A. Daroszewska

发表

Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition.

David M. Evans, D. Kiel, A. Hofman, 2014, Bone.

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.

L. Hocking, J. Mangion, S. Ralston, 2002, Human molecular genetics.

Zoledronic acid prevents pagetic-like lesions and accelerated bone loss in the p62P394L mouse model of Paget's disease

S. Ralston, A. Daroszewska, R. J. van ‘t Hof, 2018, Disease Models & Mechanisms.

Mechanisms of Disease: genetics of Paget's disease of bone and related disorders

S. Ralston, A. Daroszewska, 2006, Nature Clinical Practice Rheumatology.

Analysis of Nkx3.1:Cre-driven Erk5 deletion reveals a profound spinal deformity which is linked to increased osteoclast activity

O. Sansom, K. Blyth, I. Ahmad, 2017, Scientific Reports.

Contribution of Genetic Factors to the Pathogenesis of Paget's Disease of Bone and Related Disorders

S. Ralston, G. Lucas, A. Daroszewska, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Bone turnover in untreated polymyalgia rheumatica.

W. Fraser, T. Barnes, A. Daroszewska, 2004, Rheumatology.

Genetics of Paget's disease of bone.

S. Ralston, A. Daroszewska, 1998, Clinical science.

Novel UBA Domain Mutations of SQSTM1 in Paget's Disease of Bone: Genotype Phenotype Correlation, Functional Analysis, and Structural Consequences

L. Hocking, S. Ralston, G. Lucas, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone

P. Geusens, S. Boonen, S. Ralston, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Unilateral glossopharyngeal and hypoglossal nerve palsies due to compression by a rheumatoid pannus.

C. Mumford, A. Daroszewska, R. Mathew, 2010, Rheumatology.

Syndecan-3: A Signaling Conductor in the Musculoskeletal System

A. Pisconti, A. Daroszewska, O. Kehoe, 2021 .

Syndecan-3 enhances anabolic bone formation through WNT signalling

George Bou-Gharios, A. Pisconti, B. Poulet, 2019, bioRxiv.

Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

Niamh M. Ryan, Toshiko Tanaka, D. Kiel, 2017, Annals of the rheumatic diseases.

Molecular insights into an ancient form of Paget’s disease of bone

W. Fraser, R. Fischer, S. González, 2019, Proceedings of the National Academy of Sciences.

Identification of Sex‐Specific Associations Between Polymorphisms of the Osteoprotegerin Gene, TNFRSF11B, and Paget's Disease of Bone

S. Ralston, E. Fransen, J. Devogelaer, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Reduced expression of PML predisposes to Paget's disease of bone by increasing osteoclast differentiation and bone resorption.

S. Ralston, D. Salter, Sachin E. Wani, 2022, Disease models & mechanisms.

Susceptibility to Paget's Disease of Bone Is Influenced by a Common Polymorphic Variant of Osteoprotegerin

L. Hocking, S. Ralston, W. Fraser, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Ubiquitin‐Associated Domain Mutations of SQSTM1 in Paget's Disease of Bone: Evidence for a Founder Effect in Patients of British Descent

L. Hocking, S. Ralston, G. Lucas, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Nitisinone arrests ochronosis and decreases rate of progression of Alkaptonuria: Evaluation of the effect of nitisinone in the United Kingdom National Alkaptonuria Centre.

A. Milan, T. Cox, J. Harrold, 2018, Molecular genetics and metabolism.

Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus.

David M. Evans, D. Kiel, A. Hofman, 2014, Bone.

Severe hypercalcaemia in B-cell lymphoma: combined effects of PTH-rP, IL-6 and TNF

W. Fraser, R. Bucknall, A. Daroszewska, 1999, Postgraduate medical journal.

Open source software for semi-automated histomorphometry of bone resorption and formation parameters.

Lorraine Rose, Rob J van 't Hof, Euphemie Bassonga, 2017, Bone.

Open source software for semi-automated histomorphometry of bone resorption and formation parameters

A. Daroszewska, Lorraine Rose, 2013 .

A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice.

S. Ralston, R. Layfield, A. Daroszewska, 2011, Human molecular genetics.