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Traditional Chinese medicine may help treat ischemic stroke by targeting specific genes and pathways.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Hair analysis can show nutritional status and environmental exposure, with phosphorus being very stable in hair and differences found based on gender and conditions like depression and autism.

Asiasari radix extract may be a potential treatment for melanoma because it selectively triggers cell death in melanoma cells by affecting p53 regulation.

Androgenic alopecia, a common hair loss condition, is linked to changes in androgen metabolism and genetics, and can be treated with finasteride and minoxidil, but these treatments are only fully effective in 10% of patients.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Acetate helps reduce depression in rats with PCOS by lowering specific gene expression and DNA changes in the brain.

The salts have diverse molecular packing with significant hydrogen interactions.

Geranium sibiricum may help manage diabetic complications by inhibiting a key enzyme.

COVID-19-related hair loss may be linked to blood flow disorders and inflammation.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

Many skin patients have mental health issues, but few dermatologists are well-versed in treating these conditions.

New tests detect finasteride and dutasteride in urine quickly and easily.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Male and female skin differ in many ways, which could lead to gender-specific skin treatments.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

DA-9401 helps protect rat testis from finasteride damage.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

ILK is essential for skin development, pigmentation, and healing.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

The new ELISA method is reliable and eco-friendly for checking the quality of Pueraria candollei.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

A hormone linked to collagen helps hair grow back in mice after chemotherapy, and may also prevent bone loss.