Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

TRH stimulates human hair growth and extends the hair growth phase.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

Lack of cystatin M/E causes thin hair and dry skin.

Triple H syndrome exists and can vary in symptoms.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The α-MSH-MC1R-cAMP pathway does not protect skin cells from UVA damage.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

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

Exosomes from certain stem cells can fight hair loss by promoting hair growth and maintaining the growth phase of hair.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

A genetic variant linked to hair thinning in Japanese women was found.

The patient with severe hirsutism improved after being diagnosed with non-classic congenital adrenal hyperplasia and treated with corticosteroids.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.