1. Dhandapany PS, Sadayappan S, Xue Y, Powell GT, Rani DS, Nallari P, Rai TS, Khullar M, Soares P, Bahl A, Tharkan JM, Vaideeswar P, Rathinavel A, Narasimhan C, Ayapati DR, Ayub Q, Mehdi SQ, Oppenheimer S, Richards MB, Price AL, Patterson N, Reich D, Singh L, Tyler-Smith C, Thangaraj K. A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia. Nat Genet 2009; 41:187-91.
2. Ahluwalia TS, Ahuja M, Rai TS, Kohli HS, Bhansali A, Sud K, Khullar M. ACE Variants Interact with the RAS Pathway to Confer Risk and Protection against Type 2 Diabetic Nephropathy. DNA Cell Biol 2009; 28: 141-50.
3. Markan S, Kohli HS, Joshi K, Minz RW, Sud K, Ahuja M, Anand S, Khullar M. Up regulation of the GRP-78 and GADD-153 and down regulation of Bcl-2 proteins in primary glomerular diseases: a possible involvement of the ER stress pathway in glomerulonephritis. Mol Cell Biochem 2009; 324: 131-38.
4. Poduri A, Bahl A, Sharma YP, KK Talwar, Khullar M. Polymorphisms in statin metabolism pathway genes predict statin mediated LDL cholesterol lowering in coronary artery disease patients. J Clin Lipidol 2008; 2: S169.
5. Ahmad S, Otaal PS, Rai TS, Bahl A, Saikia UN, Manoj RK, Thungapathra M, Talwar KK, Khullar M. Circulating proinflammatory cytokines and N-terminal pro-brain natriuretic peptide significantly decrease with recovery of left ventricular function in patients with dilated cardiomyopathy. Mol Cell Biochem 2009; 324: 139-45.
6. Rai TS, Ahmad S, Bahl A, Ahuja M, Ahluwalia TS, Singh B, Talwar KK, Khullar M. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy. Mol Cell Biochem 2009; 321: 189-96.
7. Khandelwal G, Bhalla S, Khullar M, Panda NK. High frequency of heterozygosity in GJB2 mutations among patients of non-syndromic hearing loss. J Laryngol Otol 2008; 23:1-5.
8. Rai TS, Khullar M, Sehrawat BS, Ahuja M, Sharma PK, Vijayvergiya R, Grover A. Synergistic effect between apolipoprotein E and apolipoprotein A1 gene polymorphisms in the risk for coronary artery disease. Mol Cell Biochem 2008; 313:139-46.
9. Ahluwalia TS, Ahuja M, Rai TS, Kohli HS, Sud K, Bhansali A, Khullar M. Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians. Mol Cell Biochem 2008; 314:9-17.
10. Markan S, Kohli HS, Sud K, Ahuja M, Ahluwalia TS, Sakhuja V, Khullar M. Oxidative stress in primary glomerular diseases: a comparative study. Mol Cell Biochem 2008; 311: 105-10.
11. Rai TS, Dhandapany PS, Ahluwalia TS, Bhardwaj M, Bahl A, Talwar KK, Nair K, Rathinavel A, Khullar M. ACE I/D polymorphism in Indian patients with hypertrophic cardiomyopathy and dilated cardiomyopathy. Mol Cell Biochem 2008; 31: 67-72.
12. Poduri A, Mukherjee D, Sud K, Kohli HS, Sakhuja V, Khullar M. (2007). MTHFR A1298C polymorphism is associated with cardiovascular risk in end stage renal disease in North Indians. Mol Cell Biochem. Mol Cell Biochem 2008; 308: 43-50.
13. Bhalla S, Panda N, Khullar M. PCR-RFLP assay for 235delC mutation detection in non-syndromic Hearing loss subjects. Am J of Med Gen 2007; 143A:1810-1811. |