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Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Ephrin-A3 helps increase and speed up hair growth in baby mice.

Thyroid hormone receptor β1 is found in human hair follicles and helps them survive.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

A new gene, JMJD1C, may affect testosterone levels in men.

Trichotillomania may have a genetic link to psychiatric disorders.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

p63 controls Satb1 to help skin develop properly.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Sgk3 is essential for normal hair follicle growth and maintenance.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

YAP and TAZ are crucial for skin cell growth and repair.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Controlling Tslp can improve health in AEC syndrome patients.

Thyroid hormone (T3) may reverse gray hair by stimulating hair growth.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

TAZ boosts fat cell formation in goat stem cells by activating a specific signaling pathway.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A pathway helps maintain long telomeres in both stem and cancer cells.