Recent advances in studies of SLCO2A1 as a key regulator of the delivery of prostaglandins to their sites of action
T Nakanishi, Y Nakamura, J Umeno - Pharmacology & Therapeutics, 2021 - Elsevier
Solute carrier organic anion transporter family member 2A1 (SLCO2A1, also known as PGT,
OATP2A1, PHOAR2, or SLC21A2) is a plasma membrane transporter consisting of 12 …
OATP2A1, PHOAR2, or SLC21A2) is a plasma membrane transporter consisting of 12 …
Biologics for inherited disorders of keratinisation: A systematic review
MKY Chen, AL Flanagan… - Australasian Journal of …, 2024 - Wiley Online Library
Abstract Background/Objectives Recent literature highlights the potential of biologics in the
management of inherited disorders of keratinisation. In this study, we conducted a …
management of inherited disorders of keratinisation. In this study, we conducted a …
Digital clubbing, joint pain, and skin changes in a young man: primary hypertrophic osteoarthropathy
LA González, DC Quintero-González… - Clinical …, 2022 - Springer
Discussion PHO or pachydermoperiostosis is a genetic disease characterized by facial skin
thickening (pachydermia), digital clubbing, and periostosis of long bones. Arthritis occurs in …
thickening (pachydermia), digital clubbing, and periostosis of long bones. Arthritis occurs in …
Osteoartropatía hipertrófica
G Chalès, F Robin, G Coiffier, A Rouil - EMC-Aparato Locomotor, 2023 - Elsevier
La osteoartropatía hipertrófica (OAH), descrita hace 125 años por Von Bamberger (1889) y
Pierre Marie (1890), es una entidad clínica y radiológica clásicamente secundaria a …
Pierre Marie (1890), es una entidad clínica y radiológica clásicamente secundaria a …
Identification of Novel Juvenile Idiopathic Arthritis Risk Genes in Large Pedigrees
CN Avery - 2023 - search.proquest.com
Juvenile idiopathic arthritis (JIA) is a heterogenous, complex autoimmune disease with
environmental and genetic risk factors with an estimated prevalence of 1 in 1000. Efforts to …
environmental and genetic risk factors with an estimated prevalence of 1 in 1000. Efforts to …
Differential Diagnosis of Juvenile Arthritis: A Rare Disease with Hypertrophic Osteoarthropathy.
Ö BABA, H KISAOĞLU… - Turkiye Klinikleri Journal …, 2022 - search.ebscohost.com
Pachydermoperiostosis is a rare disease characterized by clubbing, periostosis, and soft
tissue swelling, caused by mutations in any of the genes involved in prostaglandin …
tissue swelling, caused by mutations in any of the genes involved in prostaglandin …