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Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

The Orenburg goat breed has unique genetics that require more detailed research and careful breeding.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

Three genes linked to the development of trichilemmal cysts were found.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Gene mutations can cause problems in male genital development.

Diet changes can protect against harmful environmental effects on fetal development.

CDP is crucial for lung and hair follicle cell development.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

New treatments targeting specific genes show promise for treating keratin disorders.

DHT, a testosterone byproduct, causes male pattern baldness.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

New cells are added to the hair's dermal papilla during the active growth phase.

Human hair follicle stem cells show signs of low oxygen levels, which may be important for hair growth and preventing baldness.