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A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

AKR1C3 could be a treatment target for metabolic issues in PCOS.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Genetic marker rs12558842 strongly linked to male hair loss.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Certain genes are linked to the risk of developing Alopecia Areata.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Mutations in the KRT16 gene can cause skin and nail disorders.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

FLCN helps control iron levels in cells.

The fuzzy gene is crucial for controlling hair growth cycles.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

BMP receptor IA is essential for proper hair cell differentiation in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Overexpression of ALK2 in hair follicles disrupts skin development and slows wound healing.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.