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A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Keratinocyte growth factor significantly alters skin and tissue development.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A KRT32 gene variant causes loose anagen hair syndrome.

The Itpr3 gene causes a specific hair pattern in mice.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

Entadfi, a mix of finasteride and tadalafil, is used for BPH.

Human hair keratins might be good for filtering out harmful substances like diclofenac and PFBS from water.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

Fisetin may help treat psoriasis and reduce skin inflammation.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Calcium reduces involucrin in rat hair bulbs but doesn't affect filaggrin and Kdap.

Scientists made nanoparticles from human hair proteins to improve drug delivery.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

Mosaic Klinefelter syndrome can affect male fertility and may be missed in routine tests.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

KID syndrome should be reclassified as an ectodermal dysplasia.

Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

KFSD can be linked to acne keloidalis nuchae and tufted hair folliculitis.

SCFF may help promote hair growth and scalp health.