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Melatonin may treat rosacea and Alzheimer's by reducing inflammation and affecting blood vessel growth.

A specific genetic variation affects wool quality in sheep.

The protein's size was reduced, but more work is needed to confirm its function.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Cathepsin L is essential for normal hair growth and development.

A new mouse mutation causes skin and hair defects due to a gene change.

pCLCA2 protein may help maintain skin structure and function.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

A gene mutation in mice causes severe skin disorder similar to a human condition.

The LMNA mutation affects skin structure even in asymptomatic carriers.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

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.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

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