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PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A specific gene mutation causes a severe skin disorder in a family.

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

CDH3-related disease causes worsening eye and hair issues.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

ARHGEF3 is essential for proper hair follicle development in mice.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

A girl had rickets due to a gene mutation affecting vitamin D response.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Researchers found a genetic region that influences the number of coat layers in dogs.

CCC1 is essential for ion balance and proper plant cell function.