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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Dermal EZH2 controls skin cell development and hair growth in mice.

Dkk4 protein helps control how hair grows and its arrangement.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A mutant FERONIA gene affects root hair growth at high temperatures.

A mutation in the human hairless gene causes alopecia universalis.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

ILC1-like cells can cause alopecia areata by themselves.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Longer CAG repeats in gene linked to more severe hair loss in females.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Specific RNA patterns are linked to alopecia areata.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A new mutation in the HR gene causes hair loss in a specific family.

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

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Fatp4 is crucial for healthy skin development and function.

MC4R gene variants not linked to female hair loss.

No clear link between specific gene and hair loss in Mexican brothers.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Ruxolitinib helped a patient with alopecia areata regrow hair.