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E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

BBS7 is essential for healthy gums and teeth by supporting cell function and blood flow.

KRT72 gene helps form hair.

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

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

cDermo-1 causes dense skin, feathers, and scales in chickens.

ILC1-like cells can cause alopecia areata by themselves.

Mouse skin cells can become sperm-like cells in the lab.

Hair follicle stem cells in cashmere goats show different gene activity during hair growth phases.

Certain gene variations may increase the risk of PCOS in South Indian women.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

Masculinization in affected individuals occurs gradually after puberty due to hormone changes.

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

PCOS is influenced by both genes and environment, but its exact genetic cause is still unclear.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Rat dermal papilla cells have unique genes crucial for hair growth.

Mutations in the hairless protein gene cause hair loss.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Lhx2 helps retinal cells respond to signals for eye development.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.