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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Two genetic variations in Moa buffalo help them adapt to heat.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

CT60 polymorphism might increase the risk of Alopecia Areata.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

The rs1128977 gene variant may affect cholesterol and body measurements.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

A KRT32 gene variant causes loose anagen hair syndrome.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Gene differences affect finasteride side effects in men with hair loss.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Nucleophilic reagents break down hair keratin, forming more lanthionine and lysinoalanine than in wool.

CAG repeat numbers in the AR gene likely don't affect hair loss in Korean men.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

A new gene mutation causes a rare type of hair loss.

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

Ptprq has multiple forms that change during inner ear development.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A specific gene mutation causes congenital hair loss.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.