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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

FOL-005 peptide may help treat excessive hair growth safely.

Mutations in the SNRPE gene cause hereditary hair loss.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

Krtap11-1 is important for hair strength and structure.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

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.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

CTIP2 may help in skin development and maintenance.

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

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

Osteopontin may help hair follicle growth during the catagen phase.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

CD2 might be a new treatment target for patchy alopecia areata.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

People with alopecia areata have higher levels of osteopontin, which might be important in the disease's development, but this doesn't relate to how severe the disease is.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

LncRNA RP11-818O24.3 may help treat hair loss by boosting hair follicle stem cell growth and differentiation.

Mutations in hKAP1 genes may cause hereditary hair disorders.

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

New biological pathways and potential treatment targets for male pattern baldness were identified.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Deleting part of a gene in mice causes wavy hair and high pup loss.