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Infrared spectral imaging can map hair growth proteins and sugars without staining.

High S100B protein levels indicate poor survival in advanced melanoma.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Alcohol dependence affects stress hormone levels more than childhood maltreatment.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Bioengineered skin models aging well, useful for studying aging and testing treatments.

HMPV causes respiratory infections, mainly managed with supportive care, and lacks a vaccine or specific treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Higher PSA levels are linked to more hirsutism in women with PCOS.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Human hair keratin scaffold material degrades in muscles mainly through the ubiquitin system with lysosome help.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

A new gene mutation is linked to monilethrix in the studied family.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Hypoxic preconditioning helps human hair follicle stem cells survive oxidative stress.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.