Fibrillin-1, a calcium binding protein of extracellular matrix. by Handford, P

Molecular pathology of the Marfan syndrome by Handford, P

Insights into fibrillin-1 structure and function from domain studies by Handford, P

Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders. by Whiteman, P, Handford, P

Fibrillin-1 misfolding and disease. by Whiteman, P, Hutchinson, S, Handford, P

Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence. by Hutchinson, S, Wordsworth, B, Handford, P

TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs. by Robertson, I, Jensen, S, Handford, P

Backbone ¹H, ¹³C and ¹⁵N resonance assignment of the C-terminal EGF-cbEGF pair of LTBP1 and flanking residues. by Robertson, I, Handford, P, Redfield, C

A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias by Jensen, S, Iqbal, S, Bulsiewicz, A, Handford, P

The N1317H substitution associated with Leber congenital amaurosis results in impaired interdomain packing in human CRB1 epidermal growth factor-like (EGF) domains. by Davis, J, Handford, P, Redfield, C

Dissecting the fibrillin microfibril: structural insights into organization and function. by Jensen, SA, Robertson, I, Handford, P

1H, 13C and 15N assignments of EGF domains 8 to 11 of human Notch-1 by Weisshuhn, P, Handford, P, Redfield, C

(1)H, (13)C and (15)N assignments of EGF domains 4 to 7 of human Notch-1 by Weisshuhn, P, Handford, P, Redfield, C

$^1$H, $^13$C and $^15$N assignments of EGF domains 8–11 of human Notch-1 by Weisshuhn, P, Handford, P, Redfield, C

Notch receptor-ligand binding and activation: Insights from molecular studies by Chillakuri, C, Sheppard, D, Lea, S, Handford, P

Notch receptor-ligand binding and activation: insights from molecular studies. by Chillakuri, C, Sheppard, D, Lea, S, Handford, P

Characterisation of fibrillin-1 cDNA clones in a human fibroblast cell line that assembles microfibrils. by Kettle, S, Card, C, Hutchinson, S, Sykes, B, Handford, P

Fibrillin-integrin interactions in health and disease. by Jovanović, J, Iqbal, S, Jensen, S, Mardon, H, Handford, P

Fibrillin: from domain structure to supramolecular assembly. by Handford, P, Downing, A, Reinhardt, D, Sakai, L

Fibrillin-integrin interactions in health and disease by Jovanovic, J, Iqbal, S, Jensen, S, Mardonf, H, Handford, P