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Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

New mouse models help study melanocytic cells for melanoma research.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

FOL-005 peptide may help treat excessive hair growth safely.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Genetic factors play a major role in acne.

PCOS in women from Karnataka is influenced by genetics, family history, and insulin resistance, requiring better diagnosis and treatment.

Ablative fractional laser treatment nearly matches the gene reduction effects of topical vismodegib in skin cancer.

Mutations in the LIPH gene cause woolly hair in a child.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

A new model uses specific blood markers to predict if children's hair loss will return.

Polygenic Score can help predict severe psoriasis and psoriatic arthritis.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

HLA-DRB5 and other genes may be linked to alopecia universalis.

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