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The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Forsythiaside A helps protect cells and liver from damage by reducing oxidative stress and boosting antioxidants.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

Sorafenib may cause hand-foot and stump syndrome, requiring early detection and management.

Finasteride helps female-pattern hair loss.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

The gene Prss53 affects hair shape and bone development in rabbits.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Rat hair follicle stem cells can improve nerve repair and muscle function after injury.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Certain microRNAs might help identify and understand Frontal Fibrosing Alopecia.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.