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Blocking certain proteins can reduce skin inflammation caused by cancer treatment.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

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

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

Targeting thyroid hormone receptor α in liver cells may help treat liver fibrosis.

Different keratins have unique expression patterns in mouse skin cells.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

NFIB and STAT5 work together to control specific genetic programs in cells.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

TSH influences keratin expression in human hair follicles.

Treg cells help repair and regenerate tissues by interacting with local cells.

LGD1069 effectively prevents breast tumors in mice without toxicity.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

New treatments may restore cancer-blocking proteins, slow prostate cancer, identify drug targets, and potentially regrow hair.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Testosterone changes how certain channels work in male rat reproductive tracts, affecting fertility-related fluid balance.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

TYK2 inhibitors show promise for treating cancer and autoimmune disorders.

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