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

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

WWP2 is crucial for tooth development in mice.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A specific gene mutation causes severe skin and nail issues and hair loss.

YAP1 is important for skin regeneration and may affect skin disorder treatments.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

Id2 gene helps keep hair follicle stem cells inactive.

Runx1 is crucial for proper hair structure and development.

PBX1 helps reduce aging and cell death in hair follicle stem cells by decreasing DNA damage, not by improving DNA repair.

A rare gene variant causes hair and nail issues in a family.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Gene linked to common hair loss found, may lead to new treatments.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

Reducing Zyxin may help treat hair loss.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

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