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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

A rabbit gene important for hair development was identified and detailed.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

IL-15 is key for T cell function and could help improve treatments for immune-related diseases.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

BMP receptor IA is essential for proper hair cell differentiation in mice.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Noncoding RNAs help determine cashmere quality in goats.

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

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Laser-capture microdissection effectively analyzes hair follicle microbiomes, revealing region-specific bacterial differences.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

LED-LLLT helps heal wounds, reduce pain, and regrow hair using specific light wavelengths.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.