Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes : Support for a genetic bottleneck von MARCHINGTON, D. R, HARTSHORNE, G. M, BARLOW, D, POULTON, J

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Evidence from Human Oocytes for a Genetic Bottleneck in an mtDNA Disease von Marchington, D.R., Macaulay, V., Hartshorne, G.M., Barlow, D., Poulton, J.

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A common mitochondrial DNA variant is associated with insulin resistance in adult life von POULTON, J, BROWTT, M. S, COOPER, A, MARCHINGTON, D. R, PHILLIPS, D. I. W

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No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI von Marchington, D.R., Scott Brown, M.S.G., Lamb, V.K., van Golde, R.J.T., Kremer, J.A.M., Tuerlings, J.H.A.M., Mariman, E.C.M., Balen, A.H., Poulton, J.

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New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation von Pulkes, T, Liolitsa, D, Eunson, L H, Rose, M, Nelson, I P, Rahman, S, Poulton, J, Marchington, D R, Landon, D N, Debono, A G, Morgan-Hughes, J A, Hanna, M G

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Do Sequence Variants in the Major Non-Coding Region of the Mitochondrial Genome Influence Mitochondrial Mutations Associated with Disease? von Marchington, David R., Poulton, Joanna, Sellar, Anneke, Holt, Ian J.

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Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility von Rovio, Anja T., Marchington, David R., Donat, Susanne, Schuppe, Hans-Christian, Abel, Josef, Fritsche, Ellen, Elliott, David J., Laippala, Pekka, Ahola, Arja L., McNay, David, Harrison, Robert F., Hughes, Barbara, Barrett, Thomas, Bailey, David M.D., Mehmet, Denise, Jequier, Anne M., Hargreave, Tim B., Kao, Shu-Huei, Cummins, James M., Barton, David E., Cooke, Howard J., Wei, Yau-Huei, Wichmann, Lars, Poulton, Joanna, Jacobs, Howard T.

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Molecular genetic characterization of an X-linked form of Leigh's syndrome von Matthews, P. M., Marchington, D. R., Squier, M., Land, J., Brown, R. M., Brown, G. K.

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Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications von Poulton, J, Marchington, DR

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Prospects for DNA-based prenatal diagnosis of mitochondrial disorders von Poulton, J., Marchington, D. R.

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Is the Bottleneck Cracked? von Poulton, J., Macaulay, V., Marchington, D.R.

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Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients von Matthews, P. M., Brown, R. M., Otero, L. J., Marchington, D. R., LeGris, M., Howes, R., Meadows, L. S., Shevell, M., Scriver, C. R., Brown, G. K.

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Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: Developing the first mouse model of mitochondrial DNA disease von Marchington, David R., Barlow, David, Poulton, Joanna

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Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases von Poulton, Joanna, Marchington, David R

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Longer-term regulation of pyruvate dehydrogenase kinase in cultured rat cardiac myocytes von Marchington, D R, Kerbey, A L, Randle, P J

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Long term culture of rat soleus muscle in vitro: Its effects on glucose utilization and insulin sensitivity von Stace, Pamela B., Marchington, David R., Kerbey, Alan L., Randle, Philip J.

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Longer-term regulation of pyruvate dehydrogenase kinase in cultured rat hepatocytes von Marchington, D R, Kerbey, A L, Giardina, M G, Jones, A E, Randle, P J

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Insulin reverses effects of starvation on the activity of pyruvate dehydrogenase kinase in cultured hepatocytes von Marchington, D R, Kerbey, A L, Jones, A E, Randle, P J

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Does a common mitochondrial DNA polymorphism underlie susceptibility to diabetes and the thrifty genotype? von Poulton, Joanna

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Mitochondrial genetics '98 is the bottleneck cracked? von Poulton, J, Macaulay, V, Marchington, D R

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