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Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

Cabergoline helped a boy with Cushing disease get better after surgery and radiotherapy didn't work.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

Adding a second method to PROTACs could improve cancer treatment.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

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

Skin cancer often starts from Lgr5+ progenitor cells.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

p2y5, now called LPA6, is a receptor important for human hair growth.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Cinnamomi cortex may help treat prostate enlargement by reducing related proteins.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

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

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Eating phenylthiocarbamide made all the rats' hair go gray, but some returned to their original color after stopping.