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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

DNA phenotyping can predict physical traits like eye, hair, and skin color, improving forensic investigations.

Certain DNA regions in alpacas are linked to fiber diameter.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Gene variation affects prostate issues and hair loss.

Different long non-coding RNAs in yaks change during hair growth cycles and are involved in key growth pathways.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

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

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

RDW is a useful, cost-effective tool for diagnosing and monitoring various diseases.

Low-penetration genes might help personalize colorectal cancer prevention.

SFRP2 and PTGDS may be key factors in female hair loss.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

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

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

New genetic locations explain much of hair color variation in Europeans.

New biomarkers and potential treatments for skin diseases were identified.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

Rabbits with high wool production have more hair follicles, influenced by specific long noncoding RNAs.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.