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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Certain genes control the color of human hair by affecting pigment production.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

Matrix changes and increased MMPs contribute to skin inflammation in hidradenitis suppurativa.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

The study found nine new hair protein genes in human hair follicles.

Boosting HGF signaling could improve the creation of hair follicles in lab-made skin.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

A peptide from hair follicle stem cells can boost hair growth.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

The PML protein helps prevent skin cancer in mice.

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

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Hairless USP mice have enlarged skin cysts as they age.

Thymic stromal lymphopoietin (TSLP) promotes hair growth by stimulating specific skin cells.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Specific keratin gene mutations can cause monilethrix.

A mouse gene mutation increases the risk of skin cancer.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Artemis protein may help control hair growth and health by influencing cell processes.