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Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Tph cells are linked to the severity of systemic lupus erythematosus.

Thyrotropin-Releasing Hormone helps heal wounds in frog and human skin.

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

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

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

Whn is crucial for hair growth in certain areas by controlling a specific gene.

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

COVID-toes show a unique immune response over time, different from vaccine-related chilblains.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

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

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Human skin cells can respond to thyroid-stimulating hormone, affecting hair and skin health.

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

Whn is essential for hair growth, and its malfunction causes hair loss.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

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

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.