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MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A new gene mutation causes long hair in some Maine Coon cats.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Researchers found a genetic region that influences the number of coat layers in dogs.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Researchers found a gene mutation responsible for a rare hair loss condition.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Circ 0020938 slows down hair growth in cashmere goats.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Methylation in specific gene region causes finasteride resistance in some BPH patients.