Search Results - WORTHAM, Noel

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  1. 1
    Analysis of the subunit organization of the eIF2B complex reveals new insights into its structure and regulation

    Analysis of the subunit organization of the eIF2B complex reveals new insights into its structure and regulation by Wortham, Noel C., Martinez, Magdalena, Gordiyenko, Yuliya, Robinson, Carol V., Proud, Christopher G.

    Published in The FASEB journal
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  2. 2
    Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter disease

    Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter disease by Wortham, Noel C, Proud, Christopher G

    Published in BMC medical genetics
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  3. 3
    Identification of Residues That Underpin Interactions within the Eukaryotic Initiation Factor (eIF2) 2B Complex

    Identification of Residues That Underpin Interactions within the Eukaryotic Initiation Factor (eIF2) 2B Complex by Wang, Xuemin, Wortham, Noel C., Liu, Rui, Proud, Christopher G.

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  4. 4
    Adult Leydig Cell Tumors of the Testis Caused by Germline Fumarate Hydratase Mutations

    Adult Leydig Cell Tumors of the Testis Caused by Germline Fumarate Hydratase Mutations by Carvajal-Carmona, Luis G., Alam, N. Afrina, Pollard, Patrick J., Jones, Angela M., Barclay, Ella, Wortham, Noel, Pignatelli, Massimo, Freeman, Alex, Pomplun, Sabine, Ellis, Ian, Poulsom, Richard, El-Bahrawy, Mona A., Berney, Daniel M., Tomlinson, Ian P. M.

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  5. 5
    Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5

    Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5 by Matsukawa, Takashi, Wang, Xuemin, Liu, Rui, Wortham, Noel C., Onuki, Yuko, Kubota, Akatsuki, Hida, Ayumi, Kowa, Hisatomo, Fukuda, Yoko, Ishiura, Hiroyuki, Mitsui, Jun, Takahashi, Yuji, Aoki, Shigeki, Takizawa, Shunya, Shimizu, Jun, Goto, Jun, Proud, Christopher G., Tsuji, Shoji

    Published in Neurogenetics
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  6. 6
    Definition of a minimal region of deletion of chromosome 7 in uterine leiomyomas by tiling-path microarray CGH and mutation analysis of known genes in this region

    Definition of a minimal region of deletion of chromosome 7 in uterine leiomyomas by tiling-path microarray CGH and mutation analysis of known genes in this region by Vanharanta, Sakari, Wortham, Noel C., Langford, Cordelia, El-Bahrawy, Mona, van der Spuy, Zephne, Sjöberg, Jari, Lehtonen, Rainer, Karhu, Auli, Tomlinson, Ian P.M., Aaltonen, Lauri A.

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  7. 7
    Evidence of increased microvessel density and activation of the hypoxia pathway in tumours from the hereditary leiomyomatosis and renal cell cancer syndrome

    Evidence of increased microvessel density and activation of the hypoxia pathway in tumours from the hereditary leiomyomatosis and renal cell cancer syndrome by Pollard, Patrick, Wortham, Noel, Barclay, Ella, Alam, Afrina, Elia, George, Manek, Sanjiv, Poulsom, Richard, Tomlinson, Ian

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  8. 8
    CDC4 mutations occur in a subset of colorectal cancers but are not predicted to cause loss of function and are not associated with chromosomal instability

    CDC4 mutations occur in a subset of colorectal cancers but are not predicted to cause loss of function and are not associated with chromosomal instability by KEMP, Zoe, ROWAN, Andrew, TOMLINSON, Ian, CHAMBERS, William, WORTHAM, Noel, HALFORD, Sarah, SIEBER, Oliver, MORTENSEN, Neil, VON HERBAY, Axel, GUNTHER, Thomas, ILYAS, Mohammad

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  9. 9
    Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia

    Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia by Murdoch, Jennifer N, Doudney, Kit, Gerrelli, Dianne, Wortham, Noel, Paternotte, Caroline, Stanier, Philip, Copp, Andrew J

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