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DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Zinc can both inhibit and stimulate mouse hair growth, and might help recover hair after chemotherapy.

Certain drugs that block specific enzymes can help treat prostate diseases.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Cow milk sugars increase fat production and inflammation in skin oil cells.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Eating healthy, exercising, and taking certain supplements can help manage Polycystic Ovary Syndrome symptoms.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Genetic testing for EGFR mutations is crucial in similar cases.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

5% topical minoxidil improves hair density and quality in monilethrix patients.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new gene mutation causes insulin resistance in a girl and her mother.