Search Results - "Chaturvedi, L"

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    De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) cases by Mukherjee, Monisha, Chaturvedi, L S, Srivastava, Sandhya, Mittal, R D, Mittal, Balraj

    Published in Experimental & molecular medicine (30-04-2003)
    “…Dinucleotide repeat polymorphism based genetic analysis is a powerful approach to gain insight into rare genetic events like germline mosaicism and de novo…”
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    Journal Article
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    COM Crystals Activate the p38 Mitogen-activated Protein Kinase Signal Transduction Pathway in Renal Epithelial Cells by Koul, Hari K., Menon, Mani, Chaturvedi, Lakshmi S., Koul, Sweaty, Sekhon, Avtar, Bhandari, Akshay, Huang, Meiyi

    Published in The Journal of biological chemistry (27-09-2002)
    “…Interaction of calcium oxalate monohydrate (COM) crystals with renal cells has been shown to result in altered gene expression, DNA synthesis, and cell death…”
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    Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients by Chaturvedi, L S, Mukherjee, M, Srivastava, S, Mittal, R D, Mittal, B

    Published in Experimental & molecular medicine (31-12-2001)
    “…Duchenne and Becker muscular dystrophies (D/BMD) are caused by mutations in the dystrophin gene. Two-thirds of patients have large intragenic deletions or…”
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    Oxalate Selectively Activates p38 Mitogen-activated Protein Kinase and c-Jun N-terminal Kinase Signal Transduction Pathways in Renal Epithelial Cells by Chaturvedi, Lakshmi S., Koul, Sweaty, Sekhon, Avtar, Bhandari, Akshay, Menon, Mani, Koul, Hari K.

    Published in The Journal of biological chemistry (12-04-2002)
    “…Oxalate, a metabolic end product, is an important factor in the pathogenesis of renal stone disease. Oxalate exposure to renal epithelial cells results in…”
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    Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene by Chaturvedi, L S, Srivastava, S, Mukherjee, M, Mittal, R D, Phadke, S R, Pradhan, S, Mittal, B

    “…Carrier detection and prenatal diagnosis is of great importance for families with one or more sons affected with Duchenne/Becker muscular dystrophy (D/BMD). In…”
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    Abstract P6-09-09: A second-generation proteasome inhibitor (SGPI) inhibits proliferation of triple negative breast cancer cells to a greater extent than doxorubicin while decreasing IL-6/NF-kB pathway inflammatory activity by Vyas, D, Lopez, N, Chaturvedi, L, Vyas, A

    Published in Cancer research (Chicago, Ill.) (15-12-2013)
    “…Background: Proteasome inhibitors limit tumor growth by lowering the capacity of cancer cells to degrade pro-apoptotic signals. Given the success of proteasome…”
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    Resolution of the Long-Term Performance Issues at the Waste Isolation Pilot Plant by Silva, M K, Rucker, D F, Chaturvedi, L

    Published in Risk analysis (01-10-1999)
    “…The Waste Isolation Pilot Plant (WIPP) is a geological repository for disposal of U.S. defense transuranic radioactive waste. Built and operated by the U.S…”
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    Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow by Mittal, B, Singh, V, Mishra, S, Sinha, S, Mittal, R D, Chaturvedi, L S, Danda, S, Pradhan, S, Agarwal, S S

    “…The molecular basis of two allelic forms of muscular dystrophy, Duchenne (DMD) and Becker (BMD), has been explained by frame shift hypothesis. In order to test…”
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    Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients by SINGH, V, SINHA, S, MISHRA, S, LAKSHMI SHANKAR CHATURVEDI, PRADHAN, S, RAMA DEVI MITTAL, MITTAL, B

    Published in Human genetics (01-02-1997)
    “…Population-based variations in frequency and distribution of dystrophin gene deletions have been recognized in Duchenne/Becker (DMD/BMD) muscular dystrophy…”
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