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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

HAP-cell-sheets improved wound healing in diabetic mice.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

Children with partial biotinidase deficiency are healthy at birth but may develop symptoms that improve with biotin therapy.

CD44 signaling can help heal wounds without scars.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Different keratins have unique expression patterns in mouse skin cells.

The new sprayable wound mask helps heal wounds without scars.

PDGF signaling is crucial for cell development, wound healing, and fluid regulation in the body.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Higher levels of the DP2 receptor may lead to hair loss.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Early diagnosis and treatment of biotinidase deficiency are crucial to prevent vision problems.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Mutations in specific genes cause different types of ectodermal dysplasias.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

HNG helps hair grow by keeping hair in the growth phase longer.

p63 is essential for activating and differentiating stem cells in the nose's olfactory tissue.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.