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Genetics play a role in acne, but how exactly they contribute is not fully understood.

The debate on direct-to-consumer pharmaceutical ads continues, with consumers finding them educational and doctors concerned about their impact on patient relationships and medication understanding.

Human hair is a significant sample for various tests in clinical, nutritional, archaeological, and forensic studies.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Acne can be managed with various treatments and requires psychological support due to its emotional impact.

Finasteride affects alcohol intake in male mice, possibly due to neurosteroids.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Neuroactive steroids show promise for treating mental and neurological disorders by targeting GABA_A receptors.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

Certain liver diseases respond well to specific treatments and have varying risks for liver cancer.

Dutasteride-loaded nanoparticles coated with Lauric Acid-Chitosan show promise for treating hair loss due to their controlled release, low toxicity, and potential to stimulate hair growth.

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

People with diabetes or obesity should manage their conditions carefully as they have a higher risk of severe COVID-19.

New skin substitutes for treating severe burns and chronic wounds are being developed, but a permanent solution for deep wounds is not yet available commercially.

Testosterone therapy can help improve mood, sexual function, and bone health in women with low androgen levels, but more research is needed to establish safe and effective guidelines.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Alopecia areata treatment varies, with no optimal method established yet.

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Melatonin-loaded nanocarriers improve melatonin delivery and effectiveness for various medical treatments.