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New insights into the causes and treatments for the autoimmune hair loss condition Alopecia areata have been made.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

FFA's causes may include environmental triggers and genetic factors.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The study found that sweat glands contain different types of stem cells that help with healing and maintaining healthy skin.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

New genetic discoveries may lead to better treatments for alopecia areata.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.