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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Using special RNA to target a mutant gene fixed hair problems in mice.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

New injectable hydrogels with gelatin, metal, and tea polyphenols help heal diabetic wounds faster by controlling infection, improving blood vessel growth, and managing oxidative stress.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

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.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Human hair follicle stem cells can be isolated using specific markers for potential therapeutic use.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Researchers made stem cells from human hair follicle cells with better efficiency than from skin cells.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

The conclusion is that the new method makes collecting cells from plucked hair to create stem cells more efficient and less invasive.

The new method using gene-modified stem cells and a 3D printed scaffold improved skin repair in mice.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Enhancing melanin's energy generation may help treat alopecia areata.

Certain metabolites can either protect against or increase the risk of hair loss.