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A specific RNA can help hair growth in baldness by boosting stem cell activity.

A new gene mutation causes a rare type of hair loss.

YAP and TAZ proteins control skin cell growth and repair.

Imaging living plant cells shows dynamic changes in actin and endoplasmic reticulum linked to root hair growth.

Skin acetyl-CoA synthesis is crucial for overall lipid balance.

Microtubules help control the direction and stability of root hair growth in Arabidopsis thaliana.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

MYC protooncogenes may be important for hair growth, but more research is needed.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Understanding the APCDD1 gene can lead to new hair loss treatments.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

A 9-year-old boy had a rare scalp condition usually seen in young men.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Basonuclin is crucial for hair follicle development and cycling in mice.

Zinc supplementation effectively treats acrodermatitis enteropathica symptoms.

Expanded CD8+ T cells are linked to Alopecia Areata and may cause relapse after treatment.

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

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

Zinc therapy improved hair health in a girl with acrodermatitis enteropathica.

Defects in certain proteins cause major heart abnormalities during early development.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

The authors clarified data overlap and corrected a figure error, apologizing for any confusion.

Mutations in hKAP1 genes may cause hereditary hair disorders.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.