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A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Two mouse mutants have defective hair cuticle cross-linking.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

Hair amino acid levels can indicate metabolic disorders.

Copper supplements during pregnancy improve survival and development in mutant mice.

A new perming method is less damaging to hair and works as well as traditional methods.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Different keratins have unique expression patterns in mouse skin cells.

N-acetylcysteine may help treat trichotillomania.

Modified wheat protein in shampoo repairs and smooths damaged hair effectively.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Poly-γ-glutamic acid may help reduce hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A wide range of proteins are integrated into the skin's protective layer.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Lack of cystatin M/E causes thin hair and dry skin.

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