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A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

PADI4 enzyme slows down cell growth in developing hair follicles.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

A new gene mutation causes a rare type of hair loss.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

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

New genes linked to male pattern baldness were found on chromosome 20p11.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.