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

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Understanding intermediate filaments helps explain hair health and related diseases.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

Collagen XVIII affects wound healing, hair growth, and bone development, with its absence speeding up processes and overexpression causing delays and abnormalities.

Keratin filaments' elasticity is influenced by their terminal domains and surrounding medium.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

H+-ATPase is crucial for plant growth and can be influenced by microbial compounds, affecting root hair development.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Minoxidil can reduce functions related to androgen receptors.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A specific gene mutation causes woolly hair and hair loss.

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

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.