Browse by UCL Departments and Centres
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Group by: Author | Type
Number of items: 50.
A
| AGUZZI, A and BRANDNER, S and SURE, U and RUEDI, D and ISENMANN, S (1994) TRANSGENIC AND KNOCK-OUT MICE - MODELS OF NEUROLOGICAL DISEASE. BRAIN PATHOL , 4 (1) 3 - 20. |
| ALBRECHT, S and VONDEIMLING, A and PIETSCH, T and GIANGASPERO, F and BRANDNER, S and KLEIHUES, P and WIESTLER, OD (1994) MICROSATELLITE ANALYSIS OF LOSS OF HETEROZYGOSITY ON CHROMOSOMES 9Q, 11P AND 17P IN MEDULLOBLASTOMAS. NEUROPATH APPL NEURO , 20 (1) 74 - 81. |
| ASHWORTH, A and CAMPBELL, T and PALMER, M and COLLINGE, J and BROWN, J (1994) G/T POLYMORPHISM IN CRYA2 GENE. HUM MOL GENET , 3 (9) 1712 - 1712. |
B
| BALL, JA and WARNER, T and REID, P and HOWARD, RS and GREGSON, NA and ROSSOR, MN (1994) CENTRAL ALVEOLAR HYPOVENTILATION ASSOCIATED WITH PARANEOPLASTIC BRAIN-STEM ENCEPHALITIS AND ANTI-HU ANTIBODIES. J NEUROL , 241 (9) 561 - 566. |
| BRANDNER, S and HEISS, E and GEHRKE, G (1994) GLIOBLASTOMA PENETRATING THE ANTERIOR SKULL BASE - CASE REPORT AND REVIEW OF THE LITERATURE. In: Samii, M, (ed.) SKULL BASE SURGERY. (pp. 156 - 160). KARGER |
C
| Chartier-Harlin, M-C and Parfitt, M and Legrain, S and Pérez-Tur, J and Brousseau, T and Evans, A and Berr, C and Vidal, O and Roques, P and Gourlet, V and Fruchart, J-C and Delacourte, A and Rossor, M and Amouyel, P (1994) Apolipoprotein E, ε4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: Analysis of the 19q13.2 chromosomal region. Human Molecular Genetics , 3 (4) 569 - 574. |
| COLLINGE, J (1994) MOLECULAR-BIOLOGY OF PRION DISEASES - PREFACE. PHILOS T ROY SOC B , 343 (1306) 353 - 353. |
| COLLINGE, J and PALMER, MS (1994) HUMAN PRION DISEASES. BAILLIERE CLIN NEUR , 3 (2) 241 - 255. |
| COLLINGE, J and PALMER, MS (1994) MOLECULAR-GENETICS OF HUMAN PRION DISEASES. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES , 343 (1306) 371 - 378. |
| Collinge, J and Palmer, MS (1994) Prion diseases. In: Burns, A and Levy, R, (eds.) Dementia. (835 - 853). Chapman and Hall: London, UK. |
| Collinge, J and Palmer, MS (1994) Human prion diseases. In: Harding, AE, (ed.) Genetics in Neurology. (241 - 257). Bailliere Tindall: London, UK. |
| COLLINGE, J and PALMER, MS and SIDLE, KCL and MAHAL, SP and CAMPBELL, T and BROWN, J and HARDY, J and BRUN, AE and GUSTAFSON, L and BAKKER, E and ROOS, R and GROEN, JJ (1994) FAMILIAL PICKS-DISEASE AND DEMENTIA IN FRONTAL-LOBE DEGENERATION OF NON-ALZHEIMER TYPE ARE NOT VARIANTS OF PRION DISEASE. J NEUROL NEUROSUR PS , 57 (6) 762 - 762. |
| COLLINGE, J and WHITTINGTON, MA and SIDLE, KCL and SMITH, CJ and PALMER, MS and CLARKE, AR and JEFFERYS, JGR (1994) PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION. NATURE , 370 (6487) 295 - 297. |
D
| DRAEGER, A and EHLER, E and JAT, PS and NOBLE, MD (1994) SEARCHING FOR PRECURSOR CELLS OF THE VASCULAR WALL. J MUSCLE RES CELL M , 15 (2) 214 - 214. |
E
| Egan, SE and Fisher, EMC and Downward, J (1994) Transformation by the mSos1 Ras exchange protein. In: J. Cell. Biochem. (pp. 234 - ?). |
| EIBL, RH and KLEIHUES, P and JAT, PS and WIESTLER, OD (1994) A MODEL FOR PRIMITIVE NEUROECTODERMAL TUMORS IN TRANSGENIC NEURAL TRANSPLANTS HARBORING THE SV40 LARGE T-ANTIGEN. AM J PATHOL , 144 (3) 556 - 564. |
F
| Fisher, EMC (1994) Genetics, molecular and cell biology. In: Kumar, PJ and Clark, ML, (eds.) Clinical Medicine. Balliere Tindall: London. |
| Fisher, EMC and Scambler, PJ (1994) Human haploinsufficiency - one for sorrow, two for joy. Nature Genetics , 7 5 - 7. |
H
| HAWKINS, PN and ROSSOR, MN and GALLIMORE, JR and MILLER, B and MOORE, EG and PEPYS, MB (1994) CONCENTRATION OF SERUM AMYLOID-P COMPONENT IN THE CSF AS A POSSIBLE MARKER OF CEREBRAL AMYLOID DEPOSITS IN ALZHEIMERS-DISEASE. BIOCHEM BIOPH RES CO , 201 (2) 722 - 726. |
| Hernandez, D and Tybulewicz, V and Fisher, EMC (1994) Modelling Down syndrome in mouse. In: Genetics Research (Camb). |
| Hernandez, D and Yulug, IG and Egan, SE and Fisher, EMC (1994) Mapping the gene which encodes phosphatidylinositol specific phospholipase C-g 2 in the human and the mouse. Genomics , 23 504 - 507. |
| HOULDEN, H and CROOK, R and HARDY, J and ROQUES, P and COLLINGE, J and ROSSER, M (1994) CONFIRMATION THAT FAMILIAL CLUSTERING AND AGE-OF-ONSET IN LATE-ONSET ALZHEIMERS-DISEASE ARE DETERMINED AT THE APOLIPOPROTEIN-E LOCUS. NEUROSCI LETT , 174 (2) 222 - 224. |
| Hoyle, J and Yulug, IG and Egan, SE and Fisher, EMC (1994) The gene which encodes the phosphatidylinositol-3 kinase regulatory subunit (p85a) maps to chromosome 13 in the mouse. Genomics , 24 400 - 402. |
I
| IKRAM, Z and NORTON, T and JAT, PS (1994) THE BIOLOGICAL CLOCK THAT MEASURES THE MITOTIC LIFE-SPAN OF MOUSE EMBRYO FIBROBLASTS CONTINUES TO FUNCTION IN THE PRESENCE OF SIMIAN-VIRUS-40 LARGE TUMOR-ANTIGEN. P NATL ACAD SCI USA , 91 (14) 6448 - 6452. |
| Isenmann, S and Brandner, S and Sure, U and Magyar, JP and Schachner, M and Aguzzi, A (1994) [Morphology and development of neural transplants of AMOG-deficient mice]. Verh Dtsch Ges Pathol , 78 433 - 437. |
| ISENMANN, S and BRANDNER, S and SURE, U and MAGYAR, JP and SCHACHNER, M and AGUZZI, A (1994) MORPHOLOGY AND DEVELOPMENT OF NEURAL TRANSPLANTS DEFICIENT OF AMOG. In: Kloppel, G, (ed.) PROCEEDINGS OF THE GERMAN SOCIETY FOR PATHOLOGY, 78TH MEETING. (pp. 433 - 437). GUSTAV FISCHER VERLAG |
K
| Karlinsky, H and Lennox, A and Rossor, M (1994) Alzheimer's disease and genetic testing. Alzheimer Dis Assoc Disord , 8 (2) 63 - 65. |
| Kennedy, AM and Brown, J and Rossor, M (1994) The genetics of Alzheimer's disease. Baillieres Clin Neurol , 3 (2) 217 - 240. |
| KENNEDY, AM and FOX, N and SEAWARD, J and NEWMAN, S and KARLINSKY, H and GEORGEHYSLOP, PS and MCLACHLAN, D and LENNOX, A and ROQUES, R and STEVENS, J and ROSSOR, MN and FRACKOWIAK, RSJ (1994) A NEUROIMAGING STUDY OF INDIVIDUALS WITH APP MUTATIONS. NEUROLOGY , 44 (4) A299 - A299. |
| KENNEDY, AM and FRACKOWIAK, RSJ and NEWMAN, S and ROQUES, P and ROSSOR, MN (1994) PRESYMPTOMATIC DEFICITS IN INDIVIDUALS AT RISK OF FAMILIAL ALZHEIMERS-DISEASE - A POSITRON EMISSION TOMOGRAPHY STUDY. ANN NEUROL , 36 (2) 308 - 308. |
| Khalili-Shirazi, A and Gregson, N and Webb, HE (1994) A study of brain gangliosides and other glycolipids after infection with Semliki Forest virus. Biochem Soc Trans , 22 (2) 87S - ?. |
L
| LANDELS, EC and PROSCHEL, C and NOBLE, MD and JAT, PS and FINE, LG and WOOLF, AS (1994) RECEPTOR TYROSINE KINASES (RTKS) EXPRESSED IN EARLY NEPHROGENESIS. J AM SOC NEPHROL , 5 (3) 721 - 721. |
| LANTOS, PL and OVENSTONE, IMK and JOHNSON, J and CLELLAND, CA and ROQUES, P and ROSSOR, MN (1994) LEWY BODIES IN THE BRAIN OF 2 MEMBERS OF A FAMILY WITH THE 717 (VAL TO ILE) MUTATION OF THE AMYLOID PRECURSOR PROTEIN GENE. NEUROSCI LETT , 172 (1-2) 77 - 79. |
| LAWRENCE, RM and RONCA, MA and TYRRELL, P and ROSSOR, MN (1994) PSYCHIATRIC-SYMPTOMS IN PATIENTS WITH FOCAL CORTICAL DEGENERATION. BEHAV NEUROL , 7 (3-4) 153 - 158. |
M
| MARINO, S and BRANDNER, S (1994) MOLECULAR ANALYSIS OF DEVELOPMENT AND NEOPLASIA - HOMOLOGOUS RECOMBINATION AND KNOCK-OUT APPROACHES, SCHLOSS-REISENBURG, GERMANY, MARCH 22ND, 1994. BRAIN PATHOL , 4 (3) 285 - 286. |
| MORGAN, JE and BEAUCHAMP, JR and PAGEL, CN and PECKHAM, M and ATALIOTIS, P and JAT, PS and NOBLE, MD and FARMER, K and PARTRIDGE, TA (1994) MYOGENIC CELL-LINES DERIVED FROM TRANSGENIC MICE CARRYING A THERMOLABILE T-ANTIGEN - A MODEL SYSTEM FOR THE DERIVATION OF TISSUE-SPECIFIC AND MUTATION-SPECIFIC CELL-LINES. DEV BIOL , 162 (2) 486 - 498. |
| MULLER, U and CRISTINA, N and LI, ZW and WOLFER, DP and LIPP, HP and RULICKE, T and BRANDNER, S and AGUZZI, A and WEISSMANN, C (1994) BEHAVIORAL AND ANATOMICAL DEFICITS IN MICE HOMOZYGOUS FOR A MODIFIED BETA-AMYLOID PRECURSOR PROTEIN GENE. CELL , 79 (5) 755 - 765. |
N
| NEWMAN, SK and WARRINGTON, EK and KENNEDY, AM and ROSSOR, MN (1994) THE EARLIEST COGNITIVE CHANGE IN A PERSON WITH FAMILIAL ALZHEIMERS-DISEASE - PRESYMPTOMATIC NEUROPSYCHOLOGICAL FEATURES IN A PEDIGREE WITH FAMILIAL ALZHEIMERS-DISEASE CONFIRMED AT NECROPSY. J NEUROL NEUROSUR PS , 57 (8) 967 - 972. |
P
| PARTRIDGE, T and MORGAN, J and PAGEL, C and BEAUCHAMP, J and PECKHAM, M and NOBLE, M and JAT, P (1994) MYOGENIC CELLS WITH STEM-CELL PROPERTIES. J CELL BIOCHEM 266 - 266. |
R
| ROSSOR, MN (1994) CLINICAL HETEROGENEITY IN FAMILIAL ALZHEIMERS-DISEASE. NEUROBIOL AGING , 15 S140 - S140. |
| ROSSOR, MN (1994) MANAGEMENT OF NEUROLOGICAL DISORDERS - DEMENTIA. J NEUROL NEUROSUR PS , 57 (12) 1451 - 1456. |
S
| Schmitt, K and Lazzeroni, LC and Vollrath, D and Foote, S and Fisher, EMC and Goradia, TM and Lange, K and Page, DC and Arnheim, N (1994) Multipoint linkage map of the human pseudoautosomal region based on single sperm typing: Do double crossovers occur during male meiosis? Am. J. Hum. Genet. , 55 423 - 430. |
| SCHOTT, J and RUTHERFORD, O (1994) CHANGES IN FATIGUABILITY AND CONTRACTILE PROPERTIES OF THE HUMAN QUADRICEPS FOLLOWING ISOMETRIC STRENGTH TRAINING. JOURNAL OF PHYSIOLOGY-LONDON , 475P P26 - P27. |
| SURE, U and BERGHORN, W and BRANDNER, S and ISENMANN, S and BERTALANFFY, H (1994) MEDULLOBLASTOMA - METASTASES AND LOCAL RECURRENCES. J NEUROSURG , 80 (2) A398 - A398. |
T
| TABRIZI, SJ and SCOTT, J and PUSEY, CD and LACEY, S and DAVIES, RAA and REES, AJ and BEYNON, H and OAKLEY, C and WHYTE, M (1994) GRAND ROUNDS - HAMMERSMITH-HOSPITAL - NOCARDIA-PERICARDITIS - A RARE OPPORTUNISTIC INFECTION. BRIT MED J , 309 (6967) 1495 - 1497. |
| TABRIZI, SJ and SCOTT, J and PUSEY, CD and LACEY, S and DAVIES, RAA and REES, AJ and BEYNON, H and OAKLEY, C and WHYTE, M (1994) GRAND ROUNDS - HAMMERSMITH-HOSPITAL - NOCARDIA-PERICARDITIS - A RARE OPPORTUNISTIC INFECTION. BRIT MED J , 309 (6967) 1495 - 1497. |
| TELLING, GC and SCOTT, M and HSIAO, KK and FOSTER, D and YANG, SL and TORCHIA, M and SIDLE, KCL and COLLINGE, J and DEARMOND, SJ and PRUSINER, SB (1994) TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE FROM HUMANS TO TRANSGENIC MICE EXPRESSING CHIMERIC HUMAN-MOUSE PRION PROTEIN. P NATL ACAD SCI USA , 91 (21) 9936 - 9940. |
Y
| Yulug, IG and Egan, SE and See, CG and Fisher, EMC (1994) Mapping GRB2, a signal transduction gene in the human and the mouse. Genomics , 22 313 - 318. |
| Yulug, IG and Hillermann, R and Fisher, EMC (1994) The SHB adaptor protein maps to human chromosome 9. Genomics , 24 615 - 617. |
| Yulug, IG and Killary, A and Athwal, R and Fisher, EMC (1994) Creating somatic cell hybrids which respond to the morphogen retinoic acid. In: Genetics Research, Camb. (pp. 160 - ?). |


