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Testosterone needs to be converted to DHT to reduce stress response in male rats.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

IL-15 promotes hair growth and protects hair follicles.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

Allopregnanolone increases growth and changes gene activity in human brain cancer cells.

Flutamide, dutasteride, and finasteride dissolve differently in supercritical carbon dioxide, with dutasteride dissolving the least.

New method measures finasteride in plasma, finds two formulations bioequivalent.

The method accurately and quickly measures silodosin and dutasteride in mixtures.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Frontal Fibrosing Alopecia involves disrupted cholesterol pathways, fibrosis, and increased mast cells.

Collagen XVII is crucial for preventing hair and pigmentation loss by maintaining melanocyte stem cells.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Blocking LFA-1 prevents hair loss in mice.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.