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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

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

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Hair follicles protect melanocytes from sun damage, helping them replenish skin.

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

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A specific gene mutation causes woolly hair and hair loss.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Understanding normal hair follicle development helps analyze abnormalities in mutant mice.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

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

FGF13 gene changes cause excessive hair growth in a rare condition.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.