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PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

CEC levels may be a useful marker for predicting prostate cancer progression.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

SQSTM1 is linked to increased risk of alopecia areata.

Touch dome keratinocytes in adult skin have traits of different skin cell types.

Steroid sulfatase in hair follicles may be a target for treating hair loss.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

SOCS3 treatment can prevent hair loss by stopping harmful immune responses.

TEDAR is crucial for skin cell differentiation and barrier formation.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Sertoli cell transplants can reduce inflammation and improve sperm quality.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Combining FTSC with TSN6 peptide greatly improves wound healing.

Granulation tissue-derived cells can aid wound healing and serve as an alternative source of stem cells for tissue repair.

CD200 is not a reliable marker for identifying stem cells in all skin types.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

CTP-543 is generally safe for treating alopecia areata.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Strontium can effectively reduce skin irritation and inflammation.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.