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Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

A new gene mutation causes insulin resistance in a girl and her mother.

Abrocitinib significantly improved hair regrowth in adolescents with alopecia areata without serious safety issues.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

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

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

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

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Alopecia areata patients have lower SOX9 and CD34 levels, affecting hair growth.

Mutations in specific llama genes may affect fiber quality for textiles.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Antibodies help identify glycoproteins in normal skin and tumor cells.

The algorithm accurately identified alopecia in women of childbearing age using claims data.

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

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

A man had bad reactions to a hair loss treatment called DNCB.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

Let-7b helps alpaca hair grow by reducing TGFβR I protein.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.