Human prostate cell lines from normal and tumourigenic epithelia differ in the pattern and control of choline lipid headgroups released into the medium on stimulation of protein kinase C
RUMSBY, M, SCHMITT, J, SHARRARD, M, RODRIGUES, G, STOWER, M, MAITLAND, N
Published in British journal of cancer (15.02.2011)
Published in British journal of cancer (15.02.2011)
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A new mode of inheritance
Koodiyedath, B, Bowen, J, Johnson, D, Sharrard, M
Published in Archives of disease in childhood (01.04.2011)
Published in Archives of disease in childhood (01.04.2011)
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High frequency of missense mutations in glycogen storage disease type VI
Beauchamp, N. J, Taybert, J, Champion, M. P, Layet, V, Heinz-Erian, P, Dalton, A, Tanner, M. S, Pronicka, E, Sharrard, M. J
Published in Journal of inherited metabolic disease (01.10.2007)
Published in Journal of inherited metabolic disease (01.10.2007)
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Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency
Olpin, S. E., Clark, S., Andresen, B. S., Bischoff, C., Olsen, R. K. J., Gregersen, N., Chakrapani, A., Downing, M., Manning, N. J., Sharrard, M., Bonham, J. R., Muntoni, F., Turnbull, D. N., Pourfarzam, M.
Published in Journal of inherited metabolic disease (01.08.2005)
Published in Journal of inherited metabolic disease (01.08.2005)
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P287 Acute metabolic presentation in heterozygote glutaryl CoA dehydrogenase mutation
Davies, E, Sharrard, M, Rao, P, Mordekar, S
Published in European journal of paediatric neurology (2009)
Published in European journal of paediatric neurology (2009)
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Coordinate changes of polyamine metabolism regulatory proteins during the cell cycle of normal human dermal fibroblasts
Bettuzzi, S., Davalli, P., Astancolle, S., Pinna, C., Roncaglia, R., Boraldi, F., Tiozzo, R., Sharrard, M., Corti, A.
Published in FEBS letters (05.03.1999)
Published in FEBS letters (05.03.1999)
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Patterns of methylation of the c-myc gene in human colorectal cancer progression
SHARRARD, R. M, ROYDS, J. A, ROGERS, S, SHORTHOUSE, A. J
Published in British journal of cancer (01.05.1992)
Published in British journal of cancer (01.05.1992)
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Evaluation of the significance of polyamines and their oxidases in the aetiology of human cervical carcinoma
FERNANDEZ, C, SHARRARD, R. M, TALBOT, M, REED, B. D, MONKS, N
Published in British journal of cancer (01.11.1995)
Published in British journal of cancer (01.11.1995)
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Carnitine‐acylcarnitine translocase deficiency ‐ a mild phenotype
Olpin, S.E., Bonham, J.R., Downing, M., Manning, N.J., Pollitt, R.J., Sharrard, M.J., Tanner, M.S.
Published in Journal of inherited metabolic disease (01.09.1997)
Published in Journal of inherited metabolic disease (01.09.1997)
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Detection of circulating prostate-specific antigen-positive cells in patients with prostate cancer by flow cytometry and reverse transcription polymerase chain reaction
FADLON, E. J, REES, R. C, MCINTYRE, C, SHARRARD, R. M, LAWRY, J, HAMDY, F. C
Published in British journal of cancer (01.08.1996)
Published in British journal of cancer (01.08.1996)
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Screening for medium chain acyl-CoA dehydrogenase deficiency has still not been evaluated
Tanner, Stuart, Sharrard, Mark, Cleary, Maureen, Walter, John, Wraith, Ed, Lee, Philip, Leonard, James, Morris, Andrew, McIntosh, Neil
Published in BMJ (13.01.2001)
Published in BMJ (13.01.2001)
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The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease
Bonham, J. R., Guthrie, P., Downing, M., Allen, J. C., Tanner, M. S., Sharrard, M., Rittey, C., Land, J. M., Fensom, A., O'Neill, D., Duley, J. A., Fairbanks, L. D.
Published in Journal of inherited metabolic disease (01.04.1999)
Published in Journal of inherited metabolic disease (01.04.1999)
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Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants
Vogel, Georg F., Mozer-Glassberg, Yael, Landau, Yuval E., Schlieben, Lea D., Prokisch, Holger, Feichtinger, René G., Mayr, Johannes A., Brennenstuhl, Heiko, Schröter, Julian, Pechlaner, Agnes, Alkuraya, Fowzan S., Baker, Joshua J., Barcia, Giulia, Baric, Ivo, Braverman, Nancy, Burnyte, Birute, Christodoulou, John, Ciara, Elzbieta, Coman, David, Das, Anibh M., Darin, Niklas, Della Marina, Adela, Distelmaier, Felix, Eklund, Erik A., Ersoy, Melike, Fang, Weiyan, Gaignard, Pauline, Ganetzky, Rebecca D., Gonzales, Emmanuel, Howard, Caoimhe, Hughes, Joanne, Konstantopoulou, Vassiliki, Kose, Melis, Kerr, Marina, Khan, Aneal, Lenz, Dominic, McFarland, Robert, Margolis, Merav Gil, Morrison, Kevin, Müller, Thomas, Murayama, Kei, Nicastro, Emanuele, Pennisi, Alessandra, Peters, Heidi, Piekutowska-Abramczuk, Dorota, Rötig, Agnès, Santer, René, Scaglia, Fernando, Schiff, Manuel, Shagrani, Mohmmad, Sharrard, Mark, Soler-Alfonso, Claudia, Staufner, Christian, Storey, Imogen, Stormon, Michael, Taylor, Robert W., Thorburn, David R., Teles, Elisa Leao, Wang, Jian-She, Weghuber, Daniel, Wortmann, Saskia
Published in Genetics in medicine (01.06.2023)
Published in Genetics in medicine (01.06.2023)
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