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Keratinocytes help keep hair follicle cells and skin cells separate in 3D cultures, which is important for hair growth research.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Genomic approach finds new possible treatments for hair loss.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Different combinations of human hair keratins affect how hair fibers form.

A 72-year-old man had severe fatigue, weight loss, and frequent loose stools.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

ILK and ELMO2 help cells move and stick together, important for wound healing and hair growth.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Lower growth factors linked to balding in androgenetic alopecia.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Mutation in hairless gene may increase hair loss risk.

LLLT helps treat hair loss by increasing blood flow, reducing inflammation, and stimulating growth factors.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Hair loss in children is diagnosed and treated differently than in adults, with different common causes and a focus on less invasive methods.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

No genetic link between prostaglandins and hair loss found.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Acitretin helped improve hand mobility and skin condition in a patient.

Pregnancy can cause unique skin issues, some of which may risk the mother and baby's health and need careful treatment.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.