UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Browse by UCL Departments and Centres

Up a level
Export as [feed] RSS 2.0 [feed] RSS 1.0 [feed] Atom
Group by: Author | Type
Jump to: C | E | G | K | L | M | O | S
Number of items: 22.

C

Chadwick, N.C.; (1998) Molecular strategies for the detection of measles virus in inflammatory bowel disease. Doctoral thesis, University of London. Green open access
file

Chang, WS; Lomas, DA; (1998) Latent alpha1-antichymotrypsin. A molecular explanation for the inactivation of alpha1-antichymotrypsin in chronic bronchitis and emphysema. J Biol Chem , 273 (6) 3695 - 3701. Gold open access

E

Elliott, PR; Abrahams, JP; Lomas, DA; (1998) Wild-type alpha 1-antitrypsin is in the canonical inhibitory conformation. J Mol Biol , 275 (3) 419 - 425. 10.1006/jmbi.1997.1458.

Elliott, PR; Bilton, D; Lomas, DA; (1998) Lung polymers in Z alpha1-antitrypsin deficiency-related emphysema. Am J Respir Cell Mol Biol , 18 (5) 670 - 674. 10.1165/ajrcmb.18.5.3065.

G

Goldring, K; Butterfield, JH; Warner, JA; (1998) Focal adhesion kinase expression in mast cells and basophils. J ALLERGY CLIN IMMUN , 101 (1) S213 - S213.

K

Kapsa, RMI; Quigley, AF; Han, TF; Jean-Francois, MJB; Vaughan, P; Byrne, E; (1998) MtDNA replicative potential remains constant during ageing: polymerase gamma activity does not correlate with age related cytochrome oxidase activity decline in platelets. Nucleic Acids Research , 26 (19) 4365 - 4373. Gold open access

Kurek, JB; Radford, AJ; Crump, DE; Bower, JJ; Feeney, SJ; Austin, L; Byrne, E; (1998) LIF (AM424), a promising growth factor for the treatment of ALS. Journal of the Neurological Sciences , 160 S106 - S113.

L

Lamande, SR; Bateman, JF; Hutchison, W; Gardner, RJM; Bower, SP; Byrne, E; Dahl, HHM; (1998) Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency. Human Molecular Genetics , 7 (6) 981 - 989.

Lomas, DA; Caine, N; Wells, FC; (1998) Lung volume reduction surgery. THORAX , 53 (2) 155 - 155.

M

Mahadeva, R; Lomas, DA; (1998) Alpha(1)-antitrypsin deficiency, cirrhosis and emphysema. THORAX , 53 (6) 501 - 505.

Mahadeva, R; Lomas, DA; (1998) Genetics and respiratory disease. 2. Alpha 1-antitrypsin deficiency, cirrhosis and emphysema. Thorax , 53 (6) 501 - 505.

Mahadeva, R; Stewart, S; Bilton, D; Lomas, DA; (1998) Alpha-1 antitrypsin deficiency alleles and severe cystic fibrosis lung disease. Thorax , 53 (12) 1022 - 1024.

Mahadeva, R; Webb, K; Westerbeek, RC; Carroll, NR; Dodd, ME; Bilton, D; Lomas, DA; (1998) Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study. BMJ , 316 (7147) 1771 - 1775.

Mahadeva, R; Westerbeek, RC; Perry, DJ; Lovegrove, JU; Whitehouse, DB; Carroll, NR; ... Lomas, DA; + view all (1998) alpha-Antitrypsin deficiency alleles and the Taq-I G -> A allele in cystic fibrosis lung disease. EUROPEAN RESPIRATORY JOURNAL , 11 (4) 873 - 879. 10.1183/09031936.98.11040873.

Mahadeva, R; Westerbeek, RC; Perry, DJ; Lovegrove, JU; Whitehouse, DB; Carroll, NR; ... Lomas, DA; + view all (1998) Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung disease. Eur Respir J , 11 (4) 873 - 879.

O

O'Brien, T; Collins, S; Dennett, X; Byrne, E; McKelvie, P; (1998) McArdle's disease resembling an inflammatory myopathy. Journal of Clinical Neuroscience , 5 (2) 210 - 212.

Ojaimi, J; Katsabanis, S; Bower, S; Quigley, A; Byrne, E; (1998) Mitochondrial DNA in stroke and migraine with aura. Cerebrovascular Diseases , 8 (2) 102 - 106.

S

Siregar, NC; Jean-Francois, MJB; Blok, RB; Byrne, E; (1998) Genotypic and phenotypic changes in exhaustively grown cell lines from mitochondrial cytopathy patients. Muscle & Nerve , 21 (5) 599 - 609.

Skinner, R; Chang, WS; Jin, L; Pei, X; Huntington, JA; Abrahams, JP; ... Lomas, DA; + view all (1998) Implications for function and therapy of a 2.9 A structure of binary-complexed antithrombin. J Mol Biol , 283 (1) 9 - 14. 10.1006/jmbi.1998.2083.

Sue, CM; Crimmins, DS; Soo, YS; Pamphlett, R; Presgrave, CM; Kotsimbos, N; ... Morris, JGL; + view all (1998) Neuroradiological features of six kindreds with MELAS tRNA(Leu) A3243G point mutation: implications for pathogenesis. Journal of Neurology, Neurosurgery and Psychiatry , 65 (2) 233 - 240.

Sue, CM; Lipsett, LJ; Crimmins, DS; Tsang, CS; Boyages, SC; Presgrave, CM; ... Morris, JGL; + view all (1998) Cochlear origin of hearing loss in MELAS syndrome. Annals of Neurology , 43 (3) 350 - 359.

Sue, CM; Quigley, A; Katsabanis, S; Kapsa, R; Crimmins, DS; Byrne, E; Morris, JGL; (1998) Detection of MELAS A3243G point mutation in muscle, blood and hair follicles. Journal of the Neurological Sciences , 161 (1) 36 - 39.

This list was generated on Sun Jul 27 03:49:45 2014 BST.