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

Hoxc13 gene is essential for hair, nail, and papilla development.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

The enzyme from human skin can cross-link proteins and needs calcium to work.

New compounds with carborane showed anti-androgen effects similar to flutamide.

Dimeric peptide derivatives could help hair growth and treat hair loss safely.

Human hair follicles have their own thyroid hormone system.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Actin filaments help stabilize and reshape cell membranes.

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

A new compound effectively inhibits human 5α-reductase 1.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Monilethrix hair issues are due to problems in the hair's internodes.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Hair and wool strength is affected by the number and type of bonds in their protein structures, with hair having more protein aggregates than wool.

Balanced tension in skin is crucial for its structure and function.

Two siblings have a rare hair condition caused by a new genetic variant.

The document's conclusion cannot be provided because the document is not available or cannot be read.

New steroids were effective in blocking male hormone receptors in hamster prostates.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

Immunofluorescence tomography is a cost-effective method for creating detailed 3-D images of tissues.