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Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

Some thymic peptides can increase human hair growth, while others may inhibit it.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Bendamustine combined with tucidinostat may effectively treat adult T-cell leukemia.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Hair loss gene linked to prostate issues.

Scientists made a mouse that can be made to lose hair and then grow it back.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

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

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

EGFR is essential for normal hair development and follicle differentiation.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Granulation tissue-derived cells can aid wound healing and serve as an alternative source of stem cells for tissue repair.