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Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

The research shows how certain drugs can form stable structures with polymers, which is important for making new pharmaceuticals.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The hair defect is due to abnormal inner root sheath keratinization.

Hair follicles and urine cell pellets are promising for transcriptome studies due to consistent quality and useful expression profiles.

Mitochondrial DNA from nails and hair can be effectively analyzed for forensic use.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Egfl6 is not needed for zebrafish face development.

Genes linked to wool fineness in sheep have been identified.

A fungal enzyme was used to make compounds more soluble, aiding drug discovery and crop protection.

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

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

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

Mutations in keratin genes cause cell fragility and various skin disorders.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.