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Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

FGF21 can help reduce skin inflammation caused by C. acnes.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Hair loss is caused by the breakdown of a protein called COL17A1 in hair follicle stem cells.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Researchers found a gene mutation responsible for a rare hair loss condition.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

DHA derivatives, especially didocosahexaenoin, effectively kill prostate cancer cells and may offer a safer cancer treatment option.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

Aging in one type of stem cell can cause aging-like changes in various organs.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

FAPD is a possible diagnosis for hair loss in patients of color and requires multiple evaluations for accurate diagnosis.

Mutations in the spike protein affect drug binding and effectiveness.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.