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Jump to: A | B | F | H | J | K | L | M | R | S | V | W | Y
Number of items: 23.

A

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.

B

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.

F

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

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

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.

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: (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.

M

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.

R

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

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

S

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.

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.

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) Erratum: An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4 (Human Molecular Genetics 4 (1101-1104)). Human Molecular Genetics , 4 (8) 1474-.

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; 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 May 20 02:29:13 2018 BST.