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

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

The Itpr3 gene causes a specific hair pattern in mice.

The WIF1 gene is crucial for hair growth in Angora rabbits.

The enzyme from human skin can cross-link proteins and needs calcium to work.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

A specific gene variant may increase the risk of developing Alopecia Areata.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

Phospholipids help plant proteins move by regulating receptor interactions.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Patched1 helps prevent tumors by controlling cell growth.

Specific gene variants affect wool traits in Chinese Tan sheep.

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

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

SQSTM1 is linked to increased risk of alopecia areata.

A new gene mutation is linked to monilethrix in the studied family.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

New genetic mutations causing hair loss were found in a Chinese family.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

CDP is crucial for lung and hair follicle cell development.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Björnstad syndrome causes twisted hair from birth.