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

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

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

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Tanshinone IIA helps protect tissue from low oxygen damage by activating certain cell pathways.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

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

AL136131.3 slows hair growth by affecting energy processes in hair loss.

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.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A new gene mutation linked to a skin condition was found in a Spanish family.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A specific mutation in PA-PLA1α causes abnormal hair growth.

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

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Nano-PROTACs could improve drug targeting and delivery by using nanotechnology.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.