College for Women Vaniyambadi - 635 751, Tamil Nadu, INDIA.
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https://public.slidesharecdn.com/v2/images/profile-picture.png Dr. Magendira Mani was born in the state of Tamil Nadu, India, on August 30, 1985. He did his schooling at Hindu Higher Secondary School, Vaniyambadi. He obtained his undergraduate and postgraduate degrees from Islamiah College, Vaniyambadi. He completed his Master of Philosophy at the University of Madras, Guindy Campus, Chennai. He received his doctoral degree from Thiruvalluvar University, Vellore. He also qualified for the Tamil Nadu State Eligibility Test (TN-SET) conducted by Mother Teresa Women's University. His research interests lie in Molecular and Clinical Toxicology. He has more than 15 years of research experience and has made several scholarly contributions. https://cdn.slidesharecdn.com/ss_thumbnails/homocystinuria-200911121730-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/homocystinuria-238455286/238455286 Homocystinuria https://cdn.slidesharecdn.com/ss_thumbnails/maplesyrupurinediseasemsud-200911121639-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/maple-syrup-urine-disease-msud/238455278 Maple syrup urine dise... https://cdn.slidesharecdn.com/ss_thumbnails/albinism-200911121407-thumbnail.jpg?width=320&height=320&fit=bounds magendiramanivinayag/albinism-238455259 Albinism