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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Hoxc genes control hair growth through Wnt signaling.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

PCOS involves genetic and immune factors, especially T cells, affecting its development.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

HSPC016 gene is important for hair growth.

Certain gene variations are found in people with polycystic ovary syndrome.

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.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

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

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A missing mK6irs1 gene causes hair loss in mice.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Armadillo Repeat Only proteins are essential for proper plant growth and response by regulating calcium channels.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

UTX is crucial for skin differentiation and health, especially in females.