CCN proteins in the musculoskeletal system: current understanding and challenges in physiology and pathology

V Giusti, K Scotlandi - Journal of Cell Communication and …, 2021 - Wiley Online Library
The acronym for the CCN family was recently revised to represent “cellular communication
network”. These six, small, cysteine‐enriched and evolutionarily conserved proteins are …

[HTML][HTML] Progressive pseudorheumatoid dysplasia involving a novel WISP3 mutation and sacroiliac and hip arthritis: a case report and literature review

W Wang, G Xiao, Q Han, J Ding, R Xie, J Jia, N Leng… - Medicine, 2023 - journals.lww.com
Medicine Log in or Register Get new issue alertsGet alerts Secondary Logo Journal Logo
Advanced Search Toggle navigation Register Login Articles & Issues Browse by Specialty …

Directed differentiation of human pluripotent stem cells into articular cartilage reveals effects caused by absence of WISP3, the gene responsible for progressive …

C Li, M Alemany-Ribes, RM Raftery, U Nwoko… - Annals of the …, 2023 - ard.bmj.com
Objectives Progressive pseudorheumatoid arthropathy of childhood (PPAC), caused by
deficiency of WNT1 inducible signalling pathway protein 3 (WISP3), has been challenging to …

Gait alterations in two young siblings with progressive Pseudorheumatoid dysplasia

S Sassi, S Faccioli, GM Farella, R Tedeschi, L Garavelli… - Children, 2022 - mdpi.com
Progressive pseudorheumatoid dysplasia (PPRD) is an autosomal recessive inherited
skeletal dysplasia characterized by progressive non-inflammatory arthropathy affecting …

[HTML][HTML] Multicentric osteolysis, nodulosis, and arthropathy in two unrelated children with matrix metalloproteinase 2 variants: genetic-skeletal correlations

H Elsebaie, MA Mansour, SM Elsayed, S Mahmoud… - Bone Reports, 2021 - Elsevier
Abstract Multicentric Osteolysis, Nodulosis, and Arthropathy (MONA) syndrome is a rare
genetic skeletal dysplasia. Its diagnosis can be deceptively similar to childhood-onset …

[HTML][HTML] Get Spliced: Uniting Alternative Splicing and Arthritis

MJH van Haaren, LB Steller, SJ Vastert… - International Journal of …, 2024 - mdpi.com
Immune responses demand the rapid and precise regulation of gene protein expression.
Splicing is a crucial step in this process;~ 95% of protein-coding gene transcripts are spliced …

Dual roles of cellular communication network factor 6 (CCN6) in the invasion and metastasis of oral cancer cells to bone via binding to BMP2 and RANKL

H Hochi, S Kubota, M Takigawa, T Nishida - Carcinogenesis, 2023 - academic.oup.com
The acquisition of motility via epithelial–mesenchymal transition (EMT) and osteoclast
induction are essential for the invasion and metastasis of oral squamous cell carcinoma …

Progressive pseudorheumatoid dysplasia: A rare entity mimicking juvenile idiopathic arthritis

K Maatallah, H Boussaa… - Clinical Case …, 2021 - Wiley Online Library
Progressive pseudorheumatoid dysplasia: A rare entity mimicking juvenile idiopathic arthritis -
Maatallah - 2021 - Clinical Case Reports - Wiley Online Library Skip to Article Content Skip to …

Multiple disc herniation in spondyloepiphyseal dysplasia tarda: A rare case report and review of the literature

Z Chen, Z Zhang, F Ye, F Lei, D Feng - BMC Musculoskeletal Disorders, 2022 - Springer
Background Spondyloepiphyseal dysplasia tarda (SEDT) is a rare, hereditary, X-linked
skeletal disorder. To our knowledge, there are few reports about orthopedic surgery in these …

Spine radiograph in dysplasias: A pictorial essay

P Gabra, M Jana, P Naranje, N Gupta… - Indian Journal of …, 2020 - thieme-connect.com
Spine radiograph is an essential component of a skeletal survey. It provides important
diagnostic clues to various types of skeletal dysplasia. In some conditions, a spine …