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Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

CD98hc's role in skin health decreases with age.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

A new method can detect mutations in mice by observing changes in hair follicle cells.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Fraser's Dolphin can heal skin wounds with minimal scarring, unlike humans.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Restoring NAD⁺ may help with aging and chronic diseases, but more research is needed.

CDP is crucial for lung and hair follicle cell development.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

RIPK1 inhibitors might help prevent alopecia areata.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A new gene mutation linked to a skin condition was found in a Spanish family.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

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

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Goat skin adapts to seasonal changes through genes that respond to daylight length, affecting hormone levels and potentially making skin cells light-sensitive.