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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.
An open access version is available from UCL Discovery
 file

Chang, WS and 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.
An open access publication

E

Elliott, PR and Abrahams, JP and 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 and Bilton, D and 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 and Butterfield, JH and Warner, JA (1998) Focal adhesion kinase expression in mast cells and basophils. J ALLERGY CLIN IMMUN , 101 (1) S213 - S213.

K

Kapsa, RMI and Quigley, AF and Han, TF and Jean-Francois, MJB and Vaughan, P and 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.
An open access publication

Kurek, JB and Radford, AJ and Crump, DE and Bower, JJ and Feeney, SJ and Austin, L and 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 and Bateman, JF and Hutchison, W and Gardner, RJM and Bower, SP and Byrne, E and 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 and Caine, N and Wells, FC (1998) Lung volume reduction surgery. THORAX , 53 (2) 155 - 155.

M

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

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

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

Mahadeva, R and Webb, K and Westerbeek, RC and Carroll, NR and Dodd, ME and Bilton, D and 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 and Westerbeek, RC and Perry, DJ and Lovegrove, JU and Whitehouse, DB and Carroll, NR and Ross-Russell, RI and Webb, AK and Bilton, D and Lomas, DA (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 and Westerbeek, RC and Perry, DJ and Lovegrove, JU and Whitehouse, DB and Carroll, NR and Ross-Russell, RI and Webb, AK and Bilton, D and Lomas, DA (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 and Collins, S and Dennett, X and Byrne, E and McKelvie, P (1998) McArdle's disease resembling an inflammatory myopathy. Journal of Clinical Neuroscience , 5 (2) 210 - 212.

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

S

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

Skinner, R and Chang, WS and Jin, L and Pei, X and Huntington, JA and Abrahams, JP and Carrell, RW and Lomas, DA (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 and Crimmins, DS and Soo, YS and Pamphlett, R and Presgrave, CM and Kotsimbos, N and Jean-Francois, MJB and Byrne, E and Morris, JGL (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 and Lipsett, LJ and Crimmins, DS and Tsang, CS and Boyages, SC and Presgrave, CM and Gibson, WPR and Byrne, E and Morris, JGL (1998) Cochlear origin of hearing loss in MELAS syndrome. Annals of Neurology , 43 (3) 350 - 359.

Sue, CM and Quigley, A and Katsabanis, S and Kapsa, R and Crimmins, DS and Byrne, E and 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 Tue May 21 07:38:44 2013 BST.