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Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

Lower SMAD2/3 activation predicts more severe skin cancer.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

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

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Slug is crucial for skin health, hair growth, and healing.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Cathepsin L is essential for normal hair growth and development.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

CDP is crucial for lung and hair follicle cell development.

Sostdc1 controls the size and number of hair and mammary gland structures.

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The SULT1A1 enzyme booster improves minoxidil effectiveness in treating hair loss, especially in females.

Enzyme booster SULT1A1 greatly enhances hair regrowth with minoxidil.

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

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Superoxide dismutases help balance cell stress and may aid cancer treatment.

The PP2A-B55α protein is essential for brain and skin development in embryos.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Suplatast tosilate successfully treated a woman's systemic sclerosis symptoms.

ARTS helps stop tumors by promoting cell death.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.