A mutation in the viral sensor 2'-5'-oligoadenylate synthetase 2 causes failure of lactation von Oakes, Samantha R, Gallego-Ortega, David, Stanford, Prudence M, Junankar, Simon, Au, Wendy Wing Yee, Kikhtyak, Zoya, von Korff, Anita, Sergio, Claudio M, Law, Andrew M K, Castillo, Lesley E, Allerdice, Stephanie L, Young, Adelaide I J, Piggin, Catherine, Whittle, Belinda, Bertram, Edward, Naylor, Matthew J, Roden, Daniel L, Donovan, Jesse, Korennykh, Alexei, Goodnow, Christopher C, O'Bryan, Moira K, Ormandy, Christopher J

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Socs2 and Elf5 Mediate Prolactin-Induced Mammary Gland Development von Harris, Jessica, Stanford, Prudence M, Sutherland, Kate, Oakes, Samantha R, Naylor, Matthew J, Robertson, Fiona G, Blazek, Katrina D, Kazlauskas, Michael, Hilton, Heidi N, Wittlin, Sergio, Alexander, Warren S, Lindeman, Geoffrey J, Visvader, Jane E, Ormandy, Christopher J

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Prolactin and the prolactin receptor: new targets of an old hormone von Harris, Jessica, Stanford, Prudence M, Oakes, Samantha R, Ormandy, Christopher J

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Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: Expansion of the disease phenotype caused by tau gene mutations von STANFORD, P. M, HALLIDAY, G. M, BROOKS, W. S, KWOK, J. B. J, STOREY, C. E, CREASEY, H, MORRIS, J. G. L, FULHAM, M. J, SCHOFIELD, P. R

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KIBRA interacts with discoidin domain receptor 1 to modulate collagen-induced signalling von Hilton, Heidi N., Stanford, Prudence M., Harris, Jessica, Oakes, Samantha R., Kaplan, Warren, Daly, Roger J., Ormandy, Christopher J.

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Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia von Stanford, Prudence M., Shepherd, Claire E., Halliday, Glenda M., Brooks, William S., Schofield, Peter W., Brodaty, Henry, Martins, Ralph N., Kwok, John B. J., Schofield, Peter R.

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Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies von STANFORD, Prudence M, BROOKS, William S, TEBER, Erdahl T, HALLUPP, Marianne, MCLEAN, Catriona, HALLIDAY, Glenda M, MARTINS, Ralph N, KWOK, John B. J, SCHOFIELD, Peter R

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Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene von Stanford, Prudence M., Halliday, Glenda M., Brooks, William S., Kwok, John B. J., Storey, Catherine E., Creasey, Helen, Morris, John G. L., Fulham, Michael J., Schofield, Peter R.

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Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation von Wszolek, Zbigniew K., Tsuboi, Yoshio, Uitti, Ryan J., Reed, Lee, Hutton, Michael L., Dickson, Dennis W., Stanford, Prudence M., Halliday, Glenda M., Brooks, William S., Kwok, John B.J., Schofield, Peter R.

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Tau gene mutations are pleiotropic: Identification of two novel mutations in the tau gene von Stanford, Prudence Mary, Halliday, Glenda M., Brooks, William S., Kwok, John Bj, Storey, Catherine E., Creasey, Helen, Morris, John Gl, Fulham, Michael J.

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