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Number of items: 67.

A

AGUZZI, A; BRANDNER, S; ISENMANN, S; STEINBACH, JP; SURE, U; (1995) TRANSGENIC AND GENE DISRUPTION TECHNIQUES IN THE STUDY OF NEUROCARCINOGENESIS. GLIA , 15 (3) 348 - 364.

ASHWORTH, A; BROWN, J; GYDESEN, S; SORENSEN, A; ROSSOR, MN; HARDY, J; ... COLLINGE, J; + view all (1995) A LOCUS FOR FAMILIAL NON SPECIFIC DEMENTIA MAPS TO CHROMOSOME-3. AM J HUM GENET , 57 (4) 1063 - 1063.

ASHWORTH, A; BROWN, J; GYDESEN, S; SORENSEN, SA; ROSSOR, MN; HARDY, J; COLLINGE, J; (1995) FRONTAL-LOBE OR NONSPECIFIC DEMENTIAS ARE GENETICALLY HETEROGENEOUS. NEUROLOGY , 45 (9) 1781 - 1781.

B

BATEMAN, D; HILTON, D; LOVE, S; ZEIDLER, M; BECK, J; COLLINGE, J; (1995) SPORADIC CREUTZFELDT-JAKOB-DISEASE IN A 18-YEAR-OLD IN THE UK. LANCET , 346 (8983) 1155 - 1156.

Bennett, C; Crawford, F; Osborne, A; Diaz, P; Hoyne, J; Lopez, R; ... Mullan, M; + view all (1995) Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causative. Am J Med Genet , 60 (1) 1 - 6. 10.1002/ajmg.1320600102.

Bermingham, N; Gilmour, F; Martin, JE; Fisher, EMC; (1995) Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5. Hum Genet , 96 671 - 673.

Bermingham, N; Hernandez, D; Balfour, A; Gilmour, F; Martin, JE; Fisher, EMC; (1995) Mapping TNNC1, the gene which encodes cardiac troponin I in the human and the mouse. Genomics , 30 620 - 622.

BRITTON, TC; ALSARRAJ, S; SHAW, C; CAMPBELL, T; COLLINGE, J; (1995) SPORADIC CREUTZFELDT-JAKOB-DISEASE IN A 16-YEAR-OLD IN THE UK. LANCET , 346 (8983) 1155 - 1155.

Brodaty, H; Conneally, M; Gauthier, S; Jennings, C; Lennox, A; Lovestone, S; ... Whitehouse, P; + view all (1995) Consensus statement on predictive testing for Alzheimer disease. ALZHEIMER DISEASE & ASSOCIATED DISORDERS , 9 (4) 182 - 187.

BROWN, J; ASHWORTH, A; GYDESEN, S; SORENSEN, A; ROSSOR, M; HARDY, J; COLLINGE, J; (1995) FAMILIAL NONSPECIFIC DEMENTIA MAPS TO CHROMOSOME-3. HUM MOL GENET , 4 (9) 1625 - 1628.

BUDKA, H; AGUZZI, A; BROWN, P; BRUCHER, JM; BUGIANI, O; COLLINGE, J; ... WILL, RG; + view all (1995) TISSUE HANDLING IN SUSPECTED CREUTZFELDT-JAKOB-DISEASE (CJD) AND OTHER HUMAN SPONGIFORM ENCEPHALOPATHIES (PRION DISEASES). BRAIN PATHOL , 5 (3) 319 - 322.

C

CLARK, RF; HUTTON, M; FULDNER, RA; FROELICH, S; KARRAN, E; TALBOT, C; ... GOATE, A; + view all (1995) THE STRUCTURE OF THE PRESENILIN-1 (S182) GENE AND IDENTIFICATION OF 6 NOVEL MUTATIONS IN EARLY-ONSET AD FAMILIES. NAT GENET , 11 (2) 219 - 222.

Collinge, J; (1995) Molecular genetics of human prion disease and the development of transgenic models. In: Prusiner, SB, (ed.) Current topics in microbiology and immunology. (35 - 36). Scientific Publishing Services (P) Ltd: Bangalore, India.

COLLINGE, J; PALMER, MS; SIDLE, KCL; GOWLAND, I; MEDORI, R; IRONSIDE, J; LANTOS, P; (1995) TRANSMISSION OF FATAL FAMILIAL INSOMNIA TO LABORATORY-ANIMALS. LANCET , 346 (8974) 569 - 570.

COLLINGE, J; PALMER, MS; SIDLE, KCL; HILL, AF; GOWLAND, I; MEADS, J; ... LANTOS, PL; + view all (1995) UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN. NATURE , 378 (6559) 779 - 783.

D

DANIEL, SE; GEDDES, JF; REVESZ, T; (1995) GLIAL CYTOPLASMIC INCLUSIONS ARE NOT EXCLUSIVE TO MULTIPLE SYSTEM ATROPHY. J NEUROL NEUROSUR PS , 58 (2) 262 - 262.

E

EHLER, E; JAT, PS; NOBLE, MD; CITI, S; DRAEGER, A; (1995) VASCULAR SMOOTH-MUSCLE CELLS OF H-2K(B)-TSA58 TRANSGENIC MICE - CHARACTERIZATION OF CELL-LINES WITH DISTINCT PROPERTIES. CIRCULATION , 92 (11) 3289 - 3296.

F

Ferris, SH; Hasegawa, K; Homma, A; Khachaturian, ZS; Post, S; Rossor, M; Whitehouse, PJ; (1995) International efforts to improve Alzheimer disease treatment. Alzheimer Disease and Associated Disorders , 9 (4) 181 - 181.

Fisher, EMC; (1995) Why aren't we all bacteria. Immunology News , 2 100 - 103.

G

GHISO, J; PLANT, GT; REVESZ, T; WISNIEWSKI, T; FRANGIONE, B; (1995) FAMILIAL CEREBRAL AMYLOID ANGIOPATHY (BRITISH TYPE) WITH NONNEURITIC AMYLOID PLAQUE-FORMATION MAY BE DUE TO A NOVEL AMYLOID PROTEIN. J NEUROL SCI , 129 (1) 74 - 75.

H

Harvey, R; Fraser, D; Bonner, D; Warnes, A; Warrington, E; Rossor, M; (1995) Dementia and driving: Results of a semi-realistic simulator study. International Journal of Geriatric Psychiatry , 10 (10) 859 - 864. 10.1002/gps.930101008.

Harvey, R; Rossor, M; (1995) Treatments for Alzheimer's disease. Practitioner , 239 (1552) 440 - 443.

HARVEY, RJ; ROSSOR, MN; (1995) DOES EARLY-ONSET ALZHEIMER-DISEASE CONSTITUTE A DISTINCT SUBTYPE - THE CONTRIBUTION OF MOLECULAR-GENETICS. ALZHEIMER DISEASE & ASSOCIATED DISORDERS , 9 S7 - S13.

Hernandez, D; Pannett, A; Tybulewicz, V; Fisher, EMC; (1995) Highly polymorphic sequence at D21S1448 mapping close to D21S55. Hum Genet , 95 721 - 722.

HOULDEN, H; CROOK, R; DUFF, K; HUTTON, M; COLLINGE, J; ROQUES, P; ... HARDY, J; + view all (1995) APOLIPOPROTEIN-E ALLELES BUT NEITHER APOLIPOPROTEIN-B NOR APOLIPOPROTEIN AI/CIII ALLELES ARE ASSOCIATED WITH LATE-ONSET, FAMILIAL ALZHEIMERS-DISEASE. NEUROSCI LETT , 188 (3) 202 - 204.

Hoyle, J; Smith, DJ; Connolly, JAC; Fisher, EMC; (1995) Characterisation of the S4 gene, a member of a highly conserved gene family involved in ubiquitinated degradation of proteins. In: Genetics Research (Camb).

I

Isenmann, S; Molthagen, M; Brandner, S; Bartsch, U; Kuhne, G; Magyar, JP; ... Aguzzi, A; + view all (1995) The AMOG/beta 2 subunit of Na,K-ATPase is not necessary for long-term survival of telencephalic grafts. GLIA , 15 (4) 377 - 388.

J

JENDROSKA, K; ROSSOR, MN; MATHIAS, CJ; DANIEL, SE; (1995) MORPHOLOGICAL OVERLAP BETWEEN CORTICOBASAL DEGENERATION AND PICKS-DISEASE - A CLINICOPATHOLOGICAL REPORT. MOVEMENT DISORD , 10 (1) 111 - 114.

K

Katsanis, N; Yaspo, ML; Fisher, EMC; (1995) cDNA selection from human chromosome 21. In: Genetics Research (Camb).

KENNEDY, AM; FRACKOWIAK, RSJ; NEWMAN, SK; BLOOMFIELD, PM; SEAWARD, J; ROQUES, P; ... ROSSOR, MN; + view all (1995) DEFICITS IN CEREBRAL GLUCOSE-METABOLISM DEMONSTRATED BY POSITRON EMISSION TOMOGRAPHY IN INDIVIDUALS AT RISK OF FAMILIAL ALZHEIMERS-DISEASE. NEUROSCI LETT , 186 (1) 17 - 20.

KENNEDY, AM; NEWMAN, SK; FRACKOWIAK, RSJ; CUNNINGHAM, VJ; ROQUES, P; STEVENS, J; ... ROSSOR, MN; + view all (1995) CHROMOSOME-14 LINKED FAMILIAL ALZHEIMERS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF A SINGLE PEDIGREE. BRAIN , 118 185 - 205.

KENNEDY, AM; ROSSOR, MN; FRACKOWIAK, RSJ; (1995) POSITRON EMISSION TOMOGRAPHY IN FAMILIAL ALZHEIMER-DISEASE. ALZ DIS ASSOC DIS , 9 (1) 17 - 20.

Klöhn, PC; Massalha, H; Neumann, HG; (1995) A metabolite of carcinogenic 2-acetylaminofluorene, 2-nitrosofluorene, induces redox cycling in mitochondria. Biochim Biophys Acta , 1229 (3) 363 - 372.

KRAUS, JA; KOOPMANN, J; KASKEL, P; MAINTZ, D; BRANDNER, S; SCHRAMM, J; ... VONDEIMLING, A; + view all (1995) SHARED ALLELIC LOSSES ON CHROMOSOMES 1P AND 19Q SUGGEST A COMMON ORIGIN OF OLIGODENDROGLIOMA AND OLIGOASTROCYTOMA. J NEUROPATH EXP NEUR , 54 (1) 91 - 95.

L

LAMMIE, GA; RAKSHI, J; ROSSOR, MN; HARDING, AE; SCARAVILLI, F; (1995) CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY (CADASIL) - CONFIRMATION BY CEREBRAL BIOPSY IN 2 CASES. CLIN NEUROPATHOL , 14 (4) 201 - 206.

LANNFELT, L; LILIUS, L; VIITANEN, M; HOULDEN, H; ROSSOR, M; HARDY, J; ... BASUN, H; + view all (1995) MICROSATELLITE D21S210 (GT-12) ALLELE FREQUENCIES IN SPORADIC ALZHEIMERS-DISEASE. ACTA NEUROL SCAND , 91 (2) 145 - 148.

M

MARINO, S; KRETSCHMER, C; BRANDNER, S; CAVARD, C; ZIDER, A; BRIAND, P; ... AGUZZI, A; + view all (1995) ACTIVATION OF HIV TRANSCRIPTION BY HUMAN FOAMY VIRUS IN TRANSGENIC MICE. LAB INVEST , 73 (1) 103 - 110.

MAZARS, GR; POWELL, A; BURNS, J; KOBRNA, A; JAT, P; (1995) REGULATION OF THE EXPRESSION OF THE CDK INHIBITOR P21 IN SENESCENCE OF RAT EMBRYO FIBROBLASTS. J CELL BIOCHEM 70 - 70.

MULLAN, M; BENNETT, C; FIGUEREDO, C; HUGHES, D; MANT, R; OWEN, M; ... CRAWFORD, F; + view all (1995) CLINICAL-FEATURES OF EARLY-ONSET, FAMILIAL ALZHEIMERS-DISEASE LINKED TO CHROMOSOME-14. AM J MED GENET , 60 (1) 44 - 52.

N

NOBLE, M; GROVES, AK; ATALIOTIS, P; IKRAM, Z; JAT, PS; (1995) THE H-2K(B)TSA58 TRANSGENIC MOUSE - A NEW TOOL FOR THE RAPID GENERATION OF NOVEL CELL-LINES. TRANSGENIC RES , 4 (4) 215 - 225.

Noble, M; Groves, AK; Ataliotis, P; Ikram, Z; Jat, PS; (1995) The H-2KbtsA58 transgenic mouse as a single source of a wide range of conditionally immortal cell lines. In: Monastersky, GM and Robl, JM, (eds.) Strategies in transgenic animal science. (325 - ?). Amer Society for Microbiology

O

ORRELL, RW; JAMESGALTON, M; STEVENS, JM; ROSSOR, MN; (1995) CEREBRAL ACHROMATOPSIA AS A PRESENTATION OF TROUSSEAUS-SYNDROME. POSTGRAD MED J , 71 (831) 44 - 46.

R

REVESZ, T; DANIEL, SE; LEES, AJ; WILL, RG; (1995) A CASE OF PROGRESSIVE SUBCORTICAL GLIOSIS ASSOCIATED WITH DEPOSITION OF ABNORMAL PRION PROTEIN (PRP). J NEUROL NEUROSUR PS , 58 (6) 759 - 760.

Rossor, MN; (1995) Catastrophe, chaos and Alzheimer's disease. The F E Williams Lecture. J R Coll Physicians Lond , 29 (5) 412 - 418.

ROSSOR, MN; (1995) CATASTROPHE, CHAOS AND ALZHEIMERS-DISEASE - THE WILLIAMS,F.E LECTURE. J ROY COLL PHYS LOND , 29 (5) 412 - 418.

ROSSOR, MN; BROWN, J; (1995) PROGRESSIVE SUPRANUCLEAR PALSY - NEUROPATHOLOGICALLY BASED DIAGNOSTIC CLINICAL-CRITERIA. J NEUROL NEUROSUR PS , 59 (3) 343 - 343.

ROSSOR, MN; WARRINGTON, EK; CIPOLOTTI, L; (1995) THE ISOLATION OF CALCULATION SKILLS. J NEUROL , 242 (2) 78 - 81.

Rutherford, OM; Beshyah, SA; Schott, J; Watkins, Y; Johnston, DG; (1995) Contractile properties of the quadriceps muscle in growth hormone-deficient hypopituitary adults. Clin Sci (Lond) , 88 (1) 67 - 71.

S

Schott, J; McCully, K; Rutherford, OM; (1995) The role of metabolites in strength training. II. Short versus long isometric contractions. Eur J Appl Physiol Occup Physiol , 71 (4) 337 - 341.

Schott, J; Puttick, M; (1995) Handedness among surgeons. BMJ , 310 (6981) 739 - ?.

SMITH, C; COLLINGE, J; (1995) MOLECULAR PATHOLOGY OF PRION DISEASES. ESSAYS BIOCHEM , 29 157 - 174.

Stoodley, MA; Warren, JD; Oatey, PE; (1995) Thalamic syndrome caused by unruptured cerebral aneurysm. Journal of Neurosurgery , 82 291 - 293.

STROMMER, KN; BRANDNER, S; SARIOGLU, AC; SURE, U; YONEKAWA, Y; (1995) SYMPTOMATIC CEREBELLAR METASTASIS AND LATE LOCAL RECURRENCE OF A CAUDA-EQUINA PARAGANGLIOMA - CASE-REPORT. J NEUROSURG , 83 (1) 166 - 169.

Sure, U; Bertalanffy, H; Isenmann, S; Brandner, S; Berghorn, WJ; Seeger, W; Aguzzi, A; (1995) Secondary manifestation of medulloblastoma: metastases and local recurrences in 66 patients. Acta Neurochir (Wien) , 136 (3-4) 117 - 126.

V

VanPaesschen, W; Sisodiya, S; Connelly, A; Duncan, JS; Free, SL; Raymond, AA; ... Jackson, GD; + view all (1995) Quantitative hippocampal MRI and intractable temporal lobe epilepsy. NEUROLOGY , 45 (12) 2233 - 2240.

VANPAESSCHEN, WIM; REVESZ, T; SISODIYA, S; CONNELLY, A; JACKSON, GD; DUNCAN, JS; (1995) QUANTITATIVE NEUROPATHOLOGY AND QUANTITATIVE MAGNETIC-RESONANCE-IMAGING OF THE HIPPOCAMPUS OF PATIENTS WITH INTRACTABLE TEMPORAL-LOBE EPILEPSY. EPILEPSIA , 36 S96 - S96.

W

Wang, W; Fisher, EMC; Jia, Q; Dunn, JM; Porfiri, E; Downward, J; Egan, SE; (1995) The Grb2 binding domain of mSos1 is not required for downstream signal transduction. Nature Genetics , 10 294 - 299.

WHITTINGTON, MA; SIDLE, KCL; GOWLAND, I; MEADS, J; HILL, AF; PALMER, MS; ... COLLINGE, J; + view all (1995) RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN. NAT GENET , 9 (2) 197 - 201.

WHITTINGTON, MA; SIDLE, KCL; GOWLAND, I; MEADS, J; HILL, AF; PALMER, MS; ... COLLINGE, J; + view all (1995) RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN, (VOL 9, PG 197, 1995). NAT GENET , 9 (4) 451 - 451.

WOOLF, AS; KOLATSIJOANNOU, M; HARDMAN, P; ANDERMARCHER, E; MOORBY, C; FINE, LG; ... GHERARDI, E; + view all (1995) ROLES OF HEPATOCYTE GROWTH FACTOR/SCATTER FACTOR AND THE MET RECEPTOR IN THE EARLY DEVELOPMENT OF THE METANEPHROS. J CELL BIOL , 128 (1-2) 171 - 184.

Y

Yulug, IG; Egan, SE; See, CG; Fisher, EMC; (1995) Mapping human SHC, a gene that encodes an adaptor protein and identifying and mapping a SHC related sequence. Hum. Genet. , 96 245 - 248.

Yulug, IG; Fisher, EMC; (1995) The frequency and position of Alu repeats in cDNAs, as determined by database searching. Genomics , 27 544 - 548.

Yulug, IG; Katsanis, N; de-Belleroche, J; Collinge, J; Fisher, EMC; (1995) An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4. Hum Mol Genet , 4 1101 - 1104.

YULUG, IG; KATSANIS, N; DEBELLEROCHE, J; COLLINGE, J; FISHER, EMC; (1995) AN IMPROVED PROTOCOL FOR THE ANALYSIS OF SOD1 GENE-MUTATIONS, AND A NEW MUTATION IN EXON-4. HUM MOL GENET , 4 (6) 1101 - 1104.

YULUG, IG; KATSANIS, N; DEBELLEROCHE, J; COLLINGE, J; FISHER, EMC; (1995) AN IMPROVED PROTOCOL FOR THE ANALYSIS OF SOD1 GENE-MUTATIONS, AND A NEW MUTATION IN EXON-4 (VOL 4, PG 1101, 1995). HUM MOL GENET , 4 (8) 1474 - 1474.

Yulug, IG; Killary, AM; Sandhu, AK; Athwal, RS; Fox, M; Fisher, EMC; (1995) Gene expression in response to retinoic acid in novel human chromosome 21 monochromosomal cell hybrids. SOMAT CELL MOLEC GEN , 21 (5) 357 - 365.

Yulug, IG; See, CG; Fisher, EMC; (1995) The DAD1 protein, whose defect causes apoptotic cell death, maps to human chromosome 14. Genomics , 26 433 - 435.

This list was generated on Sun Nov 23 12:28:45 2014 GMT.