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A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Different PADI isoforms help cells develop diverse functions.

Progerin affects cell shape but not hair or skin in mice.

Mutations in the KRT85 gene cause hair and nail problems.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Different skin cells produce unique materials, which can improve skin substitutes for healing.

HB24 helps convert IBA to IAA, promoting root hair growth.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

A woman with frontal fibrosing alopecia experienced unusual hair growth after using a specific topical lotion.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Excessive sun protection might contribute to frontal fibrosing alopecia.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Four new FGF5 gene variants cause long hair in dogs.

Antiandrogenic drugs could be a good treatment option for frontal fibrosing alopecia.

Carbamates may help treat androgen-dependent conditions by changing how certain lipid enzymes are produced.

Gefitinib treatment led to unexpected hair growth in two lung cancer patients.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Editing the FGF5 gene in sheep increases fine wool growth.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

These hair loss conditions might be part of a spectrum, not separate issues.

Human hair follicles have a unique way of using energy and might use the Cori cycle; blocking CCR5 could help treat hair loss.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Blocking α1-integrin makes adult fibroblasts more like foetal ones, improving their movement and aiding wound healing.

Hair follicles can be used to study gene expression and understand conditions like COPD.

Higher FABP4 levels may help diagnose androgenetic alopecia early.