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The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Most hirsutism patients had idiopathic hirsutism or PCOS, with hormonal imbalances and signs like acne and irregular periods.

Reversing female hair loss.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Common noncancerous skin diseases have various treatments, including topical applications, light therapy, surgery, and medications, with psychological support being important.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Skin issues can indicate immune system problems.

Targeted cancer therapies often cause skin problems that need careful management to improve patient quality of life and treatment success.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

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

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

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

The study identified key genes that regulate the growth cycle of cashmere in goats, which could help improve breeding strategies.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.