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Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

High-dose iron therapy improves anemia without affecting IBD treatment.

Mice with CBS deficiency are healthier on a low-methionine diet.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

A new mouse mutation causes skin and hair defects due to a gene change.

Finasteride increases CD8+ T cells in BPH tissues.

A new engineered treatment shows promise in curing heart fibrosis.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

High glucocorticoids cause pancreatic malfunction and malabsorption, reversible with enzyme supplements.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A form of vitamin E promotes hair growth by activating a specific skin pathway.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

Finasteride may cause floppy-iris syndrome during cataract surgery, so check patients' medical history.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Co-trimoxazole may help treat autoimmune diseases.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

A new gene mutation causes a rare type of hair loss.

CFx-δ2 from stem cells helps heal burn wounds faster.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.