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Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

Apremilast improved symptoms in patients with severe skin conditions.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

Diffuse alopecia in women may be related to androgens and iron deficiency, and basic hormone and nutrient screening is useful.

The document concludes that anticonvulsants like phenytoin may cause skin reactions by affecting tryptophan metabolism and suggests researching vitamin levels in patients with drug reactions.

Hair loss and growth can be accurately measured using computer-assisted counting.

Some patients with Alopecia Areata experience itch due to immune cells and enzymes that cause itching.

For sensitive scalp, treatment is personalized and may include specific medications and hydration, while avoiding stress and irritating products.

A woman's complete hair loss condition improved after recovering from COVID-19.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Children taking higher doses of valproic acid had lower biotinidase activity, which may lead to biotin deficiency, but biotin supplements could help.

The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

Facial hair growth from minoxidil stopped after she quit using it.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

Drinking alcohol before taking flibanserin does not increase the risk of severe low blood pressure or fainting.

Herbal alternatives like saw palmetto and green tea may offer safe, effective treatment for hormonal hair loss.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

CCCA is a common scarring hair loss in African descent women, possibly linked to genetics, hair care practices, and health issues like diabetes.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Certain DNA regions in alpacas are linked to fiber diameter.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Mechanical forces are crucial for shaping cells and forming tissues during development.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.