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

Hair loss in androgenic alopecia patients is linked to changes in certain genes that control cell growth and death.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Both HLA-B and MICA are independently linked to alopecia areata.

ILC1-like cells can independently cause alopecia areata by affecting hair follicles.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

ILC1-like cells can independently cause alopecia areata.

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Beard alopecia areata causes patchy beard hair loss, often treatable with janus kinase inhibitors.

Permanent hair loss after bone marrow transplant can be caused by chemotherapy or chronic graft-versus-host disease.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

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

A new therapy for a skin blistering condition has not been developed yet.

Mutations in the LIPH gene cause woolly hair in a child.