Search Results - "Shah, Nila"

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  1. 1

    Combined Analysis of Oligonucleotide Microarray Data from Transgenic and Knockout Mice Identifies Direct SREBP Target Genes by Horton, Jay D., Shah, Nila A., Warrington, Janet A., Anderson, Norma N., Park, Sahng Wook, Brown, Michael S., Goldstein, Joseph L.

    “…The synthesis of fatty acids and cholesterol, the building blocks of membranes, is regulated by three membrane-bound transcription factors: sterol regulatory…”
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    The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection by Maitra, Anirban, Cohen, Yoram, Gillespie, Susannah E D, Mambo, Elizabeth, Fukushima, Noriyoshi, Hoque, Mohammad O, Shah, Nila, Goggins, Michael, Califano, Joseph, Sidransky, David, Chakravarti, Aravinda

    Published in Genome research (01-05-2004)
    “…Somatic mitochondrial mutations are common in human cancers, and can be used as a tool for early detection of cancer. We have developed a mitochondrial Custom…”
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    Identification of a Mammalian Long Chain Fatty Acyl Elongase Regulated by Sterol Regulatory Element-binding Proteins by Moon, Y A, Shah, N A, Mohapatra, S, Warrington, J A, Horton, J D

    Published in The Journal of biological chemistry (30-11-2001)
    “…Fatty acids are synthesized de novo from acetyl-CoA and malonyl-CoA through a series of reactions mediated by acetyl-CoA carboxylase (ACC) and fatty acid…”
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    New developments in high-throughput resequencing and variation detection using high density microarrays by Warrington, Janet A., Shah, Nila A., Chen, Xiyin, Janis, Michael, Liu, Chunmei, Kondapalli, Sangeetha, Reyes, Vivian, Savage, Michael P., Zhang, Zhaomei, Watts, Richard, DeGuzman, Maria, Berno, Anthony, Snyder, Jim, Baid, Jyoti

    Published in Human mutation (01-04-2002)
    “…We developed a high‐throughput method for resequencing for single nucleotide polymorphism (SNP) discovery using high‐density microarrays. Over the two‐year…”
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    High-throughput variation detection and genotyping using microarrays by Cutler, D J, Zwick, M E, Carrasquillo, M M, Yohn, C T, Tobin, K P, Kashuk, C, Mathews, D J, Shah, N A, Eichler, E E, Warrington, J A, Chakravarti, A

    Published in Genome research (01-11-2001)
    “…The genetic dissection of complex traits may ultimately require a large number of SNPs to be genotyped in multiple individuals who exhibit phenotypic variation…”
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    Extensive polymorphisms observed in HIV-1 clade B protease gene using high-density oligonucleotide arrays by Kozal, Michael J, Shah, Nila, Shen, Naiping, Yang, Robert, Fucini, Raymond, Merigan, Thomas C, Richman, Douglas D, Morris, Don, Hubbell, Earl, Chee, Mark, Gingeras, Thomas R

    Published in Nature medicine (01-07-1996)
    “…Naturally occurring mutations in HIV-1-infected patients have important implications for therapy and the outcome of clinical studies. However, little is known…”
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    Evidence for homology of normal and neoplastic human placental alkaline phosphatases as determined by monoclonal antibodies to the cancer-associated enzyme by JEMMERSON, R, SHAH, N, FISHMAN, W. H

    Published in Cancer research (Chicago, Ill.) (01-07-1985)
    “…The HeLa TCRC-1 human adenocarcinoma cell line expresses a form of alkaline phosphatase that is similar to the common S-variant of placental alkaline…”
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  14. 14

    Characterization of the placental alkaline phosphatase-like (Nagao) isozyme on the surface of A431 human epidermoid carcinoma cells by JEMMERSON, R, SHAH, N, TAKEDA, M, FISHMAN, W. H

    Published in Cancer research (Chicago, Ill.) (1985)
    “…A431 human epidermoid carcinoma cells monophenotypically express the placental alkaline phosphatase (PLAP)-like enzyme shown by its catalytic and antigenic…”
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  15. 15

    Immunoelectron microscopic analysis of the binding of monoclonal antibodies to molecular variants of human placental alkaline phosphatase by Takeya, Motohiro, Jemmerson, Ronald, Shah, Nila, Fishman, William H

    Published in Biochemistry (Easton) (18-11-1986)
    “…Three monoclonal antibodies with distinct antigenic specificities were examined by electron microscopy for their binding to three common genetic variants (SS,…”
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