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The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

The HCR gene contributes to psoriasis risk.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Trps1 is essential for proper hair follicle development.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

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.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

A unique gene mutation was found in a family with monilethrix.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Ets2 gene is crucial for placental development in mice.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

BLMP-1 is important for regular molting and gene expression cycles in worms.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.