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A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Certain leukemia drugs can cause severe skin reactions that may require stopping treatment.

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

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

The Gsdma3 gene is essential for normal hair development in mice.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

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

High levels of ERK activity are key for tissue regeneration in spiny mice, and activating ERK can potentially redirect scar-forming healing towards regenerative healing in mammals.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Folate receptor β helps suppress the immune system in macrophages and affects cancer growth and hair health.

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

miR-325-3p can slow down brain tumor growth by targeting FOXM1.

Stat3 affects skin cancer development by altering keratinocyte stem cell behavior.

Ritlecitinib reduces alopecia areata symptoms by blocking JAK3/TEC signaling and T-cell activity.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Trichoscopy can help diagnose and decide when to biopsy folliculotropic mycosis fungoides.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

High testosterone levels can harm fertility by disrupting the LIF signaling pathway in the uterus.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

A mutant FERONIA gene affects root hair growth at high temperatures.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.