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PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

A mutation in the Sgkl gene causes defective hair growth in mice.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Lhx2 helps retinal cells respond to signals for eye development.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

Keratin gene regulation is similar across mammals, affecting hair follicle differentiation.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Researchers found a non-functional sheep keratin gene due to mutations.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

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

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

MEF2C is crucial for normal hair cycle progression.

CHI3L1 and CXCL5 proteins help promote hair growth.

Overexpression of certain genes can shorten hair by disrupting the hair-growth cycle.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

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

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.