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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

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

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

A specific genetic deletion in goats affects cashmere yield and thickness.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

High S100A4 levels worsen glioblastoma by promoting blood vessel growth.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Low-level laser therapy can boost cell activity and energy production.

Nab-paclitaxel chemotherapy can rarely cause lupus-like skin issues.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

The new drug delivery system effectively targets lung cancer cells.

The treatment was ineffective in humans.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

LOYON® is a safe and effective way to reduce cradle cap in infants and children.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The new composite material is safe and has anticoagulant properties.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.