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The Journal of Urology|December 22, 1999
Expanding the living related donor pool in renal transplantation: use of marginal donorsA Kumar, A Mandhani, B S Verma, et al.
Prostate Cancer and Prostatic Diseases|November 10, 2010
Prostate cancer gene expression signature of patients with high body mass indexS Sharad, A Srivastava, S Ravulapalli, et al.
International Journal of Laboratory Hematology|April 5, 2012
A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLCE S Edison, M Sathya, S V Rajkumar, et al.
Ultrasound in Medicine & Biology|July 1, 1985
Duplex scanning of the thyroidJ P Woodcock, G M Owen, E J Shedden, et al.
Journal of Applied Microbiology|December 23, 2016
Antimicrobial assay and genetic screening of selected freshwater Cyanobacteria and identification of a biomolecule dihydro-2H-pyran-2-one derivativeA Srivastava, V K Singh, S Patnaik, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 15, 2014
Association between angiotensin converting enzyme gene insertion/deletion polymorphism and intracerebral haemorrhage in North Indian population: a case control study and meta-analysisA Kumar, K Prasad, S Vivekanandhan, et al.
Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
Three novel beta-propeller mutations causing Glanzmann thrombasthenia result in production of normally stable pro-alphaIIb, but variably impaired progression of pro-alphaIIbbeta3 from endoplasmic reticulum to GolgiE J R Nelson, J Li, W B Mitchell, et al.
Endocrine Pathology|March 27, 2002
Juvenile rheumatoid arthritis with amyloid goiter: report of a case with review of the literatureA Srivastava, M Baxi, S Yadav, et al.
Cytokine|August 9, 2021
Regulation of STAT3 signaling in IFNγ and IL10 pathways and in their cross-talkU Sarma, M Maiti, A Nair, et al.
Journal of Thrombosis and Haemostasis : JTH|May 17, 2005
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutationG Jayandharan, A Viswabandya, S Baidya, et al.
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