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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Normal skin results from interactions between EGF and the Tabby mutation.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

TPA is about 50 times more effective at promoting tumors than MZ.

Transglutaminase-3 is often reduced in esophageal cancer.

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

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Ets2 gene is crucial for placental development in mice.

FOXN1 gene variants cause low T cells and immune issues from birth.

The Itpr3 gene causes a specific hair pattern in mice.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

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

Meis1 is crucial for skin health and tumor development.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

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

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

Tissue-resident memory T cells can protect against infections and cancer but may also contribute to autoimmune diseases.

High TSPEAR levels in colorectal cancer predict worse outcomes.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

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

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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