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

Plucked hair follicles can help diagnose scalp lupus.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A new DSG4 gene mutation causes hair defects in a young girl.

Autoimmune reactions may cause both alopecia areata and HAM.

Hsc70 protein may influence hair growth by responding to androgens.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A specific gene variant may increase the risk of developing Alopecia Areata.

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

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The 2012 criteria are better for diagnosing atypical lupus cases.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

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

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

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

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

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

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.