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Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

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

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

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

Chinese fine-wool sheep have genetic variations linked to traits like milk and health, with some genes under strong selection.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

A new genetic mutation was found causing hair and eye issues in a boy.

TCHHL1 is a protein important for hair growth, found in hair follicles.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Neutrophils quickly move to the site of skin injury.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.