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The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Family members have similar hair protein patterns, which could be useful for genetic studies.

Polish doctors find performance-enhancing substances unethical and want more knowledge to combat doping in sports.

Epristeride's metabolism in zebrafish helps improve doping detection methods.

The combination therapy is effective and well-tolerated for treating esophageal cancer.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

EISA uses enzymes to create precise nanostructures in cells, offering new ways to design adaptive materials and therapies.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

The new SIS-PEG sponge is a promising material for skin regeneration and hair growth.

Lack of KSR1 stops certain skin tumors in mice.

The gel effectively delivers EGCG through the skin, improving its absorption.

Balancing lipophilicity and solubility is key for effective and safe ketorolac prodrugs.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

The new gel for psoriasis is effective, stable, and easy to apply.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

Kanglaite injection with chemotherapy improves treatment and reduces side effects for advanced lung cancer.

A patient with a rare form of lupus improved after treatment for skin ulcers and hair loss on the face and scalp.