[HTML][HTML] STAT4: an immunoregulator contributing to diverse human diseases

C Yang, H Mai, J Peng, B Zhou, J Hou… - International journal of …, 2020 - ncbi.nlm.nih.gov
Signal transducer and activator of transcription 4 (STAT4) is a member of the STAT family
and localizes to the cytoplasm. STAT4 is phosphorylated after a variety of cytokines bind to …

Epigenetics as a versatile regulator of fibrosis

Y Liu, D Wen, C Ho, L Yu, D Zheng, S O'Reilly… - Journal of Translational …, 2023 - Springer
Fibrosis, a process caused by excessive deposition of extracellular matrix (ECM), is a
common cause and outcome of organ failure and even death. Researchers have made …

New insights into the genetics and epigenetics of systemic sclerosis

C Angiolilli, W Marut, M van der Kroef… - Nature Reviews …, 2018 - nature.com
Systemic sclerosis (SSc) is a severe autoimmune disease that is characterized by vascular
abnormalities, immunological alterations and fibrosis of the skin and internal organs. The …

Circulating soluble CD163, associations with cardiovascular outcomes and mortality, and identification of genetic variants in older individuals: the cardiovascular …

P Durda, LM Raffield, EM Lange, NC Olson… - Journal of the …, 2022 - Am Heart Assoc
Background Monocytes/macrophages participate in cardiovascular disease. CD163 (cluster
of differentiation 163) is a monocyte/macrophage receptor, and the shed sCD163 (soluble …

Unfolding the pathogenesis of scleroderma through genomics and epigenomics

PS Tsou, AH Sawalha - Journal of autoimmunity, 2017 - Elsevier
With unknown etiology, scleroderma (SSc) is a multifaceted disease characterized by
immune activation, vascular complications, and excessive fibrosis in internal organs …

PDGF/PDGFR: a possible molecular target in scleroderma fibrosis

C Paolini, S Agarbati, D Benfaremo… - International Journal of …, 2022 - mdpi.com
Systemic sclerosis (SSc) is a clinically heterogeneous disorder of the connective tissue
characterized by vascular alterations, immune/inflammatory manifestations, and organ …

Classical disease-specific autoantibodies in systemic sclerosis: clinical features, gene susceptibility, and disease stratification

C Yang, S Tang, D Zhu, Y Ding, J Qiao - Frontiers in medicine, 2020 - frontiersin.org
Systemic sclerosis (SSc) is an autoimmune disease characterized by abnormalities in
microcirculation, extracellular matrix accumulation, and immune activation. Autoantibodies …

HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications

R Busch, S Kollnberger, ED Mellins - Nature Reviews Rheumatology, 2019 - nature.com
Our understanding of the mechanisms underlying HLA associations with inflammatory
arthritis continues to evolve. Disease associations have been refined, and interactions of …

Pathophysiology of systemic sclerosis

B Thoreau, B Chaigne, A Renaud, L Mouthon - La Presse Médicale, 2021 - Elsevier
Systemic sclerosis (SSc) is a rare connective tissue disease characterized by vascular
remodeling, fibroblast activation and extra-cellular matrix production in excess and …

Genomics of human fibrotic diseases: disordered wound healing response

RC Stone, V Chen, J Burgess, S Pannu… - International journal of …, 2020 - mdpi.com
Fibrotic disease, which is implicated in almost half of all deaths worldwide, is the result of an
uncontrolled wound healing response to injury in which tissue is replaced by deposition of …