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Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

NSG mice had the most mites, and genetic factors affect immune response and susceptibility.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

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

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

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

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Mice with human skin protein K8 had more skin problems and cancer.

Assessing newborn scalp hair can reveal important health information.

Hair loss treatments work better with lifestyle changes.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Women with low SHBG levels and a high 3a-diol G to SHBG ratio are likely to experience female pattern baldness, possibly due to a slight excess of androgens affecting sensitive hair bulbs.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Different types of RNAs are found in varying amounts in patients with Polycystic Ovary Syndrome, suggesting they could be important in the disease's development and potentially used as disease markers.

IMA and IMA/albumin levels don't predict alopecia areata severity.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Clinical signs of hyperandrogenism are related to female pattern hair loss severity, but biochemical markers are not.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Selective breeding can enhance immunity in dairy cattle.

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

Collagen XVII is crucial for skin cell growth and nail health.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Alopecia areata involves immune activation in the scalp, suggesting treatments targeting TH1, TH2, and IL-23 pathways.

Male pattern baldness involves genetics, hormones, and needs better treatments.