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Journal of General Microbiology|September 1, 1990
Molecular cloning, expression and nucleotide sequence of the rcsA gene of Erwinia amylovora, encoding a positive regulator of capsule expression: evidence for a family of related capsule activator proteinsM Coleman, R Pearce, E Hitchin, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 10, 2001
Familial Paget's disease of bone: nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigreeD Good, F Busfield, D Duffy, et al.Australian Veterinary Journal|September 26, 2012
Coronavirus infection in intensively managed cattle with respiratory diseaseP M Hick, A J Read, I Lugton, et al.Neuroreport|December 29, 1995
A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 geneJ Perez-Tur, S Froelich, G Prihar, et al.Journal of Hepatology|April 29, 1998
The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patientsK A Stuart, F Busfield, E C Jazwinska, et al.European Journal of Human Genetics : EJHG|November 5, 1998
Generation of a transcription map distal to HLA-FS Goldwurm, B F Van der Griend, J L Banyer, et al.Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
The role of presenilin 1 in the genetics of Alzheimer's diseaseR F Clark, M Hutton, C Talbot, et al.Journal of Medical Genetics|March 10, 2006
Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14J V Warner, D R Nyholt, F Busfield, et al.Neurology|June 20, 1998
Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22C L Lendon, T Lynch, J Norton, et al.Human Mutation|January 1, 1997
E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE allelesC L Lendon, A Martinez, I M Behrens, et al.Pageof 2