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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

New mutations in the hairless gene may cause hair loss and affect bone development.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A genetic variant linked to hair thinning in Japanese women was found.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Nested PCR can reliably identify fungal infections when traditional methods fail.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Traumatic alopecia causes hair loss from pulling or rubbing, leading to broken hairs and changes in the scalp.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

A man had rare skin tumors with bone formation and cholesterol deposits.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The study found potential new DNA patterns in fertility genes, but further testing is needed.