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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Scientists discovered two versions of a new human hair keratin gene.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

p120-catenin helps control skin inflammation by regulating cadherin levels.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

CCCA can affect both genders and all ages, and it has a genetic component.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

Whn is essential for hair growth, and its malfunction causes hair loss.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

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

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.