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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

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

A new mutation in mice causes crooked whiskers and messy hair.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

A specific gene change in APCDD1 increases the risk of hair loss.

EGFR inhibitors can cause unusual localized hair growth.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Circ 0020938 slows down hair growth in cashmere goats.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

EZH2 is crucial for uterine gland development and female fertility.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

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

GhDET2 is crucial for cotton fiber growth.

Mutations in specific genes cause different types of ectodermal dysplasias.

A gene mutation in mice causes permanent hair loss and skin issues.

A young cat had a rare fungal infection caused by Microsporum gypseum.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Mice hair follicles take in the amino acid cystine.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Mutations in the HOXC13 gene cause hair and nail development issues.