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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

The new topical growth hormone formula has high skin penetration and bioavailability.

The MEST method increases cell yield and volume for regenerative medicine but needs more testing.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

Higher STAT3 levels are found in hair loss areas, but not linked to hair loss severity.

Transglutaminase-3 is often reduced in esophageal cancer.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Stat3 is essential for hair growth and wound healing.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

EGFR helps hair follicles transition properly by controlling Stathmin levels.

The Itpr3 gene causes a specific hair pattern in mice.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Stat3 activation increases hair follicle progenitors but reduces bulge region stem cells.

Sub3 is essential for fungus adherence but not for skin invasion.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

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

Lower SMAD2/3 activation predicts more severe skin cancer.

A new compound was effective for imaging prostate cancer in rats.

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

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.