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Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

Trichothiodystrophy causes unusual hair and developmental issues.

Thiazole, a sulfur and nitrogen chemical, is useful in creating potential drugs for conditions like seizures, cancer, bacterial infections, tuberculosis, inflammation, malaria, viruses, Alzheimer's, diabetes, and A1-receptor issues.

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

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

A new, efficient method creates sulfinimidate esters from sulfenamides and alcohols without metals.

A genetic hair protein variant is more common in Japanese people and is inherited.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Sphynx cats have abnormal hair follicles and keratinization affecting their skin.

Cystaselenonine causes temporary hair loss in mice by interfering with hair growth.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

Cutaneous keratocyst and steatocystoma should be called "sebaceous duct cyst" due to their similarities.

Skin cysts might help advance stem cell treatments to repair skin.

Hairless USP mice have enlarged skin cysts as they age.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Researchers developed a method to identify and analyze cyclosporin compounds and their structures effectively.

Cubosomes enhance antimicrobial peptide stability and effectiveness.

Excessive iodine from a cystic fibrosis supplement can cause hypothyroidism.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Cathepsin L deficiency causes hair and skin issues in mice.

Lack of functional CYLD in mice leads to early aging and cancer.