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Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Pangenome analysis reveals key genes for pig adaptation and traits, aiding genetic improvement.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

FGF13 gene changes cause excessive hair growth in a rare condition.

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

KRT72 gene helps form hair.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The K14 promoter is more active in skin cells than the K5 promoter.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.