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Dihydrotestosterone (DHT) mainly affects nearby cells, doesn't significantly change prostate hormonal environment or cancer risk, and doesn't play a main role in causing hair loss or acne. More research is needed on its effects on heart health, sexual function, and bone health.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

High calcium levels hinder wheat root growth, but not root hair formation.

Regenerative medicine may offer long-lasting relief for chronic pain and neuro-degenerative conditions.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Finasteride treatment changes Cx43 in rat testes, possibly causing fertility issues.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A rare EGFR mutation in newborns leads to severe health issues and early death.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

Topical treatments can deliver active molecules to skin stem cells, potentially helping treat skin and hair disorders, including skin cancers and hair loss.

A rare skin condition causing scarring was successfully treated with topical erythromycin and benzoyl peroxide.

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

Ionizable lipid nanoparticles are the best for delivering gene-editing therapies.

Telocytes in silky fowl embryos develop distinct features and connections by the 20th day of incubation.

Afoxolaner effectively treats mange in guinea pigs with one dose.

Hair grows in cycles and changes with age, starting from fetal development.

Electromagnetic energy from wound dressing paste can disrupt skin lipid droplets, possibly affecting cancer development.

Thyroid disorders are common and affect health and quality of life, especially in women, highlighting the need for more awareness and iodine intake.

Human stem cells have diverse sources and potential uses in medicine.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.