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Papulopustular rosacea is an inflammatory skin condition treatable with lifestyle changes and medications.

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.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Macroalgae compounds offer sustainable, effective benefits for cosmetics.

Nanostructured delivery systems could potentially improve hair loss treatment by targeting drugs to hair follicles, reducing side effects and dosage, but the best size, charge, and materials for these systems need further investigation.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

Men with androgenetic alopecia have different scalp oils and microbes compared to those without.

Corin helps control salt and sweat release in sweat glands.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The study found key genes and pathways involved in cashmere goat hair growth stages.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Women with polycystic ovarian syndrome often experience depression and anxiety.

Genomic approach finds new possible treatments for hair loss.

PCOS understanding and treatment are advancing, requiring continuous updates for better patient management.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Antiandrogen therapy helps treat genetic hair loss.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Understanding skin patterns can help us learn about skin diseases and their treatments.

Gene mutations can cause problems in male genital development.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

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

Atopic dermatitis in kids with alopecia areata can predict poor response to topical immunotherapy.

Use 5% minoxidil or oral finasteride for mild-to-moderate hair loss, combine with hair transplant for severe cases.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.