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Number of items: 35.

A

ANDERTON, B; COLLINGE, J; POWELL, J; PRUSINER, SB; (1992) AN INTRODUCTION TO PRION RESEARCH. In: Prusiner, S and Collinge, J and Powell, J and Anderton, B, (eds.) PRION DISEASES OF HUMANS AND ANIMALS. (pp. 3 - 4). ELLIS HORWOOD LTD

Anderton, BH; Collinge, J; Powell, J; Prusiner, SB; (1992) An introduction to prion research. In: Prusiner, SB and Collinge, J and Powell, J and Anderton, B, (eds.) Prion diseases of humans and animals. (3 - 4). Ellis Horwood: London, UK.

C

CLINE, MJ; JAT, PS; FOTI, A; (1992) MOLECULAR MECHANISMS IN THE EVOLUTION OF CHRONIC MYELOCYTIC-LEUKEMIA. LEUKEMIA LYMPHOMA , 7 (4) 283 - 287.

COLLINGE, J; BROWN, J; HARDY, J; MULLAN, M; ROSSOR, MN; BAKER, H; CROW, TJ; (1992) INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .2. CLINICAL AND PATHOLOGICAL FEATURES. BRAIN , 115 687 - 710.

COLLINGE, J; PALMER, MS; (1992) MOLECULAR-GENETICS OF INHERITED, SPORADIC AND IATROGENIC PRION DISEASE. In: Prusiner, S and Collinge, J and Powell, J and Anderton, B, (eds.) PRION DISEASES OF HUMANS AND ANIMALS. (pp. 95 - 119). ELLIS HORWOOD LTD

COLLINGE, J; PRUSINER, SB; (1992) PRIONS AND NEURODEGENERATIVE DISEASES. In: Prusiner, S and Collinge, J and Powell, J and Anderton, B, (eds.) PRION DISEASES OF HUMANS AND ANIMALS. (pp. 568 - 569). ELLIS HORWOOD LTD

COLLINGE, J; PRUSINER, SB; (1992) TERMINOLOGY OF PRION DISEASES. In: Prusiner, S and Collinge, J and Powell, J and Anderton, B, (eds.) PRION DISEASES OF HUMANS AND ANIMALS. (pp. 5 - 12). ELLIS HORWOOD LTD

CROW, TJ; POULTER, M; BAKER, HF; FRITH, CD; LEACH, M; LOFTHOUSE, R; RIDLEY, RM; (1992) FAMILIAL DEMENTIA IN RELATION TO THE 144 BP INSERT AND ITS IMPLICATIONS. In: Prusiner, S and Collinge, J and Powell, J and Anderton, B, (eds.) PRION DISEASES OF HUMANS AND ANIMALS. (pp. 200 - 214). ELLIS HORWOOD LTD

Collinge, J; Palmer, MS; (1992) Prion diseases. Curr Opin Genet Dev , 2 (3) pp. 448-454.

Collinge, J; Palmer, S; (1992) Molecular genetics of inherited, sporadic and iatrogenic prion disease. In: Prusiner, SB and Collinge, J and Powell, J and Anderton, B, (eds.) Prion diseases of humans and animals. (95 - 119). Ellis Horwood: London, UK.

Collinge, J; Prusiner, SB; (1992) Terminology of prion disease. In: Prusiner, SB and Collinge, J and Powell, J and Anderton, B, (eds.) Prion diseases of humans & animals. (5 - 12). Ellis Horwood: London, UK.

Crow, TJ; Poulter, M; Baker, HF; Frith, CD; Leach, M; Lofthouse, R; Ridley, RM; (1992) Familial dementia in relation to the 144bp insert and its implications. In: Prusiner, SB and Collinge, J and Powell, J and Anderton, B, (eds.) Prion diseases of humans & animals. (200 - 214). Ellis Horwood: London, UK.

F

Fidani, L; Rooke, K; Chartier-Harlin, MC; Hughes, D; Tanzi, R; Mullan, M; Roques, P; (1992) Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile. Hum Mol Genet , 1 (3) pp. 165-168.

G

GONOS, ES; POWELL, AJ; JAT, PS; (1992) HUMAN AND RODENT FIBROBLASTS - MODEL SYSTEMS FOR STUDYING SENESCENCE AND IMMORTALIZATION (REVIEW). INT J ONCOL , 1 (2) 209 - 213.

Gonos, ES; Powell, AJ; Ikram, Z; Cline, M; Jat, PS; (1992) A molecular genetic approach towards senescence and immortalization. In: Spandidos, DA, (ed.) Current Perspectives on Molecular and Cellular Oncology: Volume 1 (Part A) Mechanisms of Gene Regulation in Cancer. Elsevier Science Ltd: London.

H

HATTERSLEY, G; OWENS, JM; JAT, PS; NOBLE, MD; CHAMBERS, TJ; (1992) GENERATION OF CELL-LINES WITH POTENT ABILITY TO FORM BONE RESORBING OSTEOCLASTS. J BONE MINER RES , 7 S112 - S112.

Hamvas, RMJ; Zinn, A; Keer, JT; Fisher, EMC; Beer-Romero, P; Brown, SDM; Page, D; (1992) Rps4 maps near the inactivation center on the mouse X chromosome. Genomics , 12 pp. 363-367.

K

KAPOOR, R; REVESZ, T; POWELL, M; (1992) SOLITARY CERVICAL LYMPHOMA PRESENTING AS A NEUROFIBROMA. BRIT J NEUROSURG , 6 (6) 583 - 586.

Khalili-Shirazi, A; Hughes, RA; Brostoff, SW; Linington, C; Gregson, N; (1992) T cell responses to myelin proteins in Guillain-Barré syndrome. J Neurol Sci , 111 (2) pp. 200-203.

L

LANTOS, PL; LUTHERT, PJ; HANGER, D; ANDERTON, BH; MULLAN, M; ROSSOR, M; (1992) FAMILIAL ALZHEIMERS-DISEASE WITH THE AMYLOID PRECURSOR PROTEIN POSITION-717 MUTATION AND SPORADIC ALZHEIMERS-DISEASE HAVE THE SAME CYTOSKELETAL PATHOLOGY. NEUROSCI LETT , 137 (2) 221 - 224.

LANTOS, PL; MCGILL, IS; JANOTA, I; DOEY, LJ; COLLINGE, J; BRUCE, MT; WHATLEY, SA; (1992) PRION PROTEIN IMMUNOCYTOCHEMISTRY HELPS TO ESTABLISH THE TRUE INCIDENCE OF PRION DISEASES. NEUROSCI LETT , 147 (1) 67 - 71.

M

MULLAN, M; HOULDEN, H; WINDELSPECHT, M; FIDANI, L; LOMBARDI, C; DIAZ, P; ROSSOR, M; (1992) A LOCUS FOR FAMILIAL EARLY-ONSET ALZHEIMERS-DISEASE ON THE LONG ARM OF CHROMOSOME 14, PROXIMAL TO THE ALPHA-1-ANTICHYMOTRYPSIN GENE. NAT GENET , 2 (4) 340 - 342.

N

NOBLE, M; GROVES, AK; ATALIOTIS, P; JAT, PS; (1992) FROM CHANCE TO CHOICE IN THE GENERATION OF NEURAL CELL-LINES. BRAIN PATHOL , 2 (1) 39 - 46.

O

O'Sullivan, F; Rossor, M; Elston, JS; (1992) Amaurosis fugax in young people. Br J Ophthalmol , 76 (11) pp. 660-662.

OWEN, F; POULTER, M; COLLINGE, J; LEACH, M; LOFTHOUSE, R; CROW, TJ; HARDING, AE; (1992) A DEMENTING ILLNESS ASSOCIATED WITH A NOVEL INSERTION IN THE PRION PROTEIN GENE. MOL BRAIN RES , 13 (1-2) 155 - 157.

P

PALMER, MS; COLLINGE, J; (1992) HUMAN PRION DISEASES. CURR OPIN NEUROL NEU , 5 (6) 895 - 901.

POULTER, M; BAKER, HF; FRITH, CD; LEACH, M; LOFTHOUSE, R; RIDLEY, RM; SHAH, T; (1992) INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .1. GENEALOGICAL AND MOLECULAR STUDIES. BRAIN , 115 675 - 685.

Palmer, MS; Collinge, J; (1992) Human prion diseases. Baillieres Clin Neurol , 1 (3) pp. 627-651.

Palmer, MS; Collinge, J; (1992) Human prion diseases. In: Rossor, M, (ed.) Unusual dementias. (627 - 651). Bailliere Tindall: London, UK.

Prusiner, SB; Collinge, J; (1992) Prions and neurodegenerative diseases. In: Prusiner, SB and Collinge, J and Powell, J and Anderton, B, (eds.) Prion diseases of humans & animals. (568 - 569). Ellis Horwood: London, UK.

R

ROSSOR, M; (1992) ALZHEIMERS-DISEASE. POSTGRADUATE MEDICAL JOURNAL , 68 (801) pp. 528-532.

ROSSOR, MN; (1992) FAMILIAL ALZHEIMERS-DISEASE. BAILLIERE CLIN NEUR , 1 (3) 517 - 534.

ROSSOR, MN; KENNEDY, AM; NEWMAN, SK; (1992) HETEROGENEITY IN FAMILIAL ALZHEIMERS-DISEASE. In: Boller, F and Forette, F and Khachaturian, Z and Poncet, M and Christen, Y, (eds.) HETEROGENEITY OF ALZHEIMERS DISEASE. (pp. 81 - 87). SPRINGER-VERLAG BERLIN

Rossor, MN; (1992) Unusual dementias. Introduction. Baillieres Clin Neurol , 1 (3) pp. 477-483.

W

Warren, JD; Miles, TS; Türker, KS; (1992) Properties of synaptic noise in tonically active human motoneurons. Journal of Electromyography and Kinesiology , 2 (4) pp. 189-202. 10.1016/1050-6411(92)90023-C.

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