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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

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

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

DNA analysis can help tailor alopecia treatment.

Hsc70 protein may influence hair growth by responding to androgens.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Keratin-associated proteins are crucial for hair strength and structure.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

OR2AT4 helps reduce aging and cell damage in human skin cells.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

HSPC016 gene is important for hair growth.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Five molecular elements identified as potential future targets for hair loss therapy.

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

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

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

The research aims to better understand hair follicle regulation and find new treatments for hair loss.