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The fuzzy gene is crucial for controlling hair growth cycles.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

Removing SIX1 in fat cells reduces skin fibrosis.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

SIRT7 protein is crucial for starting hair growth in mice.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A mutation in the Sgkl gene causes defective hair growth in mice.

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

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Id2 gene helps keep hair follicle stem cells inactive.

A new DSG4 gene mutation causes hair defects in a young girl.

A new gene mutation causes insulin resistance in a girl and her mother.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.