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TCDD changes skin cell growth and keratin production in mice.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

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

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The new assay can help develop products for hair re-growth.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Regulatory T cells help hair growth by using the Cxcr4-Cxcl12 pathway.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Patched1 helps prevent tumors by controlling cell growth.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.