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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

New pyridine compounds effectively inhibit GSK3, a diabetes treatment target.

Mutations in the DSG4 gene cause specific hair and scalp issues.

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

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

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

γδ T cells adapt uniquely to different tissues in mice.

Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Targeting NETs may help reduce fibrosis in Crohn's disease.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Basement membrane changes are crucial for hair follicle development.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

PADI4 enzyme slows down cell growth in developing hair follicles.

Laminin-511 is essential for proper melanocyte movement and development in mice.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A new mouse mutation causes skin and hair defects due to a gene change.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

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

QLT0267 stops hair follicle cell growth and movement.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

Smad4 is crucial for muscle repair, especially in aging, by promoting cell growth over differentiation.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.