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The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Specific gene variants affect wool traits in Chinese Tan sheep.

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

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

FGF13 gene changes cause excessive hair growth in a rare condition.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

Male hormones control a specific gene in hamster skin, with different hormones having varying effects.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

Hex gene plays a crucial role in starting feather development in chick embryos.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The assay effectively detects hormonal activity of certain chemicals.

Hordenine may help hair grow by activating a specific cell growth pathway.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

MPZL3 protein is important for controlling hair growth cycles.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

Collagen XXII is a marker for tissue junctions, aiding in structural integrity and found in muscles, heart, skin, and arthritic joints.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

The patient's high testosterone was reduced by a medication that suppresses gonadotropin.

Mutations in the SNRPE gene cause hereditary hair loss.