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Number of items: 61.

A

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

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

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

B

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

Bennett, C and Crawford, F and Osborne, A and Diaz, P and Hoyne, J and Lopez, R and Roques, P and Duara, R and Rossor, M and Mullan, M (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 and Gilmour, F and Martin, JE and Fisher, EMC (1995) Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5. Hum Genet , 96 671 - 673.

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

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

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

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

BUDKA, H and AGUZZI, A and BROWN, P and BRUCHER, JM and BUGIANI, O and COLLINGE, J and DIRINGER, H and GULLOTTA, F and HALTIA, M and HAUW, JJ and IRONSIDE, JW and KRETZSCHMAR, HA and LANTOS, PL and MASULLO, C and POCCHIARI, M and SCHLOTE, W and TATEISHI, J and WILL, RG (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 and HUTTON, M and FULDNER, RA and FROELICH, S and KARRAN, E and TALBOT, C and CROOK, R and LENDON, C and PRIHAR, G and HE, C and KORENBLAT, K and MARTINEZ, A and WRAGG, M and BUSFIELD, F and BEHRENS, MI and MYERS, A and NORTON, J and MORRIS, J and MEHTA, N and PEARSON, C and LINCOLN, S and BAKER, M and DUFF, K and ZEHR, C and PEREZTUR, J and HOULDEN, H and RUIZ, A and OSSA, J and LOPERA, F and ARCOS, M and MADRIGAL, L and COLLINGE, J and HUMPHREYS, C and ASHWORTH, A and SARNER, S and FOX, N and HARVEY, R and KENNEDY, A and ROQUES, P and CLINE, RT and PHILLIPS, CA and VENTER, JC and FORSELL, L and AXELMAN, K and LILIUS, L and JOHNSTON, J and COWBURN, R and VIITANEN, M and WINBLAD, B and KOSIK, K and HALTIA, M and POYHONEN, M and DICKSON, D and MANN, D and NEARY, D and SNOWDEN, J and LANTOS, P and LANNFELT, L and ROSSOR, M and ROBERTS, GW and ADAMS, MD and HARDY, J and GOATE, A (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 and PALMER, MS and SIDLE, KCL and GOWLAND, I and MEDORI, R and IRONSIDE, J and LANTOS, P (1995) TRANSMISSION OF FATAL FAMILIAL INSOMNIA TO LABORATORY-ANIMALS. LANCET , 346 (8974) 569 - 570.

COLLINGE, J and PALMER, MS and SIDLE, KCL and HILL, AF and GOWLAND, I and MEADS, J and ASANTE, E and BRADLEY, R and DOEY, LJ and LANTOS, PL (1995) UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN. NATURE , 378 (6559) 779 - 783.

E

EHLER, E and JAT, PS and NOBLE, MD and CITI, S and 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 and Hasegawa, K and Homma, A and Khachaturian, ZS and Post, S and Rossor, M and 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.

H

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

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

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

HOULDEN, H and CROOK, R and DUFF, K and HUTTON, M and COLLINGE, J and ROQUES, P and ROSSOR, M and HARDY, J (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 and Smith, DJ and Connolly, JAC and 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 and Molthagen, M and Brandner, S and Bartsch, U and Kuhne, G and Magyar, JP and Sure, U and Schachner, M and Aguzzi, A (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 and ROSSOR, MN and MATHIAS, CJ and DANIEL, SE (1995) MORPHOLOGICAL OVERLAP BETWEEN CORTICOBASAL DEGENERATION AND PICKS-DISEASE - A CLINICOPATHOLOGICAL REPORT. MOVEMENT DISORD , 10 (1) 111 - 114.

K

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

KENNEDY, AM and FRACKOWIAK, RSJ and NEWMAN, SK and BLOOMFIELD, PM and SEAWARD, J and ROQUES, P and LEWINGTON, G and CUNNINGHAM, VJ and ROSSOR, MN (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 and NEWMAN, SK and FRACKOWIAK, RSJ and CUNNINGHAM, VJ and ROQUES, P and STEVENS, J and NEARY, D and BRUTON, CJ and WARRINGTON, EK and ROSSOR, MN (1995) CHROMOSOME-14 LINKED FAMILIAL ALZHEIMERS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF A SINGLE PEDIGREE. BRAIN , 118 185 - 205.

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

KRAUS, JA and KOOPMANN, J and KASKEL, P and MAINTZ, D and BRANDNER, S and SCHRAMM, J and LOUIS, DN and WIESTLER, OD and VONDEIMLING, A (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 and RAKSHI, J and ROSSOR, MN and HARDING, AE and 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 and LILIUS, L and VIITANEN, M and HOULDEN, H and ROSSOR, M and HARDY, J and WINBLAD, B and BASUN, H (1995) MICROSATELLITE D21S210 (GT-12) ALLELE FREQUENCIES IN SPORADIC ALZHEIMERS-DISEASE. ACTA NEUROL SCAND , 91 (2) 145 - 148.

M

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

MAZARS, GR and POWELL, A and BURNS, J and KOBRNA, A and 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 and BENNETT, C and FIGUEREDO, C and HUGHES, D and MANT, R and OWEN, M and WARREN, A and MCINNIS, M and MARSHALL, A and LANTOS, P and COLLINGE, J and GOATE, A and HOULDEN, H and CRAWFORD, F (1995) CLINICAL-FEATURES OF EARLY-ONSET, FAMILIAL ALZHEIMERS-DISEASE LINKED TO CHROMOSOME-14. AM J MED GENET , 60 (1) 44 - 52.

N

NOBLE, M and GROVES, AK and ATALIOTIS, P and IKRAM, Z and 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 and Groves, AK and Ataliotis, P and Ikram, Z and 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 and JAMESGALTON, M and STEVENS, JM and ROSSOR, MN (1995) CEREBRAL ACHROMATOPSIA AS A PRESENTATION OF TROUSSEAUS-SYNDROME. POSTGRAD MED J , 71 (831) 44 - 46.

R

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

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

Rutherford, OM and Beshyah, SA and Schott, J and Watkins, Y and 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 and McCully, K and 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 and Puttick, M (1995) Handedness among surgeons. BMJ , 310 (6981) 739 - ?.

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

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

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

W

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

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

WHITTINGTON, MA and SIDLE, KCL and GOWLAND, I and MEADS, J and HILL, AF and PALMER, MS and JEFFERYS, JGR and COLLINGE, J (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 and KOLATSIJOANNOU, M and HARDMAN, P and ANDERMARCHER, E and MOORBY, C and FINE, LG and JAT, PS and NOBLE, MD and GHERARDI, E (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 and Egan, SE and See, CG and 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 and Fisher, EMC (1995) The frequency and position of Alu repeats in cDNAs, as determined by database searching. Genomics , 27 544 - 548.

Yulug, IG and Katsanis, N and de-Belleroche, J and Collinge, J and 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 and KATSANIS, N and DEBELLEROCHE, J and COLLINGE, J and 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 and KATSANIS, N and DEBELLEROCHE, J and COLLINGE, J and 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 and Killary, AM and Sandhu, AK and Athwal, RS and Fox, M and 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 and See, CG and 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 Mon May 20 07:17:12 2013 BST.