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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

BRG1 is essential for skin cells to move and heal wounds properly.

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 ST14 gene causes a rare skin and hair disorder in a specific family.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

HB24 helps convert IBA to IAA, promoting root hair growth.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

CARASIL can cause different symptoms even with the same genetic mutation.

Certain DNA regions in alpacas are linked to fiber diameter.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

The research identified specific genes that are active in the cells crucial for hair growth.

Genes linked to wool fineness in sheep have been identified.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

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

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

A truncated protein linked to breast cancer may change cell adhesion.

Cantú syndrome may be linked to pituitary adenomas.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.