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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 conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

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

A gene mutation in mice causes permanent hair loss and skin issues.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

RXRα is crucial for proper immune response and links diet to immune function.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The CORIN gene variant causes the golden color in Siberian cats.

The HCR gene contributes to psoriasis risk.

Certain IL-18 gene variations may increase the risk of alopecia areata.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

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

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

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

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.

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

Certain genetic variations are linked to hair loss in Mexican men.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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