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Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

The new criteria for classifying lupus are more accurate and comprehensive.

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.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

pCLCA2 protein may help maintain skin structure and function.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

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

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Lower levels of MYLK and CALD1 in bladder cancer and osteosarcoma are linked to worse survival rates.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

Lack of functional CYLD in mice leads to early aging and cancer.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Dlx3 is essential for hair growth and regeneration.

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

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

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