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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Disrupted stem cell signals in hairpoor mice cause hair loss.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

The study found that specific proteins are markers of hair follicle development in human fetuses.

The research found specific genes and pathways that control fur development and color in young American minks.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

New methods to test hair growth treatments have been developed.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

More research is needed to understand how testosterone is maintained in adult males.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Certain gene variations are linked to the thickness of cashmere goat hair.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Six genetic conditions are often linked to complete scalp hair loss in children.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.