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The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

PDCD4 is important for controlling skin cell growth and healing.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

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

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Early diagnosis and treatment of congenital adrenal hyperplasia are crucial to manage symptoms and prevent complications.

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

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Researchers found genes that affect hair growth in Yangtze River Delta white goats.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

hHbl gene is active in hair shaft cells and some pilomatricomas.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.