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Proteins influence the quality and traits of cashmere goat fleece, affecting hair strength and diameter.

The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

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

HSA nanoparticles can improve tamoxifen delivery for breast cancer treatment, reducing side effects.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

Exosomes from certain stem cells can fight hair loss by promoting hair growth and maintaining the growth phase of hair.

The study found key long non-coding RNAs involved in yak hair growth cycles.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

EAAT4 decreases with age, harming skin function and calcium balance.

Ebastine may promote hair regrowth by increasing cell growth through the ERK pathway.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Different genes are linked to various types of hair loss.

A KRT32 gene variant causes loose anagen hair syndrome.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Proteins from stem cells improved hair growth in patients with hair loss.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.