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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.

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

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

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

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.

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

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

Neoplasms hide in hair follicles to avoid the immune system.

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

The 14-3-3σ gene is essential for preventing hair loss.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

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.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

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

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Keratin mutations cause skin diseases and could lead to new treatments.

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

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

New genes linked to male pattern baldness were found on chromosome 20p11.

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

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

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

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Gene mutations can cause problems in male genital development.

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