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A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A specific gene mutation causes woolly hair and hair loss.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The new synthetic retinoid RO 13-6298 effectively treated severe psoriasis at low doses with manageable side effects.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

DA-9401 protects against hair loss, improves organ function, and prevents infertility caused by finasteride.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

5-ARI therapy may help prevent prostate cancer progression.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

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DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

ADF8 and ADF11 help root hairs grow longer at high pH.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Human keratinocytes do not naturally respond to androgens.

No significant link was found between the studied genes and female hair loss in the Polish population.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.