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Aging reduces skin stem cell function, leading to changes like hair loss and slower wound healing.

Over half of young people in Saudi Arabia experience early gray hair, linked to factors like smoking, stress, and family history.

Plant extracts may help prevent or reverse hair graying.

Many popular skincare products claim to prevent aging but lack strong evidence to prove their effectiveness and safety.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Mouse skin color ranges from pink to black, depending on their hair growth cycle.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Thai rice bran extracts, especially from Tubtim Chumphae rice, can significantly reduce the activity of hair loss genes, with x-tocopherol showing potential as an anti-hair loss product.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

FOXN1 gene variants cause low T cells and immune issues from birth.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

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.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Skin-derived precursors in hair follicles come from different origins but function similarly.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.