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Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

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

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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

Mice can regenerate ear tissue without the p53 protein.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Dkk4 protein helps control how hair grows and its arrangement.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Keratin hydrogel improves nerve regeneration and motor recovery.