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Females have higher Dechlorane Plus in hair, while males have more in dorm dust.

Trichorrhexis nodosa is mainly caused by hair trauma, not a metabolic defect.

New mutations in the DSG4 gene cause a rare hair condition.

Dracorhodin perchlorate helps heal wounds in diabetic rats by reducing inflammation.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

The folate-cyclodextrin conjugate targets cancer cells more precisely, potentially reducing chemotherapy side effects.

The document's conclusion cannot be determined.

Boron/nitrogen-doped carbon nano-onions improve targeted breast cancer treatment by enhancing drug delivery and reducing side effects.

DHA-NLC may improve drug delivery and reduce side effects for cancer treatment.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Lithium chloride helps hair follicle cells become tooth cells by activating a specific signaling pathway.

The document's conclusion cannot be provided because the document is not accessible or understandable.

Small amounts of DNA can be found in the hair shaft, especially near the root, but it decreases with hair treatments and washing.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

The man has a genetic skin condition called pachyonychia congenita.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

Yorkshire Terriers with Colour Dilution Alopecia have reduced melanin and hair structure issues.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Some nail changes in chilblains can look like lichen planus and may be severe and long-lasting.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.