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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

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

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Lipase H is important for hair follicle function and shaping hair fibers.

Dlx3 is essential for hair growth and regeneration.

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

lncRNAs may regulate hair follicle development in Hu sheep.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Different keratins have unique expression patterns in mouse skin cells.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

Mutations in the HOXC13 gene cause hair and nail development issues.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

ELF5 is essential for skin cell growth and maintenance.

A specific gene mutation causes congenital hair loss.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A specific gene mutation causes sparse, brittle hair in a family.

The goat hair keratin gene is very similar to sheep's and is strongly expressed in goat hair follicles.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

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

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

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Lateral plate mesoderm helps create skin and amnion-like tissues for studying development and therapies.

Sostdc1 controls the size and number of hair and mammary gland structures.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A unique gene mutation was found in a family with monilethrix.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.