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Severe CCCA may be biologically and clinically different from milder forms.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

HLD10 can include increased body hair and Mongolian spots.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Genetic differences affect how people respond to COVID-19.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A gene variation is linked to hair thickness in Asians.

Deleting part of a gene in mice causes wavy hair and high pup loss.

CD34+ and CD34- melanocyte stem cells have different regenerative abilities.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

A new mouse mutation causes skin and hair defects due to a gene change.

CD8+ T cells drive alopecia areata, while regulatory T cells are protective.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

A specific gene change in APCDD1 increases the risk of hair loss.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.