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AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The hr gene is linked to hair loss in Valle del Belice sheep.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

MCHR2 gene duplications may be linked to alopecia areata.

AKR1C enzymes in scalp glands decrease with age, possibly affecting hair loss.

A mutation in the KRTHB5 gene causes hair and nail issues.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

EDA2R gene linked to hair loss.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

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

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

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

A new mouse mutation causes skin and hair defects due to a gene change.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Certain gene variations increase the risk of alopecia areata in Koreans.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Farudodstat can prevent hair follicle immune damage linked to alopecia areata.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

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