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R D Mittal

Showing results (21-30 of 36) with videos related to

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Clinical Genetics|November 1, 1996
High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patientsS Sinha, S Mishra, V Singh, et al.
Neurology India|December 4, 2003
Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophyG S Pandey, A Kesari, M Mukherjee, et al.
Teratogenesis, Carcinogenesis, and Mutagenesis|March 5, 2003
Assessment of microsatellite instability in bladder and thyroid malignanciesMinal Vaish, S K Mishra, Anil Mandhani, et al.
Clinical Genetics|November 15, 2000
Analysis of dinucleotide repeat loci of dystrophin gene for carrier detection, germline mosaicism and de novo mutations in Duchenne muscular dystrophyL S Chaturvedi, R D Mittal, S Srivastava, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1994
Muscular sufficiency, serum protein, enzymes and bioenergetic studies (31-phosphorus magnetic resonance spectroscopy) in chronic malnutritionR K Gupta, R D Mittal, K N Agarwal, et al.
Experimental & Molecular Medicine|January 25, 2002
Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patientsL S Chaturvedi, M Mukherjee, S Srivastava, et al.
Experimental & Molecular Medicine|May 20, 2003
De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) casesMonisha Mukherjee, L S Chaturvedi, Sandhya Srivastava, et al.
Indian Journal of Cancer|October 9, 2004
Polymorphism of GSTM1 and GSTT1 genes in prostate cancer: a study from North IndiaR D Mittal, D S L Srivastava, A Mandhani, et al.
European Urology|August 16, 2002
Role of Oxalobacter formigenes in calcium oxalate stone disease: a study from North IndiaR Kumar, M Mukherjee, M Bhandari, et al.
Cancer Epidemiology|May 28, 2013
Influence of ABCB1 genetic variants in breast cancer treatment outcomesP Chaturvedi, S Tulsyan, G Agarwal, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Clinical Genetics|November 1, 1996
High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patientsS Sinha, S Mishra, V Singh, et al.
Neurology India|December 4, 2003
Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophyG S Pandey, A Kesari, M Mukherjee, et al.
Teratogenesis, Carcinogenesis, and Mutagenesis|March 5, 2003
Assessment of microsatellite instability in bladder and thyroid malignanciesMinal Vaish, S K Mishra, Anil Mandhani, et al.
Clinical Genetics|November 15, 2000
Analysis of dinucleotide repeat loci of dystrophin gene for carrier detection, germline mosaicism and de novo mutations in Duchenne muscular dystrophyL S Chaturvedi, R D Mittal, S Srivastava, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1994
Muscular sufficiency, serum protein, enzymes and bioenergetic studies (31-phosphorus magnetic resonance spectroscopy) in chronic malnutritionR K Gupta, R D Mittal, K N Agarwal, et al.
Experimental & Molecular Medicine|January 25, 2002
Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patientsL S Chaturvedi, M Mukherjee, S Srivastava, et al.
Experimental & Molecular Medicine|May 20, 2003
De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) casesMonisha Mukherjee, L S Chaturvedi, Sandhya Srivastava, et al.
Indian Journal of Cancer|October 9, 2004
Polymorphism of GSTM1 and GSTT1 genes in prostate cancer: a study from North IndiaR D Mittal, D S L Srivastava, A Mandhani, et al.
European Urology|August 16, 2002
Role of Oxalobacter formigenes in calcium oxalate stone disease: a study from North IndiaR Kumar, M Mukherjee, M Bhandari, et al.
Cancer Epidemiology|May 28, 2013
Influence of ABCB1 genetic variants in breast cancer treatment outcomesP Chaturvedi, S Tulsyan, G Agarwal, et al.
Pageof 4