Results 71 to 80 of about 2,722 (180)
An interactive tool for real time feedback on diagnosis and treatment plan of arthritis based on C++ programing language [PDF]
, 2014 Arthritis causes joint inflammation where body’s immunity against disease or injury becomes overactive leading to swelling, pain and stiffness and it also can lead to tissue damage.
Bhatt, S
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Identifying Key Questions and Challenges in Microchimerism Biology
Advanced Science, Volume 12, Issue 48, December 29, 2025.This study identifies key unanswered questions about microchimerism, the presence of cells from one individual living in another. Experts highlight how these cells may affect health, pregnancy, and disease. This study outlines research priorities and challenges in detecting and studying these rare microchimeric cells, aiming to guide future discoveries
Kristine J. Chua +31 more
wiley +1 more source
A rare clinical case-buschke's scleredema [PDF]
, 2015 A clinical case of rare disease of the skin-Buschker's scleredema was described in the article.
Julei, L.O., Mudriak, L.V.
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Sexing the X: How the X Became the “Female Chromosome” [PDF]
, 2014 This essay examines how the X became the “female chromosome” and how the association of the X with femaleness influences research questions, models, and descriptive language in human sex chromosome research.
Richardson, Sarah S
core +2 more sources
MedComm, Volume 6, Issue 12, December 2025.Protein arginine methyltransferase 1 (PRMT1) is a pivotal enzyme that catalyzes the asymmetric dimethylation of arginine residues, thereby functioning as a critical epigenetic regulator of diverse biological processes such as gene expression, RNA splicing, and DNA repair.
Yanqun Luo +4 more
wiley +1 more source
Treatment of systemic sclerosis: potential role for stem cell transplantation. [PDF]
, 2009 Hematopoietic stem cell transplantation may reset the immune reconstitution and induce self tolerance of autoreactive lymphocytes, and has been explored in the treatments for systemic sclerosis.
Derk, Chris T, Xiong, Wen
core +2 more sources
Pediatric Dermatology, Volume 42, Issue 6, Page 1252-1254, November/December 2025.ABSTRACT Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by progressive heterotopic ossification (HO) and congenital malformation of the great toes. This case describes a 5‐year‐old Caucasian girl who initially presented with painless neck and back swelling as well as severe limitation of movement in the neck and ...
Orhan Yilmaz, Loretta Fiorillo
wiley +1 more source
Journal of Clinical and Translational Science, 2019 OBJECTIVES/SPECIFIC AIMS: To further explore the role of vWF in the pathogenesis of scleroderma by identifying its location within the tissue of sample biopsies obtained as part of routine diagnosis with the use of immuno-histochemical staining.
Natalia Vasquez Canizares +4 more
doaj +1 more source
Lokalisierte Sklerodermie (Morphea) im Kindesalter [PDF]
, 2018 Zusammenfassung: Die lokalisierte (oder zirkumskripte) Sklerodermie (LS) oder Morphea ist eine sklerosierende Bindegewebserkrankung der Haut, die auch darunterliegende Gewebe wie Subkutis, Muskulatur und Skelett betreffen kann.
Weibel, L.
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Galectin-3. One molecule for an alphabet of diseases, from A to Z [PDF]
, 2018 Galectin-3 (Gal-3) regulates basic cellular functions such as cell–cell and cell–matrix interactions, growth, proliferation, differentiation, and inflammation.
Bellotti, Carlo +8 more
core +2 more sources