Unfolded protein response markers Grp78 and eIF2alpha are upregulated with increasing alpha‐synuclein levels in Lewy body disease Por Hrabos, D, Poggiolini, I, Civitelli, L, Galli, E, Esapa, C, Saarma, M, Lindholm, P, Parkkinen, L

Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development Por Karunaratne, A, Davis, G, Hiller, J, Esapa, C, Terrill, N, Brown, S, Cox, R, Thakker, R, Gupta, H

Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone. Por Karunaratne, A, Boyde, A, Esapa, C, Hiller, J, Terrill, N, Brown, S, Cox, R, Thakker, R, Gupta, H

Islet amyloid polypeptide gene promoter polymorphisms are not associated with Type 2 diabetes or with the severity of islet amyloidosis. Por Esapa, C, Moffitt, J, Novials, A, McNamara, C, Levy, J, Laakso, M, Gomis, R, Clark, A

Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development. Por Karunaratne, A, Davis, G, Hiller, J, Esapa, C, Terrill, N, Brown, S, Cox, R, Thakker, R, Gupta, H

Mice with an N-ethyl-N-nitrosourea (ENU) induced Tyr209Asn mutation in natriuretic peptide receptor 3 (NPR3) provide a model for kyphosis associated with activation of the MAPK sig... Por Esapa, C, Piret, S, Nesbit, M, Loh, N, Thomas, G, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse models Por Esapa, C, Hannan, F, Babinsky, V, Potter, P, Thomas, G, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

SGCE missense mutations that cause myoclonus-dystonia syndrome impair ε-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA Por Esapa, C, Waite, A, Locke, M, Benson, M, Kraus, M, McIlhinney, R, Sillitoe, R, Beesley, P, Blake, D

GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasiveness. Por Gaynor, K, Grigorieva, I, Allen, MD, Esapa, C, Head, R, Gopinath, P, Christie, P, Nesbit, M, Jones, J, Thakker, R

GATA3 Mutations Found in Breast Cancers May Be Associated with Aberrant Nuclear Localization, Reduced Transactivation and Cell Invasiveness Por Gaynor, K, Grigorieva, I, Allen, MD, Esapa, C, Head, R, Gopinath, P, Christie, P, Nesbit, M, Jones, J, Thakker, R

A Mouse with a Ser1386Pro Mutation in the C-propeptide Domain of col2aI Provides a Model for Spondyloepiphyseal Dysplasia Congenita Por Esapa, C, Hough, T, Testori, S, Head, R, Crane, E, Chan, C, Brown, M, Brown, S, Croucher, P, Cox, R, Cheeseman, M, Thakker, R

A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation. Por Piret, S, Esapa, C, Gorvin, C, Head, R, Loh, N, Devuyst, O, Thomas, G, Brown, s, Brown, M, Croucher, P, Cox, R, Thakker, R

Genetic models of bone disease using ENU mutagenesis Por Brown, S, Esapa, C, Barbaric, I, Hough, T, Brown, M, Croucher, P, Head, R, Chan, C, Crane, E, Cox, R, Cheeseman, M, Thakker, R

Novel models of late onset, progressive osteoarthritis caused by point mutations in the two alpha chains of collagen type I Por Blease, A, Wisby, L, Haynes, A, Nicol, T, Falcone, S, Lad, H, Esapa, C, Horwood, N, Thorpe, C, Thakker, R, Screen, H, Vincent, T, Browny, S, Potter, P

A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis Por Esapa, C, Head, R, Jeyabalan, J, Evans, H, Hough, T, Cheeseman, M, McNally, E, Carr, A, Thomas, G, Brown, M, Croucher, P, Brown, S, Cox, R, Thakker, R

An N-ethyl-N-nitrosourea (ENU) mutagenized mouse model for autosomal dominant non-syndromic kyphoscoliosis due to vertebral fusion Por Esapa, C, Piret, S, Nesbit, A, Thomas, G, Coulton, L, Gallagher, O, Simon, M, Kumar, S, Mallon, A, Ballantuono, I, Brown, M, Croucher, P, Potter, P, Brown, S, Cox, R, Thakker, R

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and... Por Karunaratne, A, Esapa, C, Hiller, J, Boyde, A, Head, R, Bassett, J, Terrill, N, Williams, G, Brown, M, Croucher, P, Brown, S, Cox, R, Barber, A, Thakker, R, Gupta, H

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and... Por Karunaratne, A, Esapa, C, Hiller, J, Boyde, A, Head, R, Bassett, J, Terrill, N, Williams, G, Brown, M, Croucher, P, Brown, S, Cox, R, Barber, A, Thakker, R, Gupta, H

An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess. Por Bentley, L, Esapa, C, Nesbit, M, Head, R, Evans, H, Lath, D, Scudamore, C, Hough, T, Podrini, C, Hannan, F, Fraser, W, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

An N-ethyl-n-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess Por Bentley, L, Esapa, C, Nesbit, M, Head, R, Evans, H, Lath, D, Scudamore, C, Hough, T, Podrini, C, Hannan, F, Fraser, W, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R