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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

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

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

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Vinblastine and its metabolites may cause nausea and hair loss by binding to specific receptors and could lead to better chemotherapy drugs with fewer side effects.

VEGF165 influences hair follicle cell growth and movement through VEGFR-2 activation.

LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Aminoguanidine increases a specific growth signal in stored hair grafts, which may help them survive better after being transplanted.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Overexpressing AVP1 and AtNHX1 in plants improves salt tolerance and root hair development.

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

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.