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A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Drugs that block GSK-3 show promise for treating various diseases.

The alpha-helix was confirmed as a key structure in proteins.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

A specific gene mutation causes a severe skin disorder in a family.

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

LhGH promotes hair growth and prevents hair loss in mice.

The treatment effectively reduces hair loss and improves hair growth with minimal side effects.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

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

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

BRG1 is essential for skin cells to move and heal wounds properly.

Cysteine strengthens hair, and glutamine fuels hair growth.

Hair amino acid levels can indicate metabolic disorders.