Search

everythinglearnresearchcommunity

for

Search:↓

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A girl had rickets due to a gene mutation affecting vitamin D response.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Two new gene clusters important for hair formation were found on human chromosome 11.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

Two new gene clusters important for hair formation were found on human chromosome 11.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

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

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Activating PPAR-γ signalling can protect hair follicle stem cells from damage caused by chemotherapy.

HLA can be linked to autoimmune hepatitis.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.