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Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Researchers made stem cells from human hair follicle cells with better efficiency than from skin cells.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

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

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Epigenetic factors play a crucial role in skin health and disease.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Genes linked to wool fineness in sheep have been identified.

Men with baldness, ear creases, and hairy ears have a higher risk of heart disease.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Some treatments for hereditary hair loss are effective but vary in results and side effects; new therapies show promise but need more research.

Bicalutamide may help treat female pattern hair loss.