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Number of items: 53.

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; PALMER, MS; (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

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.

Bennett, C; Crawford, F; Osborne, A; Diaz, P; Hoyne, J; Lopez, R; Roques, P; ... 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) pp. 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 pp. 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 pp. 620-622.

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

C

CLARK, RF; HUTTON, M; FULDNER, RA; FROELICH, S; KARRAN, E; TALBOT, C; CROOK, R; ... 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.

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.

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-.

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

HOULDEN, H; CROOK, R; DUFF, K; HUTTON, M; COLLINGE, J; ROQUES, P; ROSSOR, M; (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.

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) pp. 859-864. 10.1002/gps.930101008.

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

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

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: (Proceedings) Mammalian Genetics and Development Workshop.

I

Isenmann, S; Molthagen, M; Brandner, S; Bartsch, U; Kuhne, G; Magyar, JP; Sure, U; ... 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

KENNEDY, AM; FRACKOWIAK, RSJ; NEWMAN, SK; BLOOMFIELD, PM; SEAWARD, J; ROQUES, P; LEWINGTON, G; ... 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; NEARY, D; ... 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.

KRAUS, JA; KOOPMANN, J; KASKEL, P; MAINTZ, D; BRANDNER, S; SCHRAMM, J; LOUIS, DN; ... 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.

Katsanis, N; Yaspo, ML; Fisher, EMC; (1995) cDNA selection from human chromosome 21. In: (Proceedings) Mammalian Genetics and Development Workshop.

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; WINBLAD, B; (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; ISENMANN, S; ... AGUZZI, A; + view all (1995) ACTIVATION OF HIV TRANSCRIPTION BY HUMAN FOAMY VIRUS IN TRANSGENIC MICE. LAB INVEST , 73 (1) 103 - 110.

Martin, J; Bermingham, N; Mileham, P; Peters, J; Fisher, EMC; (1995) A model of neurological disease with anterior horn cell degeneration - legs at odd angles. In: (Proceedings) Motor Neurone Disease Association Meeting.

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.

P

PerezTur, J; Froelich, S; Prihar, G; Crook, R; Baker, M; Duff, K; Wragg, M; ... Hutton, M; + view all (1995) A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene. NEUROREPORT , 7 (1) 297 - 301.

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 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.

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

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) pp. 67-71.

S

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.

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) pp. 337-341.

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

Stoodley, MA; Warren, JD; Oatey, PE; (1995) Thalamic syndrome caused by unruptured cerebral aneurysm. Case report. J Neurosurg , 82 (2) pp. 291-293. 10.3171/jns.1995.82.2.0291.

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) pp. 117-126.

V

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.

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

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 pp. 294-299.

Y

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; 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; 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 pp. 245-248.

Yulug, IG; Fisher, EMC; (1995) The frequency and position of Alu repeats in cDNAs, as determined by database searching. Genomics , 27 pp. 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 pp. 1101-1104.

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 pp. 433-435.

This list was generated on Sun Oct 22 03:47:34 2017 BST.