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Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

TCDD changes skin cell growth and keratin production in mice.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

Phospholipase C-δ1 is crucial for normal hair development.

A mutation in the Sgkl gene causes defective hair growth in mice.

CD8+ T cells are involved in alopecia areata and may cause disease relapse.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

FoxN1 overexpression in young mice harms immune cell and skin development.

Lower TGFß1 levels help stem cells become beige fat cells.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

TCDD reduces EGF receptors in the liver, affecting growth and development.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

TGM3 is important for skin and hair structure and may help diagnose cancer.

Activated ras can protect kidney cells from a certain substance that causes cell death.

CT60 polymorphism might increase the risk of Alopecia Areata.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

KRT72 gene helps form hair.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.