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Hispanic patients in the USA have lower survival rates for melanoma compared to non-Hispanic Whites.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A new one-step test can quickly identify skin cancer during surgery.

Hair loss treatment caused more hair loss in a man.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

SLHA can be hard to diagnose and needs teamwork between specialists.

Removing the liver tumor improved the patient's skin condition and hair growth.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Alopecia areata may be caused by antibodies targeting specific hair follicle proteins, hindering hair growth.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Hairline-lowering surgery effectively reduces a high hairline with immediate, noticeable results.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Hair testing is crucial for forensic science and public health.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.