Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research
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Indian Journal of Medical ResearchIndian Journal of Medical Research, a publication of Indian Council of Medical Research, is a peer-reviewed online journal with Monthly print on demand compilation of issues published. The journal’s full text is available online at http://www.ijmr.org.in. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository. The journal does not charge for submission, processing or publication of manuscripts and even for color reproduction of photographs.

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The journal is indexed with Caspur, CNKI (China National Knowledge Infrastructure), EBSCO Publishing's Electronic Databases, Google Scholar, Index Copernicus, Index Medicus for South-East Asia Region, Indian Science Abstracts, IndMed, MEDLINE/Index Medicus, National Science Library, OpenJGate, PubMed, Pubmed Central, Science Citation Index, Science Citation Index Expanded, Scimago Journal Ranking, SCOLOAR, SCOPUS, SIIC databases, Summon by Serial Solutions, Ulrich's International Periodical Directory and Web of Science

Impact Factor® for 2013 is 1.661

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  Articles from current issue   February 2015 | Vol 141 | Issue 2  
 
Editorial
Mesenchymal stromal cells as regulators of anti-tumour immune response
In India, breast and cervix uteri cancers are two of the leading causes of neoplasia for women, while neoplasia of lung and gastroenteric tract are a cause of mortality in men. It appears that lifesty...
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Editorial
International Epilepsy Day - A day notified for global public education & awareness
Epilepsy is a common medical disorder that can have a psychological and emotional impact on people with this disorder and their caregivers. About 65 million people worldwide have epilepsy [1] and near...
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Commentary
Low-density oligonucleotide microarrays - A major step in Wilson's disease diagnosis
Wilson's disease (WD) is a monogenic disorder of copper accumulation caused due to mutation in the copper transporting ATPase gene ATP7B[1],[2] . WD follows an autosomal recessive mode of inheritance ...
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Commentary
An understanding of spinocerebellar ataxia
Advances in molecular genetics techniques have given several approaches to diagnose most common complex genetic disorders and also these advances have helped to diagnose the rare complex disorders. Au...
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