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

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

PDGFC gene may help select goats with desirable curly wool traits.

Progesterone and allopregnanolone increase glycine release in rat brain cells.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

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

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A specific gene mutation causes a severe skin disorder in a family.

Longer CAG repeats in gene linked to more severe hair loss in females.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.