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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A vitamin D receptor mutation causes rickets and affects immune responses.

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

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

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

c-Kit is important for heart regeneration and cancer development.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.