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Possible link between androgens and COVID-19 severity; more research needed.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

The document concludes that pig iPSCs show promise for transplant therapies and the field is advancing in controlling cell behavior for biology and medicine.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Human hair keratins can be turned into useful 3D biomedical scaffolds through a freeze-thaw process.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

AMH helps estimate ovarian reserve but doesn't predict pregnancy chances; age is more important.

Recognizing and treating skin symptoms in essential thrombocythemia is crucial for patient quality of life.

Recent selection on immune response genes was identified across seven ethnicities.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Polonium poisoning is diagnosed by detecting it in urine and feces, and treated with supportive care, infection prevention, and chelation therapy.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Hair follicle stem cells help maintain skin health and could improve skin replacement therapies.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Olfactory receptors found outside the nose may offer new treatments for diseases like cancer and help in wound healing and hair growth.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.