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Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Biotinidase deficiency can mimic neuromyelitis optica and should be considered for accurate diagnosis and treatment.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Sonidegib often causes hair loss, and LC-OCT helps identify early signs.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

Anti-DFS70 antibodies can help identify nonsystemic autoimmune conditions in SLE patients.

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

JAK inhibitors can be safely used in alopecia areata patients with latent hepatitis B or tuberculosis, with proper monitoring.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Inhibiting HSP90 increases cell adaptability and survival under stress.

A human serum-enriched medium effectively supports melanocyte growth and activity without using animal-derived supplements.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

The hydrogel dressing effectively treats infected wounds by combining infection control and tissue regeneration.

Cyclohexyl salicylate may help hair growth and treat hair loss.

Hair growth genes work better with more glucose due to changes in gene-regulating markers.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Hair glycation can indicate long-term blood sugar levels and diabetic nerve issues.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

GLABRA2 represses root hair formation by inhibiting a specific gene.