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The International Journal of Biochemistry & Cell Biology|May 2, 2001
Type VIII collagen: heterotrimeric chain associationC Illidge, C Kielty, A ShuttleworthThe Journal of Biological Chemistry|August 15, 1998
The alpha1(VIII) and alpha2(VIII) chains of type VIII collagen can form stable homotrimeric moleculesC Illidge, C Kielty, A ShuttleworthBiochemical Genetics|June 1, 1985
The expression of human glycerol-3-phosphate dehydrogenase in human/rodent somatic-cell hybridsY Edwards, S L McMillan, C Kielty, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 1, 1996
Type VI collagen is present in human and bovine vitreousP Bishop, S Ayad, A Reardon, et al.Genomics|September 15, 1996
A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndromeL Lönnqvist, L Karttunen, T Rantamäki, et al.The Journal of Clinical Investigation|May 1, 1995
A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndromeD M Milewicz, J Grossfield, S N Cao, et al.Annals of Human Genetics|May 1, 1982
Mapping studies on human mitochondrial glutamate oxaloacetate transaminaseS J Jeremiah, S Povey, M W Burley, et al.The British Journal of Oral & Maxillofacial Surgery|December 5, 2016
Medical students' understanding of oral and maxillofacial surgery: an Irish perspectiveP G C Kielty, B R O'Connor, C J Cotter, et al.Human Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.Pageof 1