M. Palmer

发表

Sequences homologous to ZFY, a candidate human sex-determining gene, are autosomal in marsupials

D. Page, A. Sinclair, J. W. Foster, 1988, Nature.

Comparison of human ZFY and ZFX transcripts.

P N Goodfellow, A. Sinclair, M. Palmer, 1990, Proceedings of the National Academy of Sciences of the United States of America.

The human SRY transcript.

A. Sinclair, M. Palmer, P. Goodfellow, 1993, Human molecular genetics.

Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies

M. Palmer, J. Collinge, S. Mahal, 1996, Human mutation.

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

R. Lathe, M. Palmer, J. Collinge, 1996, Human Genetics.

Molecular genetics of human prion diseases.

M. Palmer, J. Collinge, 1994, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Human prion diseases.

M. Palmer, J. Collinge, Palmer Ms, 1992, Current opinion in neurology and neurosurgery.

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

John Collinge, M. Palmer, J. Collinge, 1991, Nature.

Mutations and polymorphisms in the prion protein gene

M. Palmer, J. Collinge, 1993, Human mutation.

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene

M. Palmer, W. Gibb, J. Collinge, 1996, Neurology.

Human trophoblast and the choriocarcinoma cell line BeWo express a truncated HLA Class I molecule.

M. Palmer, A. McMichael, S. Ellis, 1990, Journal of immunology.

Complete nucleotide sequence of a unique HLA class I C locus product expressed on the human choriocarcinoma cell line BeWo.

M. Palmer, A. McMichael, T. Strachan, 1989, Journal of immunology.

Pathogenic presenilin 1 mutations (P436S & I143F) in early‐onset Alzheimer's disease in the UK

Nick C Fox, M. Palmer, M. Rossor, 1999, Human mutation.

The T cell receptor from an influenza-A specific murine CTL clone.

M. Palmer, A. Townsend, K. Gould, 1989, Nucleic acids research.

Monoclonal antibodies against the complement control protein factor H (beta 1 H).

M. Palmer, Robert B Sim, E. Sim, 1983, Bioscience reports.

Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

M. Palmer, J. Hardy, A. Brun, 1994, Journal of neurology, neurosurgery, and psychiatry.

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

Robin Lovell-Badge, Andrew H. Sinclair, Philippe Berta, 1990, Nature.

Genetic evidence that ZFY is not the testis-determining factor

A. Sinclair, M. Palmer, P. Goodfellow, 1989, Nature.

Monoclonal antibodies against the complement control protein Factor H (β1 H)

M. Palmer, Robert B Sim, E. Sim, 1983 .

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome

M. Palmer, P. Goodfellow, P. Goodfellow, 1989, Nature.

Prion protein is necessary for normal synaptic function

M. Palmer, M. Whittington, J. Collinge, 1994, Nature.

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

M. Palmer, J. Collinge, Aidan J. Dryden, 1991, The Lancet.

Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark

M. Palmer, J. Hardy, M. Rossor, 1993, Journal of the Neurological Sciences.

Prion diseases

M. Palmer, J. Collinge, 1992, Current Biology.

Deletions in the prion protein gene are not associated with CJD.

M. Palmer, J. Collinge, A. Hill, 1993, Human molecular genetics.

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

M. Palmer, P. Lantos, J. Collinge, 1995, Nature.

Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

M. Palmer, M. Whittington, J. Collinge, 1995, Nature Genetics.

Conformational properties of the prion octa‐repeat and hydrophobic sequences

M. Palmer, J. Collinge, A. Clarke, 1997, FEBS letters.

Transmission of Creutzfeldt-Jakob disease by handling of dura mater

M. Palmer, J. Collinge, H. Tumani, 1993, The Lancet.

Liposomes for gene therapy : Receptor ligand-facilitated gene transfer: enhancement of liposome-mediated gene transfer and expression by transferrin Cheng, P-W. (1996) Hum. Gene Ther. 7, 275–282

M. Palmer, 1996 .

Prion diseases in humans and their relevance to other neurodegenerative diseases.

M. Palmer, J. Collinge, 1993, Dementia.

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

J Collinge, M. Palmer, J. Collinge, 1993, BMJ.

Binding and Functional Analysis of the Workshop T Cell Specific Set of Monoclonal Antibodies

M. Palmer, A. McMichael, P. Morris, 1986 .