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25% of women in North Sudan have traction alopecia, linked to family history and hair treatments, highlighting the need for better hair care awareness.

Nyctanthes arbor-tristis is effective for treating many health issues.

Hibiscus micranthus leaf extract is safe and effective for antibacterial and wound healing.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Kabīkaj has potential medicinal benefits for skin conditions but is less used now due to availability issues.

PCOS in women from Karnataka is influenced by genetics, family history, and insulin resistance, requiring better diagnosis and treatment.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Many children with alopecia areata also have other autoimmune diseases.

Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.

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

Women with PCOS should be screened for heart disease risk and manage their health to prevent it.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

Low iron and vitamin D levels are linked to hair loss in women.

LGBT individuals have unique skin health needs, including higher STD risks and side effects from gender-affirming treatments, requiring dermatologists to offer knowledgeable and culturally competent care.

Mutations in the KRT85 gene cause hair and nail problems.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Hormone therapies like birth control pills and spironolactone are safe and effective for treating women's adult acne.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Increasing Wnt5a in mice skin delays hair growth but doesn't stop it.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Men with male pattern baldness have a higher risk of dying from prostate cancer.

Balding men have higher heart disease risk.

Tinea capitis in adults is best treated with oral terbinafine, but other medications may be needed for resistant infections, and family and pets should be checked to prevent reinfection.

Tinea capitis can cause scalp issues in children and should be considered in similar cases; treatment with griseofulvin and selenium sulfide is effective.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A woman was the first known case to have both polycystic ovary syndrome and autoimmune polyglandular syndrome type 2, suggesting a need to check for both conditions in similar patients.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.