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Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Small molecules can help turn skin cells into sweat gland-like cells for potential skin repair.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Two new gene clusters important for hair formation were found on human chromosome 11.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

The new wound dressing improves healing and tissue repair better than conventional dressings.

A new microneedle patch helps repair spinal cord injuries by reducing scarring and promoting nerve growth.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Rac1 is essential for proper hair structure and color.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Stem cells improve nerve repair by enhancing blood vessel growth.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

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

Aging in one type of stem cell can cause aging-like changes in various organs.

Two new gene clusters important for hair formation were found on human chromosome 11.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

The chitosan-peptide system helps cartilage regeneration using fat-derived cells.

3D culture better preserves sweat gland cell identity than 2D culture.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

The composite sponge helps heal diabetic wounds by reducing inflammation and promoting new blood vessel growth.

High S100A4 levels worsen glioblastoma by promoting blood vessel growth.