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Glioblastoma cells can make androgens, which might help the tumor grow.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

A gene mutation in mice causes permanent hair loss and skin issues.

Certain genes control the color of human hair by affecting pigment production.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

IL-18 signaling helps mature Tregs move into the thymus.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Interleukin-1 increases keratin K6 production in skin cells.

The hr gene is linked to hair loss in Valle del Belice sheep.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

Genes linked to coat color and fiber length in Chinese goats were identified.

KRT72 gene helps form hair.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

GLI2 increases follistatin production in human skin cells.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.