Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 69

1.

A novel haplotype within C-reactive protein gene influences CRP levels and coronary heart disease risk in Northwest Indians.

Singh P, Singh M, Nagpal HS, Kaur T, Khullar S, Kaur G, Dhillon H, Di Napoli M, Mastana S.

Mol Biol Rep. 2014 Sep;41(9):5851-62. doi: 10.1007/s11033-014-3459-0. Epub 2014 Jun 26.

PMID:
24965144
[PubMed - in process]
2.

Unity in diversity: an overview of the genomic anthropology of India.

Mastana SS.

Ann Hum Biol. 2014 Jul-Aug;41(4):287-99. doi: 10.3109/03014460.2014.922615.

PMID:
24932744
[PubMed - in process]
3.

'From death, lead me to immortality' - mantra of ageing skeletal muscle.

Saini A, Mastana S, Myers F, Lewis MP.

Curr Genomics. 2013 Jun;14(4):256-67. doi: 10.2174/1389202911314040004.

PMID:
24294106
[PubMed]
Free PMC Article
4.

Influence of glutathione S-transferase polymorphisms (GSTT1, GSTM1, GSTP1) on type-2 diabetes mellitus (T2D) risk in an endogamous population from north India.

Mastana SS, Kaur A, Hale R, Lindley MR.

Mol Biol Rep. 2013 Dec;40(12):7103-10. doi: 10.1007/s11033-013-2833-7. Epub 2013 Nov 8.

PMID:
24203463
[PubMed - indexed for MEDLINE]
5.

The relationship of testosterone and AR CAG repeat genotype with knee extensor muscle function of young and older men.

Folland JP, Mc Cauley TM, Phypers C, Hanson B, Mastana SS.

Exp Gerontol. 2012 Jun;47(6):437-43. doi: 10.1016/j.exger.2012.03.013. Epub 2012 Mar 28.

PMID:
22484019
[PubMed - indexed for MEDLINE]
6.

Relationship of 2D:4D finger ratio with muscle strength, testosterone, and androgen receptor CAG repeat genotype.

Folland JP, Mc Cauley TM, Phypers C, Hanson B, Mastana SS.

Am J Phys Anthropol. 2012 May;148(1):81-7. doi: 10.1002/ajpa.22044. Epub 2012 Mar 15.

PMID:
22419368
[PubMed - indexed for MEDLINE]
7.

Lack of association between Glu298Asp polymorphism and coronary artery disease in North Indians.

Rai H, Fitt J, Sharma AK, Sinha N, Kumar S, Pandey CM, Agrawal S, Mastana S.

Mol Biol Rep. 2012 May;39(5):5995-6000. doi: 10.1007/s11033-011-1412-z. Epub 2011 Dec 30.

PMID:
22207178
[PubMed - indexed for MEDLINE]
8.

Lack of association of bone morphogenetic protein 2 gene haplotypes with bone mineral density, bone loss, or risk of fractures in men.

Varanasi SS, Tuck SP, Mastana SS, Dennison E, Cooper C, Vila J, Francis RM, Datta HK.

J Osteoporos. 2011;2011:243465. doi: 10.4061/2011/243465. Epub 2011 Oct 13.

PMID:
22013543
[PubMed]
Free PMC Article
9.

The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease.

Gleeson M, Bishop NC, Stensel DJ, Lindley MR, Mastana SS, Nimmo MA.

Nat Rev Immunol. 2011 Aug 5;11(9):607-15. doi: 10.1038/nri3041.

PMID:
21818123
[PubMed - indexed for MEDLINE]
10.

Modification of estrogen's association with Alzheimer's disease risk by genetic polymorphisms.

Thornton V, Warden D, Talbot C, Mastana SS, Bandelow S, Hogervorst E.

Brain Res. 2011 Mar 16;1379:213-23. doi: 10.1016/j.brainres.2010.12.074. Epub 2011 Jan 4.

PMID:
21211518
[PubMed - indexed for MEDLINE]
11.

ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetes in North Indians.

Bhatti JS, Bhatti GK, Mastana SS, Ralhan S, Joshi A, Tewari R.

Mol Cell Biochem. 2010 Dec;345(1-2):249-57. doi: 10.1007/s11010-010-0579-2. Epub 2010 Sep 4.

PMID:
20820885
[PubMed - indexed for MEDLINE]
12.

Association analysis of TNFR2, VDR, A2M, GSTT1, GSTM1, and ACE genes with rheumatoid arthritis in South Asians and Caucasians of East Midlands in the United Kingdom.

Ghelani AM, Samanta A, Jones AC, Mastana SS.

Rheumatol Int. 2011 Oct;31(10):1355-61. doi: 10.1007/s00296-010-1478-2. Epub 2010 Apr 18.

PMID:
20401725
[PubMed - indexed for MEDLINE]
13.

ACE I/D and ACTN3 R/X polymorphisms and muscle function and muscularity of older Caucasian men.

McCauley T, Mastana SS, Folland JP.

Eur J Appl Physiol. 2010 May;109(2):269-77. doi: 10.1007/s00421-009-1340-y. Epub 2010 Jan 13.

PMID:
20069311
[PubMed - indexed for MEDLINE]
14.

Paraoxonase 1 gene polymorphisms contribute to coronary artery disease risk among north Indians.

Agrawal S, Tripathi G, Prajnya R, Sinha N, Gilmour A, Bush L, Mastana S.

Indian J Med Sci. 2009 Aug;63(8):335-44. doi: 10.4103/0019-5359.55884.

PMID:
19770524
[PubMed - indexed for MEDLINE]
Free Article
15.

Tumor necrosis factor alpha -308 gene locus promoter polymorphism: an analysis of association with health and disease.

Elahi MM, Asotra K, Matata BM, Mastana SS.

Biochim Biophys Acta. 2009 Mar;1792(3):163-72. Review.

PMID:
19708125
[PubMed - indexed for MEDLINE]
16.

Human angiotensin-converting enzyme I/D and alpha-actinin 3 R577X genotypes and muscle functional and contractile properties.

McCauley T, Mastana SS, Hossack J, Macdonald M, Folland JP.

Exp Physiol. 2009 Jan;94(1):81-9. doi: 10.1113/expphysiol.2008.043075. Epub 2008 Aug 1.

PMID:
18676575
[PubMed - indexed for MEDLINE]
Free Article
17.

Vitamin D-binding protein gene microsatellite polymorphism influences BMD and risk of fractures in men.

Al-oanzi ZH, Tuck SP, Mastana SS, Summers GD, Cook DB, Francis RM, Datta HK.

Osteoporos Int. 2008 Jul;19(7):951-60. Epub 2007 Nov 24.

PMID:
18038108
[PubMed - indexed for MEDLINE]
18.

Association of PTPN22 with rheumatoid arthritis among South Asians in the UK.

Mastana S, Gilmour A, Ghelani A, Smith H, Samanta A.

J Rheumatol. 2007 Oct;34(10):1984-6. Epub 2007 Aug 1.

PMID:
17696275
[PubMed - indexed for MEDLINE]
19.

A variant of position -308 of the Tumour necrosis factor alpha gene promoter and the risk of coronary heart disease.

Elahi MM, Gilmour A, Matata BM, Mastana SS.

Heart Lung Circ. 2008 Feb;17(1):14-8. Epub 2007 Jun 19.

PMID:
17581788
[PubMed - indexed for MEDLINE]
20.

Chemokine receptor 5 (CCR5) deletion polymorphism in North Indian patients with coronary artery disease.

Sharda S, Gilmour A, Harris V, Singh VP, Sinha N, Tewari S, Ramesh V, Agrawal S, Mastana S.

Int J Cardiol. 2008 Feb 29;124(2):254-8. Epub 2007 Mar 26.

PMID:
17383752
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk