Assessing the pathological relevance of SPINK1 promoter variants
Eur J Hum Genet. 2011 Oct;19(10):1066-73. doi: 10.1038/ejhg.2011.79. Epub 2011 May 25.
2011
Assessing the pathological relevance of SPINK1 promoter variants
Eur J Hum Genet. 2011 Oct;19(10):1066-73. doi: 10.1038/ejhg.2011.79. Epub 2011 May 25.
2011
Glioblastoma cell secretome: analysis of three glioblastoma cell lines reveal 148 non-redundant proteins
J Proteomics. 2011 Sep 6;74(10):1918-25. doi: 10.1016/j.jprot.2011.05.002. Epub 2011 May 11.
2011
Relationship of APOA5, PPAR? and HL gene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood
Lipids Health Dis. 2011 May 8;10:68. doi: 10.1186/1476-511X-10-68.
2011
Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes
Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):507-12. doi: 10.1089/gtmb.2010.0207. Epub 2011 Mar 25.
2011
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Hum Mol Genet. 2011 Jun 1;20(11):2273-84. doi: 10.1093/hmg/ddr092. Epub 2011 Mar 4.
2011
Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians
J Gastroenterol Hepatol. 2011 Apr;26(4):694-9. doi: 10.1111/j.1440-1746.2010.06533.x.
2011
Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India
BMC Med Genet. Dec 15; 12:162.
2011
Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia.
Am J Hum Genet. 89:731-44
2011
Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.
DNA Cell Biol. (in press).
2011
Cellular model of Warburg effect identifies tumor promoting function of UCP2 in breast cancer and its suppression by genipin.
PLoS One 6:e24792
2011
Analysis of mitochondrial genome revealed a rare 50bp deletion and substitutions in a family with hypertension.
Mitochondrion. Jul 20. [Epub ahead of print].
2011
Indian Siddis: African Descendants with Indian Admixture.
Am J Hum Genet. 89: 154-161.
2011
No evidence for association between SLC11A1 and visceral leishmaniasis in India.
BMC Med Genet. 12:71.
2011
Contribution of muscle biopsy and genetics to the diagnosis of chronic progressive external opthalmoplegia of mitochondrial origin.
J Clin Neurosci. 18:535-538.
2011
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