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ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A specific gene mutation causes woolly hair and hair loss.

Increased PHGDH expression causes early melanin buildup in hair follicles.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Defective nuclear transport may cause gene expression changes in Progeria.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

FLCN helps control iron levels in cells.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

FGF22 helps hair follicle stem cells grow and develop.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Hex gene plays a crucial role in starting feather development in chick embryos.

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

A genetic marker linked to a type of hair loss was found in most patients studied.

Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

Egfl6 is not needed for zebrafish face development.

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

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.