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Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Amotosalen-treated donor T-cells can prevent late CMV infection after bone marrow transplants.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

The new aptamer TAGX-0003 shows promise as an effective treatment for hair loss disorder alopecia areata.

HPV8 E6 gene causes growth of certain skin stem cells.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

MsPG3 protein gathers at root hair tips, aiding growth.

Gene variations may increase oxidative stress in male pattern baldness.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

Spt4 and Spt6 are essential for fat cell development.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

Disabling the FGF5 gene in sheep leads to longer wool.

UC.145 may be a new biomarker for predicting gastric cancer.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Increasing SSAT makes skin more prone to cancer.

A gene mutation in Lama3 is linked to a common type of hair loss.

Glutamic acid helps increase hair growth in mice.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.