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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Mutations in hKAP1 genes may cause hereditary hair disorders.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

A specific gene mutation causes a severe skin disorder in a family.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

ELL is crucial for gene transcription related to skin cell growth.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

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.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.