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Group by: Author | Type
Jump to: A | B | D | F | G | H | K | L | M | R
Number of items: 26.

A

Armstrong, RA; Cairns, NJ; Myers, D; Smith, CUM; Lantos, PL; Rossor, MN; (1996) A comparison of beta-amyloid deposition in the medial temporal lobe in sporadic Alzheimer's disease, Down's syndrome and normal elderly brains. NEURODEGENERATION , 5 (1) 35 - 41.

Armstrong, RA; Cairns, NJ; Patel, R; Lantos, PL; Rossor, MN; (1996) Relationships between beta-amyloid (A beta) deposits and blood vessels in patients with sporadic and familial Alzheimer's disease. NEUROSCI LETT , 207 (3) 171 - 174.

B

Bermingham, N; Martin, JE; Fisher, EMC; (1996) The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus. Genomics , 32 pp. 266-271.

Bermingham, N; McKay, T; Hoyle, J; Hernandez, D; Martin, JE; Fisher, EMC; (1996) The gene encoding tripeptidyl peptidase II maps to chromosome 1 in the mouse. Mamm Genome , 7 390-.

Bush, MS; Goold, RG; Moya, F; GordonWeeks, PR; (1996) An analysis of an axonal gradient of phosphorylated MAP 1B in cultured rat sensory neurons. EUROPEAN JOURNAL OF NEUROSCIENCE , 8 (2) pp. 235-248. 10.1111/j.1460-9568.1996.tb01208.x.

D

David, K; Revesz, T; Path, MRC; Kratimenos, G; Krausz, T; Path, FRC; Crockard, HA; (1996) Oncogenic osteomalacia associated with a meningeal phosphaturic mesenchymal tumor - Case report. J NEUROSURG , 84 (2) 288 - 292.

Delabar, JM; Creau, N; Antonarakis, SE; Brahe, C; Estivill, X; Pritchard, M; Fisher, EMC; ... Lutfalla, G; + view all (1996) Towards an integrated chromosome 21 map: progress of the European chromosome 21 consortium. In: (Proceedings) European Society of Human Genetics - 28th Annual Meeting.

F

Fox, N; Harvey, RJ; Rossor, MN; (1996) Protein folding, nucleation phenomena and delayed neurodegeneration in Alzheimer's disease. REV NEUROSCIENCE , 7 (1) 21 - 28.

Fukutani, Y; Cairns, NJ; Rossor, MN; Lantos, PL; (1996) Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val->Ile) mutation cases. NEUROPATH APPL NEURO , 22 (5) 452 - 452.

G

Geddes, JF; Thom, M; Robinson, SFD; Revesz, T; (1996) Granular cell change in astrocytic tumors. AM J SURG PATHOL , 20 (1) 55 - 63.

H

Hernandez, D; Fisher, EMC; (1996) Down syndrome genetics: unravelling a multifactorial disorder. Hum Mol Genet , 5 pp. 1411-1416.

Hoyle, J; Fisher, EMC; (1996) Genomic organization and mapping of the mouse P26s4 ATPase gene: a member of the remarkably conserved AAA gene family. Genomics , 31 pp. 115-118.

Hoyle, J; Phelan, JP; Bermingham, N; Fisher, EMC; (1996) Localization of human and mouse N-ethylmaleimide-sensitive factor (NSF) gene: a two domain member of the AAA family which is involved in membrane fusion. Mamm Genome , 7 850-.

Hoyle, J; Yulug, IG; Johnstone, K; Scambler, PJ; Fisher, EMC; (1996) Characterisation of a short interspersed repeat (Mermaid) which has family members on human chromosome 21 and elsewhere in the human genome. Hum Genet , 97 pp. 117-120.

K

Katsanis, N; Fisher, EMC; (1996) The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome. Hum Genet , 98 497-.

Katsanis, N; Fitzgibbon, J; Fisher, EMC; (1996) Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci. Genomics , 35 pp. 101-108.

L

Lovestone, S; Wilcock, G; Rossor, M; Cayton, H; Ragan, I; (1996) Apolipoprotein E genotyping in Alzheimer's disease. The UK Alzheimer's Disease Genetic consortium. Lancet , 347 (9017) 1775 - 1776.

M

Matthews, D; Fry, L; Powles, A; Weber, J; McCarthy, M; Fisher, EMC; Davies, K; (1996) Evidence for a locus for familial psoriasis mapping to chromosome 4q. Nature genetics , 14 pp. 231-233.

Moran, TH; Reeves, RH; Rogers, D; Fisher, EMC; (1996) Ain't misbehavin' - it's genetic. Nature Genetics , 12 pp. 115-116.

R

Revesz, T; Sangha, H; Daniel, SE; (1996) The nucleus raphe interpositus in progressive supranuclear palsy. J NEUROPATH EXP NEUR , 55 (5) 117 - 117.

Rossor, MN; (1996) BSE and human disease. J ROY COLL PHYS LOND , 30 (6) 494 - 495.

Rossor, MN; (1996) Degenerative diseases - Editorial comment. CURR OPIN NEUROL , 9 (4) 251 - 253.

Rossor, MN; (1996) Degenerative diseases - Editorial comment. CURRENT OPINION IN NEUROLOGY , 9 (4) pp. 251-253. 10.1097/00019052-199608000-00001.

Rossor, MN; (1996) Mad cows and demented people. Trans Med Soc Lond , 113 pp. 34-37.

Rossor, MN; Fox, NC; Beck, J; Campbell, TC; Collinge, J; (1996) Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation. LANCET , 347 (9014) 1560 - 1560.

Rudge, P; Webster, ADB; Revesz, T; Warner, T; Espanol, T; CunninghamRundles, C; Hyman, N; (1996) Encephalomyelitis in primary hypogammaglobulinaemia. BRAIN , 119 1 - 15.

This list was generated on Sun May 20 02:29:09 2018 BST.