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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.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

A specific signal from hair cells controls the tightening of the surrounding muscle, which is necessary for hair shedding.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.

ALRV5XR effectively increases hair density in men with androgenetic alopecia without adverse effects.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Hormones control reproduction and are crucial for body balance.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Certain genes may influence hair loss differently in men and women.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Primary care is key in managing PCOS, focusing on lifestyle changes and medications like birth control and metformin.

Experts discussed hair care, genetic hair defects, hair loss treatments, nail surgery, lupus treatments, skin infections, and cosmetic allergies.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.