UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Browse by UCL Departments and Centres

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Author | Type
Jump to: B | D | G | I | M | P | S
Number of items: 12.

B

Bayston, TA; Tripodi, A; Mannucci, PM; Bock, SC; Ireland, H; Lane, DA; (1997) Over-expression of beta antithrombin in familial antithrombin deficiency caused by an ASN135 to THR mutation. THROMB HAEMOSTASIS OC765 - OC765.

D

Dangel, AW; Botcherby, MRM; Strivens, MA; Platzer, M; Heiss, N; Straw, R; Williams, GW; ... Herman, GE; + view all (1997) Comparative X chromosomal DNA sequencing to identify candidate disease genes in Xq28. AMERICAN JOURNAL OF HUMAN GENETICS , 61 (4) A233-A233.

Denny, P; Lord, CJ; Hill, NJ; Goy, JV; Levy, ER; Podolin, PL; Peterson, LB; ... Lyons, PA; + view all (1997) Mapping of the IDDM locus Idd3 to a 0.35-cM interval containing the interleukin-2 gene. Diabetes , 46 (4) pp. 695-700. 10.2337/diab.46.4.695.

G

Gandrille, S; Borgel, D; Ireland, H; Lane, DA; Simmonds, R; Reitsma, PH; Mannhalter, C; ... Alach, M; + view all (1997) Protein S deficiency: A database of mutations - For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. THROMB HAEMOSTASIS , 77 (6) 1201 - 1214.

Gilbert, HL; Flora, RS; Acharya, J; Sawyer, BM; Cotter, FE; Pearson, TC; (1997) Detection of novel genetic rearrangements in patients with myeloproliferative disorders by inter-Alu DNA fingerprinting. BLOOD , 90 (10) 4063 - 4063.

I

Ireland, H; Kunz, G; Kyriakoulis, K; Stubbs, PJ; Lane, DA; (1997) Thrombomodulin gene mutations associated with myocardial infarction. CIRCULATION , 96 (1) 15 - 18.

Ireland, H; Kunz, G; Kyriakoulis, K; Stubbs, PJ; Lane, DA; (1997) Thrombomodulin gene mutations in myocardial infarction. THROMB HAEMOSTASIS SC7 - SC7.

M

Mailly, F; Palmen, J; Muller, DPR; Gibbs, T; Lloyd, J; Brunzell, J; Durrington, P; ... Talmud, PJ; + view all (1997) Familial lipoprotein lipase (LPL) deficiency: A catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy. HUM MUTAT , 10 (6) 465 - 473.

P

Podolin, PL; Denny, P; Lord, CJ; Hill, NJ; Todd, JA; Peterson, LB; Wicker, LS; (1997) Congenic mapping of the insulin-dependent diabetes (Idd) gene, Idd10, localizes two gene mediating the Idd10 effect and eliminates the candidate Fcgr1. JOURNAL OF IMMUNOLOGY , 159 (4) pp. 1835-1843.

S

Simmonds, RE; Zoller, B; Ireland, H; Thompson, E; De Frutos, PG; Dahlback, B; Lane, DA; (1997) Thrombotic risk associated with protein S (PS) gene mutation and an explanation for the familial coexistence of type I and type III PS-deficient phenotypes. THROMB HAEMOSTASIS OC729 - OC729.

Simmonds, RE; Zoller, B; Ireland, H; Thompson, E; de Frutos, PG; Dahlback, B; Lane, DA; (1997) Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes. BLOOD , 89 (12) 4364 - 4370.

Strivens, MA; Middlehurst, P; Brown, SDM; Denny, P; (1997) HOSEpipe-a WWW-hosted data management and analysis system for STS content mapping projects. MAMMALIAN GENOME , 8 (7) pp. 467-471. 10.1007/s003359900478.

This list was generated on Sun Aug 25 06:31:05 2019 BST.