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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

A new DSG4 gene mutation causes hair defects in a young girl.

Cystatin M/E helps in the final stages of hair and nail formation by controlling certain enzymes.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Progerin affects cell shape but not hair or skin in mice.

Hairless USP mice have enlarged skin cysts as they age.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

BMI1 is essential for preventing hair greying and maintaining hair color.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

A genetic variant in the KRT25 gene causes tightly curled hair.

Injury boosts normal skin cell growth, reducing cancer cell advantage.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Sheep cells were successfully modified to include a spider silk protein gene.

EGFR and MEK inhibitors reduce PD-L1 in hair follicles, possibly causing inflammation.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.