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A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

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

CDP is crucial for lung and hair follicle cell development.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

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

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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 gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

ILC1-like cells can cause alopecia areata by themselves.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A specific gene mutation causes a severe skin disorder in a family.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.