Search

everythinglearnresearchcommunity

for

Search:↓

Chemicals called 4-(alkylthio)- and 4-(arylthio)-benzonitrile derivatives can potentially reduce oil production on skin, which could help treat conditions like acne and hair loss.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

The document explains the genetic causes and characteristics of inherited hair disorders.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Abnormal gene expression related to keratin causes hair loss in certain mice.

OXTR agonists may promote hair growth and be effective for treating hair loss.

The YH complex, made from Astragalus membranaceus and Cinnamomum cassia, may help treat hair loss by promoting hair growth and follicle development.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Janus kinase inhibitors are promising drugs for treating autoimmune and inflammatory diseases.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Alpinetin helps grow hair by turning on hair stem cells and is safe for use.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Inhibiting class I HDACs helps maintain hair growth ability in skin cells.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Autoimmune skin disorders are caused by genetic and environmental factors and are treated with various medications and preventative strategies.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Tofacitinib is a promising treatment for children with rheumatic diseases.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The girl's hair loss is due to trichotillomania, which may improve with behavioral therapy or a combination of treatments.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.