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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

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

Photodynamic therapy is the preferred treatment for skin precancer due to its effectiveness and safety.

Nested PCR can reliably identify fungal infections when traditional methods fail.

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.

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

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Menopause causes significant changes in the vaginal introitus, but less so in the labia majora, which may lead to symptoms of vaginal atrophy.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Energy healing treatment improved L-cysteine's stability, solubility, bioavailability, and shelf-life.

Male and female human hairs have different microscopic structures that can help in forensic analysis.

Hair growth and health are influenced by factors like age, environment, and nutrition, and are controlled by various molecular pathways. Red light can promote hair growth, and understanding these processes can help treat hair-related diseases.

Human hair follicle cells can grow hair when put into mouse skin if they stay in contact with mouse cells.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

MALDI Imaging Mass Spectrometry is a useful method for studying skin conditions, but sample preparation is crucial for accurate results.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Different types of stem cells and their environments are key to skin repair and maintenance.

Some drugs can cause skin reactions, which may improve when the drug is stopped, and rapid diagnosis and stopping the drug is crucial.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Non-invasive methods show promise for diagnosing skin diseases like psoriasis and lupus but need more research for regular use.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

Non-surgical procedures can help reduce wrinkles and stimulate skin repair by understanding skin aging at the molecular level.

MSC-derived exosomes can help treat COVID-19, hair loss, skin aging, and arthritis.