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Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

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

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

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

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Certain gene variations increase the risk of alopecia areata in Koreans.

The 4C32 gene may help in mouse skin development and differentiation.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new mouse mutation causes skin and hair defects due to a gene change.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

CLE14 peptide promotes root hair growth in Arabidopsis.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

PADI4 enzyme slows down cell growth in developing hair follicles.