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SIPHL1 from tomato enhances plants' response to low phosphate levels.

Lack of functional CYLD in mice leads to early aging and cancer.

miR-200c-3p could help diagnose and treat alopecia areata.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The study identified key immune cell differences between mild and severe alopecia areata.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

miR-144 affects hair growth by interacting with Lhx2.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Hair follicle stem cells need all reprogramming factors to become pluripotent.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Grape seed extract may safely and effectively help prevent lung cancer.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Prolactin affects when mice shed and grow hair.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

RCS-01 cell therapy is safe and improves skin gene expression.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

RhoA helps skin stem cells grow, aiding wound healing.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

PCOS involves immune and genetic factors, with key roles for T cells and specific genes.