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Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

H3K4me3 helps control RSPO3 to influence hair growth and development.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

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

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

Uncombable hair syndrome is linked to Zellweger syndrome.

RXRα is crucial for hair growth and skin cell function.

Different fish use the same genes to regrow teeth.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

A genetic variant in goats is linked to cashmere growth.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Integrin α6 helps identify different neural crest cell types in the skin.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.