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Katarzyna Piróg
Katarzyna Piróg
Institute of Genetic Medicine, Newcastle University, UK
在 ncl.ac.uk 的电子邮件经过验证
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Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C …
KA Piróg-Garcia, RS Meadows, L Knowles, D Heinegård, DJ Thornton, ...
Human molecular genetics 16 (17), 2072-2088, 2007
962007
A mouse model offers novel insights into the myopathy and tendinopathy often associated with pseudoachondroplasia and multiple epiphyseal dysplasia
KA Pirog, O Jaka, Y Katakura, RS Meadows, KE Kadler, ...
Human molecular genetics 19 (1), 52-64, 2010
592010
A novel form of chondrocyte stress is triggered by a COMP mutation causing pseudoachondroplasia
F Suleman, B Gualeni, HJ Gregson, MP Leighton, KA Piróg, S Edwards, ...
Human mutation 33 (1), 218-231, 2012
532012
Cartilage-specific ablation of XBP1 signaling in mouse results in a chondrodysplasia characterized by reduced chondrocyte proliferation and delayed cartilage maturation and …
TL Cameron, IL Gresshoff, KM Bell, KA Piróg, L Sampurno, CL Hartley, ...
Osteoarthritis and cartilage 23 (4), 661-670, 2015
462015
New therapeutic targets in rare genetic skeletal diseases
MD Briggs, PA Bell, MJ Wright, KA Pirog
Expert opinion on orphan drugs 3 (10), 1137-1154, 2015
382015
The utility of mouse models to provide information regarding the pathomolecular mechanisms in human genetic skeletal diseases: The emerging role of endoplasmic reticulum stress
MD Briggs, PA Bell, KA Pirog
International journal of molecular medicine 35 (6), 1483-1492, 2015
362015
Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification
C Paganini, L Monti, R Costantini, R Besio, S Lecci, M Biggiogera, K Tian, ...
Matrix Biology 81, 70-90, 2019
352019
Abnormal chondrocyte apoptosis in the cartilage growth plate is influenced by genetic background and deletion of CHOP in a targeted mouse model of pseudoachondroplasia
KA Piróg, A Irman, S Young, P Halai, PA Bell, RP Boot-Handford, ...
PloS one 9 (2), e85145, 2014
352014
Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis
PA Bell, EP Dennis, CL Hartley, RM Jackson, A Porter, RP Boot-Handford, ...
Cell Stress and Chaperones 24 (1), 159-173, 2019
252019
XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease
KA Pirog, EP Dennis, CL Hartley, RM Jackson, J Soul, JM Schwartz, ...
PLoS Genetics 15 (7), e1008215, 2019
242019
New developments in chondrocyte ER stress and related diseases
MD Briggs, EP Dennis, HF Dietmar, KA Pirog
F1000Research 9, 2020
232020
Skeletal Dysplasias Associated with Mild Myopathy—A Clinical and Molecular Review
A Katarzyna, MD Briggs
222010
microRNA-seq of cartilage reveals an overabundance of miR-140-3p which contains functional isomiRs
S Woods, S Charlton, K Cheung, Y Hao, J Soul, LN Reynard, N Crowe, ...
Rna 26 (11), 1575-1588, 2020
202020
CRELD2 is a novel LRP1 chaperone that regulates noncanonical WNT signaling in skeletal development
EP Dennis, SM Edwards, RM Jackson, CL Hartley, D Tsompani, M Capulli, ...
Journal of Bone and Mineral Research 35 (8), 1452-1469, 2020
192020
Increased hippocampal excitability in miR-324-null mice
DJ Hayman, T Modebadze, S Charlton, K Cheung, J Soul, H Lin, Y Hao, ...
Scientific reports 11 (1), 10452, 2021
102021
Mild myopathy is associated with COMP but not MATN3 mutations in mouse models of genetic skeletal diseases
KA Piróg, Y Katakura, A Mironov, MD Briggs
PloS one 8 (11), e82412, 2013
102013
Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation
PA Bell, KA Piróg, M Fresquet, DJ Thornton, RP Boot‐Handford, ...
Arthritis & Rheumatism 64 (5), 1529-1539, 2012
92012
Changes in Bcl-2 expression in vaccinia virus-infected human peripheral blood monocytes
KA Pirog, AK Kowalczyk, HB Rokita
Viral Immunology 18 (1), 224-231, 2005
32005
Pseudoachondroplasia and multiple epiphyseal dysplasia: Molecular genetics, disease mechanisms and therapeutic targets
MD Briggs, P Bell, KA Piróg
Cartilage: Volume 2: Pathophysiology, 135-153, 2017
22017
Involvement of kinesins in skeletal dysplasia-a review
R Bouchenafa, FM de Sousa Brito, KA Pirog
American Journal of Physiology-Cell Physiology, 2024
2024
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