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PDRN may reduce inflammation and complications in revision rhinoplasty for patients with high fibrinogen levels.

Low prolactin in young women may increase heart and metabolism risks.

Proxalutamide improved blood markers related to inflammation, immune response, and clotting in COVID-19 patients, potentially reducing hospitalizations.

3D bioprinting shows promise for creating skin substitutes, but standardized methods are needed for clinical use.

Most severe COVID-19 patients in Mexico experienced long-lasting symptoms that worsened their quality of life.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

People with blood group O may have a higher risk of developing post-COVID-19 syndrome.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

The buffy coat method yields higher TGF-β1 levels in PRP, especially in males.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Recombinant human hair keratin proteins can effectively stop bleeding.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Compound 6 is a promising candidate for better wound healing.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.