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Jump to: B | C | E | F | G | H | L | S | W
Number of items: 15.

B

BINNS, KE; SALT, TE; (1995) EXCITATORY AMINO-ACID RECEPTORS MODULATE HABITUATION OF THE RESPONSE TO VISUAL-STIMULATION IN THE CAT SUPERIOR COLLICULUS. VISUAL NEUROSCI , 12 (3) 563 - 571.

BINNS, KE; SALT, TE; (1995) N-METHYL-D-ASPARTATE (NMDA) RECEPTORS CORTICAL INFLUENCES ON VISUAL RESPONSES IN SUPERIOR COLLICULUS (SC) OF THE ANESTHETIZED CAT. J PHYSIOL-LONDON , 485P P11 - P12.

C

Corbett, MC; Shilling, JS; Holder, GE; (1995) The assessment of clinical investigations: The Greenwich grading system and its application to electrodiagnostic testing in ophthalmology. EYE , 9 pp. 59-64.

E

EVANS, KL; VANHEYNINGEN, V; PORTEOUS, DJ; (1995) PLACEMENT AND REFINED MAPPING OF ESTABLISHED AND NEW MARKERS ON HUMAN-CHROMOSOME 11Q USING A SMALL PANEL OF SOMATIC-CELL HYBRIDS. EUROPEAN JOURNAL OF HUMAN GENETICS , 3 (1) pp. 42-48.

F

FARRELL, MA; GREEN, AJ; SEPP, T; MISCHEL, P; VINTERS, HV; (1995) LOSS OF HETEROZYGOSITY IN SPORADIC CORTICAL DYSPLASIA FOR DNA MARKERS IN THE REGION OF THE TUBEROUS SCLEROSIS (TSC1) GENE ON CHROMOSOME 9Q34. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY , 54 (3) p. 414.

G

GREEN, AJ; SEPP, T; MISCHEL, P; VINTERS, H; FARRELL, MA; (1995) ISOLATED CORTICAL DYSPLASIA SHOWS LOSS OF HETEROZYGOSITY IN THE REGION OF THE TUBEROUS SCLEROSIS-1 GENE. AMERICAN JOURNAL OF HUMAN GENETICS , 57 (4) p. 1915.

GREEN, AJ; SEPP, T; YATES, JRW; (1995) HAMARTOMAS FROM PATIENTS WITH TUBEROUS SCLEROSIS SHOW LOSS OF HETEROZYGOSITY FOR CHROMOSOME 9Q34. JOURNAL OF MEDICAL GENETICS , 32 (2) pp. 152-153.

H

HANSON, I; BROWN, A; VANHEYNINGEN, V; (1995) A NEW PAX6 MUTATION IN FAMILIAL ANIRIDIA. JOURNAL OF MEDICAL GENETICS , 32 (6) pp. 488-489. 10.1136/jmg.32.6.488.

HOLZ, FG; EVANS, K; GREGORY, CY; BHATTACHARYA, S; BIRD, AC; (1995) AUTOSOMAL-DOMINANT MACULAR DYSTROPHY SIMULATING NORTH-CAROLINA MACULAR DYSTROPHY. ARCHIVES OF OPHTHALMOLOGY , 113 (2) pp. 178-184. 10.1001/archopht.1995.01100020062029.

L

LITTLE, M; HOLMES, G; BICKMORE, W; VANHEYNINGEN, V; HASTIE, N; WAINWRIGHT, B; (1995) DNA-BINDING CAPACITY OF THE WT1 PROTEIN IS ABOLISHED BY DENYS-DRASH SYNDROME WT1 POINT MUTATIONS. HUMAN MOLECULAR GENETICS , 4 (3) pp. 351-358. 10.1093/hmg/4.3.351.

S

SLAVOTINEK, A; MILLER, E; TAYLOR, GM; NUSSE, M; VANHEYNINGEN, V; (1995) MICRONUCLEUS FREQUENCIES IN LYMPHOBLASTOID CELL-LINES MEASURED WITH THE CYTOKINESIS-BLOCK TECHNIQUE AND FLOW-CYTOMETRY. MUTAGENESIS , 10 (5) pp. 439-445. 10.1093/mutage/10.5.439.

Shipp, S; (1995) The odd couple. Current Biology , 5 (2) pp. 124-128.

Shipp, S; Watson, JD; Frackowiak, RS; Zeki, S; (1995) Retinotopic maps in human prestriate cortex: the demarcation of areas V2 and V3. Neuroimage , 2 (2) pp. 125-132.

Shipp, S; Zeki, S; (1995) Segregation and convergence of specialised pathways in macaque monkey visual cortex. Journal of Anatomy , 187 (3) pp. 547-562.

W

WEBB, NJA; LEWIS, MA; WILLIAMSON, K; VANHEYNINGEN, V; BRUCE, J; LENDON, M; POSTLETHWAITE, RJ; (1995) DO CHILDREN WITH DIFFUSE MESANGIAL SCLEROSIS IN ASSOCIATION WITH MUTATIONS OF THE WILMS-TUMOR SUPPRESSOR GENE (WT1) REQUIRE BILATERAL-NEPHRECTOMY. PEDIATRIC NEPHROLOGY , 9 (2) pp. 252-253. 10.1007/BF00860765.

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