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Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

Retinoic acid causes gland formation instead of hair in mouse skin by altering epidermal and dermal interactions.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

Certain genetic variations are linked to hair loss in Mexican men.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

Certain gene variations may increase the risk and severity of alopecia areata.

Damage to skin releases dsRNA, which activates TLR3 and helps in skin and hair follicle regeneration.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

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

The study provides exploratory findings on miRNA changes in female hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

PDRN, derived from salmon sperm, shows promise in healing wounds, reducing inflammation, and regenerating tissues, but more research is needed to understand its mechanisms and improve its use.

Certain microRNAs are important for sheep hair follicle development and could help improve wool quality.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A genetic variant in the KRT25 gene causes tightly curled hair.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

The research helps improve wool quality and aids human hair research.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Certain miRNAs play a key role in the growth of cashmere by affecting hair follicle development and regeneration.

Gene expression affects fur development in rex rabbits.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Certain circular RNAs help cashmere goats grow more hair.

Ionizable lipid nanoparticles are the best for delivering gene-editing therapies.