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A special microbe helps plants absorb rock phosphate by growing on their root hairs.

A specific gene mutation causes congenital hair loss.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

A gene mutation causes woolly hair in a Syrian patient.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

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

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Lipases, especially gehB, are crucial for Staphylococcus aureus to enter and colonize hair follicles.

Rabbit skin analysis showed changes in hair growth and identified miRNAs that may regulate hair follicle development.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

BLMP-1 is important for regular molting and gene expression cycles in worms.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

FLCN helps control iron levels in cells.

The research mapped out the cell types and molecular processes involved in developing Cashmere goat hair follicles.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Chitosan slows root hair growth and causes a buildup of callose at low concentrations, but at high concentrations, it only inhibits growth without callose buildup.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

The research shows that skin cancer likely originates from hair follicles and that certain cell populations expand to promote skin cancer growth.

Hair analysis can somewhat track past testosterone levels but is influenced by factors like hair washing, growth rate, sex, and hair color.

Different long non-coding RNAs in yaks change during hair growth cycles and are involved in key growth pathways.

The Miniflap Hair Restoration method effectively restores hair and reduces baldness, but may cause some hair loss and increased baldness in the crown, with the Juri flap method suggested as a quicker, less risky alternative.

Using developmental signaling pathways could improve adult wound healing by mimicking scarless embryonic healing.

The Hairless gene is crucial for healthy skin and hair growth.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Circadian rhythms are crucial for stem cell function and tissue repair, and understanding them may improve aging and regeneration treatments.

Docetaxel and paclitaxel for breast cancer can cause permanent, severe hair loss.