S. Jensen

发表

Hydrophobic Domains of Human Tropoelastin Interact in a Context-dependent Manner*

A. Weiss, P. Toonkool, S. Jensen, 2001, The Journal of Biological Chemistry.

Structural changes and facilitated association of tropoelastin.

Lisa D. Muiznieks, A. Weiss, S. Jensen, 2003, Archives of biochemistry and biophysics.

TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs.

P. Handford, S. Jensen, Ian B Robertson, 2011, The Biochemical journal.

Rational design of tropoelastin peptide-based inhibitors of metalloproteinases.

A. Weiss, B. Vrhovski, S. Jensen, 2003, Archives of biochemistry and biophysics.

Aspartate/asparagine-β-hydroxylase crystal structures reveal an unexpected epidermal growth factor-like domain substrate disulfide pattern

P. Handford, U. Oppermann, M. Münzel, 2019, Nature Communications.

Evolutionary Insights into Fibrillin Structure and Function in the Extracellular Matrix

P. Handford, S. Jensen, Ian B Robertson, 2013 .

Ca2+-dependent Interface Formation in Fibrillin-1*

P. Handford, S. Jensen, C. Redfield, 2005, Journal of Biological Chemistry.

Dissecting the fibrillin microfibril: structural insights into organization and function.

P. Handford, S. Jensen, Ian B Robertson, 2012, Structure.

New insights into the structure, assembly and biological roles of 10-12 nm connective tissue microfibrils from fibrillin-1 studies.

P. Handford, S. Jensen, 2016, The Biochemical journal.

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

D. Sillence, A. Munnich, J. Casanova, 2011, American journal of human genetics.

C-terminal propeptide is required for fibrillin-1 secretion and blocks premature assembly through linkage to domains cbEGF41-43

P. Handford, S. Jensen, G. Aspinall, 2014, Proceedings of the National Academy of Sciences.

Structure and Interdomain Interactions of a Hybrid Domain: A Disulphide-Rich Module of the Fibrillin/LTBP Superfamily of Matrix Proteins

P. Handford, E. Lowe, S. Jensen, 2009, Structure.

Protein Interaction Studies of MAGP-1 with Tropoelastin and Fibrillin-1*

A. Weiss, D. Reinhardt, S. Jensen, 2001, The Journal of Biological Chemistry.

Biophysical characterisation of fibulin-5 proteins associated with disease.

P. Handford, J. McCullagh, S. Jensen, 2010, Journal of molecular biology.

Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin‐binding fragment of FBN1

P. Handford, P. Brennan, S. Jensen, 2013, American journal of medical genetics. Part A.

An N-glycan on the C2 domain of JAGGED1 is important for Notch activation

P. Handford, M. Sansom, A. H. Larsen, 2022, Science Signaling.

Fibrillin-integrin interactions in health and disease.

P. Handford, S. Jensen, H. Mardon, 2008, Biochemical Society transactions.

Coacervation characteristics of recombinant human tropoelastin.

A. Weiss, B. Vrhovski, S. Jensen, 1997, European journal of biochemistry.

Hutchinson–Gilford progeria: faithful DNA maintenance, inheritance and allelic transcription of β(1-4) galactosyltransferase

A. Weiss, S. Jensen, M. E. O'Brien, 1998, Mechanisms of Ageing and Development.

A conserved face of the Jagged/Serrate DSL domain is involved in Notch trans-activation and cis-inhibition

P. Handford, P. Roversi, Hideyuki Shimizu, 2008, Nature Structural &Molecular Biology.

Structure of the Fibrillin-1 N-Terminal Domains Suggests that Heparan Sulfate Regulates the Early Stages of Microfibril Assembly

P. Handford, D. Stoddart, S. Jensen, 2013, Structure.

Assembly assay identifies a critical region of human fibrillin-1 required for 10–12 nm diameter microfibril biogenesis

P. Handford, S. Jensen, Ondine Atwa, 2021, PloS one.

A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias

P. Handford, S. Jensen, S. Iqbal, 2015, Human molecular genetics.

Structural Consequences of Cysteine Substitutions C1977Y and C1977R in Calcium-binding Epidermal Growth Factor-like Domain 30 of Human Fibrillin-1*

P. Handford, A. Willis, S. Jensen, 2004, Journal of Biological Chemistry.

Domain 26 of Tropoelastin Plays a Dominant Role in Association by Coacervation*

A. Weiss, B. Vrhovski, S. Jensen, 2000, The Journal of Biological Chemistry.

A disease-associated mutation in fibrillin-1 differentially regulates integrin-mediated cell adhesion

W. DeGrado, P. Handford, D. Sheppard, 2019, The Journal of Biological Chemistry.

The N-Terminal Region of Fibrillin-1 Mediates a Bipartite Interaction with LTBP1

Isabelle H. Osuch, P. Handford, E. Lowe, 2017, Structure.

1H, 13C and 15N assignments of the four N-terminal domains of human fibrillin-1

P. Handford, S. Jensen, C. Redfield, 2012, Biomolecular NMR assignments.

1H, 13C and 15N resonance assignments for the fibrillin-1 EGF2-EGF3-hybrid1-cbEGF1 four-domain fragment

Isabelle H. Osuch, P. Handford, S. Jensen, 2013, Biomolecular NMR Assignments.

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

D. Sillence, A. Munnich, J. Casanova, 2011, American journal of human genetics.

Nuclear magnetic resonance characterization of the Jun leucine zipper domain: unusual properties of coiled-coil interfacial polar residues.

W. Bubb, J. Mackay, A. Weiss, 1995, Biochemistry.