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Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

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

Notch signalling helps skin cells differentiate and prevents tumors.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The Hairless gene is crucial for healthy skin and hair growth.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

CD98hc's role in skin health decreases with age.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

FOXN1 gene variants cause low T cells and immune issues from birth.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

CDP is crucial for lung and hair follicle cell development.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

TRP channels in the skin are important for sensation and health, and targeting them could help treat skin disorders.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.