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ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

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

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Long noncoding RNAs help regulate hair follicle density in rabbits.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

lncRNAs significantly influence koi carp skin color.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

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

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Phospholipase A2 enzymes play key roles in skin health and disease.

FLRG and follistatin have different roles in wound healing.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The Wave complex controls skin growth by suppressing certain signals.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

Researchers found that certain RNA sequences play a role in yak hair growth and these sequences are somewhat similar to those in cashmere goats.

Trps1 plays a key role in hair follicle development and cycling.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Two new gene mutations cause a rare hair disorder.

Researchers found a gene mutation responsible for a rare hair loss condition.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.