<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns="http://purl.org/rss/1.0/">
<channel rdf:about="http://www.inderscience.com/current_issue_rss/index.php?journal=ijis">
<title>Most recent issue published online for the International Journal of Immunological Studies.</title>
<description>International Journal of Immunological Studies</description>
<link>http://www.inderscience.com/browse/index.php?journalID=257&amp;year=2011&amp;vol=1&amp;issue=3</link>
<dc:publisher>Inderscience Publishers Ltd</dc:publisher>
<dc:language>en-uk</dc:language>
<prism:publicationName>International Journal of Immunological Studies</prism:publicationName>
<prism:issn>1754-1441</prism:issn>
<prism:eIssn>1754-145X</prism:eIssn>
<prism:copyright>&#169; 2011 Inderscience Publishers Ltd</prism:copyright>
<prism:rightsAgent>editor@inderscience.com</prism:rightsAgent>
<image rdf:resource="https://www.inderscience.com/images/files/coverImgs/ijis_scoverijis.jpg" />
<items>
<rdf:Seq>
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041721" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041722" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041723" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041724" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041725" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041726" />
<rdf:li rdf:resource="http://dx.doi.org/10.1504/IJIS.2011.041727" />
</rdf:Seq>
</items>
</channel>
<image rdf:about="https://www.inderscience.com/images/files/coverImgs/ijis_scoverijis.jpg">
<title>International Journal of Immunological Studies</title>
<url>https://www.inderscience.com/images/files/coverImgs/ijis_scoverijis.jpg</url>
<link>http://www.inderscience.com/browse/index.php?journalID=257&amp;year=2011&amp;vol=1&amp;issue=3</link>
</image>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041721">
<title>Prediction of mutations in ATM gene responsible for breast cancer in women &amp;ndash; a cancer&#45;informatics approach</title>
<link>http://www.inderscience.com/link.php?id=41721</link>
<description>Cancer is an abnormal growth of cells caused by multiple changes in gene expression. Breast cancer is a cancer of the glandular breast tissue. The BRCA1 and BRCA2 genes were considered as greatly increasing occurrence of inherited breast cancer, however, it was found that the damaged ataxia telangiectasia mutated &#40;ATM&#41; genes were also equal culprits. The ATM gene &#40;NC&amp;&#35;95;000011.8&#41; is very large and mutations occur throughout its amino acid coding portions. The present work discusses the use of bioinformatics tools in analysing the ATM gene&#39;s role in breast cancer.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41721"><b>Prediction of mutations in ATM gene responsible for breast cancer in women &amp;ndash; a cancer&#45;informatics approach</b></A><br />R. Sindhuja, R. Seenivasagam, K. Hemavathi<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 229 - 248</i><br />Cancer is an abnormal growth of cells caused by multiple changes in gene expression. Breast cancer is a cancer of the glandular breast tissue. The BRCA1 and BRCA2 genes were considered as greatly increasing occurrence of inherited breast cancer, however, it was found that the damaged ataxia telangiectasia mutated &#40;ATM&#41; genes were also equal culprits. The ATM gene &#40;NC&amp;&#35;95;000011.8&#41; is very large and mutations occur throughout its amino acid coding portions. The present work discusses the use of bioinformatics tools in analysing the ATM gene&#39;s role in breast cancer.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041721</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 229 - 248</dc:source>
<dc:creator>R. Sindhuja</dc:creator>
<dc:creator>R. Seenivasagam</dc:creator>
<dc:creator>K. Hemavathi</dc:creator>
<dc:contributor>Department of Bioinformatics, School of Chemical and Biotechnology, Shanmugha Arts Science Technology &amp;amp; Research Academy &#40;SASTRA University&#41;, Tanjore&#45;613402, Tamilnadu, India. &#39; Department of Drug Discovery, St. Joseph College, P.B. 27094, 36, Lalbagh Road, Bangalore, Karnataka 560027, India. &#39; Department of Bioinformatics, School of Chemical and Biotechnology, Shanmugha Arts Science Technology &amp;amp; Research Academy &#40;SASTRA University&#41;, Tanjore&#45;613402, Tamilnadu, India</dc:contributor>
<dc:subject>systems biology</dc:subject>
<dc:subject>in&#45;silico analysis</dc:subject>
<dc:subject>gene mutations</dc:subject>
<dc:subject>breast cancer</dc:subject>
<dc:subject>immunogenetics</dc:subject>
<dc:subject>ataxia telangiectasia</dc:subject>
<dc:subject>ATM genes</dc:subject>
<dc:subject>mutated genes</dc:subject>
<dc:subject>amino acid coding</dc:subject>
<dc:subject>bioinformatics.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>229</prism:startingPage>
<prism:endingPage>248</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041722">
<title>Hypothesis for a common&#45;cause underlying both autoimmune&#45;diseases and allergies</title>
<link>http://www.inderscience.com/link.php?id=41722</link>
<description>Although autoimmune diseases and allergies have recently been associated with each other, the results of the few studies that are available are contradictory. While some of these studies suggest that there is no evidence to assume a connection between autoimmune diseases and allergies, other studies, including some recent animal studies, suggest a connection between these diseases. In this study, we describe the possible connection between autoimmune diseases and allergies. It is important to note that, for the considerations described here, it will be necessary to consider the two types of diseases in a completely different way than has been done so far.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41722"><b>Hypothesis for a common&#45;cause underlying both autoimmune&#45;diseases and allergies</b></A><br />Borros M. Arneth<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 249 - 254</i><br />Although autoimmune diseases and allergies have recently been associated with each other, the results of the few studies that are available are contradictory. While some of these studies suggest that there is no evidence to assume a connection between autoimmune diseases and allergies, other studies, including some recent animal studies, suggest a connection between these diseases. In this study, we describe the possible connection between autoimmune diseases and allergies. It is important to note that, for the considerations described here, it will be necessary to consider the two types of diseases in a completely different way than has been done so far.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041722</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 249 - 254</dc:source>
<dc:creator>Borros M. Arneth</dc:creator>
<dc:contributor>Institute of Clinical Chemistry and Laboratory Medicine, University of Technology, Technische Universitat &amp;ndash; Dresden, Fetscherstr 74, 01307 Dresden, Germany</dc:contributor>
<dc:subject>autoimmunity</dc:subject>
<dc:subject>antigen presentation</dc:subject>
<dc:subject>food allergies</dc:subject>
<dc:subject>T&#45;lymphocytes</dc:subject>
<dc:subject>CD4&#45;T&#45;lymphocytes</dc:subject>
<dc:subject>CD8&#45;T&#45;lymphocytes</dc:subject>
<dc:subject>autoimmune diseases</dc:subject>
<dc:subject>autoimmune allergies.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>249</prism:startingPage>
<prism:endingPage>254</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041723">
<title>Hepatitis G virus &#40;HGV&#41;&#58; where we stand and what to do&#63;</title>
<link>http://www.inderscience.com/link.php?id=41723</link>
<description>Hepatitis G virus was identified in 1995. Some work was done on HGV until 1997 and the FDA declared it as a non&#45;harmful virus. This resulted in no screening of virus for blood donors and bags from 1997 until today. A review of scientific literature of the last 16 years, majority identify with polymerase chain reaction &#40;PCR&#41; has shown that HGV is quite prevalent around the globe with low to high prevalence in different countries among blood donors and other groups. It was found to be associated in hepatitis, cirrhosis of the liver and possibly present in hepatocellular carcinoma. It was also seen in hematological disorders and hematological malignancies. It is advisable that screening of blood is better than transferring HGV ignorantly to blood recipients as it was done before, where we did transfer HCV to many individuals which resulted in a lot of morbidities and mortalities.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41723"><b>Hepatitis G virus &#40;HGV&#41;&#58; where we stand and what to do&#63;</b></A><br />Q. Mughis Uddin Ahmed<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 255 - 263</i><br />Hepatitis G virus was identified in 1995. Some work was done on HGV until 1997 and the FDA declared it as a non&#45;harmful virus. This resulted in no screening of virus for blood donors and bags from 1997 until today. A review of scientific literature of the last 16 years, majority identify with polymerase chain reaction &#40;PCR&#41; has shown that HGV is quite prevalent around the globe with low to high prevalence in different countries among blood donors and other groups. It was found to be associated in hepatitis, cirrhosis of the liver and possibly present in hepatocellular carcinoma. It was also seen in hematological disorders and hematological malignancies. It is advisable that screening of blood is better than transferring HGV ignorantly to blood recipients as it was done before, where we did transfer HCV to many individuals which resulted in a lot of morbidities and mortalities.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041723</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 255 - 263</dc:source>
<dc:creator>Q. Mughis Uddin Ahmed</dc:creator>
<dc:contributor>Department of Pathology &amp;amp; Laboratory Medicine &#40;105&#41;, King Abdulaziz Hospital &#40;NGHA&#41;, P.O. Box &amp;&#35;35;2477 Al&#45;Ahsa&#45;31982, Saudi Arabia</dc:contributor>
<dc:subject>hepatitis G virus</dc:subject>
<dc:subject>HGV</dc:subject>
<dc:subject>polymerase chain reaction</dc:subject>
<dc:subject>PCR</dc:subject>
<dc:subject>blood donors</dc:subject>
<dc:subject>blood screening</dc:subject>
<dc:subject>blood doning.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>255</prism:startingPage>
<prism:endingPage>263</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041724">
<title>Cytokine therapy&#58; clinical and progressive status in cancer</title>
<link>http://www.inderscience.com/link.php?id=41724</link>
<description>Immunologic approaches to cancer therapy rely on two distinct capabilities of the immune system&#58; targeting the tumour microenvironment by recognising molecules expressed to a greater extent on tumour cells than normal cells and generating immune responses that can kill tumour cells. Immunocytokines, which are fusion proteins composed of a recombinant monoclonal antibody and a cytokine, capitalise on both of these capabilities by combining the ability of tumour&#45;specific antibodies selectively to target tumours with the broad&#45;based immunomodulatory activities of cytokines. This review hypothesises the rationale for development of immunocytokines for cancer and discusses preclinical and clinical data on specific immunocytokines being investigated as potential cancer therapies.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41724"><b>Cytokine therapy&#58; clinical and progressive status in cancer</b></A><br />Vemuri Praveen Kumar, Mamidi Sai Ratna Mounica, Tadikamalla N.L. Swetha, Gogineni V.S.N. Lakshmi, Tullimilli Anusri, Pemmaraju Lakshmi Amulya, Anne Sirisha<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 264 - 271</i><br />Immunologic approaches to cancer therapy rely on two distinct capabilities of the immune system&#58; targeting the tumour microenvironment by recognising molecules expressed to a greater extent on tumour cells than normal cells and generating immune responses that can kill tumour cells. Immunocytokines, which are fusion proteins composed of a recombinant monoclonal antibody and a cytokine, capitalise on both of these capabilities by combining the ability of tumour&#45;specific antibodies selectively to target tumours with the broad&#45;based immunomodulatory activities of cytokines. This review hypothesises the rationale for development of immunocytokines for cancer and discusses preclinical and clinical data on specific immunocytokines being investigated as potential cancer therapies.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041724</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 264 - 271</dc:source>
<dc:creator>Vemuri Praveen Kumar</dc:creator>
<dc:creator>Mamidi Sai Ratna Mounica</dc:creator>
<dc:creator>Tadikamalla N.L. Swetha</dc:creator>
<dc:creator>Gogineni V.S.N. Lakshmi</dc:creator>
<dc:creator>Tullimilli Anusri</dc:creator>
<dc:creator>Pemmaraju Lakshmi Amulya</dc:creator>
<dc:creator>Anne Sirisha</dc:creator>
<dc:contributor>Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India. &#39; Department of Biotechnology, KL University, Green Fields, Vaddeswaram, Guntur District, 522502, Andhra Pradesh, India</dc:contributor>
<dc:subject>cytokine therapy</dc:subject>
<dc:subject>cancer therapy</dc:subject>
<dc:subject>cancer treatment</dc:subject>
<dc:subject>immunocytokines</dc:subject>
<dc:subject>monoclonal antibody</dc:subject>
<dc:subject>aldesleukin</dc:subject>
<dc:subject>tumour microenvironment</dc:subject>
<dc:subject>IL&#45;2</dc:subject>
<dc:subject>hu14.18&#45;IL&#45;2</dc:subject>
<dc:subject>huKS&#45;IL&#45;2</dc:subject>
<dc:subject>immunology</dc:subject>
<dc:subject>tumour cells.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>264</prism:startingPage>
<prism:endingPage>271</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041725">
<title>Expression of different filarial parasite adult stage antigens during course of DEC treatment in mouse model of Brugian filariasis</title>
<link>http://www.inderscience.com/link.php?id=41725</link>
<description>Filariasis is a tropical disease with high morbidity rate due to lack of permanent cure. Here, we investigated specific filarial parasite antigens useful in treatment strategies for filariasis in areas where the chances of constant stimulations are at high peak. This study highlighted alterations in antigen recognition in the people living in endemic countries and receiving the orthodox treatments with diethylcarbamazine. We found that reinfection with L&amp;lt;SUB align&#61;right&amp;gt;3 stage in pre&#45;DEC treated mouse sera recognises 62 kDa, 45 kDa and 32 kDa antigens, which was not present in control animal sera. Further investigation shows that 62 kDa antigen was present in microfilaria while 45 kDa and 31 kDa was part of adult stage. These findings demonstrated that reinfection during the course of DEC treatment unmask specific parasite antigen, which do not express during initial stage of infections. Our findings argued that mapping of these new antigens would be helpful in the development of treatment strategies through appropriate vaccine.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41725"><b>Expression of different filarial parasite adult stage antigens during course of DEC treatment in mouse model of Brugian filariasis</b></A><br />Mohammad A. Khan, M. Saleemuddin, Puvadda K. Murthy<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 272 - 284</i><br />Filariasis is a tropical disease with high morbidity rate due to lack of permanent cure. Here, we investigated specific filarial parasite antigens useful in treatment strategies for filariasis in areas where the chances of constant stimulations are at high peak. This study highlighted alterations in antigen recognition in the people living in endemic countries and receiving the orthodox treatments with diethylcarbamazine. We found that reinfection with L&amp;lt;SUB align&#61;right&amp;gt;3 stage in pre&#45;DEC treated mouse sera recognises 62 kDa, 45 kDa and 32 kDa antigens, which was not present in control animal sera. Further investigation shows that 62 kDa antigen was present in microfilaria while 45 kDa and 31 kDa was part of adult stage. These findings demonstrated that reinfection during the course of DEC treatment unmask specific parasite antigen, which do not express during initial stage of infections. Our findings argued that mapping of these new antigens would be helpful in the development of treatment strategies through appropriate vaccine.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041725</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 272 - 284</dc:source>
<dc:creator>Mohammad A. Khan</dc:creator>
<dc:creator>M. Saleemuddin</dc:creator>
<dc:creator>Puvadda K. Murthy</dc:creator>
<dc:contributor>Department of Medicine, Stanford University, Palo Alto, 94304, California, USA. &#39; Department Biotechnology, Aligarh Muslim University, Aligarh, 202 002, UP, India. &#39; Department of Parasitology, Central Drug Research Institute, Lucknow 226 001, UP, India</dc:contributor>
<dc:subject>Brugia malayi</dc:subject>
<dc:subject>microfilaria</dc:subject>
<dc:subject>L3</dc:subject>
<dc:subject>reinfection</dc:subject>
<dc:subject>diethylcarbamazine treatment</dc:subject>
<dc:subject>Brugian filariasis</dc:subject>
<dc:subject>parasite antigens</dc:subject>
<dc:subject>tropical diseases</dc:subject>
<dc:subject>vaccines.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>272</prism:startingPage>
<prism:endingPage>284</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041726">
<title>Analysis of essential trace elements in some traditional Indian medicinal plants using instrumental neutron activation analysis and atomic absorption spectroscopy techniques</title>
<link>http://www.inderscience.com/link.php?id=41726</link>
<description>Specific parts &#40;fruits and leaves&#41; of different medicinal plants often used in Indian Ayurvedic system were analysed for 18 elements &#40;K, Mn, Na, Fe, Zn, Cu, Co, Br, Sm, Cl, La, Al, Cr, Ca Cd, Ni, Pb and Hg&#41; by employing instrumental neutron activation analysis &#40;INAA&#41; and atomic absorption spectroscopy &#40;AAS&#41; techniques. The samples were irradiated with thermal neutrons in a nuclear reactor and the induced activities were counted by &amp;gamma;&#45;ray spectrometry using efficiency calibrated high resolution high purity germanium &#40;HPGe&#41; detector. Most of the medicinal plants were found to be rich in one or more of the elements under study. The elemental concentration in different part of medicinal plants and their biological effects on human beings are discussed.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41726"><b>Analysis of essential trace elements in some traditional Indian medicinal plants using instrumental neutron activation analysis and atomic absorption spectroscopy techniques</b></A><br />Ram S. Lokhande, Mahadeo L. Andhale, Pravin U. Singare<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 285 - 296</i><br />Specific parts &#40;fruits and leaves&#41; of different medicinal plants often used in Indian Ayurvedic system were analysed for 18 elements &#40;K, Mn, Na, Fe, Zn, Cu, Co, Br, Sm, Cl, La, Al, Cr, Ca Cd, Ni, Pb and Hg&#41; by employing instrumental neutron activation analysis &#40;INAA&#41; and atomic absorption spectroscopy &#40;AAS&#41; techniques. The samples were irradiated with thermal neutrons in a nuclear reactor and the induced activities were counted by &amp;gamma;&#45;ray spectrometry using efficiency calibrated high resolution high purity germanium &#40;HPGe&#41; detector. Most of the medicinal plants were found to be rich in one or more of the elements under study. The elemental concentration in different part of medicinal plants and their biological effects on human beings are discussed.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041726</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 285 - 296</dc:source>
<dc:creator>Ram S. Lokhande</dc:creator>
<dc:creator>Mahadeo L. Andhale</dc:creator>
<dc:creator>Pravin U. Singare</dc:creator>
<dc:contributor>Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz, Mumbai 400098, India. &#39; Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz, Mumbai 400098, India. &#39; Department of Chemistry, Bhavan&#39;s College, Munshi Nagar, Andheri, Mumbai 400058, India</dc:contributor>
<dc:subject>instrumental neutron activation analysis</dc:subject>
<dc:subject>INAA</dc:subject>
<dc:subject>atomic absorption spectroscopy</dc:subject>
<dc:subject>AAS</dc:subject>
<dc:subject>medicinal plants</dc:subject>
<dc:subject>trace elements</dc:subject>
<dc:subject>inter&#45;elemental correlations</dc:subject>
<dc:subject>healthcare</dc:subject>
<dc:subject>Ayurvedic medicine</dc:subject>
<dc:subject>biological effects</dc:subject>
<dc:subject>curative properties</dc:subject>
<dc:subject>India.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>285</prism:startingPage>
<prism:endingPage>296</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
<item rdf:about="http://dx.doi.org/10.1504/IJIS.2011.041727">
<title>Therapeutic impacts of Indian and Korean ginseng on human beings &amp;ndash; a review</title>
<link>http://www.inderscience.com/link.php?id=41727</link>
<description>Withania somnifera &#40;Ashwagandha or Indian ginseng&#41; is a small woody shrub or herb of the Solanaceae family. Ashwagandha is an herb which can compare favourably to the world&#39;s most renowned herbal tonics such as ginseng &#40;Panax ginseng&#41;, astragalus &#40;Astragalus membranaceus&#41; and South American suma &#40;Pfaffia paniculata&#41;. All these have been held in high regard for its ability to increase vitality, energy, endurance and stamina. Korean ginseng &#40;Panax ginseng&#41; is used in China as a preventative tonic to stimulate the entire body to overcome stress, fatigue and weakness. It contains 13 different ginsenosides. Panaxans help to lower blood sugar, polysaccharides work to enhance the immune system and its antioxidant properties are immune&#45;stimulating to protect the body from disease and stress. It balances the release of stress hormones by supporting the organs that produce them. This article investigates the therapeutic and clinical effects of Indian and Korean ginseng.</description>
<content:encoded><![CDATA[<p><a href="http://www.inderscience.com/link.php?id=41727"><b>Therapeutic impacts of Indian and Korean ginseng on human beings &amp;ndash; a review</b></A><br />R. Seenivasagam, S. Sathiyamoorthy, K. Hemavathi<br /><i>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 297 - 317</i><br />Withania somnifera &#40;Ashwagandha or Indian ginseng&#41; is a small woody shrub or herb of the Solanaceae family. Ashwagandha is an herb which can compare favourably to the world&#39;s most renowned herbal tonics such as ginseng &#40;Panax ginseng&#41;, astragalus &#40;Astragalus membranaceus&#41; and South American suma &#40;Pfaffia paniculata&#41;. All these have been held in high regard for its ability to increase vitality, energy, endurance and stamina. Korean ginseng &#40;Panax ginseng&#41; is used in China as a preventative tonic to stimulate the entire body to overcome stress, fatigue and weakness. It contains 13 different ginsenosides. Panaxans help to lower blood sugar, polysaccharides work to enhance the immune system and its antioxidant properties are immune&#45;stimulating to protect the body from disease and stress. It balances the release of stress hormones by supporting the organs that produce them. This article investigates the therapeutic and clinical effects of Indian and Korean ginseng.</p>]]></content:encoded>
<dc:identifier>10.1504/IJIS.2011.041727</dc:identifier>
<dc:source>International Journal of Immunological Studies, Vol. 1, No. 3 (2011) pp. 297 - 317</dc:source>
<dc:creator>R. Seenivasagam</dc:creator>
<dc:creator>S. Sathiyamoorthy</dc:creator>
<dc:creator>K. Hemavathi</dc:creator>
<dc:contributor>Division of Drug Discovery and Development, Center of Molecular and Computational Biology, Department of Botany, St. Joseph College, P.B. 27094, 36, Langford Road, Bangalore, Karnataka 560027, India. &#39; Korean Ginseng Center and Ginseng Genetic Resource Bank, Kyung Hee University, Yongin, 449&#45;701, South Korea. &#39; Department of Bioinformatics, School of Chemical and Biotechnology, SASTRA University, Thanjavur&#45;613 401, India</dc:contributor>
<dc:subject>traditional medicine</dc:subject>
<dc:subject>cancer</dc:subject>
<dc:subject>immunology&#58; medicinal plants</dc:subject>
<dc:subject>ginseng alkaloids</dc:subject>
<dc:subject>herbal medicine</dc:subject>
<dc:subject>India</dc:subject>
<dc:subject>Korea</dc:subject>
<dc:subject>Withania somnifera</dc:subject>
<dc:subject>Ashwagandha</dc:subject>
<dc:subject>Panax ginseng</dc:subject>
<dc:subject>China</dc:subject>
<dc:subject>herbal tonics</dc:subject>
<dc:subject>therapeutic effects</dc:subject>
<dc:subject>clinical effects.</dc:subject>
<dc:date>2011-08-01T23:20:50-05:00</dc:date>
<prism:volume>1</prism:volume>
<prism:number>3</prism:number>
<prism:startingPage>297</prism:startingPage>
<prism:endingPage>317</prism:endingPage>
<prism:publicationDate>2011-08-01T23:20:50-05:00</prism:publicationDate>
</item>
</rdf:RDF>

