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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Stem cell niche exit in C. elegans is influenced by Sh1 cell membrane protrusions.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

The Foxn1 gene is essential for normal nail and hair development.

Human thymus has stem cells that can self-renew and maintain their identity.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Monilethrix is linked to a gene cluster on chromosome 12.

sPLA2-X is crucial for normal hair growth and follicle health.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Neutrophils are important for causing chronic itch in atopic dermatitis, and blocking the CXCR3 receptor may reduce this itch.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Gene expression affects fur development in rex rabbits.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

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

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

Janus kinase inhibitors may help treat cutaneous T-cell lymphoma, but more research is needed.

EH-MSCs may help treat hair loss by reducing inflammation.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

CCC1 is essential for pH balance and normal cell function in plants.

Fatty acid transport protein 4 is essential for skin and hair development.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Krox20 is crucial for hair growth and maintaining skin stem cells.

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

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.