Coronavirus infection in intensively managed cattle with respiratory disease von Hick, PM, Read, AJ, Lugton, I, Busfield, F, Dawood, KE, Gabor, L, Hornitzky, M, Kirkland, PD

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The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families von Goate, A, Kosik, K, Talbot, C, Axelman, K, Roberts, G.W, Dickson, D, Mehta, N, Harvey, R, Winblad, B, Adams, M.D, Lantos, P, Karran, E, Arcos, M, Wragg, M, Froelich, S, Busfield, F, Morris, J, Martinez, A, Prihar, G, Zehr, C, Poyhonen, M, Viitanen, M, Myers, A, He, C, Behrens, M.I, Mann, D, Neary, D, Venter, J.C, Snowden, J, Korenblat, K, Duff, K, Ashworth, A, Rossor, M, Forsell, L, Cowburn, R, Ossa, J, Haltia, M, Pearson, C, Cline, R.T, Madrigal, L, Clark, R.F, Hutton, M, Johnston, J, Fuldner, M, Kennedy, A, Sarner, S, Lannfelt, L, Hardy, J, Roques, P, Collinge, J, Fox, N, Norton, J, Lilius, L, Lendon, C, Lincoln, S, Philips, C.A, Baker, M, Humphreys, C, Perez-Tur, J, Lopera, F, Crook, R, Houlden, H, Ruiz, A

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Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3–14 von Warner, J V, Nyholt, D R, Busfield, F, Epstein, M, Burgess, J, Stranks, S, Hill, P, Perry-Keene, D, Learoyd, D, Robinson, B, Teh, B T, Prins, J B, Cardinal, J W

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A Genomewide Search for Type 2 Diabetes–Susceptibility Genes in Indigenous Australians von Busfield, Frances, Duffy, David L., Kesting, Janine B., Walker, Shelley M., Lovelock, Paul K., Good, David, Tate, Heather, Watego, Denise, Marczak, Maureen, Hayman, Noel, Shaw, Joanne T.E.

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Hereditary dysphasic disinhibition dementia : A frontotemporal dementia linked to 17q21-22 von LENDON, C. L, LYNCH, T, WILHELMSEN, K. C, HANSEN, L, MORRIS, J. C, GOATE, A. M, NORTON, J, MCKEEL, D. W, BUSFIELD, F, CRADDOCK, N, CHAKRAVERTY, S, GOPALAKRISHNAN, G, SHEARS, S. D, GRIMMETT, W

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Carotid artery intimal medial thickness, brachial artery flow-mediated vasodilation and cardiovascular risk factors in diabetic and non-diabetic indigenous Australians von Chan, Lionel, Shaw, Andrew G., Busfield, Frances, Haluska, Brian, Barnett, Adrian, Kesting, Janine, Short, Leanne, Marczak, Maureen, Shaw, Joanne T.E.

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Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree von Good, David A., Duffy, David L., Good, Manuela, Xia Guo, Cheng, Busfield, Frances, Shaw, Anthony, Shaw, Joanne T. E.

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Haemochromatosis and HLA-H von Jazwinska, Elizabeth C, Cullen, Lara M, Busfield, Frances, Pyper, Wendy R, Webb, Sonja I, Powell, Lawrie W, Morris, C. Philip, Walsh, Terence P

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Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees von Good, David A, Busfield, Frances, Fletcher, Barbara H, Lovelock, Paul K, Duffy, David L, Kesting, Janine B, Andersen, John, Shaw, Joanne T.E

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Linkage of Paget Disease of Bone to a Novel Region on Human Chromosome 18q23 von Good, David A., Busfield, Frances, Fletcher, Barbara H., Duffy, David L., Kesting, Janine B., Andersen, John, Shaw, Joanne T.E.

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A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene von Perez-Tur, Jordi, Froelich, Susanne, Prihar, Guy, Crook, Richard, Baker, Matt, Duff, Karen, Wragg, Michelle, Busfield, Frances, Lendon, Corinne, Clark, Robert F, Roques, Penelope, Fuldner, Rebecca A, Johnston, Janet, Cowburn, Richard, Forsell, Charlotte, Axelman, Karin, Lilius, Lena, Houlden, Henry, Karran, Eric, Roberts, Gareth W, Rossor, Martin, Adams, Mark D, Hardy, John, Goate, Alison, Lannfelt, Lars, Hutton, Michael

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THE STRUCTURE OF THE PRESENILIN-1 (S182) GENE AND IDENTIFICATION OF 6 NOVEL MUTATIONS IN EARLY-ONSET AD FAMILIES von CLARK, RF, HUTTON, M, FULDNER, RA, FROELICH, S, KARRAN, E, TALBOT, C, CROOK, R, LENDON, C, PRIHAR, G, HE, C

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Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease von Wragg, M, Talbot, C, Hutton, M, Goate, Alison

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Complete analysis of the presenilin 1 gene in early onset Alzheimerʼs disease von Hutton, Mike, Busfield, Frances, Wragg, Michelle, Crook, Richard, Perez-Tur, Jordi, Clark, Robert F, Prihar, Guy, Phillips, Helen, Wright, Kristal, Baker, Matt, Lendon, Corinne, Duff, Karen, Martinez, Alonso, Houlden, Henry, Nichols, Andy, Karran, Eric, Roberts, Gareth, Roques, Penelope, Rossor, Martin, Venter, J Craig, Adams, Mark D, Cline, Robin T, Phillips, Cheryl A, Fuldner, Rebecca A, Hardy, John, Goate, Alison

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The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients von Stuart, Katherine A., Busfield, Frances, Jazwinska, Elizabeth C., Gibson, Peter, Butterworth, Lesley A., Cooksley, W.Graham, Powell, Lawrie W., Crawford, Darrell H.G.

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Familial Paget's Disease of Bone: Nonlinkage to the PDB1 and PDB2 Loci on Chromosomes 6p and 18q in a Large Pedigree von Good, David, Busfield, Frances, Duffy, David, Lovelock, Paul K., Kesting, Janine B., Cameron, Donald P., Shaw, Joanne T. E.

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E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles von Lendon, Corinne L., Martinez, Alonso, Behrens, Isabel Maria, Kosik, Kenneth S., Madrigal, Lucia, Norton, Joanne, Neuman, Rosalind, Myers, Amanda, Busfield, Frances, Wragg, Michelle, Arcos, Mauricio, Viana, Juan Carlos Arango, Ossa, Jorge, Ruiz, Andres, Goate, Alison M., Lopera, Francisco

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Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22 von Lendon, C. L., Lynch, T., Norton, J., McKeel, D. W., Busfield, F., Craddock, N., Chakraverty, S., Gopalakrishnan, G., Shears, S. D., Grimmett, W., Wilhelmsen, K. C., Hansen, L., Morris, J. C., Goate, A. M.

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Generation of a transcription map distal to HLA-F von Goldwurm, Stefano, Van der Griend, Benjamin FH, Banyer, Joanne L, Cullen, Lara M, Zournazi, Anna, Menzies, Moira L, Busfield, Frances, Little, Peter FR, Jazwinska, Elizabeth C

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Molecular genetics of hereditary dysphasic dementia von Lendon, C.L., Shears, S., Busfield, F., Talbot, C.J., Renner, J., Morris, J.C., Goate, A.M.

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