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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Two specific genes are more active during hair growth in mice.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The Enterobacter isolate AMS1-S8 is effective for removing selenium from wastewater.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

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

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Reducing SOX2 in colorectal cancer cells decreases tumor growth and self-renewal.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

ARTS helps stop tumors by promoting cell death.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A specific gene mutation causes Olmsted syndrome.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

AQB reduces harmful skin changes in systemic sclerosis.