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The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Cornu cervi pantotrichum pharmacopuncture solution helps mice grow hair by increasing hair follicle cell growth and a growth factor important for hair development.

Tacrolimus is a better option than cyclosporine due to fewer side effects.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

New method makes important drug ingredients more easily without needing extra purification steps.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

KRT72 gene helps form hair.

Rat vibrissae structure relates to their sensory function.

Many high school girls in Zanjan have polycystic ovarian syndrome.

Tortoiseshell tomcats with XX/XY chimerism can be fertile.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

The new assay can help develop products for hair re-growth.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

Clofazimine may be effective for treating ashy dermatosis.

Ceramide Synthase 4 is crucial for healthy skin barrier function.

Compound 1 showed promising anticancer activity.

Tailoring facelift techniques to individual needs improves patient satisfaction.

The new bioreactor improves skin grafts by evenly stretching cells and monitoring conditions for better growth.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

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