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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

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

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

Researchers found a new mutation causing total hair loss from birth.

A gene variation is linked to hair thickness in Asians.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

MPA increases cancer spread by boosting Eph A2 activity.

CXCR2 in skin cells promotes tumor growth.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.