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A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

LHX2, with other markers, can identify hair placodes in rats.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Nerve growth factor helps cashmere goat hair cells grow by activating a specific protein.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A specific genetic deletion in goats affects cashmere yield and thickness.

NFIC helps human dental stem cells grow and become tooth-like cells.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

Defective protein folding due to a mutation is key in ANE syndrome.

NIPP1 is important for healthy skin and could help treat skin inflammation.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

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

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

XEDAR triggers a specific signaling pathway in cells.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.