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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A mutant FERONIA gene affects root hair growth at high temperatures.

AP-2α and AP-2β are crucial for healthy skin and hair.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A truncated protein linked to breast cancer may change cell adhesion.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Rac1 is essential for proper hair structure and color.

A specific genetic deletion in goats affects cashmere yield and thickness.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The goat hair keratin gene is very similar to sheep's and is strongly expressed in goat hair follicles.

Mice without certain skin proteins had abnormal skin and hair development.