|
 |
Scientist 'E'
Molecular Endocrinology
Phone : +( 91-22) 2419 2009
Email : maitraa@nirrh.res.in
Academic Background
- M.Sc. University of Bombay
(Biochemistry, 1972)
- Ph.D. University of Bombay (Biochemistry, 1984)
Professional Experience
| Research Scientist |
University of Virginia Health,
Sciences Centre |
1992-1993 |
| Visiting Scientist |
ABC Life Technology Centre,
Hamburg , Germany |
2004-2005 |
| Scientist |
NIRRH |
1974- Till date |
Research Interests
- Reproductive Endocrinology
- Molecular Genetics
Awards & Achievements
- Awarded “Medical innovation” Grant by ICMR ( 2006-2007)
- Awarded Indian National Science Academy Bilateral Exchange Grant for Germany (2004-2005)
- Awarded Research Training grant ( 1992-1993) by the World Health Organization (WHO), for training in USA in the field of Molecular Biology
- Awarded WHO Re-entry Grant (1995-1998 ) for studies on “Molecular Regulation of Steroidogenesis in Ovaries”.
- Professor B.D. Tilak Visiting Fellowship Endowment (2007-2008) - University Institute of Chemical Technology, Mumbai.
Publications (Last 10)
-
Pusalkar M, Meherji P, Gokral J, Chinnaraj S, Maitra A. CYP11A1 and CYP17 Promoter Polymorphisms Associate with Hyperandrogenemia in Polycystic Ovary Syndrome. Fertility Sterility.In Press – Available on-line
-
Chatterjee S, Maitra A , Kadam S, Patel Z, Gokral J and Meherji P. CGG repeat sizing in the FMR1 gene in Indian women with premature ovarian failure . Reproductive BioMedicine Online. - Accepted
-
S.Mukherjee and A.Maitra. Molecular and genetic factors contributing to insulin resistance in polycystic ovary syndrome. Indian Journal of Medical Reseach - Accepted
-
Singh N, Dubey S, Chinnaraj S, Golani A and Maitra A . Study of NAT2 gene polymorphisms in an Indian population: Their association with plasma isoniazid concentration in a cohort of tuberculosis patients. Molecular Diagnosis and Therapy 13 :1: 2009.
-
Dubey S , Idicula-Thomas S, Anwaruddin M, Saravanan C, Varma RR and Anurupa Maitra A novel 9-bp insertion detected in steroid 21-hydroxylase gene (CYP21A2): prediction of its structural and functional implications by computational methods Journal of Biomedical Science 16 :3 : 2009.
-
Pathak S, Kedia-Mokashi N, Saxena M, D’Souza R, Maitra A, Parte P, Gill Sharma M, Balasinor N.Effect of tamoxifen treatment on global and Insulin-like growth factor 2-H19 locus specific DNA methylation in rat spermatozoa and its association with embryo loss. Fertility and Sterility 9:5 : 2253-2263, 2009
-
Mukherjee S, Shaikh N, Khavale S, Shinde G, Meherji P, Shah N, and Maitra A. G enetic variation in exon 17 of INSR is associated with insulin resistance and hyperandrogenemia among lean Indian women with polycystic ovary syndrome .
Eur J Endocrinol.160 (5):855-62:2009.
-
Sarkar C and Maitra A. Deciphering the cis-regulatory elements of co-expressed genes in PCOS by in silico analysis. Gene 408 : 72-84 , 2008
-
Abid S, Maitra A, Gokral J, Meherji P, Pires E, Kadam S and Modi D. Altered expression of Progesterone recptor in infertile man. Reproductive BioMedicine Online 17 : 2, 2008
-
Singh N, Golani A, Patel Z and Maitra A . Transfer of Isoniazid from circulation to breast milk in lactating women on chronic treatment for tuberculosis.
British Journal of Clinical Pharmacology65: 418-422, 2008
Present students
- Ms.Heena Shirwalkar
- Ms.Madhavi Pusalkar
- Ms. Shadaan Abid
- Ms. Neera Singh
- Mr. Chiradeep Sarkar
Past students
- Ms.Vrushali Tanavde
- Mr. Rahul Pingle
Projects
- Genomic studies on polycystic Ovaries and Congenital Adrenal Hyperplasia (Funded by ICMR “Genomic” Fund)
- Model to Predict Milk/Plasma ratios of therapeutic drugs (Funded by ICMR “Genomic” Fund)
- Molecular characterization and nucleotide polymorphism (SNP) profiling in Congenital Adrenal Hyperplasia : A study with specific emphasis on steroid 21-Hydroxylase gene. (Funded by DST)
- A genetic analysis of polycystic ovary syndrome with special emphasis on genes involved in insulin resistance (Funded by DST)
- Development of a Rapid Molecular Technique for Diagnosis of Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency (ICMR Medical Innovation Fund)
|
|
|