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Higher CRHR1 levels in AA patients lead to increased inflammation.

The gene Prss53 affects hair shape and bone development in rabbits.

CRF can cause hair loss, but blocking its receptors might prevent this.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

CXCR2 in skin cells promotes tumor growth.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

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

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The Celsr1 gene is crucial for normal hair patterning in mice.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

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

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Copper supplements during pregnancy improve survival and development in mutant mice.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

FLCN helps control iron levels in cells.

Researchers found a new mutation causing total hair loss from birth.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

CRH promotes fat production in skin cells, affecting conditions like acne.