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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A new gene mutation causes long hair in some Maine Coon cats.

Androgen use may increase the risk of stroke, but more research is needed.

Skin cells show flexibility in healing wounds and forming tumors, with potential for treating hair disorders and chronic ulcers.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Keratin proteins are crucial for hair structure and strength.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

New treatments like nanotechnology show promise in improving skin cancer therapy.

Different types of fibroblasts play specific roles in wound healing and cancer, which could help improve treatments.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The Middle East and Africa need better data, treatment consensus, and support for Alopecia Areata.

Trichoscopy effectively diagnoses and assesses the severity of androgenetic alopecia.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.