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Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Four new FGF5 gene variants cause long hair in dogs.

Mutations in the HOXC13 gene cause hair and nail development issues.

Skin-derived precursors in hair follicles come from different origins but function similarly.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Environmental factors affect reproductive traits by altering the SRD5A1 gene.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

CEC levels may be a useful marker for predicting prostate cancer progression.

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

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Different forms of FGF5 either promote or inhibit hair growth.

A new gene variant causes glucocorticoid resistance in a mother and son.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Different types of fibroblasts play specific roles in wound healing and cancer, which could help improve treatments.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Genetic predictions of baldness in Europeans don't apply well to African men.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

Not having enough cystatin M/E protein causes less hair growth and dry skin.