Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells von Reynolds, Nicola, Collier, Brian, Maratou, Klio, Bingham, Victoria, Speed, Robert M., Taggart, Mary, Semple, Colin A., Gray, Nicola K., Cooke, Howard J.

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A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis von Ma, Kun, Inglis, John D., Sharkey, Andrew, Bickmore, Wendy A., Hill, Robert E., Prosser, E.Jane, Speed, Robert M., Thomson, Eric J., Jobling, Mark, Taylor, Kay, Wolfe, Jonathan, Cooke, Howard J., Hargreave, Timothy B., Chandley, Ann C.

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Expression profiling of the developing testis in wild-type and Dazl knockout mice von Maratou, Klio, Forster, Thorsten, Costa, Yael, Taggart, Mary, Speed, Robert M., Ireland, John, Teague, Peter, Roy, Douglas, Cooke, Howard J.

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Partial rescue of the Dazl knockout mouse by the human DAZL gene von Vogel, T., Speed, R.M., Ross, A., Cooke, H.J.

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A Human DAZ Transgene Confers Partial Rescue of the Mouse Dazl Null Phenotype von Slee, R., Grimes, B., Speed, R. M., Taggart, M., Maguire, S. M., Ross, A., McGill, N. I., Saunders, P. T. K., Cooke, H. J.

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Meiotic Studies of a Human Male Carrier of the Common Translocation, t(11;22), Suggests Postzygotic Selection rather than Preferential 3:1 MI Segregation as the Cause of Liveborn O... von Armstrong, Susan J., Goldman, Alastair S.H., Speed, Robert M., Hultén, Maj A.

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Deficiency of Trp53 rescues the male fertility defects of Kit(W-v) mice but has no effect on the survival of melanocytes and mast cells von Jordan, S A, Speed, R M, Bernex, F, Jackson, I J

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Mice with Y chromosome deletion and reduced Rbm genes on a heterozygous Dazl1 null background mimic a human azoospermic factor phenotype von Vogel, T., Speed, R.M., Teague, P., Cooke, H.J.

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Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis : meiotic studies in a man with a deletion of distal Xp von MOHANDAS, T. K, SPEED, R. M, PASSAGE, M. B, YEN, P. H, CHANDLEY, A. C, SHAPIRO, L. J

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The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes von SPEED, R. M

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Different distributions of homologous chromosomes in adult human Sertoli cells and in lymphocytes signify nuclear differentiation von Chandley, A C, Speed, R M, Leitch, A R

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Evidence of disturbed meiosis in a man referred for intracytoplasmic sperm injection von Pieters, MHEC, Speed, RM, de Boer, P, Vreeburg, JTM, Dohle, G, Veld, PA in't

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Prophase of meiosis in human spermatocytes analysed by EM microspreading in infertile men and their controls and comparisons with human oocytes von SPEED, R. M, CHANDLEY, A. C

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Oocyte development in XO fœtuses of man and mouse: the possible role of heterologous X-chromosome pairing in germ cell survival von SPEED, R. M

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Morphological and temporal sequence of meiotic prophase development at puberty in the male mouse von GOETZ, P, CHANDLEY, A. C, SPEED, R. M

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Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation von Guichaoua, M R, Quack, B, Speed, R M, Noel, B, Chandley, A C, Luciani, J M

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A reassessment of Y chromosomal behaviour in germ cells and Sertoli cells of the mouse as revealed by in situ hybridisation von Chandley, A C, Speed, R M

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Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs) von Chandley, A C, Gosden, J R, Hargreave, T B, Spowart, G, Speed, R M, McBeath, S

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The prophase stages in human foetal oocytes studied by light and electron microscopy von SPEED, R. M

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Pericentric inversion in human chromosome 1 and the risk for male sterility von Chandley, A C, McBeath, S, Speed, R M, Yorston, L, Hargreave, T B

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